СТАБИЛИЗИРОВАННЫЕ РАСТВОРЫ БРОМНОВАТИСТОЙ КИСЛОТЫ

Изобретение относится к стабилизированным растворам бромноватистой кислоты, предназначенным для обработки воды. Способ получения стабилизированного маточного раствора бромноватистой кислоты включает стадии получения раствора хлорноватистой кислоты с рН менее 7,5, раствора бромида с рН менее 7,0, смешивание растворов хлорноватистой кислоты и бромида с получением раствора бромноватистой кислоты, введение в качестве стабилизатора циануровой кислоты не более 1 част./млн, с получением стабилизированного маточного раствора бромноватистой кислоты с рН 8-9. Стабилизированный маточный раствор имеет концентрацию бромноватистой кислоты менее 30 мас.% и содержит в качестве стабилизатора циануровую кислоту в количестве, не превышающем 1 част./млн. Раствор можно применять для обработки воды любого типа, но предпочтительно его применяют для обработки питьевой воды и оросительной воды. Технический результат заключается в том, что стабилизированный раствор можно применять в широком диапазоне значений рН ...

ГЕТЕРОЦИКЛИЧЕСКИЕ ИНГИБИТОРЫ МЕК И СПОСОБЫ ИХ ПРИМЕНЕНИЯ

Изобретение относится к новым соединениям, включая его разделенные энантиомеры, диастереоизомеры, сольваты, и к фармацевтически приемлемым солям, имеющим формулу: ! ! где Х представляет собой N или CR10; Y представляет собой NR3; R1, R2, R8, R9 и R10 независимо представляют собой водород, гидрокси, галоген, -SR11, -OR3, -NR3R4, C1-С10алкил, С3-С10циклоалкил, С3-С10циклоалкилалкил, арил, арилалкил, гетероарил, гетероарилалкил, гетероциклил или гетероциклилалкил; R7 представляет собой водород, C1-С10алкил, С3-С10циклоалкил, С3-С10циклоалкилалкил, арил, арилалкил, гетероарил, гетероарилалкил, гетероциклил или гетероциклилалкил, где любые из указанных алкильных, циклоалкильных, арильных, арилалкильных, гетероарильных, гетероарилалкильных, гетероциклильных и гетероциклилалкильных фрагментов возможно замещены одной или более чем одной группой, независимо выбранной из оксо (при условии, что она не замещена на ариле или гетероариле), галогена, циано, нитро, SO2NR11R12, -C(O)R11, C(O)OR11, -C(O) ...

ПРОИЗВОДНЫЕ БЕНЗОЛСУЛЬФОНАМИДА

Настоящее изобретение относится к производным бензолсульфонамида формулы I и их применимым в сельском хозяйстве солям. В формуле I X1 означает водород или галоген; X2 - хлор; X3 означает водород; Y означает группу -С(А)В; А означает кислород; В означает кислород; R1 означает C1-С6-алкил, который может быть необязательно замещен C1-С6-алкоксилом, C1-С6-алкилкарбонилом, С3-С7-циклоалкил, фенил-С1-С4-алкил; Q означает остаток Q21; А8, А9 означают кислород; R29 означает C1-С6-алкил; R30, R31 означают водород, C1-С6-галогеналкил. Изобретение также относится к способу получения производных бензолсульфонамида формулы I, гербицидному средству на их основе, способу получения гербицидно активных средств, способу борьбы с нежелательным ростом растений, применению в качестве гербицидов и к бензолсульфонилизоцианатам формулы II. 7 н. и 1 з.п. ф-лы, 4 табл. ! , ...

БИОЦИДНЫЕ КОМПОЗИЦИИ И СПОСОБЫ ИХ ПРИМЕНЕНИЯ

Синергетическая композиция для борьбы с ростом микроорганизмов в водной или водосодержащей системе включает: 2,2-дибром-3-нитрилопропионамид и биоцидное соединение, выбранное из группы, состоящей из 1-(3-хлораллил)-3,5,7-триаза-1-азониаадамантана, трис(гидроксиметил)-нитрометана и гексагидротриазина. Или композиция включает 2,2-дибром-3-нитрилопропионамид, 1-(3-хлораллил)-3,5,7-триаза-1-азониаадамантан и 2-бром-2-нитропропан-1,3-диол. Весовое соотношение 2,2-дибром-3-нитрилопропионамида к дополнительному соединению составляет между 100:1 и 1:100. Изобретение позволяет повысить эффективность борьбы с микроорганизмами в водных или водосодержащих системах. 3 н. и 6 з.п. ф-лы, 10 табл.,6 пр.

ФУНГИЦИДНЫЙ ПРЕПАРАТ НА ОСНОВЕ ПРОПИКОНАЗОЛА

Изобретение относится к области защиты растений и может быть использовано для получения фунгицида в форме концентрата коллоидного раствора. Предлагается использовать препарат на основе пропиконазола, содержащий в качестве вспомогательных добавок фенилсульфонат кальция и оксиэтилированный моноалкилфенол на основе тримеров пропилена формулы R - C6H4О(C2H4О)nН, где n = 10, 12, R - углеводородный радикал, имеющий 9 атомов углерода, причем их соотношение соответственно равно 0,4 - 1,0 при массовом соотношении компонентов, мас. %: пропиконазол 50 - 20, фенилсульфонат кальция 20 - 30, оксиэтилированный моноалкилфенол на основе тримеров пропилена 30 - 50. 2 табл.

СРЕДСТВО БОРЬБЫ С ВИРУСАМИ РАСТЕНИЙ

Использование: сельское хозяйство, химические средства защиты растений. Сущность изобретения: для борьбы с вирусами растений используют синергитическое средство, содержащее 2,4-диоксогексагидро-1,3,5-триазин и маннаны из клеток дрожжей Candida sp. При массовом соотношении (0,025 - 10) : 1. 9 табл.

СПОСОБЫ ПОДАВЛЕНИЯ РОСТА СОРНЯКОВ, ГЕРБИЦИДНЫЕ КОМПОЗИЦИИ И ПРОДУКТ

Описывается способ подавления роста сорняков в локусе, который включает применение в локусе синергичного гербицидно-эффективного количества а) 2-циано-3-циклопропил-1-(2-метилсульфонил-4-трифторметилфенил)-пропан-1,3-диона и в) одного из членов группы, включающей атразин, гербицидное производное хлорацетамида, пендиметалин, аклонифен, который представляет собой 2-хлор-6-нитро-3-феноксианилин, диурон, который представляет собой 3-(3,4-дихлорфенил)-1,1-диметилкарбамид и гербицидное производное гидроксибензонитрила. Описываются также гербицидные композиции и продукт. Технический результат - повышение эффективности гербицидной композиции за счет появления синергичного эффекта. 5 с. и 10 з.п. ф-лы, 11 табл.

ГЕРБИЦИДНЫЕ КОМПОЗИЦИИ НА ОСНОВЕ КАРБАМОИЛТРИАЗОЛИНОНА И СПОСОБЫ ИХ ПРИМЕНЕНИЯ

ФУНГИЦИДНЫЙ ПРОТРАВИТЕЛЬ СЕМЯН "ТУРИОН"

Изобретение относится к химическим средствам защиты растений, в частности к протравителям посадочного материала в качестве средства защиты от возбудителей заболеваний культуры и регуляторов роста растений. Фунгицидный протравитель семян содержит имазалил, прохлораз, тритиконазол, гетероауксин, неионогенные и анионогенные поверхностно-активные вещества в соотношении от 1:4 до 3:1, антифриз, краситель катионовый красный и растворитель. Изобретение расширяет область применения при одновременном обеспечении снижения расхода протравителя при обработке семян. 4 з.п. ф-лы, 21 табл.

ПЕСТИЦИДНЫЕ КОМПОЗИЦИИ

... 1. Молекула следующей формулы:в которой:(а) Arпредставляет собой(1) фуранил, фенил, пиридазинил, пиридил, пиримидинил, тиенил или(2) замещенный фуранил, замещенный фенил, замещенный пиридазинил, замещенный пиридил, замещенный пиримидинил или замещенный тиенил,где указанный замещенный фуранил, замещенный фенил, замещенный пиридазинил, замещенный пиридил, замещенный пиримидинил и замещенный тиенил имеют один или несколько заместителей, независимо выбираемых из следующих: H, F, Cl, Br, I, CN, NO, C-Cалкил, С-Сгалогеналкил, С-Сциклоалкил, С-Сгалогенциклоалкил, С-Сциклоалкокси, С-Сгалогенциклоалкокси, С-Салкокси, С-Сгалогеналкокси, С-Салкенил, С-Салкинил, S(=O)(С-Салкил), S(=O)(С-Сгалогеналкил), OSO(С-Салкил), OSO(С-Сгалогеналкил), С(=O)NRR, (C-Cалкил)NRR, C(=O)(C-Cалкил), С(=O)O(C-Cалкил), C(=O)(C-Cгалогеналкил), С(=O)O(C-Cгалогеналкил), C(=O)(C-Cциклоалкил), С(=O)O(C-Cциклоалкил), C(=O)(C-Cалкенил), С(=O)O(C-Cалкенил), (C-С-алкил)О(C-Cалкил), (C-Салкил)S(C-Cалкил), С(=O)(C-Cалкил)С(=О)О(C-Cалкил ...

Замещенные фенилурацилы

... 1. Замещенные фенилурацилы общей формулы (I) в которой Q означает О (кислород), S (серу), SO или SO2; R1 означает водород, амино, алкил с 1-4 атомами углерода, при необходимости, замещенный циано, галогеном или алкокси с 1-4 атомами углерода, или алкенил или алкинил с 2-4 атомами углерода, соответственно, при необходимости, замещенные галогеном; R2 означает циано, карбокси, карбамоил, тиокарбамоил, или алкил или алкоксикабонил с 1-4 атомами углерода, соответственно, при необходимости, замещенные циано, галогеном или алкокси с 1-4 атомами углерода; R3 означает водород, галоген или алкил с 1-4 атомами углерода, при необходимости, замещенный галогеном; R4 означает водород, нитро, циано или галоген; R5 означает циано, тиокарбамоил, бром, или алкил или алкокси с 1-4 атомами углерода, соответственно, при необходимости, замещенные галогеном; R6 означает азотсодержащую гетероциклическую группу из ряда: пирролил, пиразолил, имидазолил, триазолил, триазолинил, пиридинил, пиразинил, пиридазинил, пиримидинил ...

Способ получения производных 1Н-1,2,4-триазола

Изобретение касается производных 1Н-1,2,4-триазола, в частности получения соединений общей формулы } HC-N CH-N- С(К) орто-R,-napa-R., где К - (-0-СН - -CHR-0-);Ri, RI - галоид; R - алкенил, С -С -алкил, замещенный галоидом , С -С -алкил, замещенный фенилом , феноксиметил, (галоидфенил)окси- метил, (метилфенил)метил, -С -Су-алкил, (галоидфенил)метил, (С1-С4-алкил)-ОСНз, (С2-Сз- алкенил)фенил, СН,,0-бензил, СН,0-(мо- но- или дигалоидбензил), (,-алкил), фенилтиом етил, (галоидфенил ) тиометил, или их стериоизоме- ров, или фармацевтически приемлемых солей, обладающих антимикробным действием , что может быть использовано в медицине. Цель изобретения - создание новых более активных веществ указанного класса. Синтез ведут реакцией IН-1,2,4-триазола с соответствующим галоидзамещр.нным диоксаланом при 100-150 с в диполярном апротонном растворителе - дйметилформамиде или диметилсульфоксиде в присутствии основания . Целевой продукт вьщеляют в свободном виде или в виде необходимой соли. Новые вещества ...

Фунгицидное средство

Способ борьбы с нежелательной растительностью

Способ получения производных 1,4-ди- окиси 1,2,4-бензтриазина

Способ получения производных 1,2,4-триазола

Гербицидное средство

Способ получения производных имидазола или 1,2,4-триазола или их солей

Гербицидное средство

ГЕРБИЦИДНОЕ СРЕДСТВО, содержащее активное вещество - замещенный анилид карбоновой кислоты, растворитель и поверхностно-активное вещество, отличающее|с я тем, что, с целью снижения фйтотоксичности , оно содержит в замещенного анилида карбогде R и R одинаковые или различные и означают метил или этил, ; R - метоксиметил, метоксиизопропил , 1-пйразрлилметил, 1-имидаЗОЛИЛМ8ТЙЛ , ,4-триазолил-1-метил , R - 1,2,4-триазолил-1-, имидазолил-1-4 ,5-дихлоримидазолил-1, пиразолил-1 I 6 качестве растворителя - ксилол, а в качестве поверхностно активного вещества - оксиэтилированный N-моноэтаноламид олеиновой кислоты , кальциевую соль додецилбензолсульфокислоты и оксизтилированное касторовое масло при массовом соот :н шении 20:64t8:4:4 соответственно. :л :п :о ...

1-(2,4-DIFLUORPHENYL)-1-(1-FLUORCYCLOPROPYL)-2-(1,2,4-TRIAZOL-1-YL)-ETHAN-1-OL.

SUBSTITUTED ALKANYL-AZOLYL CARBAMATES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS INSECTICIDES, ACARICIDES AND NEMATOCIDES

FUNGIZIDE MITTEL

OXIMINO-TRIAZOLYL ETHANES, PROCESS FOR THEIR PREPARATION AND THEIR USE AS FUNGICIDES

TRIAZOLYL DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PLANT GROWTH REGULATION AGENTS CONTAINING THEM

ACETANILIDE

3-SUBSTITUIERTE 1-AZOLYL-3-METHYL-1-PHENOXY-BUTAN-2-ONE UND -OLE, VERFAHREN ZU IHER HERSTELLUNG UND IHRE VERWENDUNG ALS FUNGIZIDE

Substituted diphenyl ethers

Novel substituted diphenyl ethers of the formula in which R<1>, R<2>, R<3>, R<4>, R<5>, Y, m and n have the meaning given in the description, a plurality of processes for the preparation of the novel substances, and their use as herbicides. Novel intermediates and processes for their preparation.

TRISUBSTITUTED BENZYL-OXIME ETHERS, PROCESS FOR THEIR PREPARATION AND THEIR USE AS FUNGICIDES

1-HYDROXYETHYL-AZOLE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR USE IN THE REGULATION OF PLANT GROWTH AND AS FUNGICIDES

DESINFIZIERUNS- UND DESODORIERUNGSVERFAHREN

(1,2,3,4,5,6H)-TRIAZIN-2,4-DIONE, VERFAHREN ZU IHRER HERSTELLUNG SOWIE IHRE VERWENDUNG ALS INSEKTIZIDE

1,2,4-TRIAZOLYL-ENOLETHER, VERFAHREN ZU IHRER HERSTELLUNG UND IHRE VERWENDUNG ALS FUNGIZIDE

SUBSTITUIERTE TRIAZOLYLMETHYL-TERT.-BUTYL-CARBINOLE, VERFAHREN ZU IHRER HERSTELLUNG UND IHRE VERWENDUNG ALS PFLANZENSCHUTZMITTEL SOWIE ALS ZWISCHENPRODUKTE

HETEROCYCLISCHE VERBINDUNGEN.

SODIUM DICHLOROISOCYANURATE DIHYDRATE TABLET

... 1437925 Sodium dichloroisocyanurate tablet FMC CORP 2 Aug 1974 [6 Aug 1973] 34104/74 Heading C2C A rapidly - soluble, structurally - strong, storage-stable tablet of sodium dichloroisocyanurate dihydrate which resists deterioration or dimensional change due to moisture is produced by placing the compound into a structureforming apparatus, compressing with a pressure of 2000-10,000 p.s.i. and recovering the desired tablet. The pressure used is preferably 5000 p.s.i. The tablet is used as a bactericidal composition especially in swimming pools.

AGRICULTURAL BIOCIDES

... 1431880 Pesticidal application of triazines COALITE & CHEMICAL PRODUCTS LTD 29 Nov 1973 [14 Dec 1972] 57641/72 Heading A5E A method for the treatment of growing plants, seeds or agricultural or horticultural land, which comprises applying, as a biocide, to the plants, seeds or land a triazine of formula: wherein R<1> is H or an organic group such as alkyl and R is an organic group such as alkyl, cycloalkyl or HO(CH2)m[O(CH2)n]pwherein m, n and p are from 1 to 6. Typical biocides are the diglycolamine-formaldehyde, methylamine-formaldehyde and ethylamine-formalde- 'hyde condensates.

ANTIFUNGAL AGENTS

ANTIFUNGAL AGENTS

BLEACHES CONTAINING TRICHLOROISOCYANURIC ACID AND HYDRATED SODIUM DICHLOROISOCYANURATE

... 1409385 Bleach composition FMC CORP 21 Nov 1973 [24 Nov 1972 2 May 1973] 53934/73 Heading C2C [Also in Division D1] A dry bleach composition contains trichloroisocyanuric acid stabilized with sodium dichloroisocyanurate monohydrate and/or dihydrate. The hydrate is preferably present in an amount of at least 1% by weight of the composition and may comprise up to 90% by weight thereof.

TRIAZINE-2,4-DIONES AND THEIR USE AS INSECTICIDES

TRIAZOLES AND IMIDAZOLES USEFUL AS PLANT FUNGICIDES AND GROWTH REGULATING AGENTS

Stabilised hypobromous acid solutions.

Procedure for protecting plant propagation products and the plants obtained from them.

The invention relates to the protection ...

Heterocyclic and phenyl compounds.

A compound of formula (i)r-s(o)nch2ch2ch=cf2, or a salt thereof, wherein n is 0, 1 or 2; and r is a group of formulae (ii)to (xxi), wherein: the s ch2ch2ch=cf2 group is at least one of r1 (when attached to a carbon atom). R2, r3, r4, r5 or r6; r1 (when attached to a ca atom)r2, r3 r4, r5 and r6 are each independently hydrogen, optionally substituted alkyl, optionally substituted alkenyl, alkynyl, cycloalkyl, alkylcycloalkyl, alkoxy, alkenyloxy, alkynyloxy, hydroxyalkyl, alkoxyalkyl, optionally substituted aryl, optionally substituted arylalkyl, optionally substituted heteroaryl, optionally substituted heteroarylalkyl, optionally substituted aryloxy, optionally substituted arylalkoxy, optionally substituted aryloxyalkyl, optionally substituted heteroaryloxy, optionally substituted heteroarylalkoxy, optionally substituted heteroaryloxyalky, haloalkyl, haloalkenyl, haloalkynyl, haloalkoxy, haloalkenyloxy, haloalkynyloxy, halogen, hydroxy, cyano, notro, -nr7r8, -nr7cor8, -nr7csr8, -nr7so2r8 ...

Vehicle used to apply chemical Compounds to wood.

... the invention relates to a vehicle comprising toluence (40-70 %),xylene (6-40%), benzophenone (3-18%), butylglycol (2-9%), cetyl acetate (1-7%), cetyl acetate (1-7% and methanol (0.3-4%). the inventive vehicle has ahigh wood penetration index and can be used to prepare wood treatment composition which contain one or more chemical compounds, e.g. insecticide and/or fungicides, and which are used to treat or prevent damage caused by attacks by biological agents that are harmful to wood.

Heterocyclic and phenyl compounds

Stabilised hypobromous acid solutions.

PESTICIDAL COMPOSITIONS

Pesticidal compositions.

Pesticidal compositions.

Derivatives 1-hydroxyethyl-azolic, their process of production like their use like substances of growth of the plants and fungicides.

Useful news 6-amino-s-triazinediones like weedkillers.

Derived from céto-alpha (1-triazolyl) with fungicidal activity.

New derivatives arylamines, proceeded for their manufacture and use as a microbicides.

Use of derived from the malonic acid to improve the output of the cultures.

A method for raising the content glucids of the plants by means of derived from substitution the phénoxyalcoïques ones or cyclohexanedione.

Biologically active triazolyl derivatives.

Compositions for synergic purpose for the regulation of the growth of the plants.

“Proceeded to protect the products from multiplication of the plants and plants while resulting”.

Weedkillers, weedkillers compositions and process for their preparation.

Herbicide for paddy fields.

Process of prevention and fight against the undesirable vegetation in the pineapple cultures.

(4,4-Difluorobut-3-enylthio)-substituted heterocyclic or carbocyclic ring compounds having pesticidal activity

Herbicidal 1-aryl-4-substituted-1,4-dihydro-5h-tetrazole-5-ones and sulfur analogs thereof.

New triazine-diones and their application to the fight weedkiller.

New triazine-diones, their method of preparation and their application like weedkillers.

Stabilised hypobromous acid solutions.

Fungicidal and growth regulant compounds.

Selective weedkiller containing L-methyl-3-cyclohexyl-6-diméthylamino-S-triazine-2,4 (14,3H) - dione.

Weedkillers compositions.

Stabilised hypobromous acid solutions.

Pesticidal compositions.

Vehicle used to apply chemical compounds to wood

Derivatives of A 1-phenyltriazole as antiparasiticagents

Heterocyclic and phenyl compounds

3-substituted-[1,2,3] benzotriazinone compounds for enhancing glutamatergic synaptic responses

Pesticidal compositions.

Pesticidal compositions.

Stabilised hypobromous acid solutions.

Vehicle used to apply chemical compounds to wood

PROCEDURE FOR PROTECTING PLANT PROPAGATION PRODUCTS AND THE PLANTS OBTAINED FROM THEM

Pesticidal compositions.

HERBICIDES COMPOSITION FOR THE FIGHT AGAINST UNWANTED PLANT GROWTH, IN PARTICULAR AGAINST GRASS-WELL-BEHAVED AND BREITBLAETTERIGEN WEEDS

INSECTICIDE MEANS

FUNGICIDE MEANS

3-HETEROCYCLYL-SUBSTITUIERTE of BENZOIC ACID DERIVATIVES

2-HALOGENACETAMID-HERBIZIDE

USE OF (E) - 5 (4-CHLORBENZYLIDEN) - 2.2 - DIMETHYL-1 (1H-1,2,4-TRIAZOL-1 YLMETHYL) CYCLOPENTANOL FOR the FIGHT of the RUST INFESTATION AT SOJAPFLANZEN

MEANS WITH FUNGICIDAL ONE, BACTERICIDAL ONE AND WUCHSREGULATORI EFFECT AT PLANTS

MEANS TO THE MUSHROOM FIGHT

MEANS FOR THE FIGHT OF PHYTOPATHOGENER MUSHROOMS

HERBIZIDES MITTEL

CHLORHALTIGES TROCKENBLEICHMITTEL

SUBSTITUTED PHENYL SULFAMOYL CARBOXAMIDE ONE

VERFAHREN ZUR INSEKTENBEKÄMPFUNG

BEKAEMPFUNG PHYTOPATHOGENER PILZE

2-HALOGENACETAMID-HERBIZIDE 2-HALOGENACETAMID-HERBIZIDE

MITTEL ZUR REGULIERUNG DES PFLANZENWACHSTUMS

VERFAHREN ZUR HERSTELLUNG NEUER HEXAHYDROTRIAZINONDERIVATE

Method for reducing sunburn damage in plants

The present invention relates to methods, use and compositions for reducing sunburn damage in plants. More specifically, it relates to methods and compositions for controlling, preventing, or treating sunburn damage using UV filters.

Synergistic Fungicidal Composition And Methods Of Use

Described is a broad spectrum, synergistic fungicidal composition when used for the preservation of a glued wood product comprising as active ingredients: 2. The fungicidal composition according to wherein the weight ratio of (A):(B) is from about 20:1 to about 2.5:1.3. The fungicidal composition according to wherein the weight ratio of (A):(B) is from about 20:1 to about 6:1.4. The fungicidal composition according to wherein the application rate for (A) is from about 100 gai/mto about 5 claim 3 ,000 gai/mand the application rate for (B) is from about 10 gai/mto about 1 claim 3 ,000 gai/m.5. The fungicidal composition according to further comprising one or more biocides selected from the group comprising insecticides claim 1 , fungicides claim 1 , mouldicides claim 1 , anti-sapstain compounds claim 1 , bactericides and algaecides.6. The fungicidal composition according to wherein the further biocide is an insecticide.7. The fungicidal composition according to comprising about 0.1% to about 60% of active ingredient (A) and about 0.1% to about 60% of active ingredient (B) on a weight basis.8. The fungicidal composition according to formulated as a suspension claim 1 , an emulsion claim 1 , a solution claim 1 , a microcapsule claim 1 , a concentrate claim 1 , a powder claim 1 , a granule claim 1 , a gel claim 1 , or a dispersion.9. The fungicidal composition according to wherein the mean particle size of the composition is from about 0.1 microns to about 20 microns.10. The fungicidal composition according to when used as a glueline preservative for glued wood products.11. The fungicidal composition according to when used as an optional claim 10 , additional surface treatment for glued wood products.12. The fungicidal composition according to wherein the glued wood product is selected from:(i) an engineered wood product comprising glued solid timber and glued wood veneers, such products including glued laminated timber, laminated veneer lumber and plywood,(ii) a ...

FUNGICIDAL COMPOSITIONS FOR TURF TREATMENT AND IMPROVEMENT

The present invention relates to novel compositions comprising: a fungicide that inhibits mitochondrial respiration at the QoI site (QoI inhibitor), a contact fungicide, a demethylation inhibitor, and pigments, which are highly suitable for controlling unwanted phytopathogenic fungi. Moreover, the fungicidal compositions are able to control mold and fungus infection in grasses and in particular turf grasses. 1. A synergistic composition , comprising:(i) at least two fungicides selected from the group consisting of a QoI inhibitor fungicide, a contact fungicide, and a demethylation inhibitor; and(ii) a phthalocyanine pigment.2. The synergistic composition of claim 1 , wherein:the QoI inhibitor fungicide is trifloxystrobin,the contact fungicide is iprodione,the demethylation inhibitor is triticonazole, andthe pigment is phthalocyanine green pigment (Green 7).3. A method for improving turf quality after snow cover release in spring claim 1 , comprising: the synergistic composition comprising:', '(i) at least two fungicides selected from the group consisting of a QoI inhibitor fungicide, a contact fungicide, and a demethylation inhibitor; and', '(ii) a phthalocyanine pigment to turf grass., 'administering a synergistic composition,'}4. The method of claim 3 , wherein:the QoI inhibitor fungicide is trifloxystrobin,the contact fungicide is iprodione,the demethylation inhibitor is triticonazole, andthe pigment is phthalocyanine green pigment (Green 7). The present application is a continuation of U.S. application Ser. No. 12/761,144, filed on Apr. 15, 2010, which claims priority to U.S. Provisional Application No. 61/178,711, filed on May 15, 2009, the entire contents of each are herein incorporated by reference in their entireties.This application describes fungicidal compositions that control mold and fungus infection in grasses, in particular turf grasses. More specifically, the compositions comprise a fungicide that inhibits mitochondrial respiration at the QoI site ( ...

METHOD OF CONTROLLING PEST

Provided is a method which exerts an excellent effect in controlling a pest in a field of soybean, corn or cotton, using a SDHI compound and a PPO-inhibiting compound. A method of controlling a pest (a weed and/or a plant pathogen) in a field of soybean, corn or a cotton, including treating a field before, at or after seeding with a seed of soybean, corn or cotton treated with one or more compounds selected from the group consisting of SDHI compounds, with one or more PPO-inhibiting compounds selected from the group consisting of flumioxazin, sulfentrazone, saflufenacil, oxyfluorfen, fomesafen and a compound of the formula: 3. The method of controlling a pest according to or , wherein the SDHI compound is selected from the group consisting of sedaxane , penflufen , carboxin , boscalid , furametpyr , flutolanil , fluxapyroxad , isopyrazam , fluopyram and thifluzamide.4. The method of controlling a pest according to or , wherein the SDHI compound is sedaxane , penflufen or carboxin.5. The method of controlling a pest according to claim 4 , wherein the PPO-inhibiting compound is flumioxazin.6. The method of controlling a pest according to claim 2 , comprising a step of treating the field before seeding with the seed of soybean claim 2 , corn or cotton claim 2 , with the PPO inhibitory compound.7. The method of controlling a pest according to claim 2 , comprising a step of treating the field to be seeded claim 2 , with the PPO-inhibiting compound simultaneously at seeding with the seed of soybean claim 2 , corn or cotton.8. The method of controlling a pest according to claim 2 , comprising a step of treating the field after seeding with the seed of soybean claim 2 , corn or cotton claim 2 , with the PPO-inhibiting compound.9. The method of controlling a pest according to claim 2 , wherein the pest is a weed and/or a plant pathogen.10. The method of controlling a pest according to claim 2 , wherein the pest is a weed. 1. Field of the InventionThe present invention ...

Plant Health Compositions Comprising a Water-Soluble Pesticide and a Water-Insoluble Agrochemical

Compositions for improving plant health, the compositions comprising at least one water-soluble pesticide and at least one non-herbicidal water-insoluble agrochemical, are described. Also described are processes for preparing the compositions and methods of improving agronomic crop plant health using the compositions. 1. A microemulsion concentrate composition comprising (i) an aqueous carrier phase comprising at least one water-soluble pesticide in solution in the carrier phase , (ii) a surfactant phase comprising (a) a surfactant component comprising at least one surfactant and (b) at least one water-insoluble agrochemical , and (iii) a water-immiscible organic solvent ,wherein,the water soluble pesticide concentration is at least 400 grams active equivalent per liter of the concentrate composition, andthe weight ratio of the water-immiscible organic solvent to the water-insoluble agrochemical on an active equivalent basis is less than 3:1.23-. (canceled)4. The composition of wherein the weight ratio of the water-immiscible organic solvent to the water-insoluble agrochemical on an active equivalent basis is less than 2.5:1.5. The composition of wherein the weight ratio of the water-soluble pesticide on an active equivalent basis to water-insoluble agrochemical on an active equivalent basis is from about 1:1 to about 100:1.6. The composition of wherein at least 50% by weight of the water-insoluble agrochemical is present as a solute in the surfactant component.710-. (canceled)11. The composition of wherein the water-soluble pesticide comprises at least one water-soluble herbicide selected from the group consisting of glyphosate claim 1 , dicamba claim 1 , 2 claim 1 ,4-D claim 1 , MCPA claim 1 , quizalofop claim 1 , glufosinate claim 1 , diclofop-methyl claim 1 , derivatives thereof and combinations thereof.1214-. (canceled)15. The composition of wherein the water-insoluble agrochemical is a fungicide selected from the group consisting of triazoles claim 1 , ...

HERBICIDES CONTAINING SUBSTITUTED THIEN-3-YL-SULFONYLAMINO(THIO)CARBONYL-TRIAZOLIN(THI)ONE

The invention relates to herbicidal compositions, their preparation, and their use for controlling unwanted vegetation. The compositions include an effective amount of an active compound combination that includes: 2. A method for controlling unwanted plants comprising allowing an effective amount of a composition according to to act on the unwanted plants and/or their habitat.3. A composition according to in which substituted thien-3-yl-sulphonylaminocarbonyltriazolinone is in the form of a sodium claim 1 , potassium claim 1 , magnesium claim 1 , calcium claim 1 , ammonium claim 1 , C1-C4-alkylammonium claim 1 , di-(C1-C4-alkyl)ammonium claim 1 , tri-(C1-C4-alkyl)ammonium claim 1 , tetra-(C1-C4-alkyl)ammonium claim 1 , tri-(C1-C4-alkyl)sulphonium claim 1 , C5 or C6-cycloalkylammonium claim 1 , or di-(C1-C2-alkyl)benzyl ammonium salt.4. A composition according to in which substituted thien-3-yl-sulphonylaminocarbonyltriazolinone is in the form of a sodium salt.5. A composition of claim 1 , further comprising a safener (c).6. A process for preparing a herbicidal composition comprising mixing a composition according to with one or more surfactants and/or extenders.7. A method for selective claim 1 , semi-selective and/or nonselective control of monocotyledonous and/or dicotyledonous plants comprising allowing an effective amount of a composition according to to act on the monocotyledonous and/or dicotyledonous plants and/or their habitat.8Chenopodium, Abutilon, Bromus, Veronica, Viola, Setaria, Avena, Alopecurus, Cyperus, Matricaria, Xanthium, Cassia, Ipomoea, Digitaria, Polygonum, Eriochloa, Gatium EriochloaLotium. A method of claim 7 , wherein said plants are at least one selected from the group consisting of claim 7 , and and said method is used to protect at least one crop selected from the group consisting of cotton claim 7 , barley claim 7 , potatoes claim 7 , maize claim 7 , oil seed claim 7 , rape seed claim 7 , rice claim 7 , rye claim 7 , soy beans claim 7 , ...

Active compounds combinations Comprising Prothioconazole and fluxapyroxad

The present invention relates to active compound combinations, in particular within a fungicide composition, which comprises (A) prothioconazole and (B) fluxapyroxad and optionally (C) a further fungicidally active compound. Moreover, the invention relates to a method for curatively or preventively controlling the phytopathogenic fungi of plants or crops (e.g. cereals such as wheat, barley, rye, oats, millet and triticale; soya beans; rice; com/maize; oil seed rape including canola; beans, peas, peanuts; sugar beet, fodder beet, beetroot; potatoes; cotton), and to the use of a combination according to the invention for the treatment of seed, to a method for protecting a seed and not at least to the treated seed. 1. An active compound combination comprising (A) prothioconazole and (B) Fluxapyroxad.2. Active compound combination according to comprising an additional third fungicidally active compound (C).3. Method for controlling phytopathogenic fungi in crop protection claim 1 , comprising applying an active compound combination according to to seed claim 1 , plant claim 1 , to fruit of a plant and/or to soil on which a plant grows or is supposed to grow.4. Method according to claim 3 , wherein the plant claim 3 , the fruit of a plant or soil on which the plant grows or is intended to grow is treated.5. Method according to claim 3 , wherein claim 3 , in the treatment of leaves from 0.1 to 10 000 g/ha claim 3 , and in the treatment of seed from 2 to 200 g per 100 kg of seed are employed.6. Active compound combination according to for controlling unwanted phytopathogenic fungi in crop protection.7. Active compound combination according to for treating seed claim 1 , seed of transgenic plants and transgenic plants.8. Seed treated with an active compound combination according to .9AlternariaAlternaria triticina, Ascochyta tritici, Athelia rolfsi, Bipolaris sorokiniana, Blumeria graminis, Cephalosporium gramineum, Ceratobasidium cereale, CladosporiumCladosporium herbarum, ...

SYNERGISTIC FUNGICIDAL COMBINATION

Compositions and methods employing combinations of synergistically effective amounts of folpet and epoxiconazole are provided. 1. A fungicidal combination comprising folpet (I) and epoxiconazole (II) in a synergistically effective amount.2. The fungicidal combination according to claim 1 , wherein the weight ratio of folpet (I) to epoxiconazole (II) is from 1:1 to 10:1.3. A method for controlling phytopathogenic fungi claim 1 , wherein the fungi claim 1 , their habitat claim 1 , plants claim 1 , soil claim 1 , or seed to be protected against fungal attack are treated with an effective amount of the fungicidal combination according to .4Mycosphaerella graminicola. The method according to claim 3 , wherein the phytopathogenic fungi is controlled.5. The method according to claim 3 , wherein the folpet (I) and epoxiconazole (II) of the fungicidal combination according to are applied as an admixture or separately.6. The method according to claim 3 , wherein folpet (I) and epoxiconazole (II) of the fungicidal combination according to are applied as a ready-mixed admixture composition or as a tank admixture.7. The method according to claim 3 , wherein the fungicidal combination comprising folpet (I) and epoxiconazole (II) according to are applied as an admixture in an amount from 25 g/ha to 2000 g/ha.8. The method according to claim 3 , wherein the fungicidal combination comprising folpet (I) and epoxiconazole (II) according to are applied separately claim 3 , in either order claim 3 , in an amount from 10 to 1500 g/ha of folpet. (I) claim 3 , from 10 to 500 g/ha of epoxiconazole II.9. The method according to claim 3 , wherein the fungicidal combination of folpet (I) and epoxiconazole (II) according to are applied in an amount of from 1 g to 1000 g per 100 kg of seed claim 3 , either separately or as an admixture.10. The use of the combination of folpet (I) and epoxiconazole (II) according to for preparing a composition suitable for controlling harmful fungi claim 1 , ...

Fungicide Active Substance Combinations

The novel active compound combinations comprising 2-[2-(1-chorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazole-3-thione of the formula 15.-. (canceled)7. The composition of wherein the weight ratio of the active compound of formula (I) to the compound of formula (III) is from 1:0.33 to 1:3.8. A method for controlling fungi comprising applying the composition according to or to the fungi and/or their habitat.10. A method for controlling fungi comprising applying the composition according to to the fungi and/or their habitat.11. The method according to wherein the fungi is a cereal disease.12Erysiphe, PucciniaFusarium.. The method according to wherein the cereal disease is selected from the group consisting of claim 11 , and13. The method according to wherein the composition is applied to plant parts at a rate between 10 and 1000 g/ha.14. The method according to wherein the composition is applied to soil at a rate between 1 and 5000 g/ha.16. The method according to wherein the weight ratio of active compound of the formula (I) to the active compound of the formula (III) is from 1:0.33 to 1:3.17. The method according to wherein the weight ratio of active compound of the formula (I) to the active compound of the formula (III) is from 1:1 to 1:3.18. The method according to wherein the fungi is a cereal disease.19Erysiphe, PucciniaFusarium.. The method according to wherein the cereal disease is selected from the group consisting of claim 18 , and20. The method according to wherein the composition is applied to plant parts at a rate between 10 and 1000 g/ha.21. The method according to wherein the composition is applied to soil at a rate between 1 and 5000 g/ha.22. The method according to wherein the composition is applied to plant parts at a rate between 25 to 1000 g/ha. The present invention relates to novel active compound combinations which consist of the known 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro[1,2,4 ...

Use of Strobilurins for Increasing the Gluten Strength in Winter Cereals

The present invention relates to the use of a strobilurin (compound A) selected from the group consisting of pyraclostrobin, azoxystrobin, dimoxystrobin, enestroburin, fluoxastrobin, kresoxim-methyl, metominostrobin, orysastrobin, picoxystrobin, pyribencarb, trifloxystrobin, pyrametostrobin, pyraoxystrobin, coumoxystrobin, coumethoxystrobin, triclopyricarb (chlorodincarb), fenaminstrobin (diclofenoxystrobin), fenoxystrobin, 2-(2-(6-(3-chloro-2-methyl-phenoxy)-5-fluoro-pyrimidin-4-yloxy)-phenyl)-2-methoxyimino-N-methyl-acetamide, 3-methoxy-2-(2-(N-(4-methoxy-phenyl)-cyclopropane-carboximidoylsulfanylmethyl)-phenyl)-acrylic acid methyl ester, methyl (2-chloro-5-[1-(3-methylbenzyloxyimino)ethyl]benzyl)carbamate and 2-(2-(3-(2,6-dichlorophenyl)-1-methyl-allylideneaminooxymethyl)-phenyl)-2-methoxyimino-N methyl-acetamide for increasing the gluten strength in winter cereals. 116-. (canceled)17. A method for increasing the gluten strength in winter cereals wherein the plant , the locus where the plant is growing or is expected to grow or plant propagation material from which the plant grows is treated with an effective amount of a strobilurin (compound A) selected from the group consisting of pyraclostrobin , azoxystrobin , dimoxystrobin , enestroburin , fluoxastrobin , kresoxim-methyl , metominostrobin , orysastrobin , picoxystrobin , pyribencarb , trifloxystrobin , pyrametostrobin , pyraoxystrobin , coumoxystrobin , coumethoxystrobin , triclopyricarb (chlorodincarb) , fenaminstrobin (diclofenoxystrobin) , fenoxystrobin , 2-(2-(6-(3-chloro-2-methyl-phenoxy)-5-fluoro- pyrimidin-4-yloxy)-phenyl)-2-methoxyimino-N-methyl-acetamide , 3-methoxy-2-(2-(N-(4- methoxy-phenyl)-cyclopropane-carboximidoylsulfanylmethyl)-phenyl)-acrylic acid methyl ester , methyl (2-chloro-5-[1-(3-methylbenzyloxyimino)ethyl]benzyl)carbamate and 2-(2-(3- (2 ,6-dichlorophenyl)-1-methyl-allylideneaminooxymethyl)-phenyl)-2-methoxyimino-N methyl-acetamide.18. The method according to claim 17 , wherein the ...

Pyridine Compounds for Controlling Invertebrate Pests II

The present invention relates to novel pyridine compounds of the formulae I and II, to their salts, to their tautomers, to their N-oxides, and to the salts of these N-oxides or tautomers. The compounds are useful for combating or controlling invertebrate pests, in particular arthropod pests. The invention also relates to a method for controlling in-vertebrate pests by using these compounds. The invention further relates to plant propagation material and to agricultural compositions comprising said compounds. 125-. (canceled)27. The compound as claimed in claim 26 , which is a compound of the formula I.28. The compound as claimed in claim 27 , wherein Xin formula I is oxygen.29. The compound as claimed in claim 26 , wherein Ris hydrogen claim 26 , C-C-alkyl claim 26 , C-C-haloalkyl claim 26 , C-C-alkylene-CN claim 26 , heterocyclyl-C-C-alkyl claim 26 , hetaryl-C-C-alkyl claim 26 , C-C-alkylen-ORor C-C-cycloalkyl-C-C-alkyl.30. The compound as claimed in claim 29 , wherein Ris hydrogen claim 29 , C-C-alkyl claim 29 , C-C-haloalkyl claim 29 , C-C-alkylen-O—C-C-alkyl or C-C-alkylene-CN.31. The compound as claimed in claim 26 , wherein both radicals Rand Rare hydrogen.32. The compound as claimed in claim 26 , wherein Z is NR.33. The compound as claimed in claim 32 , where Ris selected from the group consisting of hydrogen claim 32 , C-C-alkyl claim 32 , C-C-haloalkyl claim 32 , C-C-alkoxy-C-C-alkyl claim 32 , C-C-alkylene-CN claim 32 , C-C-cycloalkyl claim 32 , C-C-cycloalkyl-C-C-alkyl claim 32 , heterocyclyl-C-C-alkyl claim 32 , where the cycloalkyl or heterocyclyl moieties in the last three mentioned radicals are unsubstituted or carry 1 or 2 radicals selected from the group consisting of halogen claim 32 , CN claim 32 , C-C-alkyl and C-C-haloalkyl;{'sub': 1', '4', '1', '2', '1', '2', '1', '2', '1', '2, 'phenyl and phenyl-C-C-alkyl, where the phenyl moiety in the last two mentioned radicals is unsubstituted or carries 1 or 2 radicals selected from the group consisting ...

HERBICIDAL COMPOSITION

Provided are technologies for controlling weeds, specifically, a herbicidal composition comprising as active ingredients pyrasulfotole, mefenpyr-diethyl, and one or more compounds selected from Group A has a herbicidal effect, 2. The herbicidal composition according to claim 1 , wherein the weight ratio of the one or more compounds selected from Group A to pyrasulfotole is from 1:0.001 to 1:100.3. The herbicidal composition according to claim 1 , wherein the weight ratio of the one or more compounds selected from Group A to mefenpyr-diethyl is from 1:0.0005 to 1:100.4. The herbicidal composition according to any one of to claim 1 , wherein the one or more compounds selected from Group A is flumioxazin.6. The method according to claim 5 , wherein the weight ratio of the one or more compounds selected from Group A to pyrasulfotole is within the range of from 1:0.001 to 1:100.7. The method according to claim 5 , wherein the weight ratio of the one or more compounds selected from Group A to mefenpyr-diethyl is within the range of from 1:0.0005 to 1:100.8. The method according to any one of to claim 5 , wherein the one or more compounds selected from Group A is flumioxazin.9. The method according to claim 5 , wherein the place where weeds grow or are to grow is a soybean field claim 5 , a cotton field claim 5 , or a corn field.10. The method according to claim 5 , wherein the place where weeds grow or are to grow is a tree land.11. The weed control method according to claim 9 , wherein the soybean of the soybean field or the cotton of the cotton field is transgenic soybean or transgenic cotton.12. The weed control method according to claim 9 , wherein the soybean of the soybean field or the cotton of the cotton field is transgenic soybean imparted with resistance to herbicides or transgenic cotton imparted with resistance to herbicides.13. The weed control method according to claim 9 , wherein the soybean of the soybean field or the cotton of the cotton field is ...

SELECTIVE HERBICIDES BASED ON SUBSTITUTED THIEN-3-YL-SULPHONYLAMINO(THIO)CARBONYLTRIAZOLIN(THI)ONES AND SAFENERS

The invention relates to selective herbicidal compositions that comprise an effective amount of an active compound combination comprising 2. A method for controlling undesirable plants comprising allowing an effective amount of a composition according to claim 1 , to act on undesirable plants and/or their habitat.3. A process for preparing a herbicidal composition comprising mixing a composition according to claim 1 , with one or more surfactants and/or extenders.4. A composition of claim 1 , wherein the ratio of said at least one compound that improves crop plant compatibility per part by weight of said compound of formula I or a salt thereof is from 0.1 to 50. This application is a Continuation of U.S. application Ser. No. 10/489,092, filed Sep. 7, 2004, which is a §371 National Stage Application of PCT/EP2002/010104, filed Sep. 10, 2002, which claims priority to German Application No. 101 46 590.4, filed Sep. 21, 2001, the content of all of which are incorporated herein by reference in their entireties.1. Field of the InventionThe invention relates to novel selective herbicidal active compound combinations which comprise substituted thien-3-ylsulphonylamino(thio)carbonyltriazolin(ethi)ones and at least one compound which improves crop plant compatibility and which can be used with particularly good results for the selective control of weeds in various crops of useful plants.2. Description of Related ArtSubstituted thien-3-ylsulphonylamino(thio)carbonyltriazoline(ethi)ones are already known as effective herbicides (cf. WO-A-01/05788). However, the activity of these compounds and/or their compatibility with crop plants are not entirely satisfactory under all conditions.Surprisingly, it has now been found that certain substituted thien-3-ylsulphonylamino(thio)carbonyltriazolin(ethi)ones, when used together with the crop-plant-compatibility-improving compounds (safeners/antidotes) described below, prevent damage to crop plants extremely well and can be used ...

INSECTICIDAL COMPOUNDS

The present invention relates to novel triazole derivatives of formula (I) having insecticidal activity, to processes and intermediates for preparing them, to insecticidal, acaricidal, nematicidal or molluscicidal compositions comprising them and to methods of using them to combat and control insect, acarine, nematode or mollusc pests wherein A, A, A, A, R, G, Qand Qare as defined in claim ; or salts or N-oxides thereof. 2. A compound according to claim 1 , characterized in that{'sup': 1', '2', '3', '4, 'A, A, Aand Aare C—X and each X is independently selected from hydrogen, halogen, cyano, methyl, trifluoromethyl and methoxy.'}3. A compound according to claim 2 , characterized in that{'sup': '1', 'Ris hydrogen, methyl, ethyl or acetyl;'}{'sup': '2', 'Ris hydrogen, methyl, trifluoromethyl or halogen;'}{'sup': '1', 'Gis oxygen;'}{'sup': '1', 'Qis aryl or heteroaryl; each optionally substituted by one to five substituents independently selected from cyano, nitro, hydroxy, bromo, chloro, fluoro, methyl, trifluoromethyl, methoxy, trifluoromethoxy, methylthio, methylsulfinyl, methylsulfonyl and phenyl;'}{'sup': 5', '10', '10, 'sub': 1', '6', '1', '6', '2', '6', '2', '6, 'Ris hydrogen, C-Chaloalkyl, C-Calkyl, C-Calkenyl, C-Calkynyl, phenyl or phenyl substituted by one to five substituents R, which may be the same or different, pyridyl or pyridyl substituted by one to five substituents R, which may be the same or different;'}{'sup': 7', '6, 'sub': 1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4, 'Rand Rare independently hydrogen, cyano, halogen, C-Calkyl, C-Cperfluoroalkyl, C-Cperfluoroalkylthio, C-Cperfluoroalkylsulfinyl or C-C-perfluoroalkylsulfonyl preferably independently C-Cperfluoroalkyl, C-Cperfluoroalkylthio, C-C-perfluoroalkylsulfinyl or C-C-per-fluoroalkylsulfonyl even more preferably independently C-C-perfluoroalkyl, C-C-perfluoroalkylthio, or C-C-perfluoroalkylsulfonyl.'}4. A compound ...

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

This document discloses molecules having the following formula (“Formula One”): 3. A composition according to further comprising:(a) one or more compounds having acaricidal, algicidal, avicidal, bactericidal, fungicidal, herbicidal, insecticidal, molluscicidal, nematicidal, rodenticidal, or virucidal properties; or(b) one or more compounds that are antifeedants, bird repellents, chemosterilants, herbicide safeners, insect attractants, insect repellents, mammal repellents, mating disrupters, plant activators, plant growth regulators, or synergists; or(c) both (a) and (b).4. A composition according to wherein further comprising one or more compounds selected from: (3-ethoxypropyl)mercury bromide claim 2 , 1 claim 2 ,2-dichloropropane claim 2 , 1 claim 2 ,3-dichloropropene claim 2 , 1-methylcyclopropene claim 2 , 1-naphthol claim 2 , 2-(octylthio)ethanol claim 2 , 2 claim 2 ,3 claim 2 ,5-tri-iodobenzoic acid claim 2 , 2 claim 2 ,3 claim 2 ,6-TBA claim 2 , 2 claim 2 ,3 claim 2 ,6-TBA-dimethylammonium claim 2 , 2 claim 2 ,3 claim 2 ,6-TBA-lithium claim 2 , 2 claim 2 ,3 claim 2 ,6-TBA-potassium claim 2 , 2 claim 2 ,3 claim 2 ,6-TBA-sodium claim 2 , 2 claim 2 ,4 claim 2 ,5-T claim 2 , 2 claim 2 ,4 claim 2 ,5-T-2-butoxypropyl claim 2 , 2 claim 2 ,4 claim 2 ,5-T-2-ethylhexyl claim 2 , 2 claim 2 ,4 claim 2 ,5-T-3-butoxypropyl claim 2 , 2 claim 2 ,4 claim 2 ,5-TB claim 2 , 2 claim 2 ,4 claim 2 ,5-T-butomethyl claim 2 , 2 claim 2 ,4 claim 2 ,5-T-butotyl claim 2 , 2 claim 2 ,4 claim 2 ,5-T-butyl claim 2 , 2 claim 2 ,4 claim 2 ,5-T-isobutyl claim 2 , 2 claim 2 ,4 claim 2 ,5-T-isoctyl claim 2 , 2 claim 2 ,4 claim 2 ,5-T-isopropyl claim 2 , 2 claim 2 ,4 claim 2 ,5-T-methyl claim 2 , 2 claim 2 ,4 claim 2 ,5-T-pentyl claim 2 , 2 claim 2 ,4 claim 2 ,5-T-sodium claim 2 , 2 claim 2 ,4 claim 2 ,5-T-triethylammonium claim 2 , 2 claim 2 ,4 claim 2 ,5-T-trolamine claim 2 , 2 claim 2 ,4-D claim 2 , 2 claim 2 ,4-D-2-butoxypropyl claim 2 , 2 claim 2 ,4-D-2-ethylhexyl claim 2 , 2 claim 2 ,4-D-3 ...

Fungicide Active Substance Combinations

The novel active compound combinations comprising 2-[2-(1-chlorocyclopropyl)3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazole-3-thione of the formula 15.-. (canceled)7. The composition of claim 6 , wherein the weight ratio of the active compound of formula (I) to the compound of formula (XXIII) is from 1:0.1 to 1:108. The composition of claim 6 , wherein the weight ratio of the active compound of formula (I) to the compound of formula (XXIII) is from 1:0.2 to 1:5.9. The composition of claim 6 , further comprising at least one solid carrier.10. The composition of claim 9 , wherein the solid carrier is selected from the group consisting of kaolin claim 9 , clay claim 9 , talc claim 9 , chalk claim 9 , quartz claim 9 , attapulgite claim 9 , montmorillonite earth claim 9 , diatomaceous earth claim 9 , silica claim 9 , alumina claim 9 , and silicate.11. A method for controlling fungi claim 6 , comprising applying the composition of to the fungi claim 6 , to plants claim 6 , to plant parts claim 6 , to seed claim 6 , or to soil.12. The method of claim 11 , wherein the fungi is selected from the group consisting of Plasmodiophoromycetes claim 11 , Oomycetes claim 11 , Chytridiomycetes claim 11 , Zygomycetes claim 11 , Ascomycetes claim 11 , Basidiomycetes claim 11 , and Deuteromycetes.13. The method according to claim 11 , wherein the fungi is a cereal disease.14Erysiphe, PucciniaFusarium.. The method according to claim 13 , wherein the cereal disease is selected from the group consisting of claim 13 , and15. The method according to claim 11 , wherein the composition is applied to plant parts at a rate between 10 and 1000 g/ha.16. The method according to claim 11 , wherein the composition is applied to seed at a rate between 0.01 and 10 g per kilogram of seed.17. The method according to claim 11 , wherein the composition is applied to soil at a rate between 1 and 5000 g/ha. The present invention relates to novel active compound combinations which consist of ...

PLANT GROWTH REGULATION

The present invention relates to a method for improving the plant growth regulation of and/or enhancing crop plants, by applying to the crop plants a mixture of a plant growth regulator, and jasmonic acid or a salt or ester thereof. 1. A method for regulating the growth of and/or enhancing crop plants , comprising applying to the plants , plant parts , plant propagation material , or a plant growing locus , a plant growth regulator and jasmonic acid or a salt or ester thereof , wherein the crop plants are cereals , sugar cane , rice or corn.2. A method according to claim 1 , wherein the plant growth regulator and jasmonic acid or a salt or ester thereof claim 1 , are applied in a synergistically effective amount.3. A method according to claim 1 , wherein the plant growth regulator is selected from the group consisting of trinexapac-ethyl claim 1 , prohexadione-calcium claim 1 , paclobutrazol claim 1 , uniconazole claim 1 , flurprimidol claim 1 , mefluidide claim 1 , mepiquat-chloride claim 1 , chlormequat-chloride claim 1 , and a mixture thereof.4. A method according to claim 3 , wherein the plant growth regulator is trinexapac-ethyl.5. A method according to claim 3 , wherein the plant growth regulator is paclobutrazol.6. A method according to claim 1 , wherein the jasmonic acid is in the form of methyl jasmonate.7. A method according to claim 1 , wherein the crop plants are cereals.8. A method according to claim 1 , wherein the plant growth regulator and jasmonic acid or a salt or ester thereof claim 1 , are applied in the form of a composition comprising an agriculturally acceptable carrier.9. A method according to claim 1 , wherein the plant growth regulator and jasmonic acid are applied to the plant in a weight ratio from about 1:1 to about 1:10.10. A method according to claim 1 , wherein the plant growth regulator is applied at a rate from about 50 to about 100 g ai/ha.11. A method according to claim 1 , wherein the jasmonic acid is applied at a rate from about ...

INHIBITION AND DISPERSION OF BIOFILMS IN PLANTS WITH IMIDAZOLE-TRIAZOLE DERIVATIVES

Disclosure is provided for methods of preventing, removing or inhibiting microbial biofilm formation or microbial infection in a plant or plant part thereof, including applying thereto a treatment effective amount of an active compound as described herein, or an agriculturally acceptable salt thereof. Methods of enhancing a microbicide (e.g., including a copper, antibiotic, bacteriophage, etc.) and/or plant defense activator are also provided, including applying an active compound as described herein. Compositions comprising an active compound as described herein in an agriculturally acceptable carrier are also provided, and in some embodiments the compositions further include a microbicide (e.g., including copper, antibiotic, bacteriophage, etc.) and/or plant defense activator. 2. The method of claim 1 , wherein said plant is a fruit crop plant or a vegetable crop plant.320.-. (canceled)21. The method of claim 1 , wherein said microbial biofilm formation or microbial infection is caused by a fungi.22alternaria. The method of claim 1 , wherein said compound is applied to said plant in an amount effective to treat or control a fungal disease selected from the group consisting of rots claim 1 , leaf molds claim 1 , blights claim 1 , wilts claim 1 , damping-off claim 1 , spot claim 1 , root rot claim 1 , stem rot claim 1 , mildew claim 1 , brown spot claim 1 , gummosis claim 1 , melanose claim 1 , post-bloom fruit drop claim 1 , scab claim 1 , claim 1 , canker claim 1 , flyspeck claim 1 , fruit blotch claim 1 , dieback claim 1 , downy mildews claim 1 , ear rots claim 1 , anthracnose bunts claim 1 , smut claim 1 , rust claim 1 , eyespot and pecky rice.2334.-. (canceled)36. The composition of claim 35 , further comprising a microbicide.37. The composition of claim 36 , wherein said microbicide comprises copper.38. (canceled)39. The composition of claim 35 , further comprising an antibiotic.40. The composition of claim 35 , further comprising a bacteriophage.41. The ...

SUBSTITUTED 1,2,4-TRIAZOLE COMPOUNDS AS A SEED TREATMENT TO CONTROL PESTS

Methods of using substituted 1,2,4-triazole compounds as a seed treatment to control pests, such as insects and mites. 2. The method of claim 1 , wherein contacting at least one seed with at least one substituted 1 claim 1 ,2 claim 1 ,4-triazole compound comprises contacting the at least one seed with the at least one substituted 1 claim 1 ,2 claim 1 ,4-triazole compound to control members of Phylum Arthropoda.3. The method of claim 2 , wherein contacting the at least one seed with the at least one substituted 1 claim 2 ,2 claim 2 ,4-triazole compound comprises contacting the at least one seed with the at least one substituted 1 claim 2 ,2 claim 2 ,4-triazole compound to control members of at least one of Class Insecta and Class Arachnida.4Coleoptera, Dermaptera, Dictyoptera, Diptera, Hemiptera, Homoptera, Hymenoptera, Isoptera, Lepidoptera, Orthoptera, Thysanoptera, ThysanuraAcari.. The method of claim 3 , wherein contacting the at least one seed with the at least one substituted 1 claim 3 ,2 claim 3 ,4-triazole compound comprises contacting the at least one seed with the at least one substituted 1 claim 3 ,2 claim 3 ,4-triazole compound to control at least one of members of Orders claim 3 , and5HomopteraAcari.. The method of claim 4 , wherein contacting the at least one seed with the at least one substituted 1 claim 4 ,2 claim 4 ,4-triazole compound comprises contacting the at least one seed with the at least one substituted 1 claim 4 ,2 claim 4 ,4-triazole compound to control at least one of members of Orders and6AphisMyzus. The method of claim 5 , wherein contacting the at least one seed with the at least one substituted 1 claim 5 ,2 claim 5 ,4-triazole compound comprises contacting the at least one seed with the at least one substituted 1 claim 5 ,2 claim 5 ,4-triazole compound to control at least one of spp. and spp.7Allium, Antirrhinum, Arachis, Asparagus, Avena, Begonia, Beta, Betholettia, Brassica, Capsicum, Carthamus, Chrysanthemum, Cicer, Cichorium, ...

INSECTICIDAL COMPOUNDS

The present invention relates to novel triazole derivatives of formula (I) having insecticidal activity, to processes and intermediates for preparing them, to insecticidal, acaricidal, nematicidal or molluscicidal compositions comprising them and to methods of using them to combat and control insect, acarine, nematode or mollusc pests wherein A, A, A, A, R, R, G, Qand Qare as defined in claim ; or salts or N— oxides thereof. 2. A compound according to claim 1 , characterized in that A claim 1 , A claim 1 , Aand Aare C—X and each X is independently selected from hydrogen claim 1 , halogen claim 1 , cyano claim 1 , methyl claim 1 , trifluoromethyl and methoxy;3. A compound according to claim 2 , characterized in that{'sup': '1', 'Ris hydrogen, methyl, ethyl or acetyl;'}{'sup': '2', 'Ris hydrogen, methyl, trifluoromethyl or halogen;'}{'sup': '1', 'Gis oxygen;'}{'sup': '1', 'sub': 3', '10', '1', '8, 'Qis aryl or heterocyclyl or C-Ccycloalkyl or C-Calkyl; each optionally substituted by one to five substituents independently selected from cyano, nitro, hydroxy, bromo, chloro, fluoro, methyl, trifluoromethyl, methoxy, trifluoromethoxy, methylthio, methylsulfinyl, methylsulfonyl and phenyl;'}{'sup': 5', '10', '10, 'sub': 1', '6', '1', '6', '2', '6', '2', '6, 'Ris hydrogen, C-Chaloalkyl, C-Calkyl, C-Calkenyl, C-Calkynyl, phenyl or phenyl substituted by one to five substituents R, which may be the same or different, pyridyl or pyridyl substituted by one to five substituents R, which may be the same or different;'}{'sup': 7', '6, 'sub': 1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4, 'Rand Rare independently hydrogen, cyano, halogen, C-Calkyl, C-Cperfluoroalkyl, C-Cperfluoroalkylthio, C-Cperfluoroalkylsulfinyl or C-C-perfluoroalkylsulfonyl preferably independently C-Cperfluoroalkyl, C-Cperfluoroalkylthio, C-C-perfluoroalkylsulfinyl or C-C-per-fluoroalkylsulfonyl even more preferably independently C-C- ...

Novel Herbicides Based on Substituted Thien-3-yl-Sulphonylamino(thio)Carbonyl-Triazolin(thi)ones and 4-HPPD-Inhibitors

The invention relates to herbicidal compositions comprising an effective amount of an active ingredient combination composed of 15-. (canceled)7. The composition as claimed in claim 6 , wherein the crop plant tolerance promoter compound is selected from the active ingredients benoxacor claim 6 , mefenpyr-diethyl claim 6 , fenchlorazole-ethyl claim 6 , isoxadifen-ethyl claim 6 , cloquintocet-mexyl claim 6 , and the compound N-cyclopropyl-4-[[(2-methoxybenzoyl)amino]sulfonyl]benzamide.8. A method of controlling weeds claim 6 , comprising applying the composition of to weeds and/or their habitat claim 6 , wherein said composition further comprises surface active agents and/or extenders.9. A process for producing a herbicidal composition comprising claim 6 , mixing a composition of with surface-active agents and/or extenders.10. A composition according to claim 6 , wherein Ris CH; Ris —OCH; and Ris CH. The invention relates to novel herbicidal synergistic active ingredient combinations which comprise known substituted thien-3-ylsulfonylamino(thio)carbonyltriazolin(thi)ones on the one hand and one or more known herbicidal compounds on the other hand and, if desired, additionally a crop plant tolerance promoter compound and can be used with particular success for weed control in various crops of useful plants or else for controlling monocotyledonous and dicotyledonous weeds in the semiselective and nonselective segment.Substituted thien-3-ylsulfonylamino(thio)carbonyltriazolin(thi)ones are known to be effective herbicides (cf. WO-A-01/05788). Additionally, herbicides comprising these compounds and other known herbicides or safeners are known (cf. WO-A-03/026427 and WO-A-03/026426). The action of these herbicides, however, is not entirely satisfactory under all conditions.Surprisingly it has now been found that a series of active ingredients from the class of the substituted thien-3-ylsulfonylamino(thio)carbonyltriazolin(thi)ones, when applied jointly with certain ...

SYNERGISTIC ANTIMICROBIAL COMPOSITION

A synergistic antimicrobial composition comprising: (a) 3-iodo-2-propynyl-butylcarbamate; and (b) flumetsulam. A synergistic antimicrobial composition comprising: (a) 3-iodo-2-propynyl-butylcarbamate; (b) diclosulam. 1. A synergistic antimicrobial composition comprising: (a) 3-iodo-2-propynyl-butylcarbamate; and (b) diclosulam; wherein a weight ratio of 3-iodo-2-propynyl-butylcarbamate to diclosulam is from 10:1 to 4:1.2. The composition of which is a building material claim 1 , paint claim 1 , coating claim 1 , polymer claim 1 , plastic claim 1 , synthetic or natural rubber claim 1 , paper product claim 1 , fiberglass sheet claim 1 , insulation claim 1 , exterior insulating finishing system claim 1 , roofing and flooring felt claim 1 , building plaster claim 1 , wood product or wood-plastic composite.3. The composition of which is a dry film coating. This invention relates to combinations of biocides, the combinations having greater activity than would be observed for the individual antimicrobial compounds.Use of combinations of at least two antimicrobial compounds can broaden potential markets, reduce use concentrations and costs, and reduce waste. In some cases, commercial antimicrobial compounds cannot provide effective control of microorganisms, even at high use concentrations, due to weak activity against certain types of microorganisms, e.g., those resistant to some antimicrobial compounds. Combinations of different antimicrobial compounds are sometimes used to provide overall control of microorganisms in a particular end use environment. For example, U.S. Pat. No. 6,197,805 discloses a combination of 3-iodo-2-propynyl-butylcarbamate (IPBC) and 2-(methoxycarbonylamino)benzimidazole, but this reference does not suggest any of the combinations claimed herein. Moreover, there is a need for additional combinations of antimicrobial compounds having enhanced activity against various strains of microorganisms to provide effective control of the microorganisms, ...

Pesticidal Compound Mixtures

The present invention relates to novel pesticidal compositions comprising Hither as component A: clothianidin, as component B: ipconazole Or as component A: clothianidin, as component B: ipconazole as component C: metalaxyl that show surprisingly good insecticidal, acaricidal, nematicidal and fungicidal activities. In particular, these compositions are suited for the treatment of seed. 1. A composition comprising clothianidin and ipconazole.2. A composition comprising clothianidin , ipconazole and metalaxyl.3. The composition according to claim 1 , wherein the ratio of clothianidin and ipconazole is between 100:1 and 1:1000.4. The composition according to claim 2 , wherein the ratio of clothianidin and the sum of ipconazole and metalaxyl is between 100:1 and 1:1000.510-. (canceled)11. A composition comprising seed claim 2 , clothianidin and ipconazole.12. The composition according to wherein the seed is transgenic seed.13. The composition according to wherein the seed is selected from the group consisting of corn seed claim 11 , soybean seed claim 11 , cotton seed claim 11 , rice seed and canola seed.14. The composition according to claim 11 , further comprising metalaxyl.15. The composition according to wherein the seed is transgenic seed.16. The composition according to wherein the seed is selected from the group consisting of corn seed claim 15 , soybean seed claim 15 , cotton seed claim 15 , rice seed and canola seed.17. A method for protecting a seed and/or shoots and foliage of a plant grown from the seed from damage by an animal pest claim 1 , the method comprising treating an unsown seed with the composition according to .18. The method according to wherein the unsown seed is treated separately with clothianidin and ipconazole.19. The method according to wherein said composition further comprises metalaxyl.20. The method according to wherein the unsown seed is treated separately with clothianidin claim 19 , ipconazole and metalaxyl. The present invention ...

Composition for Inhibition of Insect Host Sensing

The present invention provide chemical modulators of insect olfactory receptors. In particular, compounds and compositions are provided that can inhibit host targeting functions in insects such as mosquitoes. Method of employing such agents, and articles incorporating the same, are also provided. 1. A method of disrupting host-seeking behavior in an insect comprising providing to an insect environment a compound that binds to and/or agonizes , an ORco ion channel.2. The method of claim 1 , wherein said insect is selected from a Culicine mosquito claim 1 , an Anopheline mosquito claim 1 , a Dipteran insect claim 1 , an Ixodida insect claim 1 , and a Lepidopteran insect.36-. (canceled)7. The method of claim 1 , wherein said insect is a crop pest.8. The method of claim 1 , wherein said insect is an airborne insect.9. The method of claim 1 , wherein said insect is a blood-sucking insect.10. The method of claim 1 , wherein providing comprises contacting a host surface located in said environment with said compound.11. The method of claim 1 , wherein providing comprises aerosol or mist delivery to said environment.12. The method of claim 1 , wherein providing comprises application to a water surface in said environment.13. The method of claim 1 , wherein providing comprises application to a shelter or clothing surface in said environment.14. The method of claim 1 , wherein providing comprises use of a shelter or article of clothing containing said compound in said environment.15. The method of claim 1 , wherein providing comprises depositing a solid form of said compound in said environment.16. The method of claim 1 , wherein said compound is VUAA1.17. The method of claim 1 , further comprising provision of an insect repellent to said environment.18. The method of claim 17 , wherein said insect repellent is a mosquito repellent.19. A container comprising a VUAA1 in a liquid or gaseous dispersion.20. The container of claim 19 , wherein said gaseous dispersion is an aerosol ...

Mycotoxin accumulation inhibition method and mycotoxin accumulation inhibitor

An fungicide capable of inhibiting the accumulation of the mycotoxin in a crop effectively and a mycotoxin accumulation inhibition method using said fungicide are provided. The mycotoxin accumulation inhibition method according to the invention is a mycotoxin accumulation inhibition method for inhibiting the accumulation of the mycotoxin in a grain after cropping comprising a first fungicide treatment step for treating the cereal plant after the flowering stage with a fungicide containing metconazole as an active ingredient.

ARYLOAZOL-2-YL CYANOETHYLAMINO COMPOUNDS, METHOD OF MAKING AND METHOD OF USING THEREOF

The present invention relates to novel aryloazol-2-yl-cyanoethylamino derivatives of formula (I): 3. The aryloazol-2-yl-cyanoethylamine of claim 2 , wherein{'sub': 2', '8', '9', '10', '11', '1', '6', '2', '6', '2', '6', '3', '7', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '3', '7', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '2', '1', '6', '2', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6, 'R, R, R, Rand Reach, independently of one another, is hydrogen, amino, amido, cyano, nitro, halogen, C-C-alkyl, C-C-alkenyl, C-C-alkynyl, C-C-cycloalkyl, hydroxy-C-C-alkyl, halo-C-C-alkyl, C-C-alkylthio, halo-C-C-alkylthio arylthio, C-C-alkoxy, phenoxy, C-C-alkoxy-C-C-alkoxy, C-C-cycloalkyloxy, halo-C-C-alkoxy, C-C-alkylcarbonyl, halo-C-C-alkylcarbonyl, C-C-alkylsulfinyl, halo-C-C-alkylsulfinyl, C-C-alkylsulfonyl, C-C-alkylamino, di(C-C-alkyl)amino, C-C-alkylcarbonylamino, C-C-alkylamino-C-C-alkoxy, di-C-C-alkylamino-C-C-alkoxy, C-C-alkylamino-C-C-alkyl, di-C-C-alkylamino-C-C-alkyl, amino-C-C-alkyl, formyl, HOC—, C-C-alkyl-OC—, unsubstituted or substituted aryl or unsubstituted or substituted phenoxy, whereby the substituents may each be independent of one another and are selected from the group consisting of cyano, nitro, halogen, C-C-alkyl, halo-C-C-alkyl, C-C-alkylthio, halo-C-C-alkylthio, arylthio, C-C-alkoxy, halo-C-C-alkoxy, C-C-alkylcarbonyl, halo-C-C-alkylcarbonyl, C-C-alkylsulfinyl, halo-C-C-alkylsulfinyl, C-C-alkylsulfonyl and halo-C-C-alkylsulfonyl;'}{'sub': 3', '4', '6, 'R, Rand Rare H;'}{'sub': '5', 'Ris methyl;'}{'sub': 7', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', ...

TEBUCONAZOLE-CONTAINING PESTICIDE COMPOSITION FOR CONTROLLING FUSARIUM HEAD BLIGHTAND APPLICATION THEREOF

A pesticide composition for controlling head blight, which contains 1 to 150 parts by weight of jinggangmycin and 1 to 30 parts by weight of tebuconazole. The pesticide composition of the present invention has an obvious synergistic effect when used for controlling head blight, can remarkably enhance the effect of controlling head blight, and increase the ability of the human being in controlling head blight of grain crops. 110-. (canceled)11. A process for administrating a pesticide composition on crops , the pesticide composition containing jinggangmycin and tebuconazole in reducing DON toxin biosynthesis , characterized in that the pesticide composition comprises jinggangmycin and tebuconazole according to the weight ratio of (1-150):(1-30);{'i': fusarium', 'fusarium', 'fusarium', 'fusarium', 'Fusarium', 'fusarium., 'the DON toxin is caused by head blight; the head blight is wheat scab and barley scab, and the head blight includes bud rot, seedling blight, ear rot or ear blight of triticeae crops caused by pathogenic fungi (spp.) of carbendazim-resistant'}12. The process according to claim 11 , characterized in that the pesticide composition comprises jinggangmycin and tebuconazole according to the weight ratio of (5-85):(3-24).13. The process according to claim 11 , characterized in that the pesticide composition comprises jinggangmycin and tebuconazole according to the weight ratio of (5-30):(6-18).14. A process for administrating an agricultural fungicide on crops claim 11 , the agricultural fungicide containing jinggangmycin and tebuconazole in reducing DON toxin biosynthesis claim 11 , characterized in that the agricultural fungicide contains 0.1 to 90.0 percent by weight of pesticide composition according to any one of - claim 11 , and the balance is a light calcium carbonate carrier and/or an adjuvant chosen from ethylene glycol claim 11 , propylene glycol claim 11 , NNO-1 claim 11 , NNO-7 claim 11 , polyethylene glycol claim 11 , glycerin claim 11 , ...

FORMULATIONS

This invention relates to a formulation comprising a compound of formula (I) where R1 is hydrogen, methyl, ethyl, propyl or butyl; R2 is methyl or ethyl; R3 is hydrogen, methyl or ethyl; and n is 1, 2 or 3; to the use of a compound of formula (I) as a solvent; and to certain novel compounds of formula (I). 2. A formulation as claimed in where Ris hydrogen.3. A formulation as claimed in where Ris hydrogen.4. A formulation as claimed in claim 1 , where n is 1.5. A formulation as claimed in claim 1 , or where the formulation is an emulsifiable concentrate or an emulsion.6. A formulation as claimed in claim 1 , where the formulation further comprises an agrochemical.7. A formulation as claimed in where the agrochemical is a strobilurin claim 6 , a triazole or a succinate dehydrogenase inhibitor.8. A formulation as claimed in where the agrochemical is azoxystrobin claim 7 , difenoconazole or isopyrazam.10. A compound of formula (I) as claimed in where Ris hydrogen.11. A compound of formula (I) as claimed in where Ris hydrogen.12. A compound of formula (I) as claimed in claim 9 , where n is 1.13. A compound of formula (I) as claimed in claim 9 , where Ris methyl. This invention relates to the use of certain alkylene glycol benzoate compounds as solvents, especially in formulations, particularly in agrochemical formulations and in environmentally friendly formulations; and to certain novel compounds. The solvents of the present invention are found to be particularly effective when solubilising pesticides of the families strobilurins, triazoles and succinate dehydrogenase inhibitors (SDHI) (particularly pyrazoles; suitably pyrazam chemistry).Nowadays, the Formulation Chemist is required to address a number of environmental criteria when developing new formulations. Ideally, a suitable solvent will display many or all of the following properties: an excellent dissolving power for pesticides or other organic molecules; made from plant or animal renewable resources; low skin ...

FUNGICIDAL COMPOSITIONS

The invention relates to fungicidal compositions comprising as active ingredient a combination of components A) and B) as defined in the patent claims, to a method of controlling phytopathogenic diseases on crop plants using such a composition and to a method of protecting natural substances of vegetable and/or animal origin and/or their processed forms using such a composition. 2. The method according to claim 1 , wherein component Ris difluoromethyl and Ris hydrogen.4. The method according to claim 3 , wherein{'sub': I', 'II, 'the mixture of compounds of formula Iand formula Iis from 65 to 99% by weight of component A).'}6. The fungicidal composition of claim 5 , wherein the weight ratio of A) to B) is between 2000:1 and 1:1000.7. A method of protecting natural substances of vegetable and/or animal origin and/or their processed forms claim 1 , which have been taken from the natural life cycle claim 1 , which comprises applying to said natural substances of vegetable and/or animal origin or their processed forms a combination of components A) and B) according to in a synergistically effective amount. This application is a divisional of U.S. patent application Ser. No. 15/953,825 filed Apr. 16, 2018, which is a divisional of U.S. patent application Ser. No. 15/363,501 filed Nov. 29, 2016, now issued U.S. Pat. No. 9,949,482, issued Apr. 24, 2018, which is a divisional of U.S. patent application Ser. No. 14/017,632 filed Sep. 4, 2013, now issued U.S. Pat. No. 9,538,755 issued Jan. 10, 2017, which is a divisional of U.S. patent application Ser. No. 11/573,277 filed Feb. 6, 2007, now issued U.S. Pat. No. 8,536,089 issued Sep. 17, 2013, which is a 371 of International Application No. PCT/EP2005/008748 filed Aug. 11, 2005, which claims priority to GB 0418047.7 filed Aug. 12, 2004, all the contents of which are incorporated herein by reference.The present invention relates to novel fungicidal compositions for the treatment of phytopathogenic diseases of useful plants, ...

Fungicidal Active Compound Combinations

Safeners for herbicides are suitable for increasing the microbicidal activity of fungicides. 1. Use of a safener for increasing the microbicidal activity of a fungicide.4. Use according to one or more of to for dressing seed.5. Use according to one or more of to in transgenic plants.6. Fungicidal composition , comprising one or more compounds of group 1 according to and one or more compounds of groups 2 to 24 according to , except for the following combinations:daimuron and metominostrobin,oxabetrinil and metalaxyl,N-methylsulphonyloxyphenyl-N-methylthiolcarbamate and kasugamycin.7. Fungicidal composition according to claim 6 , where the fungicide is selected from the group consisting of prothioconazole claim 6 , tebuconazole claim 6 , fluoxastrobin claim 6 , trifloxystrobin and spiroxamine.8. Fungicidal composition according to or claim 6 , where the safener is mefenpyr.9. Fungicidal composition according to claim 8 , where the fungicide is selected from the group consisting of prothioconazole claim 8 , tebuconazole claim 8 , fluoxastrobin claim 8 , trifloxystrobin and spiroxamine.10. Method for controlling unwanted phytopathogenic fungi claim 8 , characterized in that a fungicidal composition according to one or more of to is applied to the unwanted phytopathogenic fungi and/or their habitat and/or seed. The invention relates to the use of safeners for increasing the activity of fungicides, to combinations of fungicides and safeners and to their use for controlling unwanted microorganisms.Numerous triazole derivatives, strobilurins, aniline derivatives, dicarboximides, carboxamides and other chemical compounds are already used for controlling unwanted microorganisms (see, for example, The Pesticide Manual, 13th Edition, Farnham, 2003).However, since the environmental and economic requirements imposed on modern-day fungicides are continually increasing, with regard, for example, to the spectrum of action, toxicity, selectivity, application rate, formation of ...

FUNGICIDAL BARK SPRAYS FOR TREES

The present invention generally relates to methods for controlling tree and vine fungal pathogens comprising spraying the bark of trees and vines with an effective amount of at least one inhibitor of succinate-dehydrogenase (“SDHI”) fungicide with an adjuvant 1. A method of controlling fungal pathogens comprising spraying the bark of a tree with an effective amount of a SDHI fungicide selected from the group consisting of penflufen , isopyrazam , bixafen , sedaxane , fluxapyroxad , fluopyram , penthiopyrad , boscalid , N-[1-(2 ,4-dichlohenyl)-1-methoxypropan-2-yl]-3-(difluoromethyl) -1-methyl-1H-pyrazole-4-carboxamide , N-[9-(dichloromethylene)-1 ,2 ,3 ,4-tetrahydro -1 ,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide , N-[(1S ,4R)-9-(dichlormethylen)-1 ,2 ,3 ,4-tetrahydro-1 ,4-methanonaphthalen-5-yl]-3-(difluorinethyl)-1-methyl-1H-pyrazol-4-carboxamide , and N-[1R ,4S) -9-(dichlormethylen)-1 ,2 ,3 ,4-tetrahydro-1 ,4-methanonaphthalen-5-yl]-3 (difluormethyl)-1-methyl-1H-pyrazol-4-carboxamide , and an adjuvant.2. The method of wherein the adjuvant is a surfactant.3. The method of wherein the effective amount of SDHI fungicide is from about from about 0.0001 to about 1 gram per centimeter of the trunk diameter at breast height.4. The method of wherein the effective amount of SDHI fungicide is from about 0.001 to about 0.01 grams per centimeter of the trunk diameter at breast height.5. The method of wherein the tree is selected from the group consisting of apple claim 1 , almond claim 1 , pear claim 1 , plum claim 1 , apricot claim 1 , peach claim 1 , nectarine claim 1 , cherry claim 1 , coconut claim 1 , palm claim 1 , olive claim 1 , fig claim 1 , banana claim 1 , cashew claim 1 , walnut claim 1 , pecan claim 1 , persimmon claim 1 , pomegranate claim 1 , avocado claim 1 , mango claim 1 , papaya claim 1 , pistachio claim 1 , citrus.6. The method of wherein the tree is sprayed when the tree is dormant.7. The method of wherein the tree is ...

METHODS FOR APPLE SCAB CONTROL

The present invention relates to methods for controlling apple scab caused by comprising spraying the bark of an apple tree with an effective amount of 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide and a surfactant. 1Venturia inaequalis. A method of controlling apple scab caused by comprising spraying the bark of an apple tree with an effective amount of 3-(difluoromethyl)-1-methyl-N-[(3R)-1 ,1 ,3-trimethyl-2 ,3-dihydroinden-4-yl]pyrazole-4-carboxamide and a surfactant.2. The method of wherein the effective amount of 3-(difluoromethyl)-1-methyl-N-[(3R)-1 claim 1 ,1 claim 1 ,3-trimethyl-2 claim 1 ,3-dihydroinden-4-yl]pyrazole-4-carboxamide is from about 0.0001 to about 1 gram of 3-(difluoromethyl)-1-methyl-N-[(3R)-1 claim 1 ,1 claim 1 ,3-trimethyl-2 claim 1 ,3-dihydroinden-4-yl]pyrazole-4-carboxamide per centimeter of the trunk diameter at breast height.3. The method of wherein the effective amount of 3-(difluoromethyl)-1-methyl-N-[(3R)-1 claim 2 ,1 claim 2 ,3-trimethyl-2 claim 2 ,3-dihydroinden-4-yl]pyrazole-4-carboxamide is from about 0.001 to about 0.01 grams of 3-(difluoromethyl)-1-methyl-N-[(3R)-1 claim 2 ,1 claim 2 ,3-trimethyl-2 claim 2 ,3-dihydroinden-4-yl]pyrazole-4-carboxamide per centimeter of the trunk diameter at breast height.4. The method of wherein the apple tree is selected from the group consisting of braeburn claim 1 , cameo claim 1 , cortland claim 1 , crabapple claim 1 , empire claim 1 , Fuji claim 1 , gala claim 1 , ginger gold claim 1 , golden delicious claim 1 , granny smith claim 1 , honeycrisp claim 1 , idared claim 1 , jonagold claim 1 , jonathan claim 1 , McIntosh claim 1 , mutsu claim 1 , nittany claim 1 , pink lady claim 1 , rome claim 1 , red delicious claim 1 , stayman claim 1 , winesap claim 1 , and york.5. The method of wherein the tree is sprayed when the tree is dormant.6. The method of wherein the tree is sprayed on the lower 150 centimeters of the trunk.7. The method of wherein ...

COMPOSITIONS FOR POWDERY MILDEW CONTROL AND METHODS OF THEIR USE

The present invention relates to compositions and methods for controlling apple powdery mildew comprising treating an apple tree with a silicone containing surfactant and 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide. 1. A method of controlling apple powdery mildew comprising applying an effective amount of a silicone containing surfactant and 3-(difluoromethyl)-1-methyl-N-[(3R)-1 ,1 ,3-trimethyl-2 ,3-dihydroinden-4-yl]pyrazole-4-carboxamide to an apple tree.2. The method of wherein the effective amount of 3-(difluoromethyl)-1-methyl-N-[(3R)-1 claim 1 ,1 claim 1 ,3-trimethyl-2 claim 1 ,3-dihydroinden-4-yl]pyrazole-4-carboxamide is from about 0.0001 to about 1 claim 1 ,000 grams per hectare.3. The method of wherein the effective amount of 3-(difluoromethyl)-1-methyl-N-[(3R)-1 claim 2 ,1 claim 2 ,3-trimethyl-2 claim 2 ,3-dihydroinden-4-yl]pyrazole-4-carboxamide is from about 0.001 to about 250 grams per hectare.4. The method of wherein the silicone containing surfactant is selected from the group consisting of: a mixture of 3-(3-hydroxypropyl)-heptamethyltrisiloxane-ethoxylated acetate claim 1 , polyethylene glycol monallyl acetate and polyethylene glycol diacetate; modified poly trisiloxanes; polyalkyleneoxide modified heptamethyltrisiloxanes; a mixture of silicone-polyether copolymers claim 1 , propylene glycol claim 1 , and dimethylpolysiloxane; alcohol ethoxylates; polyether-polymethylsiloxane-copolymer and polyether; and combinations thereof.5. The method of wherein the silicone containing surfactant is a mixture of 3-(3-hydroxypropyl)-heptamethyltrisiloxane-ethoxylated acetate claim 4 , polyethylene glycol monallyl acetate and polyethylene glycol diacetate.6. The method of wherein the amount of silicone containing surfactant is from about 100 to about 1 claim 1 ,000 milliliters per hectare.7. The method of wherein the amount of silicone containing surfactant is from about 250 to about 750 milliliters per hectare ...

USE OF QUINOLINE DERIVATIVES FOR IMPROVING PLANT YIELD

Compounds (A) can be used for increasing the yield of useful plants or crop plants with respect to their harvested plant organs, wherein the Compound (A) is selected from compounds of the formula (I) and hydrates or salts thereof, 2. The compound as claimed in claim 1 , wherein Compound (A) is 1-methylhexyl (5-chloro-8-quinolinoxy)acetate (“cloquintocet-mexyl”).3. The compound as claimed in claim 1 , that is capable of increasing grain yield of crop plants selected from group consisting of cereals claim 1 , canola claim 1 , soybean and cotton crops.4. The compound as claimed in claim 1 , that is capable of increasing grain yield of crop plants selected from group consisting of wheat claim 1 , barley claim 1 , rye or triticale plants.5. The compound as claimed in claim 1 , that is capable of increasing gluten content of seed kernels of crop plants selected from group consisting of cereals claim 1 , canola and soybean crops.6. The compound as claimed in claim 1 , that is capable of increasing gluten content of seed kernels of crop plants selected from group consisting of cereal crops.7. The compound as claimed in claim 1 , that is capable of increasing protein content of seed kernels of crop plants selected from group consisting of cereals claim 1 , canola and soybean crops.8. The compound as claimed in claim 1 , that is capable of increasing yield of the amount by weight of beets of beet plants.9. The compound as claimed in claim 1 , that is capable of increasing sugar content of sugar plants.10. The compound as claimed in claim 1 , that is capable of increasing germination and emergence of cereal crops.11. The compound as claimed in claim 1 , that is capable of increasing biomass yield of maize plants growing in absence of extraordinary environmental conditions.12. The compound as claimed in claim 1 , that is capable of increasing biomass yield of sugar plants.13. A method for increasing yield of useful plants and/or crop plants with respect to their harvested plant ...

SUBSTITUTED IMIDAZOLE AND (1,2,4)TRIAZOLE COMPOUNDS AS FUNGICIDES

The present invention relates to compounds of the formula I 114-. (canceled)16: The compound of claim 15 , wherein A is N.17: The compound of claim 15 , wherein A is CH.18: The compound of claim 15 , wherein D is SR.19: The compound of claim 15 , wherein D is halogen.20: The compound of claim 17 , wherein D is H.21: The compound of claim 20 , wherein Ris selected from halogen claim 20 , OH claim 20 , CN claim 20 , nitro claim 20 , C-C-cycloalkyl and C-C-halocycloalkyl claim 20 , n+m is 1 claim 20 , 2 claim 20 , 3 claim 20 , 4 claim 20 , 5 claim 20 , 6 claim 20 , 7 claim 20 , 8 or 9 and for n=0 and m=1 claim 20 , Ris not 4-Cl claim 20 , 4-F or 4-Br claim 20 , and for n=1 with R=2-Cl and m=1 claim 20 , Ris not 4-Cl.22: The compound of claim 21 , wherein n is 1 claim 21 , 2 claim 21 , 3 or 4 and m is 1 claim 21 , 2 claim 21 , 3 claim 21 , 4 or 5 with the said proviso.23: The compound I of claim 15 , wherein D is SH claim 15 , A is N claim 15 , Ris H claim 15 , Ris CH claim 15 , (R)is 4-Cl and (R)is 2-Cl or 2-CF; the compounds I wherein D is SH claim 15 , A is N claim 15 , Ris H claim 15 , Ris CH(CH) claim 15 , (R)is 4-Cl and (R)is 2-Cl or 2-CF; the compounds I wherein D is SH claim 15 , A is N claim 15 , Ris H claim 15 , Ris cyclopropyl claim 15 , (R)is 4-Cl and (R)is 2-Cl or 2-CF; the compound I wherein D is SH claim 15 , A is N claim 15 , Ris H claim 15 , Ris C═CCH claim 15 , (R)is 4-Cl and (R)is 2-Cl; and the compound I wherein D is SH claim 15 , A is N claim 15 , Ris CH claim 15 , Ris CH claim 15 , (R)is 4-Cl and (R)is 2-CF.24: A composition comprising one compound of formula I claim 15 , as defined in claim 15 , an N-oxide or an agriculturally acceptable salt thereof.25: The composition according to claim 24 , comprising additionally a further active substance.26: A method for combating harmful fungi claim 24 , comprising treating the fungi or the materials claim 24 , plants claim 24 , the soil or seeds to be protected against fungal attack with an effective ...

NOVEL HALOGEN-SUBSTITUTED COMPOUNDS

The invention relates inter alia to halogen-substituted compounds of the general formula (I) 7. A compound of formula (I) capable of being used for controlling insects , arachnids and nematodes.8. Pharmaceutical composition comprising at least one compound according to .9. Compound according to that comprises a medicament.10. A compound according to capable of being used for preparing a pharmaceutical composition for controlling parasites on animals.11. Process for preparing crop protection compositions comprising mixing a compound according to and one or more customary extenders and/or surfactants.12. Method for controlling pests claim 1 , comprising allowing a compound according to to act on the pests and/or a habitat thereof.13. A compound according to capable of being used for protecting propagation material of a plant. The present application relates to novel halogen-substituted compounds, to processes for their preparation and to their use for controlling animal pests, in particular arthropods and especially insects, arachnids and nematodes.It is known that certain halogen-substituted compounds have herbicidal action (cf. J. Org. Chem. 1997, 62(17), 5908-5919, J. Heterocycl. Chem. 1998, 35(6), 1493-1499, WO 2004/035545, WO 2004/106324, US 2006/069132, WO 2008/029084).Furthermore, it is known that certain halogen-substituted compounds are insecticidally active (EP1911751, WO2012-069366, WO2012-080376 & WO2012-107434).In addition, it is known that certain halogen-substituted compounds have FAAH-inhibitory activities (WO 2009/151991).Modern crop protection compositions have to meet many demands, for example in relation to efficacy, persistence and spectrum of their action and possible use. Questions of toxicity, the combinability with other active compounds or formulation auxiliaries play a role, as well as the question of the expense that the synthesis of an active compound requires. Furthermore, resistances may occur. For all these reasons, the search for novel ...

PLANT DISEASE CONTROL COMPOSITION AND PLANT DISEASE CONTROL METHOD

The present invention provides a plant disease control composition that has excellent plant disease controlling effects and that contains a carboxamide compound represented by formula (1) and an azole compound represented by formula (2) [wherein Rrepresents a C1-6 alkyl group, Rrepresents a hydrogen atom or the like, A represents a nitrogen atom or the like, Yrepresents a halogen atom, and n represents 0 or 1]. The present invention also provides a plant disease control method that includes a step for treating a plant or the soil in which a plant is being cultivated with an effective dose of the carboxamide compound represented by formula (1) and of the azole compound represented by formula (2). 3. The composition for controlling a plant disease according to wherein the compound represented by the formula (2a) is the compound wherein Yrepresents a chlorine atom in the formula (2a).4. The composition for controlling a plant described in wherein a weight ratio of the compound represented by the formula (1) to the compound represented by the formula (2) is 1:0.0125 to 1:500.6. The method for controlling a plant disease according to wherein the step of application to a plant or a soil for cultivating the plant is a step of application to a seed. This application claims priority to and the benefit of Japanese Patent Application Nos. 2015-158974 filed on Aug. 11, 2015 and 2015-253223 filed on Dec. 25, 2015, the entire contents of which are incorporated herein by reference.The present invention relates to a composition for controlling plant diseases and a method for controlling plant diseases.Hitherto, some compounds have been known as active ingredient for a composition for controlling plant diseases (see Patent Documents 1 and 2).Patent Document 1: WO 2011/162397 pamphletPatent Document 2: WO 2012/169516 pamphletAn object of the present invention is to provide a composition for controlling plant diseases and a method for controlling plant diseases, each having an ...

PESTICIDALLY ACTIVE PYRAZOLE DERIVATIVES

Compounds of formula (I) as defined herein, to processes for preparing them, to pesticidal, in particular insecticidal, acaricidal, molluscicidal and nematicidal compositions comprising them and to methods of using them to combat and control pests such as insect, acarine, mollusc and nematode pests. 10. A pesticidal composition claim 1 , which comprises at least one compound according to claim 1 , or an agrochemically acceptable salt or N-oxide thereof claim 1 , as active ingredient and at least one auxiliary.11. The composition according to claim 10 , which further comprises one or more other insecticidally claim 10 , acaricidally claim 10 , nematicidally and/or fungicidally active agents.12. A method for controlling pests claim 10 , which comprises applying a composition according to to the pests or their environment with the exception of a method for treatment of the human or animal body by surgery or therapy and diagnostic methods practised on the human or animal body.13. A method for the protection of plant propagation material from the attack by pests claim 10 , which comprises treating the propagation material or the site claim 10 , where the propagation material is planted claim 10 , with a composition according to .14. A coated plant propagation material claim 1 , wherein the coating of the plant propagation material comprises a compound as defined in . The present invention relates to pyrazole derivativees, to processes for preparing them, to intermediates for preparing them, to pesticidal, in particular insecticidal, acaricidal, molluscicidal and nematicidal compositions comprising those derivatives and to methods of using them to combat and control pests such as insect, acarine, mollusc and nematode pests.It has now surprisingly been found that certain pyrazole derivatives have highly potent insecticidal properties. Other compounds in this area are known from WO2014/122083, WO2012/107434, WO2015/067646, WO2015/067647, WO2015/067648, WO2015/150442, WO2015 ...

Carbonates of alcohol alkoxylates as adjuvants for crop protection

The present invention relates to an agrochemical composition comprising a pesticide and an alkoxylate of the formula (I) as defined below. The invention further relates to said alkoxylate. The invention further relates to a method of preparing said composition by bringing the alkoxylate and the pesticide into contact. Finally, the invention relates to a method of controlling phytopathogenic fungi and/or undesired plant growth and/or undesired insect or mite attack and/or for regulating the growth of plants, wherein said composition is allowed to act on the respective pests, their environment or the crop plants to be protected from the respective pest, on the soil and/or on undesired plants and/or on the crop plants and/or on their environment; and to seed containing said composition.

FUNGICIDAL COMBINATIONS

A combination comprising a multi-site contact fungicide, a succinate dehydrogenase inhibitor fungicide and a second systemic fungicide and a method using the same. 1. A fungicidal combination comprising at least one multi-site contact fungicide , a first systemic fungicide; and a second systemic fungicide; wherein:the multi-site contact fungicide is sulfur;the first systemic fungicide is a succinate dehydrogenase inhibitor; andthe second systemic fungicide is selected from an ergosterol biosynthesis inhibitor, a quinone outside inhibitor, and a respiration process inhibitor fungicide.2. The fungicidal combination as claimed in claim 1 , wherein the succinate dehydrogenase inhibitor is selected from the group consisting of benodanil claim 1 , flutolanil claim 1 , mepronil claim 1 , fluopyram claim 1 , fenfuram claim 1 , carboxin claim 1 , oxycarboxin claim 1 , thifluzamide claim 1 , bixafen claim 1 , fluxapyroxad claim 1 , furametpyr claim 1 , isopyrazam claim 1 , penflufen claim 1 , penthiopyrad claim 1 , sedaxane and boscalid.3. The fungicidal combination as claimed in claim 1 , wherein the(i) the quinone outside inhibitor is selected from fenamidone, famoxadone, azoxystrobin, mandestrobin, coumoxystrobin, enoxastrobin, flufenoxystrobin, pyraoxystrobin, dimoxystrobin, enestrobin, fluoxastrobin, kresoxim-methyl, metominostrobin, orysastrobin, picoxystrobin, pyrametostrobin, triclopyricarb, fenaminstrobin, pyraclostrobin and trifloxystrobin;(ii) the ergosterol biosynthesis inhibitor is selected from triflumizole, triforine, pyridinitrile, pyrifenox, fenarimol, nuarimol, triarimol, climbazole, clotrimazole, imazalil, oxpoconazole, prochloraz, prochloraz-manganese, triflumizole, azaconazole, bitertanol, bromuconazole, cyproconazole, diclobutrazol, difenoconazole, diniconazole, diniconazole-M, epoxiconazole, etaconazole, fenbuconazole, fluotrimazole, fluquinconazole, flusilazole, flutriafol, furconazole, furconazole-cis, hexaconazole, imibenconazole, ipconazole, ...

PARAFFINIC OIL-IN-WATER EMULSIONS FOR CONTROLLING INFECTION OF CROP PLANTS BY FUNGAL PATHOGENS

This disclosure features fungicidal combinations that include a paraffinic oil and an emulsifier. The combinations can further include one or more of the following: pigments, silicone surfactants, anti-settling agents, conventional fungicides such as demethylation inhibitors (DMI) and quinone outside inhibitors (Qol) and water. The fungicidal combinations are used for controlling infection of a crop plant by a fungal pathogen. 153.-. (canceled)54. A method of controlling infection of a crop plant by a fungal pathogen , the method comprising applying a fungicidal composition to the plant , wherein the fungicidal composition comprises a paraffinic oil-in-water emulsion , the paraffinic oil-in-water emulsion including a paraffinic oil and an emulsifier.55. The method of claim 54 , wherein the crop plant is wheat claim 54 , barley claim 54 , soybean claim 54 , or corn.56. The method of claim 54 , wherein the plant is monocotyledonous.57. The method of claim 56 , wherein the plant is of the order Poaceae.58Triticum, Secale, Hordeum, Oryza, ZeaElymus.. The method of claim 57 , wherein the plant is of the genus claim 57 , or59. The method of claim 54 , wherein the fungal pathogen is of the order Pucciniales.60Puccinia.. The method of claim 59 , wherein the fungal pathogen is of the genus61Puccinia graminis, Puccinia triticinaPuccinia sriiformis.. The method of claim 60 , wherein the fungal pathogen is of the species claim 60 , or62. (canceled)63. (canceled)64Bipolaris sorokiniana, Fusarium graminearumPyrenophora triticirepentis.. The method of claim 54 , wherein the fungal pathogen is selected from the group consisting of claim 54 , and -65. (canceled)66. (canceled)67. The method of claim 54 , wherein the plant is dicotyledonous.68. The method of claim 67 , wherein the plant is of the order Fabaceae.69. The method of claim 68 , wherein the plant is of the species Glycine max.70Phakopsora.. The method of claim 67 , wherein the fungal pathogen is of the genus71Phakopsora ...

Controlling charcoal rot with flutriafol

This invention relates to the use of flutriafol for controlling or preventing pathogenic damage caused by the fungi Macrophomina phaseolina in a plant propagation material, a plant, part of a plant and/or plant organ that grow or grows at a later point in time. The use comprises applying a composition of flutriafol on the plant, part of the plant, plant organ, plant propagation material or a surrounding area.

METALLOENZYME INHIBITOR COMPOUNDS

The present disclosure describes compounds having agricultural fungicidal activity. 2. The method of claim 1 , wherein Ris fluoro.3. The method of claim 1 , wherein Ris fluoro.4. The method of claim 1 , wherein Rand Rare fluoro.5. The method of claim 1 , wherein Ris phenyl optionally substituted with 0 claim 1 , 1 claim 1 , 2 or 3 independent R.6. The method of claim 1 , wherein Ris phenyl optionally substituted with 0 claim 1 , 1 claim 1 , 2 or 3 independent halo.7. The method of claim 1 , wherein Ris phenyl optionally substituted with 0 claim 1 , 1 claim 1 , 2 or 3 independent fluoro.8. The method of claim 1 , wherein Ris 2 claim 1 ,4-difluorophenyl.9. The method of claim 1 , wherein Ris H.10. The method of claim 1 , wherein Ris —P(O)(OH) claim 1 , —CH—O—P(O)(OH) claim 1 , or —C(O)alkyl optionally substituted with amino.11. The method of claim 1 , wherein:{'sub': '1', 'Ris fluoro;'}{'sub': '2', 'Ris fluoro;'}{'sub': '4', 'Ris 2,4-difluorophenyl; and'}{'sub': '5', 'Ris H.'}12. The method of claim 11 , wherein:{'sub': 3', '2', '7', '3', '7', '7', '8, 'each Ris independently H, alkyl, cycloalkyl, cyano, haloalkyl, alkoxy, halo, haloalkoxy, alkoxyalkyl, haloalkoxyalkyl, aryloxyalkyl, thioalkyl, hydroxyl, halothioalkyl, thiocyanate, S(O)R, nitro, C(═O)CF, C(═O)OR, C(═O)NRR, amino, cyclic amino (such as morpholino, pyrrolidino, piperidino, N-alkyl piperidino), and'}n is 1 or 2.13. The method of claim 11 , wherein:{'sub': 3', '2', '7', '3', '7', '7', '8, 'each Ris independently alkoxyalkyl, haloalkoxyalkyl, aryloxyalkyl, thioalkyl, hydroxyl, halothioalkyl, thiocyanate, S(O)R, nitro, C(═O)CF, C(═O)OR, C(═O)NRR, amino, cyclic amino (such as morpholino, pyrrolidino, piperidino, N-alkyl piperidino), and'}n is 1.14. The method of claim 1 , which is one of:4-(6-(2-(2,4-Difluorophenyl)-1,1-difluoro-2-hydroxy-3-(1H-tetrazol-1-yl)propyl) pyridin-3-yl)benzonitrile (1);2-(2,4-Difluorophenyl)-1,1-difluoro-3-(1H-tetrazol-1-yl)-1-(5-(4-(trifluoromethyl) phenyl)pyridin-2-yl)propan-2-ol ...

USE OF CYCLODEXTRINS AS AGROCHEMICAL DELIVERY SYSTEM

The present invention relates to the use of cyclodextrins for increasing biological activity and improving retention and/or bioavailability of agrochemicals such as pesticides. 1. A composition comprising an effective amount of (i) a pesticide selected from the group consisting of tau-fluvalinate , prothioconazole , and a mixture thereof , and (ii) cyclodextrin , wherein the pesticide molecules interact chemically with the cyclodextrin molecular matrix through intermolecular force (s).2. The composition of claim 1 , wherein the cyclodextrin is α (alpha)-cyclodextrin claim 1 , β (beta)-cyclodextrin claim 1 , or γ (gamma)-cyclodextrin.3. The composition of claim 1 , wherein the cyclodextrin is alkylated.4. The composition of claim 1 , wherein the cyclodextrin is a methyl-beta-cyclodextrin claim 1 , a hydroxypropyl-beta-cyclodextrin claim 1 , or a hydroxypropyl-gamma-cyclodextrin.7. The composition of claim 1 , wherein the pesticide has a log P value between 1 to 7.811-. (canceled)12. The composition of any one of - claim 1 , wherein:a the concentration of the cyclodextrin in the composition is between 0.1 to 20 g/kg,b. the concentration of the pesticide in the composition is between 0.1 to 20 g/kg,c. the amount of the cyclodextrin in the composition is 10-90% by weight based on the total weight of the composition, and/ord. the amount of the pesticide in the composition is 10-50% by weight based on the total weight of the composition.13. The composition of claim 1 , wherein:a the weight ratio between the pesticide and the cyciodextrin in the composition is from 1:5 to 1:1, and/orb) the molar ratio between the pesticide and the cyclodextrin in the composition is from 1:1 to 1:10.14. (canceled)15. The composition of claim 1 , wherein the pesticide molecules are complexed with or encapsulated within the cyclodextrin molecular matrix.16. The composition of claim 1 , wherein the composition further comprises an agriculturally acceptable carrier claim 1 , at least one ...

Method of controlling sudden death syndrome with flutriafol

This invention relates to the use of the compound flutriafol for protecting plants and plant propagation material from Sudden Death Syndrome. The use comprises applying a composition comprising flutriafol to the soil from which the plant propagation material, a plant, part of a plant and/or plant organ grow or grows at a later point in time.

Crystalline form of 4-amino-N-tert-butyl-4,5-dihydro-3-isopropyl-5-oxo-1,2,4-1H-triazole-1-carboxamide and a process for producing thereof

The invention provides a novel crystalline form of 4-amino-N-tert-butyl-4,5-dihydro-3-isopropyl-5-oxo-1,2,4-1H-triazole-1-carboxamide and a process for preparation of said crystalline form. The invention also relates to formulations and method for controlling weeds using said formulations. 2. The crystalline form as claimed in designated as Form C is further characterized by an X-ray powder diffractogram pattern having at least six of the following reflections values 6.8 claim 1 , 7.0 claim 1 , 7.6 claim 1 , 8.3 claim 1 , 11.2 claim 1 , 11.3 claim 1 , 12.4 claim 1 , 12.8 claim 1 , 15.6 claim 1 , 16.5 claim 1 , 16.6 claim 1 , 17.4 claim 1 , 17.5 claim 1 , 18.5 claim 1 , 19.6 claim 1 , 20.1 claim 1 , 23.5 claim 1 , 24.2 and 26.7 degrees 2θ (±0.2 degrees).3. A process for production of a crystalline form of 4-amino-N-tert-butyl-4 claim 1 ,5-dihydro-3-isopropyl-5-oxo-1 claim 1 ,2 claim 1 ,4-1H-triazole-1-carboxamide claim 1 , comprising:i) providing a solution of 4-amino-N-tert-butyl-4,5-dihydro-3-isopropyl-5-oxo-1,2,4-1H-triazole-1-carboxamide in an organic solvent;ii) effecting crystallisation by subjecting said solution to pre-determined crystallisation conditions thereby obtaining said crystalline form C.4. A process for the production of a crystalline form C of 4-amino-N-tert-butyl-4 claim 3 ,5-dihydro-3-isopropyl-5-oxo-1 claim 3 , 2 claim 3 ,4-1H-triazole-1-carboxamide as claimed in wherein said process comprisesi) providing a solution of 4-amino-N-tert-butyl-4,5-dihydro-3-isopropyl-5-oxo-1,2,4-1H-triazole-1-carboxamide in an organic solvent at a first temperature;ii) effecting crystallisation by subjecting the said solution to a second temperature at a pre-determined rate thereby obtaining said crystalline form C.5. The process as claimed in wherein said first temperature is in a range from about 30° to about 100° C.6. The process as claimed in wherein said second temperature is in a range from about −20° to about 30° C.7. The process as claimed in wherein said ...

METHOD OF TREATING FUNGAL INFECTIONS, FUNGICIDAL COMPOSITIONS AND THEIR USE

A fungicidal composition comprising a triazole fungicide and a micronutrient is provided. Further, there is provided a method of improving fungi control and reducing phytotoxicity caused by triazoles, comprising applying a triazole fungicide and micronutrients to the plant or a part thereof, or to surroundings thereof. The triazole fungicide is preferably tebuconazole. 1. A fungicidal composition comprising a triazole fungicide and a micronutrient.2. The composition according to claim 1 , wherein the triazole fungicide is selected from azaconazole claim 1 , bitertanol claim 1 , bromuconazole claim 1 , cyproconazole claim 1 , diclobutrazole claim 1 , difenoconazole claim 1 , diniconazole claim 1 , enilconazole claim 1 , epoxiconazole claim 1 , etaconazole claim 1 , fenbuconazole claim 1 , fluquinconazole claim 1 , flusilazole claim 1 , flutriafol claim 1 , hexaconazole claim 1 , imibenconazole claim 1 , ipconazole claim 1 , metconazole claim 1 , myclobutanil claim 1 , paclobutrazol claim 1 , penconazole claim 1 , propiconazole claim 1 , prothioconazole claim 1 , simeconazole claim 1 , tebuconazole claim 1 , tetraconazole claim 1 , triadimefon claim 1 , triadimenol claim 1 , triticonazole claim 1 , and mixtures thereof.3. The composition according to claim 2 , wherein the triazole fungicide is selected from tebuconazole claim 2 , epoxiconazole claim 2 , difenoconazole claim 2 , cyproconazole and hexaconazole.4. The composition according to claim 3 , wherein the triazole fungicide is tebuconazole.5. The composition according to claim 1 , wherein the micronutrient comprises a salt comprising a cation of a Group I metal claim 1 , a Group II metal claim 1 , a transition metal claim 1 , or an ammonium cation.6. The composition according to claim 5 , wherein the micronutrient comprises a salt comprising a cation of Na claim 5 , K claim 5 , Fe claim 5 , Mn claim 5 , Zn claim 5 , Cu claim 5 , or Mo.7. The composition according to claim 1 , wherein the micronutrient comprises ...

Fungicidal amides

Disclosed are compounds of Formula 1, including all stereoisomers, N-oxides, and salts thereof, wherein G is phenyl, pyridinyl, pyridazinyl or pyrazinyl substituted with Q meta or para to the —C(R 2a )R 2b — radical, and optionally substituted with up to 3 substituents selected from R 3 ; and A, Z, R 1 , R 2a , R 2b , R 3 and Q are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula 1 and methods for controlling plant disease caused by a fungal plant pathogen comprising applying an effective amount of a compound or a composition of the invention.

METHOD FOR THE CONTROL OF PLANT BACTERIAL DISEASES USING CARBOXAMIDE DERIVATIVES

The present invention relates to methods and to the uses of N-cyclo-propyl-N-[substituted-benzyl]-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide or thiocarboxamide derivatives of formula (I) in order to control bacterial plant pathogens and plant bacterial diseases. 2. The method according to claim 1 , wherein the compound A of formula (I) is selected from the group consisting of:N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(2-isopropylbenzyl)-1-methyl-1H-pyrazole-4-carboxamide (compound A1),N-cyclopropyl-N-(2-cyclopropylbenzyl)-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide (compound A2),N-(2-tert-butylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide (compound A3),N-(5-chloro-2-ethylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide (compound A4),N-(5-chloro-2-isopropylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide (compound A5),N-cyclopropyl-3-(difluoromethyl)-N-(2-ethyl-5-fluorobenzyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide (compound A6),N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(5-fluoro-2-isopropylbenzyl)-1-methyl-1H-pyrazole-4-carboxamide (compound A7),N-cyclopropyl-N-(2-cyclopropyl-5-fluorobenzyl)-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide (compound A8),N-(2-cyclopentyl-5-fluorobenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide (compound A9),N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(2-fluoro-6-isopropylbenzyl)-1-methyl-1H-pyrazole-4-carboxamide (compound A10),N-cyclopropyl-3-(difluoromethyl)-N-(2-ethyl-5-methylbenzyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide (compound A11),N-cyclopropyl-3-(difluoromethyl)-5-fluoro-N-(2-isopropyl-5-methylbenzyl)-1-methyl-1H-pyrazole-4-carboxamide (compound A12),N-cyclopropyl-N-(2-cyclopropyl-5-methylbenzyl)-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide (compound A13),N-(2-tert-butyl-5-methylbenzyl)-N- ...

FUNGICIDAL MIXTURES BASED ON TRIAZOLES

A fungicidal mixture, comprising 2. The synergistic fungicidal mixture of claim 1 , wherein the weight ratio of prothioconazole to fluquinconazole is from 20:1 to 1:20.3. The synergistic fungicidal composition of claim 1 , further comprising a solid or liquid carrier.4. A fungicidal kit for making a synergistic mixture of fungicides comprising claim 1 , in separate containers claim 1 , prothioconozole claim 1 , or salt or adduct thereof claim 1 , and fluquinconazole claim 1 , or salt or adduct thereof claim 1 , wherein the fungicidal kit contains each of said prothioconozole claim 1 , or salt or adduct thereof claim 1 , and fluquinconazole claim 1 , or salt or adduct thereof claim 1 , in amounts sufficient to produce a synergistic mixture when combined.6. The method of claim 5 , comprising applying said synergistic fungicidal mixture to said harmful fungi claim 5 , their habitat or the plants claim 5 , seeds claim 5 , soils claim 5 , areas claim 5 , materials or spaces to be kept free from said harmful fungi in an amount of from 0.01 to 8 kg/ha.7. The synergistic fungicidal mixture of claim 1 , wherein the prothioconazole and the fluquinconazole has a purity of at least 90%.8. The synergistic fungicidal mixture of claim 1 , wherein the weight ratio of prothioconazole to fluquinconazole is from 5:1 to 1:5.9. The method of claim 5 , wherein the prothioconazole and the fluquinconazole are applied simultaneously or successively.10. The method of claim 5 , comprising applying said synergistic fungicidal mixture to said harmful fungi claim 5 , their habitat or the plants claim 5 , seeds claim 5 , soils claim 5 , areas claim 5 , materials or spaces to be kept free from said harmful fungi claim 5 , wherein the fluquinconazole of formula II is applied in an amount of from 0.01 to 1 kg/ha.11. The method of claim 5 , wherein the synergistic mixture is applied to a plant claim 5 , a seed claim 5 , or a soil before or after sowing of the plants claim 5 , or before or after plant ...

METCONAZOLE-CONTAINING PESTICIDE COMPOSITION FOR PREVENTING AND CONTROLLING FUSARIUM HEAD BLIGHT AND APPLICATION THEREOF

It relates to a pesticide composition for preventing and controlling head blight, which contains 1 to 150 parts by weight of jinggangmycin and 1 to 20 parts by weight of metconazole per mu. The pesticide composition of the present invention has an obvious synergistic effect when used for preventing and controlling head blight, and can remarkably enhance the effect of preventing and controlling head blight, increasing the ability of the human being in preventing and controlling head blight of triticeae crops. 1fusarium. An application of a pesticide composition in preventing and controlling head blight , characterized in that the pesticide composition comprises jinggangmycin and metconazole according to a weight ratio of (1-150):(1-20).2. The application according to claim 1 , characterized in that the pesticide composition comprises jinggangmycin and metconazole according to a weight ratio of (30-100):(3-18).3. The application according to claim 1 , characterized in that the pesticide composition comprises jinggangmycin and metconazole according to a weight ratio of (50-65):(6-16).4. The application according to claim 1 , characterized in that the pesticide composition comprises a carrier and/or an adjuvant acceptable in pesticides claim 1 , and a mixture which is composed of jinggangmycin and metconazole according to a weight ratio of 1-150:1-20 accounts for 0.1 to 90.0 percent of the total weight of the pesticide composition.5. The application according to claim 4 , characterized in that the mixture which is composed of jinggangmycin and metconazole according to a weight ratio of 1-150:1-20 accounts for 10 to 75.0 percent of the total weight of the pesticide composition.6. The application according to claim 4 , characterized in that the mixture which is composed of jinggangmycin and metconazole according to a weight ratio of 1-150:1-20 accounts for 26.0 to 58.0 percent of the total weight of the pesticide composition.7. The application according to claim 4 , ...

HERBICIDAL COMPOSITIONS COMPRISING SULFENTRAZONE plus PROPYZAMIDE AND SULFENTRAZONE PLUS PROPYZAMIDE PLUS ETHALFLURALIN

Provided herein are herbicidal compositions containing (a) sulfentrazone and (b) propyzamide and (a) sulfentrazone and (b) propyzamide and (c) ethalfluralin. The compositions provide synergistic weed control of undesirable vegetation, e.g., in wheat, barley, oats, rye, sorghum, corn or maize, oilseed rape, mustard crops, soybeans, vegetables, pulse crops (e.g., common bean, field pea, chickpea, lentil and faba bean), pastures, grasslands, rangelands, fallow land, turf, tree and vine orchards, industrial vegetation management or rights-of-way. 3. The composition of claim 1 , wherein the weight ratio of the compound of formula (I) to the compound of formula (II) is within the range from about 1:18 to about 1:4.4. The composition of claim 2 , wherein the weight ratio of the compound of formula (I) to the compound of formula (II) to the compound of formula (III) is within the range from about 1:18:22 to about 1:4:5.54. The composition of any of - claims 1 , further comprising an agriculturally acceptable adjuvant or carrier.64. The composition of any of - claims 1 , which is synergistic as determined by the Colby equation.74. A method of controlling undesirable vegetation which comprises contacting the vegetation or the locus thereof with or applying to the soil to prevent the emergence or growth of vegetation the composition of any of -.10. The method of or claims 1 , wherein the undesirable vegetation is controlled in wheat claims 1 , barley claims 1 , oats claims 1 , rye claims 1 , sorghum claims 1 , corn claims 1 , maize claims 1 , pulse crops (e.g. claims 1 , common bean claims 1 , field pea claims 1 , chickpea claims 1 , lentil and faba bean) claims 1 , canola claims 1 , oilseed rape claims 1 , mustard crops claims 1 , soybeans claims 1 , pastures claims 1 , grasslands claims 1 , rangelands claims 1 , fallow land claims 1 , turf claims 1 , tree and vine orchards claims 1 , industrial vegetation management or rights-of-way.11. The method of or claims 1 , wherein ...

NOVEL T CELL RECEPTORS ANDIMMUNE THERAPY USING THE SAME

The present invention relates to novel compositions comprising certain pyrazolecarboxylic acid alkoxyamides according to formula (I) in combination with certain fungicides, to a process for preparing these compositions and to the use thereof as biologically active compositions, especially for the control of harmful microorganisms in plants and in the protection of materials and as plant growth regulators. 2. A composition according to wherein (A) is a compound according to formula (I) claim 1 , wherein Xrepresents a hydrogen atom claim 1 , Xrepresents a hydrogen atom and Xrepresents a chlorine atom.5. A composition according to and further comprising one or more auxiliaries claim 1 , solvents claim 1 , carriers claim 1 , surfactants and/or extenders.6. Method for controlling harmful microorganisms claim 1 , comprising applying a composition according to to the harmful microorganisms and/or a habitat thereof.7. A composition according to for control of harmful microorganisms.8. A composition according to as a plant growth regulator.9. Process for producing a composition for controlling harmful microorganisms claim 1 , comprising mixing a composition according to with one or more auxiliaries claim 1 , solvents claim 1 , carriers claim 1 , surfactants and/or extenders.10. A composition according to for treatment of transgenic plants.11. A composition according to for treatment of seed and of seed of transgenic plants.12. Seeds which have been treated and comprise a composition according to . The present invention relates to novel compositions, to a process for preparing these compositions and to the use thereof as biologically active compositions, especially for the control of harmful microorganisms in plantsIt is already known that certain pyrazolecarboxylic acid alkoxyamides can be used as fungicides (see WO-A 2010/063700).The production of these compounds is described in WO-A 2010/063700, in WO-A 2013127764 and in WO-A 2013/167651.Moreover, it is known that these ...

PESTICIDAL MIXTURES COMPRISING ISOXAZOLINE DERIVATIVES

The present invention relates to pesticidal mixtures comprising a component A and a component B, wherein component A is a compound of formula (I) wherein A, A, L, p, R, R, R, Rand Rare as defined in claim and component B is a fungicide. The present invention also relates to methods of using said mixtures for the control of plant pests. 2. A pesticidal mixture according to claim 1 , wherein Aand Aare C—H; Ris trifluoromethyl claim 1 , and Ris hydrogen.3. A pesticidal mixture according to claim 1 , wherein Aand Aare C—H; Ris trifluoromethyl claim 1 , Ris methyl claim 1 , Ris hydrogen claim 1 , each Ris chlorine claim 1 , p is 2.4. A pesticidal mixture according to claim 1 , wherein Ris independently hydrogen claim 1 , methyl claim 1 , ethyl claim 1 , propyl claim 1 , butyl claim 1 , cyclopropyl claim 1 , cyclopropyl-methyl claim 1 , cyclobutyl claim 1 , cyclobutyl-methyl claim 1 , oxetanyl claim 1 , thietanyl claim 1 , trifluoroethyl claim 1 , difluoroethyl claim 1 , allyl claim 1 , propargyl claim 1 , cyanomethyl claim 1 , cyanoethyl claim 1 , benzyl claim 1 , benzyl substituted by one to three R claim 1 , or Ris pyridyl-methyl- or pyridyl-methyl-substituted by one to three R claim 1 , and each Ris independently fluoro claim 1 , chloro claim 1 , bromo claim 1 , trifluoromethyl claim 1 , trifluoromethoxy claim 1 , cyano or methoxy.6. A pesticidal mixture according to claim 1 , wherein component B is a fungicide selected froma strobilurin fungicide including those selected from the group consisting of: Azoxystrobin, Dimoxystrobin, Enestrobin, Fluoxastrobin, Kresoxim-methyl, Metominostrobin, Orysastrobin, Picoxystrobin, Pyraclostrobin and Trifloxystrobin; oran azole fungicide including those selected from the group consisting of: Azaconazole, Bromuconazole, Cyproconazole, Difenoconazole, Diniconazole, Diniconazole-M, Epoxiconazole, Fenbuconazole, Fluquinconazole, Flusilazole, Flutriafol, Hexaconazole, Imazalil, Imibenconazole, Ipconazole, Metconazole, Myclobutanil, ...

Desiccant and Defoliant Composition for Crops

Provided is a safer and higher-performance desiccant and defoliant composition. The disclosed desiccant and defoliant composition comprises two or more different kinds selected from the group consisting of protoporphyrinogen oxidase-inhibiting herbicides as active ingredients. 1. A desiccant and defoliant composition comprising two or more different kinds selected from the group consisting of protoporphyrinogen oxidase-inhibiting herbicides as active ingredients.2. The desiccant and defoliant composition according to claim 1 , at least comprising pyraflufen-ethyl or an agriculturally acceptable salt or ester thereof as a first active ingredient; and one or more kinds of compounds selected from the group consisting of carfentrazone claim 1 , sulfentrazone claim 1 , flumioxazin claim 1 , fomesafen claim 1 , acifluorfen claim 1 , oxyfluorfen claim 1 , fluthiacet-methyl claim 1 , butafenacil claim 1 , saflufenacil and agriculturally acceptable salts or esters thereof as a second active ingredient.3. The desiccant and defoliant composition according to claim 1 , at least comprising carfentrazone or an agriculturally acceptable salt or ester thereof as a first active ingredient; and one or more kinds of compounds selected from the group consisting of sulfentrazone claim 1 , flumioxazin claim 1 , fomesafen claim 1 , acifluorfen claim 1 , oxyfluorfen claim 1 , fluthiacet-methyl claim 1 , butafenacil claim 1 , saflufenacil and agriculturally acceptable salts or esters thereof as a second active ingredient.4. The desiccant and defoliant composition according to claim 1 , at least comprising sulfentrazone or an agriculturally acceptable salt or ester thereof as a first active ingredient; and one or more kinds of compounds selected from the group consisting of flumioxazin claim 1 , fomesafen claim 1 , acifluorfen claim 1 , oxyfluorfen claim 1 , fluthiacet-methyl claim 1 , butafenacil claim 1 , saflufenacil and agriculturally acceptable salts or esters thereof as a second active ...

CHEMICALLY STABLE DISPERSIONS OF PROTHIOCONAZOLE AND PROCESSES FOR PREPARING THEM

Chemically stable aqueous dispersions of prothioconazole and processes for preparing them are provided. The dispersions comprise prothioconazole present in an aqueous medium, and a sulfur-containing compound present in an amount effective to render the dispersion chemically stable. 1. A process for preparing a chemically stable aqueous dispersion of prothioconazole , the process comprising:(a) introducing prothioconazole to an aqueous medium to yield an aqueous dispersion of prothioconazole; and(b) introducing a sulfur-containing compound to the aqueous dispersion in an amount effective to render the dispersion chemically stable.2. The process of claim 1 , wherein the prothioconazole is present in the aqueous dispersion in an amount of 0.05 to 2.0 percent by weight claim 1 , based on the total weight of the aqueous dispersion.3. The process of claim 1 , wherein the sulfur-containing compound is present in the aqueous dispersion in an amount up to 5 percent by weight claim 1 , based on the total weight of the aqueous dispersion.4. The process of claim 1 , wherein sulfur-containing compound comprises a sulfur-containing amino acid or peptide claim 1 , a sulfur-containing amido acid claim 1 , a sulfur-containing amino acid salt claim 1 , a sulfur-containing amino acid ester claim 1 , and/or derivatives thereof.5. The process of claim 4 , wherein the sulfur-containing compound comprises cysteine claim 4 , homocysteine claim 4 , a salt thereof claim 4 , a hydrate thereof claim 4 , an ester thereof claim 4 , and/or a substituted derivative thereof.6. The process of claim 4 , wherein the sulfur-containing compound comprises a mixture of two or more different sulfur-containing compounds having similar chemical structures.7. The process of claim 6 , wherein the different sulfur-containing compounds have similar functional groups.8. The process of claim 6 , wherein the sulfur-containing compound comprises a mixture of isomers.9. A chemically stable aqueous dispersion of ...

METHODS AND COMPOSITIONS FOR HERBICIDE TOLERANCE IN PLANTS

The invention relates to biotechnology and provides novel recombinant DNA molecules and engineered proteins for conferring tolerance to protoporphyrinogen oxidase-inhibitor herbicides. The invention also provides herbicide tolerant transgenic plants, seeds, cells, and plant parts containing the recombinant DNA molecules, as well as methods of using the same. 1. A recombinant DNA molecule comprising a heterologous promoter operably linked to a nucleic acid molecule encoding a protein that has at least 85% sequence identity to amino acid sequence selected from the group consisting of: SEQ ID NOs:1-2 and SEQ ID NOs:6-12 , wherein the protein has herbicide-insensitive protoporphyrinogen oxidase activity.2. The recombinant DNA molecule of claim 1 , wherein the nucleic acid molecule comprises a sequence selected from the group consisting of SEQ ID NOs:26-27 claim 1 , 31-32 claim 1 , 36-46 claim 1 , and 47-48.3. The recombinant DNA molecule of claim 1 , wherein the protein comprises a sequence selected from the group consisting of SEQ ID NOs:1-2 and SEQ ID NOs:6-12.4. The recombinant DNA molecule of claim 1 , wherein the heterologous promoter is functional in a plant cell.5. The recombinant DNA molecule of claim 4 , wherein the nucleic acid molecule is operably linked to a DNA molecule encoding a targeting sequence that functions to localize an operably linked protein within a cell.6. A DNA construct comprising the recombinant DNA molecule of .7. The DNA construct of claim 6 , wherein the recombinant DNA molecule further comprises an operably linked DNA molecule encoding a targeting sequence that functions to localize the protein within a cell.8. The DNA construct of claim 7 , wherein the protein confers PPO herbicide tolerance to said cell.9. The DNA construct of claim 6 , wherein the DNA construct is present in the genome of a transgenic plant claim 6 , seed claim 6 , or cell.10. A recombinant polypeptide that comprises at least 85% sequence identity to the full length ...

METALAXYL AND PROTHIOCONAZOLE COCRYSTALS AND METHODS OF MAKING AND USING

The invention relates to co-crystals of metalaxyl and prothioconazole, to methods of making them, to compositions containing them and to the methods of using said co-crystals and said compositions to treat crops and plants. 1. A cocrystal comprising prothioconazole and metalaxyl.2. The cocrystal of claim 1 , wherein said cocrystal has a melting point of about 100.8° when measured with a Differential Scanning calorimeter.3. The cocrystal of claim 1 , wherein said cocrystal has a water solubility less than the water solubility of metalaxyl alone.4. The cocrystal of claim 1 , wherein the diameter of said cocrystal is about 0.1 μm to about 100 μm.5. The cocrystal of claim 1 , wherein said cocrystal exhibits the Differential Scanning calorimeter profile of when crystallized from butyrolactone.6. The cocrystal of claim 1 , wherein said cocrystal exhibits the Differential Scanning calorimeter profile of when crystallized from acetone.7. A method of making a cocrystal comprising(a) dissolving metalaxyl and prothioconazole in a solvent; and(b) crystallizing the dissolved metalaxyl and prothioconazole.8. The method of claim 7 , wherein the dissolved metalaxyl and prothioconazole is crystallized in step (b) by the addition of water.9. The method of claim 7 , wherein the dissolved metalaxyl and prothioconazole is crystallized in step (b) by freezing.10. The method of claim 7 , wherein the dissolved metalaxyl and prothioconazole is crystallized in step (b) by seeding a solution with preformed metalaxyl and prothioconazole cocrystals.11. The method of claim 7 , wherein said cocrystal has a melting point at about 100.8° when measured with a Differential Scanning calorimeter.12. The method of claim 7 , wherein said cocrystal has a water solubility less than the water solubility of metalaxyl alone.13. A method of reducing damage or infestation to a crop caused by weeds claim 7 , fungi claim 7 , or pests by applying a cocrystal comprising a combination prothioconazole and metalaxyl ...

FUNGICIDAL ALKYL- AND ARYL-SUBSTITUTED 2-[2-CHLORO-4-(DIHALO-PHENOXY)-PHENYL]-1-[1,2,4]TRIAZOL-1-YL-ETHANOL COMPOUNDS

The present invention relates to alkyl- and aryl-substituted 2-[2-chloro-4-(dihalo-phenoxy)-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds of formula I as defined in the description, and the N-oxides, and salts thereof, processes and intermediates for preparing these compounds and also to compositions comprising at least one such compound. The invention also relates to the use of such compounds and compositions for combating harmful fungi and seed coated with at least one such compound. 115-. (canceled)17. The compound according to claim 16 , wherein Xand Xare independently of each other selected from F and Cl.18. The compound according to claim 16 , wherein Xis hydrogen claim 16 , F or Cl.19. The compound according to claim 16 , wherein Ris hydrogen claim 16 , C-C-alkyl claim 16 , allyl claim 16 , C-C-alkynyl claim 16 , cyclopropyl claim 16 , cyclopropylmethyl claim 16 , phenyl claim 16 , benzyl claim 16 , phenylethenyl or phenylethynyl.20. The compound according to claim 16 , wherein Ris hydrogen.21. The compound of claim 16 , wherein the substituents have the following meanings:{'sup': 3', '1', '2', '2', '1, 'sub': '3', 'Xis hydrogen, Xand Xare Cl, Ris H and Ris CH;'}{'sup': 3', '1', '2', '2', '1, 'sub': '3', 'Xis hydrogen, Xand Xare Cl, Rand Rare CH;'}{'sup': 3', '1', '2', '2', '1, 'Xis hydrogen, Xand Xare Cl, Rand Rare H;'}{'sup': 3', '1', '2', '2', '1, 'sub': '3', 'Xis hydrogen, Xand Xare Cl, Ris CHand Ris H; and'}{'sup': 3', '1', '2', '2', '1, 'sub': '3', 'Xis hydrogen, Xand Xare F, Ris H and Ris CH.'}27. An agrochemical composition comprising an auxiliary and at least one compound of formula I claim 16 , as defined in claim 16 , an N-oxide or an agriculturally acceptable salt thereof.28. The compositions according to claim 27 , comprising additionally a further active substance.29. A method for combating phytopathogenic fungi comprising contacting the fungi claim 16 , or their food supply claim 16 , habitat or breeding grounds with a compound of .30. The ...

Composition comprising a pesticide and a hydroxyalkyl polyoxylene glycol ether

A composition having a pesticide and a hydroxyalkyl polyoxylene glycol ether of the general formula (I) where R 1 is a saturated or unsaturated, linear or branched alkyl having 6 to 18 carbon atoms; R 2 is ethylene, propylene, butylene or a mixture thereof; R 3 is a saturated or unsaturated, linear or branched alkyl having 6 to 18 carbon atoms; and n has a value of from 1 to 100. The composition may be used as an adjuvant in in pesticide-comprising spray mixtures. In a method for controlling phytopathogenic fungi and/or undesirable plant growth and/or undesirable insect or mite infestation and/or for regulating the growth of plants, the composition is allowed to act on the respective pests, the habitat thereof or the plants to be protected from the respective pest, on the soil and/or on undesirable plants and/or the crop plants and/or the habitat thereof. Seed may also include the composition.

ASYMMETRIC FORMALES AND ACETALES AS ADJUVANTS FOR CROP PROTECTION

The present invention relates to an agrochemical composition comprising a pesticide and an alkoxylate of the formula (I) 117.-. (canceled)19. The composition according to claim 18 , wherein Ris a linear or branched claim 18 , saturated or unsaturated C-Calkyl.20. The composition according to claim 18 , wherein m is 1 to 3.21. The composition according to claim 18 , wherein n is 1.5 to 30.22. The composition according to claim 18 , wherein Ris a linear or branched claim 18 , saturated or unsaturated C-Calkyl.23. The composition according to claim 18 , wherein AO is ethylenoxy claim 18 , or a mixture of ethyleneoxy and propyleneoxy.24. The composition according to claim 18 , wherein Rand Rare independently from another H or methyl.25. The composition according to claim 18 , wherein the ratio of n to m is from 30/1 to 1/1.26. The composition according to claim 18 , wherein{'sup': '1', 'sub': 8', '20, 'Ris a linear or branched, saturated or unsaturated C-Calkyl,'}{'sup': '2', 'sub': 1', '8, 'Ris a linear or branched, saturated or unsaturated C-Calkyl'}{'sup': 3', '4, 'sub': 1', '4, 'Rand Rare H or C-Calkyl,'}AO is ethyleneoxy, or a mixture of ethyleneoxy and propyleneoxy,n is from 2 to 80, andm is from 1 to 3.27. A method of preparing the composition according to claim 18 , by bringing the pesticide and the alkoxylate of the formula (I) into contact.28. An alkoxylate of the formula (I) as defined in claim 18 , where Ris a saturated and branched Calkyl claim 18 , or a mixture thereof claim 18 , and Ris C-Calkyl claim 18 , Rand Rare H or C-Calkyl claim 18 , AO is ethyleneoxy claim 18 , or ethyleneoxy and propyleneoxy claim 18 , n is from 2 to 80 claim 18 , and m is from 1 to 3.29. The alkoxylate of claim 28 , where Ris C-Calkyl.30. The alkoxylate of claim 28 , where n has a value from 3 and 5.31. An alkoxylate of the formula (I) as defined in claim 18 , where Ris 2-propylheptyl.32. The alkoxylate of claim 31 , where Ris C-Calkyl claim 31 , Rand Rare H or C-Calkyl claim 31 ...

Emulsifiable concentrate comprising pesticide, fatty amide and lactamide

Subject matter of the present invention is an emulsifiable concentrate comprising a water-insoluble pesticide, an amide of the formula (I) as defined herein, and a lactamide of the formula (II) as defined herein. The invention further relates to a process for the preparation of said concentrate; an emulsion obtainable by mixing water, a water-insoluble pesticide, the amide of the formula (I) and the lactamide of the formula (II); and to a method for controlling phytopathogenic fungi and/or undesired vegetation and/or undesired attack by insects or mites and/or for regulating the growth of plants, where the concentrate or the emulsion is allowed to act on the respective pests, their environment or on the crop plants to be protected from the respective pests, on the soil and/or on undesired plants and/or on the crop plants and/or their environment.

METHODS OF APPLYING ONE OR MORE CERTAIN HETEROARYL-1,2,4-TRIAZOLE AND HETEROARYL-TETRAZOLE COMPOUNDS TO CONTROL DAMAGE ON PLANTS, PROPAGATION MATERIAL THEREOF, AND PLANT DERIVED PRODUCTS

Novel methods of applying certain heteroaryl-1,2,4-triazole and heteroaryl-tetrazole compounds, and to their use in the control of certain pests found in plants, plant propagation material thereof and plant derived products, wherein the heteroaryl-1,2,4-triazole and heteroaryl-tetrazole compound is of the formula (I) as defined in claim . 2. The method according to claim 1 , wherein Y is a direct bond in the compound.3. The method according to claim 1 , wherein X is O in the compound.4. The method according to claim 1 , wherein Ris methyl in the compound.5. The method according to claim 1 , wherein Qis N claim 1 , Qis CRand Ris H claim 1 , methyl claim 1 , or (CHCHO)CH— in the compound.6. The method according to claim 1 , wherein Ris 2-pyridine claim 1 , or 2-pyrimidine optionally substituted by C-Calkoxy in the compound.7. The method according to claim 6 , wherein Ris 2-pyrimidine in the compound.8. The method according to claim 1 , wherein Ris cyclopropyl-CH— claim 1 , n-propyl claim 1 , CFCHCH— claim 1 , FCHCH— claim 1 , FCHCHCH— claim 1 , 2 claim 1 ,2-difluorocyclopropyl-CH— claim 1 , 2 claim 1 ,2-dichlorocyclopropyl-CH— claim 1 , H claim 1 , CH claim 1 , (CH)SiCH— claim 1 , CHCH— claim 1 , or CNCH— in the compound.9. The method according to claim 8 , wherein Ris cyclopropyl-CH— claim 8 , CH≡CCH— claim 8 , H claim 8 , or CHin the compound.10. The method according to claim 1 , wherein Ris 3 claim 1 ,5-bis(trifluoromethyl)phenyl claim 1 , 3 claim 1 ,5-dichlorophenyl claim 1 , 3-trifluoromethoxyphenyl claim 1 , 3-chloro-5-trifluoromethylphenyl claim 1 , 3-cyanophenyl claim 1 , 3-chloro-5-trifluoromethoxyphenyl claim 1 , 5-trifluoromethylpyridin-3-yl claim 1 , 3-bromo-5-trifluoromethylphenyl claim 1 , 3-cyano-5-trifluoromethyl phenyl or 2 claim 1 ,6-bis(trifluoromethyl)pyridin-4-yl in the compound.11. The method according to claim 10 , wherein Ris 3 claim 10 ,5-bis(trifluoromethyl)phenyl.12. The method according to claim 1 , wherein the compound or salt thereof is ...

BIOCIDAL-FUNCTIONALIZED CORROSION INHIBITORS

In one aspect, the disclosure is directed to a biocidal-functionalized corrosion inhibitor. The biocidal-functionalized corrosion inhibitor includes a biocidal group linked to a corrosion inhibitor group. The corrosion inhibitor group includes a triazole ring for copper (Cu) corrosion inhibition. In another aspect, the disclosure is directed to a process of forming a biocidal-functionalized corrosion inhibiting small molecule. In yet another aspect, the disclosure is directed to a process of forming a biocidal-functionalized corrosion inhibiting polymeric material. 1. A biocidal-functionalized corrosion inhibitor that includes a biocidal group linked to a corrosion inhibitor group , the corrosion inhibitor group including a triazole ring for copper (Cu) corrosion inhibition.2. The biocidal-functionalized corrosion inhibitor of claim 1 , wherein the corrosion inhibitor group includes a 1H-1 claim 1 ,2 claim 1 ,3-Triazole or a 1H-1 claim 1 ,2 claim 1 ,3-Triazole derivative.3. The biocidal-functionalized corrosion inhibitor of claim 2 , wherein the 1H-1 claim 2 ,2 claim 2 ,3-Triazole derivative includes a 1H-1 claim 2 ,2 claim 2 ,3-Benzotriazole (BtaH).4. The biocidal-functionalized corrosion inhibitor of claim 1 , wherein the biocidal group is linked to the corrosion inhibitor group via a linking group that is degradable to release a biocidal compound from the biocidal-functionalized corrosion inhibitor.5. The biocidal-functionalized corrosion inhibitor of claim 4 , wherein the linking group includes a hydrolysable ester linkage.6. The biocidal-functionalized corrosion inhibitor of claim 4 , wherein the biocidal compound includes an antimicrobial functional group selected from the group consisting of: a hydroxyl group claim 4 , a carboxyl group claim 4 , and an amino group.7. A process of forming a biocidal-functionalized corrosion inhibiting small molecule claim 4 , the process comprising:providing a biocidal compound that includes a first reactive functional group; ...

HERBICIDAL COMPOUNDS

The present invention relates to compounds of Formula (I), or an agronomically acceptable salt of said compounds wherein A1, A2, R, R, Rand Rare as defined herein. The invention further relates to herbicidal compositions which comprise a compound of Formula (I), to their use for controlling weeds, in particular in crops of useful plants, and to intermediates used to synthesise said compounds. 2. A compound according to claim 1 , wherein Aand Aare both N.3. A compound according to claim 1 , wherein Ris selected from the group consisting of methyl claim 1 , ethyl and propyl.4. A compound according claim 1 , wherein Ris selected from the group consisting of hydroxyl and —NHR.5. A compound according to claim 1 , wherein Ris chlorine.6. A compound according to claim 1 , wherein Ris methyl.7. A compound according to claim 1 , wherein Ris phenyl optionally substituted with one or more substituents selected from the group consisting of halogen claim 1 , C-Calkyl claim 1 , cyano claim 1 , nitro claim 1 , C-Chaloalkyl- claim 1 , C-Calkyl-S(O)p- claim 1 , aryl-S(O)p- claim 1 , C-Calkoxy- and C-Chaloalkoxy-;8. A compound according to claim 1 , wherein Ris methyl.9. A herbicidal composition comprising a compound according to and an agriculturally acceptable formulation adjuvant.10. A herbicidal composition according to claim 9 , further comprising at least one additional pesticide.11. A herbicidal composition according to claim 10 , wherein the additional pesticide is a herbicide.12. A method of controlling weeds at a locus comprising application to the locus of a weed controlling amount of a composition according to .13. (canceled)14. A compound according to wherein R1 is methyl claim 1 , ethyl or propyl; R2 is chlorine claim 1 , hydroxyl claim 1 , or —NHR; R3 is methyl or phenyl optionally substituted with one or more substituents selected from the group consisting of halogen claim 1 , C-Calkyl claim 1 , cyano claim 1 , nitro claim 1 , C-Chaloalkyl- claim 1 , C-Calkyl-S(O)p- ...

WOOD PRESERVATIVE FORMULATION

The present invention relates to a preservative formulation for use in treating wood or other cellulosic materials, said formulation comprising: at least one biocidal metal compound; at least one preservative; and an aqueous carrier, wherein the preservative formulation has an uptake in the sapwood of less than about 220 l/myet achieves substantially full penetration of the sapwood. Preferably, the preservative formulation is copper/tebuconazole in a ratio of about 25/1 w/w; and the wood is around 25 mm in thickness—for instance, decking timber. 1. A preservative formulation for treating wood or other cellulosic materials , said formulation comprising:at least one biocidal metal compound;at least one preservative; andan aqueous carrier being water,one or more water-miscible co-solvents,{'sup': '3', 'wherein said preservative formulation has an uptake in the sapwood of less than about 220 L/mand achieves substantially full sapwood penetration thereby facilitating maintenance of dimensional stability of the wood or other cellulosic materials being treated.'}2. A formulation according to claim 1 , wherein said preservative formulation has an uptake in the sapwood of less than about 150 L/m claim 1 , or in the range of about 70 to about 150 L/m.3. A formulation according to claim 1 , wherein said preservative formulation has an uptake in the sapwood of less than about 120 L/m.4. A formulation according to claim 3 , wherein said preservative formulation has an uptake in the sapwood of less than about 100 L/m.5. A formulation according to claim 4 , wherein said preservative formulation has an uptake in the sapwood of less than about 80 L/m.6. A formulation according to claim 1 , wherein said metal compound is a compound of a metal selected from the group consisting of: copper claim 1 , aluminium claim 1 , manganese claim 1 , iron claim 1 , cobalt claim 1 , nickel claim 1 , zinc claim 1 , silver claim 1 , cadmium claim 1 , tin claim 1 , antimony claim 1 , mercury claim 1 , ...

SOYBEAN DISEASE CONTROL COMPOSITION AND SOYBEAN DISEASE CONTROL METHOD

There are provided a soybean disease control composition containing, as active ingredients, (a) fluazinam or a salt thereof and (b) at least one fungicide selected from the group consisting of carboxamide-based compounds and azole-based compounds; and a method for controlling a soybean disease, which includes applying the soybean disease control composition to a soybean plant or soil. 1. A soybean disease control composition comprising , as active ingredients , (a) fluazinam or a salt thereof and (b) at least one fungicide selected from the group consisting of carboxamide-based compounds and azole-based compounds ,wherein the azole-based compound is oxpoconazole fumarate, azaconazole, bromuconazole, cyproconazole, diclobutrazol, difenoconazole, epoxiconazole, etaconazole, fenbuconazole, fluquinconazole, furconazole, hexaconazole, imibenconazole, metconazole, myclobutanil, propiconazole, prothioconazole, quinconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, or triticonazole.2. The soybean disease control composition according to claim 1 , wherein the carboxamide-based compound is tolfenpyrad claim 1 , fenfuram claim 1 , carboxin claim 1 , oxycarboxin claim 1 , thifluzamide claim 1 , benzovindiflupyr claim 1 , bixafen claim 1 , fluxapyroxad claim 1 , furametpyr claim 1 , isopyrazam claim 1 , penflufen claim 1 , penthiopyrad claim 1 , sedaxane claim 1 , or boscalid.3. The soybean disease control composition according to claim 1 , wherein the carboxamide-based compound is benzovindiflupyr or fluxapyroxad.4. The soybean disease control composition according to claim 1 , wherein the azole-based compound is cyproconazole claim 1 , epoxiconazole claim 1 , prothioconazole claim 1 , or tebuconazole.5. The soybean disease control composition according to claim 1 , wherein the mixing weight ratio of (a) fluazinam or the salt thereof to (b) the fungicide is from 1:10 claim 1 ,000 to 10 claim 1 ,000:1.6. A method for controlling a soybean disease claim 1 , which ...

PLANT GROWTH ACCELERATOR

A plant growth accelerator or an agent for growing vigourous seedlings, which comprises a compound represented by formula (1) as an active ingredient: 2. A method for accelerating a plant growth by using 3-(3-bromo-6-fluoro-2-methylindol-1-ylsulfonyl)-N ,N-dimethyl-1H-1 ,2 ,4-triazole-1-sulfonamide as an active ingredient as an active ingredient for accelerating a plant growth.3. The method for accelerating a plant growth according to claim 1 , wherein the method is for seed treatment.5. A method for growing vigourous seedlings by using 3-(3-bromo-6-fluoro-2-methylindol-1-ylsulfonyl)-N claim 1 ,N-dimethyl-1H-1 claim 1 ,2 claim 1 ,4-triazole-1-sulfonamide as an active ingredient as an active ingredient for growing vigourous seedlings.6. The method for growing vigourous seedlings according to claim 4 , wherein the method is for seed treatment.7. The method for accelerating a plant growth according to claim 2 , wherein the method is for seed treatment.8. The method for growing vigourous seedlings according to claim 5 , wherein the method is for seed treatment. The present invention relates to a plant growth accelerator or an agent for growing vigourous seedlings.This application is a Continuation of U.S. application Ser. No. 14/425,113, which is a National Stage application of PCT/JP2013/005204, filed on Sep. 3, 2013, which claims priority to Japanese Patent Application No. 2012-195757, filed on Sep. 6, 2012, the disclosures of which are hereby incorporated by reference.For example, the box seedling method of rice leads to a super-dense seeding due to being adapted to a rice transplanter. Thus, making a mistake in controlling temperature, humidity, and the like can result in the poor growth of rice seedlings and the reduced quality of seedlings. After being transplanted to a paddy field, the seedlings having reduced quality are easily affected by pests and pathogens and are less resistant to changes in weather conditions because of their poor survival properties. Thus, ...

USE OF PHENYLPYRAZOLIN-3-CARBOXYLATES FOR IMPROVING PLANT YIELD

Compounds (A) can be used for increasing the yield of useful plants or crop plants with respect to their harvested plant organs, wherein the Compound (A) is selected from compounds of the formula (I) or salts thereof, 2. The method according to claim 1 , wherein{'sup': 1', '1', '1, 'sub': n', '3, '(R)is n radicals Rwhere the Rare identical or different and are each F, Cl, Br or CF.'}n is 2 or 3.{'sup': '2', 'sub': 1', '4, 'Ris hydrogen or (C-C)-alkyl.'}{'sup': '3', 'sub': 1', '4', '2', '4', '2', '4, 'Ris hydrogen, (C-C)-alkyl, (C-C)-alkenyl or (C-C)-alkynyl.'}{'sup': '4', 'sub': 1', '8, 'Ris hydrogen or (C-C)-alkyl.'}3. The method according to claim 1 , wherein compound (A) is mefenpyr-diethyl.4. The method according to claim 1 , wherein Compound (A) is applied in combination with one or more compounds selected from the group of fungicides claim 1 , insecticides and plant growth regulators.5. The method according to claim 1 , comprising increasing the grain yield of crop plants selected from group consisting of cereals claim 1 , canola claim 1 , soybean and cotton crops.6. The method according to claim 1 , comprising increasing the grain yield of crop plants selected from group consisting of wheat claim 1 , barley claim 1 , rye or triticale plants. The method according to claim 1 , comprising increasing the gluten content of seed kernels of crop plants selected from group consisting of cereals claim 1 , canola and soybean crops.8. The method according to claim 1 , comprising increasing the gluten content of seed kernels of crop plants selected from group consisting of cereal crops.9. The method according to claim 1 , comprising increasing the protein content of seed kernels of crop plants selected from group consisting of cereals claim 1 , canola and soybean crops.10. The method according to claim 1 , comprising increasing the yield of the amount by weight of beets of beet plants.11. The method according to claim 1 , comprising increasing the sugar content of sugar ...

Fungicidal substituted 1--1H-[1,2,4]triazole compounds

The present invention relates to substituted 1-{2-[2-halo-4-(4-halogen-phenoxy)phenyl]-2-ethoxy-ethyl}-1H-[1,2,4]triazole compounds of formula I as defined in the description, and the N-oxides, and salts thereof, processes and intermediates for preparing these compounds and also to compositions comprising at least one such compound. The invention also relates to the use of such compounds and compositions for combating harmful fungi and seed coated with at least one such compound. 115-. (canceled)17. The compound according to claim 16 , wherein Xis Cl.18. The compound according to claim 16 , wherein Xis Cl.19. The compound according to claim 16 , wherein Ris C-C-alkyl claim 16 , that is unsubstituted or substituted by 1 claim 16 , 2 claim 16 , 3 or up to the maximum possible number of identical or different groups R.20. The compound according to claim 16 , wherein Ris unsubstituted.21. The compound according to claim 16 , wherein Xand Xare Cl claim 16 , Ris unsubstituted and Ris CH claim 16 , CH claim 16 , cyclopropyl claim 16 , C≡CH claim 16 , CHCHCHCH claim 16 , C≡CCHor CH(CH).27. An agrochemical composition comprising an auxiliary and at least one compound of claim 16 , an N-oxide or an agriculturally acceptable salt thereof.28. The composition according to claim 27 , comprising additionally a further active substance.29. Seed coated with at least one compound of in an amount of from 0.1 g to 10 kg per 100 kg of seed.30. A method for controlling phytopathogenic harmful fungi claim 16 , which comprises treating the fungi claim 16 , their habitat or the plants to be protected against fungal attack claim 16 , the soil or seeds with a compound of .31. The method of claim 30 , wherein Xis Cl.32. The method of claim 30 , wherein Xis Cl.33. The method of claim 30 , wherein Ris C-C-alkyl claim 30 , that is unsubstituted or substituted by 1 claim 30 , 2 claim 30 , 3 or up to the maximum possible number of identical or different groups R.34. The method of claim 30 , wherein ...

Fungicidal Active Compound Combinations

The invention relates to active compound combinations comprising firstly the known fluoxastrobin and secondly further known fungicidal active compounds, which combinations are highly suitable for controlling unwanted phytopathogenic fungi. 18-. (canceled)9. A composition comprising fluoxastrobin and at least one second active compound selected from the group consisting of 2-3 (difenoconazole) , 2-14 (ipoconazole) , 4-3 (thiram) , 4-5 (ziram) , 13-6 (fenamidone) , and 14-1 (thiophanate-methyl).10. The composition according to claim 9 , wherein the composition comprises fluoxastrobin and the at least one second active compound in synergistically effective amounts.11. The composition of claim 9 , that comprises fluoxastrobin and the at least one second active compound as the only active compounds. The invention relates to active compound combinations comprising firstly the known fluoxastrobin and secondly further known fungicidal active compounds, which combinations are highly suitable for controlling unwanted phytopathogenic fungi.It is already known that the compound of the formula (I)(fluoxastrobin)has fungicidal properties (WO 97/27189).Furthermore, it is already known that numerous triazole derivatives, aniline derivatives, dicarboximides and other heterocycles can be employed for controlling fungi (cf. EP-A 0 040 345, DE-A 22 01 063, DE-A 23 24 010, Pesticide Manual, 9th Edition (1991), pages 249 and 827, EP-A 0 382 375 and EP-A 0 515 901). However, at low application rates, the activity of these compounds is also not always sufficient.Furthermore, it is already known that 1-(3,5-dimethylisoxazol-4-sulphonyl)-2-chloro-6,6-di-fluoro-[1,3]-dioxolo-[4,5f]-benzimidazole has fungicidal properties (cf. WO 97/06171).Finally, it is also known that substituted halopyrimidines have fungicidal properties (cf. DE-A1-196 46 407, EP-B-712 396).We have now found novel active compound combinations having very good fungicidal properties, comprising fluoxastrobin (group 1)and at ...

HERBICIDAL COMPOSITIONS COMPRISING CARFENTRAZONE-ETHYL AND BROMOXYNIL

Herbicidal compositions comprising a component A, carfentrazone-ethyl and a component B, mixed heptanoate-octanoate ester of bromoxynil 1. Herbicidal composition comprisinga component A, carfentrazone-ethyl anda component B, mixed heptanoate-octanoate ester of bromoxynil.2. Herbicidal composition according to claim 1 , comprising component A and component B in a weight ratio of 1:50 to 50:1.3. Herbicidal composition according to claim 1 , comprising component A and component B in a weight ratio of 1:50 to 6:1.4. Herbicidal composition according to claim 1 , comprising component A and component B in a weight ratio of 1:37.5 to 2:1.5. Herbicidal composition according to claim 1 , comprising in addition glyphosate or a salt thereof.6. Method for controlling volunteer Canola or weed plants in one or more crops of oilseed rape plants claim 1 , comprising applying a herbicidal composition according to to the volunteer Canola and/or weed plants claim 1 , oilseed rape plants claim 1 , oilseed plant parts claim 1 , or oilseed plant seeds and/or to an area on which the volunteer Canola and/or weed plants grow.7Brassica napus, Brassica rapaBrassica juncea.. Method according to claim 6 , wherein the oilseed rape plants claim 6 , plant parts or seeds are from the group consisting of and8. Method according to claim 6 , wherein the oilseed rape plants claim 6 , plant parts or seeds are Canola plants claim 6 , plant parts or seeds.9. Method according to wherein the oilseed rape plant is tolerant to one or more of the herbicides selected from the group of glufosinate (tradename Liberty) claim 6 , glyphosate (tradename RoundupReady) claim 6 , imazamethabenz claim 6 , imazamethabenz-methyl claim 6 , imazamox claim 6 , imazamox-ammonium claim 6 , imazapic claim 6 , imazapic-ammonium claim 6 , imazapyr claim 6 , imazapyr-isopropyl-ammonium claim 6 , imazaquin claim 6 , imazaquin-ammonium claim 6 , imazethapyr claim 6 , imazethapyr-ammonium claim 6 , atrazine claim 6 , simazine ...

Use of Tetrazolinones for Combating Resistant Phytopathogenic Fungi on Cereals

The present invention relates to the use of use of tetrazolinones optionally in combination with further pesticides for combating resistant phytopathogenic fungi on cereals. 111-. (canceled)12. A method for combating phytopathogenic fungi on cereals , wherein the fungi , their habitat , breeding grounds , their locus or the plants to be protected against fungal attack , the soil or plant propagation material are treated with an effective amount of a 1-[2-[[1-(4-chlorophenyl)pyrazol-3-yl]oxymethyl]-3-methyl-phenyl]-4-methyl-tetrazol-5-one (compound I) , such fungi containing a mutation in the mitochondrial cytochrome b gene conferring resistance to Qo inhibitors , wherein the mutation is G143A or F129L.13. The method of claim 12 , wherein the cereal plant is wheat.14. The method of claim 12 , wherein the cereal plant is barley.15Microduchium nivale, Blumeria graministritici, Septoria tritici, Phaesphaeria nodorumPyrenophora triticirepentis. The method of claim 12 , wherein the phytopathogenic fungi are selected from the group consisting of f. sp. and -and wherein the cultivated plant is wheat.16Septoria tritici.. The method claim 15 , wherein the phytopathogenic fungus is17Blumeria graminishordei, Pyrenophora teres, Ramularia collocygniRhynchosporium secalis. The method of claim 12 , wherein the phytopathogenic fungus is f. sp. -or and the cultivated plant is barley.18Rhynchosporium secalis.. The method of claim 17 , wherein the phytopathogenic fungus is19Pyrenophora teres.. The method of claim 17 , wherein the phytopathogenic fungus is20. The method of claim 17 , wherein compound I as defined is applied in the form of a mixture with second compound II claim 17 , which is selected from the group consisting of 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1 claim 17 ,2 claim 17 ,4-triazol-1-yl)propan-2-ol claim 17 , 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-3-methyl-1-(1 claim 17 ,2 claim 17 ,4-triazol-1-yl)butan-2-ol claim 17 , 1-[4-(4-chlorophenoxy)-2 ...

Biocide Compositions Comprising Derivatives Of Pyroglutamic Acid

Described are agrochemical compositions, comprising (a) esters and/or amides of pyroglutamic acid, and (b) biocides. The compositions are clear and exhibit an improved stability even when stored at temperatures between 5° and 40° C. over a longer period. 2. (canceled)3. The composition according to claim 1 , wherein component (a) comprises an ester selected from the group consisting of pyroglutamic acid methyl ester claim 1 , pyroglutamic acid ethyl ester claim 1 , pyroglutamic acid propyl ester(s) claim 1 , pyroglutamic acid butyl ester(s) claim 1 , pyroglutamic acid n-octyl ester claim 1 , pyroglutamic-2-ethylhexyl ester claim 1 , pyroglutamic acid furfuryl ester claim 1 , pyroglutamic acid tetrahydrofurfuryl ester claim 1 , and mixtures thereof.4. (canceled)5. The composition according to claim 1 , wherein the biocide is selected from the group consisting of herbicides claim 1 , fungicides claim 1 , insecticides claim 1 , and plant growth regulators.6. The composition according to claim 1 , wherein the biocide is selected from the group consisting of azoles claim 1 , oxyfluorfen claim 1 , propanil claim 1 , chlorpyrifos claim 1 , bifenthrin claim 1 , novaluron claim 1 , phenmedipham claim 1 , deltamethrin claim 1 , acetochlore claim 1 , lambda-cyhalothrin claim 1 , glyphosate and its salts claim 1 , and glufosinate and its salts.7. The composition according to claim 1 , further comprising(c) an oil component or a co-solvent.8. The composition according to claim 1 , further comprising(d) an emulsifier.10. The composition according to claim 1 , wherein the composition has an active matter content of 5% b.w. to 50% b.w.11. A method of dispersing a biocide claim 1 , the method comprising using an ester of pyroglutamic acid as a solvent or dispersant.12. The method of claim 2 , wherein the ester of pyroglutamic acid is selected from the group consisting of pyroglutamic acid methyl ester claim 2 , pyroglutamic acid ethyl ester claim 2 , pyroglutamic acid propyl ester(s ...

SELECTIVE HERBICIDES BASED ON SUBSTITUTED THIEN-3-YL-SULPHONYLAMINO(THIO)CARBONYLTRIAZOLIN(THI)ONES AND SAFENERS

The invention relates to selective herbicidal compositions that comprise an effective amount of an active compound combination comprising 2. The composition of claim 1 , wherein the ratio of isoxadifen-ethyl per part by weight of said compound of formula I or a salt thereof is from 1 to 25.3. The composition of claim 1 , further comprising one or more of extenders claim 1 , solid carriers claim 1 , emulsifiers claim 1 , foam-formers claim 1 , dispersants claim 1 , tackifiers claim 1 , colorants claim 1 , mineral oil claim 1 , or vegetable oil.4. The composition of claim 1 , further comprising another herbicide claim 1 , fungicide claim 1 , insecticide claim 1 , acaricide claim 1 , nematicide claim 1 , bird repellent claim 1 , growth factor claim 1 , and/or plant nutrient and agent.5. The composition of claim 1 , wherein component (a) and component (b) are the only two actives present in the composition.6. The composition of claim 1 , wherein component (a) is the only herbicide present in the composition.7. A method for controlling undesirable plants comprising allowing an effective amount of the composition according to to act on undesirable plants and/or their habitat.8. A process for preparing a herbicidal composition comprising mixing the composition according to with one or more surfactants and/or extenders.9. The method according to claim 7 , wherein the undesired plants are controlled in areas of growing maize.10. The method according to claim 9 , wherein 0.001 to 5 kg per ha of the composition are applied.11. The method according to claim 9 , wherein 0.001 to 1 kg per ha of the composition are applied.12. The method according to claim 9 , wherein 0.003 to 0.5 kg per ha of the composition are applied.13. The method according to claim 9 , wherein the composition is applied pre-emergence.14. The method according to claim 9 , wherein the composition is applied post-emergence. This application is a Continuation of U.S. application Ser. No. 14/950,588, filed Nov. ...

HERBICIDAL COMBINATION

An herbicidal combination including a photosystem II inhibitor, an ALS inhibitor, and a chlorophyll and heme biosynthesis inhibitor, a composition comprising the combination, and methods of using these combinations are described.

Methods and Compositions for PPO Inhibitor Tolerance in Soybeans

This invention relates generally to the detection of genetic differences among soybeans. More particularly, the invention relates to soybean quantitative trait loci (QTL) for tolerance to protoporphyrinogen oxidase inhibitors, to soybean plants possessing these QTLs, which map to a novel chromosomal region, and to genetic markers that are indicative of phenotypes associated with protoporphyrinogen oxidase inhibitor tolerance. Methods and compositions for use of these markers in genotyping of soybean and selection are also disclosed. 1. A method of selecting a soybean plant or germplasm with tolerance or improved tolerance to herbicides that inhibit protoporphyrinogen oxidase function , the method comprising:a) detecting in a soybean plant or germplasm at least one allele of a marker locus that is associated with the tolerance or improved tolerance to herbicides that inhibit protoporphyrinogen oxidase function, wherein the one or more marker locus is localized within a chromosome interval defined by and including markers SATT495 and SATT613 on linkage group L; andb) selecting the soybean plant or germplasm comprising the at least one allele of one or more marker locus, thereby selecting a soybean plant with tolerance or improved tolerance to herbicides that inhibit protoporphyrinogen oxidase function.2. The method of claim 1 , wherein the herbicide is selected from the group consisting of diphenylethers claim 1 , N-phenylpthalamides claim 1 , pyrimidindiones claim 1 , oxadiazoles claim 1 , and triazolinones.3. The method of claim 2 , wherein the herbicide is selected from the group consisting of sulfentrazone claim 2 , carfentrazone-ethyl claim 2 , azafeniden claim 2 , aciflourfen claim 2 , lactofen claim 2 , fomesafen claim 2 , flumioxazin claim 2 , flumiclorac-pentyl claim 2 , oxadiazon claim 2 , fluthiacet claim 2 , benzfendizone claim 2 , butagenacil claim 2 , saflufenacil claim 2 , and oxyfluorfen.4. The method of claim 1 , wherein the selection occurs as part ...

TRANSPARENT OR SEMITRANSPARENT INVERSE MICROLATICES OF POLYACRYLAMIDE AS OIL EMULSION DRIFT REDUCING AGENT

The present disclosure provides compositions comprising polyacrylamide microemulsions, for example transparent or semitransparent inverse microlatices of polyacrylamide, and methods and formulations using the compositions for management of crop pests. 1. A composition comprising a polyacrylamide microemulsion and at least one or both of a pesticide and a crop protection enhancing adjuvant.2. The composition of claim 1 , wherein the polyacrylamide microemulsion is an inverse microemulsion.3. The composition of or claim 1 , wherein the polyacrylamide microemulsion is a transparent/semitransparent inverse microlatice polyacrylamide.4. The composition of any of - claim 1 , wherein the polyacrylamide microemulsion comprises polyacrylamide having less than 30 mole percent anionic charge.5. The composition of any of - claim 1 , wherein the polyacrylamide microemulsion comprises polyacrylamide having 0-22 mole percent anionic charge.6. The composition of any of - claim 1 , wherein the polyacrylamide microemulsion comprises polyacrylamide having 3-18 mole percent anionic charge.7. The composition of any of - claim 1 , wherein the polyacrylamide microemulsion comprises polyacrylamide having 7-15 mole percent anionic charge.8. The composition of any of - claim 1 , wherein the polyacrylamide microemulsion comprises polyacrylamide having 15-22 mole percent anionic charge.9. The composition of any of - claim 1 , wherein the crop protection enhancing adjuvant is selected from the group consisting of: crop oil concentrates claim 1 , modified vegetable oils claim 1 , drift retardants claim 1 , soil or foliage penetrants claim 1 , buffering agents claim 1 , wetting agents claim 1 , surfactants claim 1 , nitrogen fertilizers claim 1 , compatibility agents claim 1 , defoamers claim 1 , deposition agents claim 1 , or combinations thereof.10. The composition of any of - claim 1 , wherein the crop protection enhancing adjuvant is a lipophilic adjuvant.11. The composition of any of - claim ...

METHOD OF PROTECTING FIELD CORN FROM DAMAGE BY A PLANT PATHOGEN

The present invention can provide a method having superior safety for protecting field corn from damage by a plant pathogen. The method includes a step of applying mefentrifluconazole to foliage of field corn, seeds of field corn or a soil of the cultivation area of field corn, wherein the application rate of mefentrifluconazole is 20 to 500 g per hectare of cultivation area. 1. A method of protecting field corn from damage by a plant pathogen in a cultivation area of field corn , the method comprising a step of applying mefentrifluconazole to foliage of field corn , seeds of field corn or a soil of the cultivation area of field corn , wherein the application rate of mefentrifluconazole is 20 to 500 g per hectare of the cultivation area.2. The method according to claim 1 , wherein mefentrifluconazole is applied to foliage of field corn. This application claims priority to and the benefit of Japanese Patent Application No. 2019-066003 filed on Mar. 29, 2019 and U.S. patent application Ser. No. 16/396,506 filed on Apr. 26, 2019, the entire contents of which are incorporated herein by reference.The present invention relates to a method of protecting field corn from damage by a plant pathogen.Hitherto, a method of applying mefentrifluconazole has been known, as a method for controlling a plant pathogen on corn (see Patent Literature 1). Also, various types of corn such as field corn, sweet corn, popcorn, and waxy corn are known (see Non-Patent Literatures 1, 2). However, it is not known that field corn, especially, can be safely protected from damage by a plant pathogen by applying mefentrifluconazole at certain application rate.An object of the present invention is to provide a method having superior safety for protecting field corn from damage by a plant pathogen.The present inventor has found out that field corn can be safely protected from damage by a plant pathogen by applying mefentrifluconazole at certain application rates to foliage of field corn, seeds of field ...

COMPOSITION COMPRISING A PESTICIDE AND ISONONANOIC ACID N,N-DIMETHYL AMIDE

A composition comprising a pesticide and a certain carboxylic acid amide, i.e. isononanoic acid N,N-dimethyl amide, is described herein. Also disclosed is a method for controlling phytopathogenic fungi and/or undesirable plant growth and/or undesirable insect or mite infestation and/or for regulating the growth of plants, wherein the composition is allowed to act on the respective pests, the habitat thereof or the plants to be protected from the respective pest, on the soil and/or on undesirable plants and/or the crop plants and/or the habitat thereof. Furthermore, use of the carboxylic acid amide as a solvent for pesticides with no or low phytotoxicity is described. 2. The composition according to claim 1 , wherein said composition further comprises at least one emulsifier.3. The composition according to claim 2 , wherein the at least one emulsifier is at least one non-ionic emulsifier.4. The composition according to claim 2 , wherein the at least one emulsifier is a combination of at least one non-ionic emulsifier and at least one anionic emulsifier.5. The composition according to claim 1 , wherein the pesticide is selected from fungicides claim 1 , herbicides and insecticides.6. The composition according to claim 1 , wherein the composition comprises of from 0.1% by weight to 90% by weight of the carboxylic acid amide according to formula (I).7. The composition according to claim 2 , wherein the composition comprises5 to 60% by weight of pesticide,1 to 30% by weight of emulsifier,0 to 90% by weight of oil components and/or co-solvents, and0.1 to 90% by weight of carboxylic acid amide according to formula (I),on the condition that the amounts add to 100% by weight.8. The composition according to claim 1 , wherein the composition further comprises water.9. A method for treating plants and/or for controlling phytopathogenic fungi and/or undesirable plant growth and/or undesirable insect or mite infestation and/or for regulating the growth of plants claim 1 , wherein ...

AZOLE DERIVATIVE, METHOD FOR PRODUCING SAME, INTERMEDIATE COMPOUND, AND AGRICULTURAL OR HORTICULTURAL CHEMICAL AGENT AND INDUSTRIAL MATERIAL PROTECTING AGENT

Provided is an azole derivative superior in disease-controlling activity contained as an active ingredient in agricultural or horticultural chemical agents. 2. The azole derivative according to claim 1 , wherein claim 1 , in General Formula (I) above claim 1 , Rrepresents COORand Rrepresents a C-C-alkyl group claim 1 , a C-C-alkenyl group claim 1 , or a C-C-alkynyl group.3. The azole derivative according to claim 1 , wherein claim 1 , in General Formula (I) above claim 1 , Rrepresents CONRR claim 1 , and Rand Reach independently represent a hydrogen atom claim 1 , a C-C-alkyl group claim 1 , a C-C-alkenyl group claim 1 , or a C-C-alkynyl group.4. The azole derivative according to claim 1 , wherein claim 1 , in General Formula (I) above claim 1 , Rrepresents a halogen atom-substituted C-C-alkyl group.5. The azole derivative according to claim 1 , wherein claim 1 , in General Formula (I) above claim 1 , Rrepresents an unsubstituted alkyl group.6. The azole derivative according to claim 1 , wherein claim 1 , in General Formula (I) above claim 1 , the number of carbons in Ris 1 to 4.7. The azole derivative according to claim 1 , wherein claim 1 , in General Formula (I) above claim 1 , Y represents a halogen atom and m is 1.18. An agricultural or horticultural chemical agent or an industrial material-protecting agent claim 1 , comprising the azole derivative according to as an active ingredient.19. The agricultural or horticultural chemical agent according to claim 18 , for use in seed treatment.20. Seeds treated with the agricultural or horticultural chemical agent according to . The present invention relates to a new azole derivative. It also relates to an agricultural or horticultural chemical agent and an industrial material-protecting agent containing the derivative as an active ingredient, and a method for producing the derivative. It also relates to an intermediate compound thereof.Some kinds of 2-substituted-5-benzyl-1-azolylmethylcyclopentanol derivatives are ...

APPLICATION OF TETRAHYDROBENZAZOLE IN PREPARATION OF AGRICULTURAL FUNGICIDE OR FUNGICIDE COMPOSITION AND PREPARATION METHOD THEREOF

An application of tetrahydrobenzazole in the preparation of an agricultural fungicide or a fungicide composition and a preparation method therefor. A 4-((-(2-chloro-4-(4-chlorophenoxy)phenyl)-4-methyl-1,3-dioxapentan-2-yl)methyl)-4H-1,2,4-triazole(tetrahydrobenzazole) compound has application in agricultural fungicides, having the structural formula shown in formula I is provided. Also, the embodiments transform waste that can usually only be treated as a hazardous organic waste solid, accounting for 35-40% of the production process of an agricultural fungicide difenoconazole, into a useful pesticide, significantly reducing discharge of hazardous organic waste solids, and alleviating environmental protection pressure on manufacturers. The preparation method of the embodiments can also increase the yield of difenoconazole and reduce costs. 110-. (canceled)12. The application of 4-((-(2-chloro-4-(4-chlorophenoxy) phenyl)-4-methyl-1 claim 11 ,3-dioxapentan-2-yl) methyl)-4H-1 claim 11 ,2 claim 11 ,4-triazole (tetrahydrobenzazole) compound in agricultural fungicide according to claim 11 , wherein the application is for preventing and treating various diseases caused by Ascomycetes claim 11 , Basidimycetes claim 11 , fungi imperfecti including Alternaria claim 11 , Ascochyta claim 11 , Cercospora claim 11 , Colletotrichum claim 11 , Guignardia claim 11 , Phoma claim 11 , Ramularia and Venturia claim 11 , Erysiphe claim 11 , Uredinales and some pathogens.13. The application of 4-((-(2-chloro-4-(4-chlorophenoxy) phenyl)-4-methyl-1 claim 11 ,3-dioxapentan-2-yl) methyl)-4H-1 claim 11 ,2 claim 11 ,4-triazole (tetrahydrobenzazole) compound in agricultural fungicide according to claim 11 , wherein a dose is 5˜500 grams of the compound per hectare.14. The application of 4-((-(2-chloro-4-(4-chlorophenoxy) phenyl)-4-methyl-1 claim 11 ,3-dioxapentan-2-yl) methyl)-4H-1 claim 11 ,2 claim 11 ,4-triazole (tetrahydrobenzazole) compound in agricultural fungicide according to claim 11 , ...

STABILISED FORMULATIONS CONTAINING PROTHIOCONAZOLE WITH A LOW 2-(1-CHLOROCYCLOPROPYL)-1-(2-CHLOROPHENYL)-3-(1H-1,2,4-TRIAZOL-1-YL)PROPAN-2-OL CONTENT

The invention relates to storage-stable prothioconazole-containing formulations having a particularly low content of 2-(1-chlorocyclopropyl)-1-(2-chlorophenyl)-3-( H-1,2,4-triazol-1-yl)propan-2-ol based on organic vinyl compounds, to a process for their preparation, to a method for controlling phytopathogenic fungi in crop protection and to their use as crop protection agents. 6. The formulation as claimed in claim 1 , wherein the proportion of component b) is 1% by weight to 50% by weight.7. The formulation as claimed in claim 1 , wherein the proportion of component a) is 1% by weight to 50% by weight.9. The formulation as claimed in claim 8 , comprising a nonionic (c1) and/or anionic (c2) emulsifier.10. The formulation as claimed in claim 8 , wherein said one or more active agrochemical ingredients d) are one or more active insecticidal or fungicidal ingredients.11. The formulation as claimed in claim 8 , wherein the further active agrochemical ingredient d) is bixafen.12. The formulation as claimed in claim 10 , comprising not more than 5% by weight of water.13. A process for preparing the formulation as claimed in comprising mixing components a) and b) and optionally one or more further additives.14. A method of controlling one or more harmful organisms claim 1 , comprising contacting the harmful organisms claim 1 , a habitat claim 1 , one or more hosts claim 1 , optionally plants and seed claim 1 , and/or soil claim 1 , an area and/or an environment in which said organisms grow or could grow claim 1 , and/or one or more materials claim 1 , plants claim 1 , seeds claim 1 , soil claim 1 , surfaces or spaces which are to be protected from attack or infestation by organisms that are harmful to plants claim 1 , with an effective amount of the formulation as claimed in .15. The use of the formulations as claimed in for protection of plants including seed claim 1 , and/or optionally useful plants claim 1 , from infestation by one or more harmful organisms.16. The ...

COMPOSITION COMPRISING A PESTICIDE AND A HYDROXYALKYL POLYOXYLENE GLYCOL ETHER

A composition having a pesticide and a hydroxyalkyl polyoxylene glycol ether of the general formula (I) 2. The composition according to claim 1 , wherein the hydroxyalkyl polyoxylene glycol ether is of the general formula (II){'br': None, 'sup': 1', '2a', '2b', '2c', '3, 'sub': 2', 'x', 'y', 'z, 'R—CH(OH)—CH—[O—R]—[O—R]—[O—R]—O—R\u2003\u2003(II)'}where{'sup': 1', '3, 'claim-ref': {'@idref': 'CLM-00001', 'claim 1'}, 'Rand Rare as defined in ;'}{'sup': 1a', '2b', '2c, 'R, Rand Rare independently ethylene, propylene, or butylene;'}x, y and z are independently a value from 0 to 100; andx, y and z sum up to a value of from 1 to 100.3. The composition according to claim 1 , wherein Ris a saturated or unsaturated claim 1 , linear or branched alkyl having 8 to 14 carbon atoms.4. The composition according to claim 1 , wherein Ris a saturated linear alkyl having 8 to 12 carbon atoms.5. The composition according to claim 1 , wherein Ris ethylene or a mixture of ethylene and propylene.6. The composition according to claim 1 , wherein Ris ethylene.7. The composition according to claim 1 , wherein Ris a saturated or unsaturated claim 1 , linear or branched alkyl having 8 to 12 carbon atoms.8. The composition according to claim 1 , wherein Ris a saturated branched alkyl having 8 to 12 carbon atoms.9. The composition according to claim 1 , wherein n has a value of from 3 to 50.10. The composition according to claim 2 , wherein R claim 2 , Rand Rare independently ethylene or propylene.11. The composition according to claim 2 , wherein x claim 2 , y and z sum up to a value of from 3 to 50.12. The composition according to claim 1 , wherein the pesticide comprises at least one fungicide.13. The composition according to claim 12 , wherein the fungicide is selected from the group consisting of carboxamides claim 12 , triazoles claim 12 , pyrazole-4-carboxamides and strobilurins.14. A method of preparing the composition as defined in claim 1 , by bringing the pesticide and the ...

Methods for Apple Scab Control

The present invention relates to methods for controlling apple scab caused by comprising spraying the bark of an apple tree with an effective amount of 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydroinden-4-yl]pyrazole-4-carboxamide and a surfactant. 1Venturia inaequalis. A method of controlling apple scab caused by comprising spraying the bark of an apple tree with an effective amount of 3-(difluoromethyl)-1-methyl-N-[(3R)-1 ,1 ,3-trimethyl-2 ,3-dihydroinden-4-yl]pyrazole-4-carboxamide and a surfactant.2. The method of wherein the effective amount of 3-(difluoromethyl)-1-methyl-N-[(3R)-1 claim 1 ,1 claim 1 ,3-trimethyl-2 claim 1 ,3-dihydroinden-4-yl]pyrazole-4-carboxamide is from about 0.0001 to about 1 gram of 3-(difluoromethyl)-1-methyl-N-[(3R)-1 claim 1 ,1 claim 1 ,3-trimethyl-2 claim 1 ,3-dihydroinden-4-yl]pyrazole-4-carboxamide per centimeter of the trunk diameter at breast height.3. The method of wherein the effective amount of 3-(difluoromethyl)-1-methyl-N-[(3R)-1 claim 2 ,1 claim 2 ,3-trimethyl-2 claim 2 ,3-dihydroinden-4-yl]pyrazole-4-carboxamide is from about 0.001 to about 0.01 grams of 3-(difluoromethyl)-1-methyl-N-[(3R)-1 claim 2 ,1 claim 2 ,3-trimethyl-2 claim 2 ,3-dihydroinden-4-yl]pyrazole-4-carboxamide per centimeter of the trunk diameter at breast height.4. The method of wherein the apple tree is selected from the group consisting of braeburn claim 1 , cameo claim 1 , cortland claim 1 , crabapple claim 1 , empire claim 1 , Fuji claim 1 , gala claim 1 , ginger gold claim 1 , golden delicious claim 1 , granny smith claim 1 , honeycrisp claim 1 , idared claim 1 , jonagold claim 1 , jonathan claim 1 , McIntosh claim 1 , mutsu claim 1 , nittany claim 1 , pink lady claim 1 , rome claim 1 , red delicious claim 1 , stayman claim 1 , winesap claim 1 , and york.5. The method of wherein the tree is sprayed when the tree is dormant.6. The method of wherein the tree is sprayed on the lower 150 centimeters of the trunk.7. The method of wherein ...

Active compound combinations

The present invention relates to active compound combinations, in particular within a fungicide composition, which comprises (A) Prothioconazole and (B) Iprodione. Moreover, the invention relates to a method for curatively or preventively controlling the phytopathogenic fungi of plants or crops, to the use of a combination according to the invention for the treatment of seed, to a method for protecting a seed and not at least to the treated seed.

Fungicidal substituted 1--1H [1,2,4]triazole compounds

The present invention relates to substituted 1-{2-[2-halo-4-(4-halogen-phenoxy)-phenyl]-2-alkoxy-3-methyl-butyl}-1H-[1,2,4]triazole compounds of formula I as defined in the description, and the N-oxides, and salts thereof, processes and intermediates for preparing these compounds and also to compositions comprising at least one such compound. The invention also relates to the use of such compounds and compositions for combating harmful fungi and seed coated with at least one such compound. 115-. (canceled)17. The compounds according to claim 16 , wherein Xis Cl.18. The compounds according to claim 16 , wherein Xis Cl.19. The compounds according to claim 16 , wherein Ris unsubstituted.20. The compounds according to claim 16 , wherein Ris C-C-alkyl claim 16 , that is unsubstituted or substituted by 1 claim 16 , 2 claim 16 , 3 or up to the maximum possible number of identical or different groups R.21. The compounds according to claim 16 , wherein Xand Xare C claim 16 , Ris CH(CH)and Ris CH claim 16 , CH claim 16 , CHCH═CHor CHCCH.27. An agrochemical composition comprising an auxiliary and at least one compound of claims.28. The compositions according to claim 27 , comprising additionally a further active substance.29. A method for combating harmful insects and/or phytopathogenic fungi claim 16 , which comprises contacting plants claim 16 , seed claim 16 , soil or habitat of plants in or on which the harmful insects and/or phytopathogenic fungi are growing or may grow claim 16 , plants claim 16 , seed or soil to be protected from attack or infestation by said harmful insects and/or phytopathogenic fungi with an effective amount of the agrochemical formulation of claim comprising a compound of .30. The method of claim 29 , wherein Xis Cl.31. The method of claim 29 , wherein Xis Cl.32. The method of claim 29 , wherein Ris unsubstituted.33. The method of claim 29 , wherein Ris C-C-alkyl claim 29 , that is unsubstituted or substituted by 1 claim 29 , 2 claim 29 , 3 or up to ...

Fungicidal substituted 1--1H-[1,2,4]triazole compounds

The present invention relates to substituted 1-{2-[2-halo-4-(4-halogen-phenoxy)-phenyl]-2-alkoxy-2-cyclyl-ethyl}-1H-[1,2,4]triazole compounds of formula I as defined in the description, and the N-oxides, and salts thereof, processes and intermediates for preparing these compounds and also to compositions comprising at least one such compound. The invention also relates to the use of such compounds and compositions for combating harmful fungi and seed coated with at least one such compound. 117-. (canceled)19. The compound according to claim 18 , wherein Xis Cl.20. The compound according to claim 18 , wherein Xis Cl.21. The compound according to claim 18 , wherein Ris phenyl claim 18 , benzyl claim 18 , phenylethenyl or phenylethynyl.22. The compound according to claim 18 , wherein Ris C-C-cycloalkyl or C-C-cycloalkyl-C-C-alkyl.23. The compound according to claim 18 , wherein Ris unsubstituted.24. The compound according to claim 18 , wherein Ris C-C-alkyl claim 18 , that is unsubstituted or substituted by 18 claim 18 , 19 claim 18 , 20 or up to the maximum possible number of identical or different groups R.25. The compound of claim 18 , wherein Xand Xare Cl claim 18 , Ris unsubstituted cyclopropyl and Ris CH claim 18 , CH claim 18 , CHCH═CH claim 18 , CHCΞCH claim 18 , CHCHor CHCHand the compound wherein Xand Xare Cl claim 18 , Ris CH═CHCHand Ris CHCΞCH.31. An agrochemical composition comprising an auxiliary and at least one compound of claim 18 , an N-oxide or an agriculturally acceptable salt thereof.32. The compositions according to claim 31 , comprising additionally a further active substance.33. Seed coated with at least one compound of in an amount of from 0.1 g to 10 kg per 100 kg of seed.34. A method for controlling phytopathogenic harmful fungi claim 18 , which comprises treating the fungi claim 18 , their habitat or the plants to be protected against fungal attack claim 18 , the soil or seeds with a compound of .35. The method of claim 34 , wherein Xis Cl. ...

FUNGICIDAL COMPOSITION

A fungicidal composition is provided, the composition comprising: 1. A fungicidal composition comprising:Component (A): prothioconazole; andComponent (B): chlorothalonil.2. The composition according to claim 1 , wherein the total amount of the component (A) prothioconazole and the component (B) chlorothalonil present in the composition is from 5% to 99% by weight.3. The composition according to claim 1 , wherein prothioconazole is present in an amount of at least 0.5% by weight.4. The composition according to claim 1 , wherein chlorothalonil is present in an amount of at least 0.5% by weight.5. The composition according to claim 1 , wherein prothioconazole is present in an amount of from 1 to 50% by weight.6. The composition according to claim 1 , wherein the weight ratio of prothioconazole to chlorothalonil is from 1:30 to 1:1.7. The composition according to claim 1 , further comprising one or more auxiliaries selected from extenders claim 1 , carriers claim 1 , solvents claim 1 , surfactants claim 1 , stabilizers claim 1 , anti-foaming agents claim 1 , anti-freezing agents claim 1 , preservatives claim 1 , antioxidants claim 1 , colorants claim 1 , thickeners claim 1 , solid adherents and inert fillers.8. The composition according to claim 1 , wherein the formulation is a water-soluble concentrate (SL) claim 1 , an emulsifiable concentrate (EC) claim 1 , an oil-in-water emulsion (EW) claim 1 , a micro-emulsion (ME) claim 1 , a suspension concentrate (SC) claim 1 , an oil-based suspension concentrate (OD) claim 1 , a flowable concentrate (FS) claim 1 , water-dispersible granules (WG) claim 1 , water-soluble granules (SG) claim 1 , a wettable powder (WP) claim 1 , a water soluble powder (SP) claim 1 , granules (GR) claim 1 , encapsulated granules (CG) claim 1 , fine granules (FG) claim 1 , macrogranules (GG) claim 1 , an aqueous suspo-emulsion (SE) claim 1 , a capsule suspension (CS) or microgranules (MG).9. A method for the control and/or prevention of fungal ...

METHOD OF PROTECTING DETERMINATE SOYBEAN FROM DAMAGE BY A PLANT PATHOGEN

The present invention can provide a method having superior safety for protecting determinate soybean from damage by a plant pathogen. The method includes a step of applying mefentrifluconazole to foliage of determinate soybean, seeds of determinate soybean or a soil of the cultivation area of determinate soybean, wherein the application rate of mefentrifluconazole is 20 to 500 g per hectare of cultivation area. 1. A method of protecting determinate soybean from damage by a plant pathogen in a cultivation area of determinate soybean , the method comprising a step of applying mefentrifluconazole to foliage of determinate soybean , seeds of determinate soybean or a soil of the cultivation area of determinate soybean , wherein the application rate of mefentrifluconazole is 20 to 500 g per hectare of the cultivation area.2. The method according to claim 1 , wherein mefentrifluconazole is applied to foliage of determinate soybean. This application claims priority to and the benefit of Japanese Patent Application No. 2019-073972 filed on Apr. 9, 2019 and U.S. patent application Ser. No. 16/396,343 filed on Apr. 26, 2019, the entire contents of which are incorporated herein by reference.The present invention relates to a method of protecting determinate soybean from damage by a plant pathogen.Hitherto, a method of applying mefentrifluconazole has been known, as a method for controlling a plant pathogen on soybean (see Patent Literature 1). Also, several types of soybean such as determinate soybean, indeterminate soybean and semi-determinate soybean are known (see Non Patent Literature 1). However, it is not known that determinate soybean, especially, can be safely protected from damage by a plant pathogen by applying mefentrifluconazole at certain application rate.An object of the present invention is to provide a method having superior safety for protecting determinate soybean from damage by a plant pathogen.The present inventor has found out that determinate soybean can ...

PLANT SUPPORT FORMULATION, VEHICLE FOR THE DELIVERY AND TRANSLOCATION OF PHYTOLOGICALLY BENEFICIAL SUBSTANCES AND COMPOSITIONS CONTAINING SAME

A plant supporting formulation which is also suitable for use as a delivery vehicle, or a component of a delivery vehicle, for the delivery of one or more phytologically beneficial substances to a plant, and for enhancing the translocation of such delivered substance(s) in or on the plant, the formulation comprising a micro-emulsion constituted by a dispersion of vesicles or microsponges of a fatty acid based component in an aqueous carrier, the fatty acid based component comprising at least one long chain fatty acid based substance selected from the group consisting of free fatty acids and derivatives of free fatty acids. The dispersion is preferably characterized in that at least 50% of the vesicles or microsponges are of a diametrical size of between 50 nm and 5 micrometer. The dispersion is further also characterized in that the micro-emulsion has a zeta potential of between −25 mV and −60 mV. 1. A plant supporting formulation which is physiologically beneficial comprising a micro-emulsion constituted by a dispersion of vesicles or microsponges of a fatty acid based component in an aqueous carrier , the fatty acid based component comprising at least one long chain fatty acid based substance selected from the group consisting of oleic acid , linoleic acid , alpha-linolenic acid , gamma-linolenic acid , arachidonic acid , eicosapentaenoic acid [C20:5ω3] , decosahexaenoic acid [C22:6ω3] , and ricinoleic acid , and derivatives thereof selected from the group consisting of Cto Calkyl esters thereof , glyceropolyethylene glycol esters thereof , and reaction products of hydrogenated and unhydrogenated natural oils composed largely of ricinoleic acid based oils with ethylene oxide and which incorporates a gas dissolved in the fatty acid mixture.2. A plant supporting formulation according to claim 1 , wherein said ricinoleic acid is castor oil.3. A plant supporting formulation according to wherein the dispersion is characterized in that at least 95% of the vesicles or ...

METHODS FOR MODULATING PLANT RESPONSE TO ENVIRONMENTALLY-INDUCED STRESS

Compounds and methods are described herein that are effective to modulate plant response (e.g., plant susceptibility) to environmentally-induced stress. The compounds and methods described herein advantageously may be used to modulate environmental stress resistance in a wide variety of plants. Environmental stresses include, for example, high light intensity (UV exposure), temperature (e.g., high heat), high soil salinity, and low soil moisture (e.g., drought). As used herein, environmental stresses include any conditions that result in increased generation of reactive oxygen species (ROS) and accumulation of ROS in the plant cells. The compounds described herein that are effective to modulate resistance to the stress prevent, directly or indirectly, or increase phosphorylation of Tyrof the RACK1A protein. 1. A method for modulating environmental stress resistance in a plant , the method comprising applying to plant material , area of cultivation , or combination thereof an amount of a compound effective to increase Tyr248 phosphorylation of RACK1A in response to the environmental stress.2. The method of claim 1 , wherein the plant material comprises foliage claim 1 , stem claim 1 , roots claim 1 , soil claim 1 , or a combination thereof.6. The method according to claim 1 , wherein the environmental stress is selected from the group consisting of high light intensity claim 1 , high soil salinity claim 1 , low soil moisture claim 1 , and heat.7. The method according to claim 1 , wherein the compound is diluted in liquid media prior to application to the plant material or area of cultivation.8. A method for increasing resistance to environmental stress in a plant claim 1 , the method comprising applying to plant material claim 1 , area of cultivation claim 1 , or combination thereof an amount of a compound effective to decrease Tyr248 phosphorylation of RACK1A in response to the environmental stress.9. The method of claim 8 , wherein the plant material comprises ...

LIQUID SUSPENSION CONCENTRATE FORMULATION COMPRISING MEFENTRIFLUCONAZOLE

An object of the present invention is to provide an aqueous suspension concentrate, which shows excellent plant disease control. An aqueous suspension concentrate comprising mefentrifluconazole, a surfactant, a thickener, and water, wherein an amount of mefentrifluconazole is less than 20% by weight of the aqueous suspension concentrate. 1. An aqueous suspension concentrate comprising mefentrifluconazole , a surfactant , a thickener , and water , wherein an amount of mefentrifluconazole is less than 20% by weight of the aqueous suspension concentrate.2. A method for controlling plant diseases comprising a step of applying the aqueous suspension concentrate according to to plants or their habitat. This application is a Continuation-in-Part of U.S. application Ser. No. 16/926,434 filed on Jul. 10, 2020, which is a Continuation application of U.S. application Ser. No. 16/507,720, filed on Jul. 10, 2019, which claims the benefit under 35 U.S.C. § 119(a) to Patent Application No. 2019-102246, filed in Japan on May 31, 2019, all of which are hereby expressly incorporated by reference into the present application.The present invention relates to a liquid suspension concentrate formulation comprising mefentrifluconazole.Conventionally, as one of forms of pesticide formulations, aqueous suspension concentrates referred to as SCs, in which particles of a solid pesticidally active ingredient are suspended in water, are known.Mefentrifluconazole is known as a fungicidal active ingredient of a plant disease control agent (see, for example, US Patent Application Publication No. 2014/0155262 A and WO 2017/102905).Patent Document 1: US-2014-0155262-A1Patent Document 2: WO 2017/102905-A1An object of the present invention is to provide an aqueous suspension concentrate comprising mefentrifluconazole at less than 20% by weight, which shows excellent plant disease controlling effect.The present inventor has intensively studied so as to find an aqueous suspension concentrate comprising ...

PLANTS HAVING INCREASED TOLERANCE TO HERBICIDES

The present invention refers to a method for controlling undesired vegetation at a plant cultivation site, the method comprising the steps of providing, at said site, a plant that comprises at least one nucleic acid comprising a nucleotide sequence encoding a wild-type hydroxyphenyl pyruvate dioxygenase or a mutated hydroxyphenyl pyruvate dioxygenase (mut-HPPD) which is resistant or tolerant to a HPPD-inhibiting herbicide and/or a nucleotide sequence encoding a wild-type homogentisate solanesyl transferase or a mutated homogentisate solanesyl transferase (mut-HST) which is resistant or tolerant to a HPPD-inhibiting herbicide, applying to said site an effective amount of said herbicide. The invention further refers to plants comprising mut-HPPD, and methods of obtaining such plants. 1. A method for controlling undesired vegetation at a plant cultivation site , the method comprising the steps of: (i) a nucleotide sequence encoding a wild-type hydroxyphenyl pyruvate dioxygenase or a mutated hydroxyphenyl pyruvate dioxygenase (mut-HPPD) which is resistant or tolerant to a HPPD-inhibiting herbicide and/or', '(ii) a nucleotide sequence encoding a wild-type homogentisate solanesyl transferase or a mutated homogentisate solanesyl transferase (mut-HST) which is resistant or tolerant to a HPPD-inhibiting herbicide, 'a) providing, at said site, a plant that comprises at least one nucleic acid comprising'}b) applying to said site an effective amount of said herbicide. the amino acid corresponding to or at position 236 is other than alanine;', 'the amino acid corresponding to or at position 411 is other than glutamic acid;', 'the amino acid corresponding to or at position 320 is other than leucine;', 'the amino acid corresponding to or at position 403 is other than glycine;', 'the amino acid corresponding to or at position 334 is other than leucine;', 'the amino acid corresponding to or at position 353 is other than leucine;', 'the amino acid corresponding to or at position 321 ...

AZOLE DERIVATIVES, METHODS FOR PRODUCING THE SAME, INTERMEDIATE THEREOF, AGRO-HORTICULTURAL AGENTS

An azole derivative according to the invention is represented by Formula (I), wherein each of Rand Rdenotes a hydrogen atom, or a C-Calkyl group, a C-Calkenyl group or a C-Calkynyl group; Rand Rmay be substituted with Xor Xwhich is a halogen atom; each of nand ndenotes 0 or the number of X- or X-substituted hydrogen atoms among the hydrogen atoms in Ror R; each Y denotes a halogen atom, a C-Calkyl group, a C-Chaloalkyl group, a C-Calkoxy group, a C-Chaloalkoxy group, a phenyl group, a cyano group or a nitro group; m denotes 0 to 5; and A denotes a nitrogen atom or a methyne group. 4. The compound according to claim 2 , wherein each of the alkyl group claim 2 , the alkenyl group and the alkynyl group in Rdenotes a C-Calkyl group claim 2 , a C-Calkenyl group and a C-Calkynyl group;{'sup': 'a', 'each of Xdenotes a fluorine atom, a chlorine atom or a bromine atom;'}{'sup': 'a', 'ndenotes 0 to 5;'}{'sub': 1', '3', '1', '3', '1', '3', '1', '3, 'each Y denotes a halogen atom, a C-Calkyl group, a C-Chaloalkyl group, a C-Calkoxy group or a C-Chaloalkoxy group;'}m denotes 0 to 3;A denotes a nitrogen atom.5. The compound according to claim 2 , wherein the alkyl group in Rdenotes a C-Calkyl group;{'sup': 'a', 'each of Xdenotes a chlorine atom or a bromine atom;'}{'sup': 'a', 'ndenotes 0 to 3;'}{'sub': 1', '2', '1', '2', '1', '2, 'each Y denotes a halogen atom, a C-Calkyl group, a C-Chaloalkyl group or a C-Chaloalkoxy group;'}m denotes 0 to 2.6. The compound according to claim 2 , wherein each of nand m denotes 0 to 1 claim 2 , and each Y denotes a halogen atom. This application is a Divisional of co-pending application Ser. No. 13/508,269 filed on May 25, 2012 which is a National Phase of PCT International Application No. PCT/JP/2010/007118 filed on Dec. 7, 2010, which claims the benefit of Japanese Application No. 2009-278593 filed on Dec. 8, 2009. The entire contents of all of the above applications are hereby expressly incorporated by reference.The present invention relates ...

Agroformulation comprising copolymer of acrylic acid, poly(alkylene glycol) (meth)acrylate, and alkyl (meth)acrylate

The present invention provides a composition comprising a pesticide and a copolymer, which contains in polymerized form acrylic acid and/or methacrylic acid (monomer A); a mono C-Calkyl terminated poly(C6 alkylene glycol)(meth)acrylate (monomer B); and a C-Calkyl(meth)acrylate (monomer C). Further on, it provides a process for preparing said composition by contacting the pesticide and the copolymer; a method for controlling phytopathogenic fungi and/or unwanted plant growth and/or unwanted insect or mite infestation and/or for regulating the growth of plants, wherein said composition is caused to act on the respective pests, their habitat or the plants to be protected from the respective pest, to the soil and/or to unwanted plants and/or the crop plants and/or their habitat; and a plant propagation material comprising said composition. 115-. (canceled)16. A composition comprising a pesticide and a copolymer , wherein the copolymer contains in polymerized form3 to 40 wt % of acrylic acid and/or methacrylic acid (monomer A);{'sub': 12', '22', '2-6, '10 to 45 wt % of a mono C-Calkyl terminated poly(Calkylene glycol)(meth)acrylate (monomer B);'}{'sub': 1', '8, '20 to 80 wt % of a C-Calkyl(meth)acrylate (monomer C); and'}up to 15 wt % further monomers D;wherein the sum of monomers A, B, C and D equals 100%,wherein the sum of monomers B and C is at least 50 wt %, based on the total amount of monomers,wherein the pesticide is a water-insoluble pesticide which has a solubility in water of up to and including 10 g/l at 20° C., andwherein the composition contains up to 10 wt % water.17. The composition according to claim 16 , wherein the sum of monomers B and C is at least 60 wt % claim 16 , based on the total amount of monomers.18. The composition according to claim 16 , wherein the copolymer contains5 to 30 wt % monomer A,20 to 40 wt % monomer B,30 to 70 wt % monomer C, andup to 10 wt % further monomers D,wherein the sum of monomers A, B, C and D equals 100%.19. The ...

Jinggangmycin and Ipconazole Fungicidal Composition and Applications Thereof

A jinggangmycin and ipconazole fungicidal composition, a weight ratio of jinggangmycin to ipconazole being (1-68):(40-1). The fungicidal composition of the present invention has a remarkable synergistic effect in preventing and controlling head blight of wheat and barley, powdery mildew of wheat and barley, rust of wheat and barley, sheath blight of wheat and barley, leaf blight of wheat and barley, rice blast, rice false smut and rice sheath blight, particularly the synergistic effect in preventing and controlling head blight of wheat and barley is more remarkable, and the contamination level of DON toxin in grains can be significantly decreased. 1. A jinggangmycin and ipconazole fungicidal composition , characterized in that a weight ratio of jinggangmycin to ipconazole is 1:68 to 40:1.2. The jinggangmycin and ipconazole fungicidal composition according to claim 1 , characterized in that the weight ratio of jinggangmycin to ipconazole is 1:34 to 20:1.3. The jinggangmycin and ipconazole fungicidal composition according to claim 1 , characterized in that the weight ratio of jinggangmycin to ipconazole is 1:17 to 10:1.4. The jinggangmycin and ipconazole fungicidal composition according to claim 1 , characterized in that the percentage by weight of jinggangmycin and ipconazole is 2 to 80 percent of the total content of the fungicidal composition claim 1 , and the rest is a carrier and/or adjuvant acceptable in pesticides.5. The jinggangmycin and ipconazole fungicidal composition according to claim 4 , characterized in that the percentage by weight of jinggangmycin and ipconazole is 10 to 70 percent of the total content of the fungicidal composition claim 4 , and the rest is a carrier and/or adjuvant acceptable in pesticides.6. The jinggangmycin and ipconazole fungicidal composition according to claim 1 , characterized in that a fungicidal composition preparation is wettable powder claim 1 , a suspending agent claim 1 , microemulsion or a water-dispersible granule ...

USE OF SAFENERS WITH PPO INHIBITOR HERBICIDES

Methods, compositions, and methods for making compositions for reducing crop injury by applying to crops a composition containing one or more safeners and an herbicide composition containing a protoporphyrinogen oxidase (PPO) inhibitor are disclosed. In particular aspects, the safener composition contains cloquintocet-mexyl and/or mefenpyr-diethyl. 1. A method of selectively controlling weeds in a crop , comprising applying to the crop weeds a herbicidally effective amount of a herbicidal composition comprising a quick acting herbicide and an effective amount of a safener composition.2. A method of claim 1 , wherein the safener composition comprising one or more safeners selected from the group consisting of cloquintocet-mexyl claim 1 , mefenpyr-diethyl claim 1 , benoxacor claim 1 , dichlormid claim 1 , isoxadifen-ethyl claim 1 , cyprosulfamide claim 1 , fenclorim claim 1 , fenchlorazole-ethyl claim 1 , fluxofenim claim 1 , naphthalic anhydride claim 1 , cyometrinil claim 1 , oxabetrinil claim 1 , flurazole claim 1 , furilazole claim 1 , daimuron claim 1 , cumyluron claim 1 , dimepiperate claim 1 , and dietholate.3. A method of claim 1 , wherein the quick acting herbicide is selected from the group consisting of protoporphyrinogen oxidase (PPO) inhibitor claim 1 , diquat claim 1 , paraquat claim 1 , glufosinate-ammonium claim 1 , bialaphos claim 1 , or mixtures thereof.4. A method of claim 1 , comprising applying to the crop weeds a herbicidally effective amount of a herbicidal composition comprising a protoporphyrinogen oxidase (PPO) inhibitor and an effective amount of a safener composition.5. The method of claim 4 , wherein the safener composition comprises cloquintocet-mexyl claim 4 , mefenpyr-diethyl claim 4 , or a mixture thereof.6. The method of claim 4 , wherein the protoporphyrinogen oxidase inhibitor is selected from the group consisting of carfentrazone claim 4 , carfentrazone-ethyl claim 4 , sulfentrazone claim 4 , fluthiacet-methyl claim 4 , ...

FUNGICIDAL FORMULATION

Liquid fungicidal compositions and methods for reducing phytotoxic effects of repeated exposure of vegetation to a demethylation inhibitor (DMI) fungicide are provided. The fungicidal composition comprises a mixture of at least one DMI fungicide and at least one succinate dehydrogenase inhibiting (SDHI) fungicide. Methods include applying the fungicidal composition on and/or near vegetation having or susceptible to a fungal infestation. 1. A liquid fungicidal composition comprising at least one demethylation inhibitor (DMI) fungicide and at least one succinate dehydrogenase inhibiting (SDHI) fungicide.2. The liquid fungicidal composition of claim 1 , wherein the at least one DMI fungicide comprises a triazole compound.3. The liquid fungicidal composition of claim 2 , wherein the triazole compound is tebuconazole.4. The liquid fungicidal composition of claim 1 , wherein the at least one SDHI fungicide comprises a phenyl-oxo-ethyl thiophene amide compound.5. The liquid fungicidal composition of claim 4 , wherein the phenyl-oxo-ethyl thiophene amide compound is isofetamid.6. The liquid fungicidal composition of claim 1 , wherein the relative weight ratio of the at least one DMI fungicide to the at least one SDHI fungicide is from about 0.5:1 to about 10:1.7. The liquid fungicidal composition of claim 1 , wherein the at least one DMI fungicide and the at least one SDHI fungicide are dispersed in an aqueous carrier.8. The liquid fungicidal composition of claim 1 , wherein the liquid fungicidal composition further comprises one or more surfactants.9. The liquid fungicidal composition of claim 1 , wherein the liquid fungicidal composition is a liquid fungicidal formulation.10. A method of reducing the incidence of fungal infestations in vegetation comprising the step of applying claim 1 , in the locus of the vegetation claim 1 , a fungicidal composition comprising at least one demethylation inhibitor (DMI) fungicide and at least one succinate dehydrogenase inhibiting (SDHI ...

Fungicidal substituted 1--1H-[1,2,4]triazole compounds

The present invention relates to substituted 1-{2-[2-halo-4-(4-halogen-phenoxy)-phenyl]-2-alkoxy-2-alkynyl-ethyl}-1H-[1,2,4]triazole compounds of formula I as defined in the description, and the N-oxides, and salts thereof, processes and intermediates for preparing these compounds and also to compositions comprising at least one such compound. The invention also relates to the use of such compounds and compositions for combating harmful fungi and seed coated with at least one such compound. 117-. (canceled)19. The compound of claim 18 , wherein Xis Cl.20. The compound of claim 18 , wherein Xis Cl.21. The compound of claim 18 , wherein Ris C-C-alkenyl.22. The compound of claim 18 , wherein Ris C-C-alkynyl.23. The compound of claim 18 , wherein Ris unsubstituted.24. The compound of claim 18 , wherein Ris C-C-alkyl.25. The compound of claim 18 , wherein Xand Xare Cl claim 18 , Ris CΞCH and Ris CH claim 18 , CH claim 18 , CHCΞCH claim 18 , CHCH claim 18 , or CHCHCH; and compounds wherein Xand Xare Cl claim 18 , Ris CH═CHand Ris CH claim 18 , CHCH═CH claim 18 , or CHCΞCH; and compounds wherein Xand Xare Cl claim 18 , Ris CΞCCHand Ris CH claim 18 , CH claim 18 , CHCH═CH claim 18 , CHCΞCH or CHC(Cl)═CHCl; and compounds wherein Xand Xare Cl claim 18 , Ris CHCΞCH and Ris CHCΞCH.31. An agrochemical composition comprising an auxiliary and at least one compound of claim 18 , an N-oxide or an agriculturally acceptable salt thereof.32. The composition according to claim 31 , comprising additionally a further active substance.33. Seed coated with at least one compound of claim 18 , in an amount of from 0.1 g to 10 kg per 100 kg of seed.34. A method for controlling phytopathogenic harmful fungi claim 18 , which comprises treating the fungi claim 18 , their habitat or the plants to be protected against fungal attack claim 18 , the soil or seeds with a compound of .35. The method of claim 34 , wherein Xis Cl.36. The method of claim 34 , wherein Xis Cl.37. The method of claim 34 , ...