БАКТЕРИЦИДНЫЕ КОМПОЗИЦИИ

Группа изобретений относится к области медицины, а именно к дезинфектологии, и предназначена для подавления роста микроорганизмов или более высоких форм водной флоры и фауны. Водная бактерицидная композиция включает (а) 1,5 мас.% смеси 5-хлор-2-метил-4-изотиазолин-3-она и 2-метил-4-изотиазолин-3-она и (б) 5 мас.% неионного ПАВ, содержащего Cалкильную группу, 5 молей полимеризованных звеньев пропиленоксида и 9 молей полимеризованных звеньев этиленоксида, причем массовое соотношение указанной смеси и указанного неионного ПАВ составляет 1:3,3. Также обеспечивается синергетическая бактерицидная композиция, включающая (а) смесь 5-хлор-2-метил-4-изотиазолин-3-она и 2-метил-4-изотиазолин-3-она и (б) неионное ПАВ структуры RO(CHCH(CH)O)(CHCHO)H, где R означает Cалкильную группу, х равен 5, а у равен 9, причем массовое соотношение указанной смеси и указанного неионного ПАВ составляет 1:3,3. Использование группы изобретений позволяет повысить эффективность подавления и контроля роста микроорганизмов ...

СПОСОБ РЕГУЛИРОВАНИЯ РОСТА РАСТЕНИЙ И ПРИМЕНЕНИЕ КЛОМАЗОНА ДЛЯ УЛУЧШЕНИЯ РОСТА РАСТЕНИЙ

Для улучшения роста целевых растений к участку, где растение растет, применяют соединение (I):.Изобретение позволяет улучшить рост сахарного тростника, риса, видов сои, масличного рапса и картофеля. 2 н. и 10 з.п. ф-лы, 5 пр.

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Изобретение относится к соединению общей формулы [1] или его фармацевтической приемлемой соли где R1 и R2 могут быть одинаковыми или разными и каждый из них представляет собой C1-С10-алкильную группу; R3 и R4 каждый представляет собой атом водорода; R5 и R6 могут быть одинаковыми или разными и каждый из них представляет собой атом водорода или C1-С10-алкильную группу; Y представляет собой 5-6-членную ароматическую гетероциклическую группу или конденсированную ароматическую гетероциклическую группу, содержащую один или несколько гетероатомов, выбранных из атома азота, атома кислорода и атома серы, причем гетероциклическая группа может быть замещена 0-6 одинаковыми или разными группами, выбранными из следующей группы заместителей α, и т.д.; n принимает целые значения от 0 до 2; [группа заместителей α]: гидроксильная группа; атомы галогена; С1-С10-алкильные группы; C1-С10-алкильные группы, каждая из которых монозамещена группой, выбранной из следующей группы заместителей β; С1-С4-галогеналкильные ...

ГЕРБИЦИДНЫЕ СРЕДСТВА И СПОСОБ БОРЬБЫ С СОРНЯКАМИ

Описывается гербицидное средство, содержащее (А) соединение формулы (I) где V означает остаток из группы (V2)-(V3): R2 означает атом водорода, алкил с 1-4 атомами углерода или алкоксил с 1-4 атомами углерода; R3 означает атом водорода или алкилсульфонил с 1-4 атомами углерода; R4 означает метил, этил или н-пропил; R6 означает гидроксил; m означает О; и Z означает остаток (ZI): , где R9 одинаковые или разные, означают галоген, галогеналкил с 1-4 атомами углерода, галогеналкоксиалкил с 1-4 атомами углерода в галогеналкоксильной части и 1-4 атомами углерода в алкильной части, алкилсульфонил с 1-4 атомами углерода или 4,5-дигидроизоксазол-3-ил, замещенный цианометилом; q означает 2 или 3; и (Б) поверхностно-активное вещество формулы (II): причем компоненты (А) и (В) взяты в синергетически эффективном соотношении. Описывается также способ борьбы с сорняками. Предлагаемые гербицидные средства обладают гербицидной активностью против широкого спектра экономически важных однодольных и двудольных ...

СИНЕРГИЧЕСКИЕ МИКРОБИЦИДНЫЕ КОМПОЗИЦИИ

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ИЗОКСАЗОЛИНОВЫЕ СОЕДИНЕНИЯ И ИХ ПРИМЕНЕНИЕ В БОРЬБЕ С ВРЕДИТЕЛЯМИ

Изобретение относится к соединениям общей формулы (1), где R1 представляет собой С1-С4галогеналкильную группу, R2 представляет собой атом галогена, R3 представляет собой C1-С6алкильную группу, C1-С6алкоксигруппу или атом галогена, m равно целому числу от 0 до 5, n равно целому числу от 0 до 4, М представляет собой атом кислорода или атом серы, R4 является таким, как определено в формуле изобретения. Также изобретение относится к способу борьбы с насекомыми, к применению соединений формулы (1) и композиции, содержащей соединения формулы (1), для борьбы с насекомыми. Технический результат - соединения формулы (1) для борьбы с насекомыми. 5 н. и 15 з.п. ф-лы, 119 пр.

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Изобретение относится карбоновокислым производным бензогетероциклилпиридинов и бензогетероциклилпиримидинов общей формулы (I)причем А означает остаток, из группы, состоящей из A3 и А15:Rозначает водород или алкил с 1-4 атомами углерода, Rозначает хлор, Rозначает водород, Rозначает водород, Rозначает водород или галоген, Rозначает водород или галоген, Rозначает водород, галоген или алкил с 1-3 атомами углерода, Rозначает водород или алкил с 1-3 атомами углерода, X означает N, СН или CF, и n означает 0, 1 или 2, и их применению в качестве гербицидов. 4 н. и 3 з.п. ф-лы, 44 табл.

КОМПОЗИЦИЯ ДЛЯ БОРЬБЫ С БОЛЕЗНЬЮ РАСТЕНИЯ И СПОСОБ БОРЬБЫ С БОЛЕЗНЬЮ РАСТЕНИЯ

Изобретение относится к сельскому хозяйству. Композиция для борьбы с болезнями растений, вызванных грибами, включает соединение, описывающееся следующей формулой (1):,соединение, описывающееся следующей формулой (2):,и соединение, описывающееся следующей формулой (3):где комбинация R, R, Rи Rявляется комбинацией, в которой Rозначает метильную группу, Rозначает трифторметильную группу и оба Rи Rозначают атом фтора, или комбинацией, в которой оба Rи Rозначают дифторметильную группу, Rозначает атом хлора и Rозначает метансульфонилоксигруппу. Способ борьбы с болезнями растений включает стадию нанесения эффективного количества соединения, описывающегося указанной выше формулой (1), соединения, описывающегося указанной выше формулой (2), и соединения, описывающегося указанной выше формулой (3) на семя растения. Изобретение позволяет повысить эффективность борьбы с грибными болезнями. 4 н. и 3 з.п. ф-лы, 2 табл., 2 пр.

ОРГАНИЧЕСКИЕ СОЕДИНЕНИЯ

Изобретение относится к соединениям формулы (Iа) и (Ib), где X представляет собой S или O, один из Xи Xпредставляет собой СR' и второй представляет собой N или независимо СR', n представляет собой целое число 1, 2 или 3; Rпредставляет собой C-галогеналкил, Rвыбран из галогена и C-C-галогеналкила; R' представляет собой H, C-C-алкил, галоген, цианогруппу, или фенил, незамещенный или замещенный галогеном, C-C-алкоксигруппой, C-C-галогеналкоксигруппой, C-C-галогеналкильной группой; Z представляет собой галоген, радикал Q или группу -C(O)-NRR; Rпредставляет собой H или C-C-алкил, Rпредставляет собой H; Q', C-C-алкил, незамещенный или замещенный галогеном, цианогруппой, C-C-алкоксигруппой, C-C-алкоксикарбонилом, C-C-алканоилом, аминокарбонилом, N-моно- или N,N-ди-C-C-алкиламинокарбонилом, C-C-алкилтиогруппой, группой -C(O)NHRили радикалом Q"; или C-C-циклоалкил, замещенный группой -C(O)NHR; или C-C-алкинил; Q, Q'и Q" являются такими, как указано в формуле изобретения; Rпредставляет собой C-C-алкил ...

БИОЦИДНАЯ КОМПОЗИЦИЯ (ВАРИАНТЫ) И СПОСОБ ИНГИБИРОВАНИЯ БАКТЕРИАЛЬНОГО РОСТА

Изобретение относится к биоцидным композициям. Биоцидная композиция содержит 1-(3-хлораллил)-3,5,7-триаза-1-азониаадамантан хлорид и диспергирующий агент, содержащий сополимер этиленоксида и пропиленоксида в качестве стабилизатора цвета и фазового стабилизатора для 1-(3-хлораллил)-3,5,7-триаза-1-азониаадамантан хлорида; носитель, содержащий полиэтиленгликоль, кэпированный простым моноэфиром, или полипропиленгликоль, и загуститель, содержащий полиэтиленгликоль. Композиция ингибирует бактериальный рост в среде. Изобретение позволяет повысить стабильность композиции. 4 н. и 9 з.п. ф-лы, 1 табл., 12 пр.

5-ФТОРПИРИМИДИНОВЫЕ ПРОИЗВОДНЫЕ В КАЧЕСТВЕ ФУНГИЦИДОВ

Изобретение относится к новым 5-фторпиримидинам общей формулы I, обладающим фунгицидной активностью. В соединениях формулы IRпредставляет собой -N(R)R; Rпредставляет собой -OR;Rпредставляет собой: H; C-C-алкил, необязательно замещенный 1-3 группами R; C-C-алкенил, необязательно замещенный 1-3 группами R; 5- или 6-членный гетероароматический цикл, выбранный из группы, состоящей из фуранила, пиридинила, пиримидинила, пиридазинила, пиразинила, тиазолила, тиадиазолила, оксазолила, изоксазолила, триазолила; при этом каждый гетероароматический цикл необязательно замещен 1-3 группами R; 3H-изобензофуран-1-онил; -C(=O)R; -C(=S)R; -C(=S)NHR; -(=O)N(R)R; -OR; -P(O)(OR); -S(O)R;-SR; -Si(R); -N(R)R; -(CHR)ORили -C(=NR)SR; где m равно целому числу от 1 до 3; Rпредставляет собой: H; C-C-алкил, необязательно замещенный 1-3 группами R; или -C(=O)R; в качестве альтернативы Rи R, взятые вместе, могут образовывать: 5- или 6-членный насыщенный или ненасыщенный цикл, содержащий 1-2 гетероатома, выбранных из ...

ГЕРБИЦИДНАЯ КОМПОЗИЦИЯ

Изобретение относится к сельскому хозяйству. Гербицидная композиция содержит (A) метобромурон или его соль и (B) по меньшей мере одно гербицидное соединение, выбранное из группы, включающей хлорпрофам, флуфенацет, пироксасульфон, никосульфурон, просульфокарб, тиобенкарб и инданофан, или его алкиловый сложный эфир или его соль. Изобретение позволяет эффективность композиции. 2 н. и 7 з.п. ф-лы, 33 табл., 32 пр.

БИОЦИДНАЯ КОМПОЗИЦИЯ, СПОСОБ ПОЛУЧЕНИЯ ТАКОЙ КОМПОЗИЦИИ И СПОСОБ ПОДАВЛЕНИЯ РОСТА МИКРООРГАНИЗМОВ В ВОДООСНОВНЫХ СИСТЕМАХ

Изобретение относится к биоцидным композициям. Биоцидная композиция содержит: эффективное количество биоцида, выбранного из одного или нескольких 3-йод-2-пропинилбутилкарбамата (IPBC), октилизотиазолинона (OIT), дийодметил-р-толилсульфона (DIMTS), биоцидов на основе триазина, таких как тербутрин, цибутрин и прометрин, азолов, таких как пропиконазол, дифеноконазол, ципроконазол и тебуконазол, 2,2-дибром-3-нитрилопропионамида (DBNPA), 2-бром-2-нитропропан-1,3-диола (бронопола), и 2,2-дибром-3-нитрилопропионамида; и алкилполигликолевую жидкость-носитель формулы (I) R-O-(AO)-H, где R является С-Салкилом; АО является этиленоксидной группой и n является средним числом повторяющихся АО элементарных звеньев и равно, по меньшей мере, 4. Композицию получают смешиванием ингредиентов. Композицию добавляют в водоосновные системы для подавления роста микроорганизмов. Изобретение позволяет понизить вязкость и летучесть композиции при высоких концентрациях активных веществ. 3 н. и 7 з.п. ф-лы. 8 табл., ...

КОМПОЗИЦИЯ НА ОСНОВЕ КОМБИНАЦИИ ЛИПО-ХИТООЛИГОСАХАРИДА ДЛЯ УСИЛЕНИЯ УРОЖАЙНОСТИ РАСТЕНИЙ

Изобретение относится к сельскому хозяйству. Композиция для повышения урожайности бобовых и небобовых культур включает липо-хитоолигосахариды в комбинации с флавоноидными соединениями, таким как дайдзеин. Способ повышения урожайности бобовых и небобовых культур включает обработку композицией семян и/или растений либо одновременно, либо последовательно. 3 н. и 41 з.п. ф-лы, 16 табл., 16 пр.

ПЕСТИЦИДНЫЕ КОМПОЗИЦИИ

Изобретение относится к сельскому хозяйству. Соединение формулы двагде (a) Arпредставляет собой замещенный фенил, содержащий один или несколько заместителей, независимо выбранных из C-Сгалогеналкила и C-Сгалогеналкокси; (b) Het представляет собой 1,2,4-триазолил(c) Arпредставляет собой фенил; (d) R1 представляет собой Н или C-Cалкил; (g) R4 представляет собой фенил, замещенный одним или несколькими заместителями, независимо выбранными из F, Cl, Br, I и C-Салкила; (h) R5 представляет собой 1-членную насыщенную углеводородную связь. Изобретение позволяет повысить эффективность борьбы с вредителями. 2 н. и 2 з.п. ф-лы, 5 табл., 24 пр.

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Изобретение относится к способу получения водной дисперсии, которая включает один или более загустителей и твердые частицы 1,2-бензизотиазолин-3-она. Способ включает стадии: (а) образования водной смеси (I), включающей воду, растворенную соль 1,2-бензизотиазолин-3-она, при этом рН водной смеси (I) составляет 8,5 или более, (b) последующего образования водной дисперсии при смешивании в любой последовательности компонентов, включающих кислоту, водную смесь (I) и один или более загустителей, добавляемых либо на стадии (а), и/или на стадии (b), причем рН указанной дисперсии составляет от 1,5 до 7,5. Также изобретение относится к водной дисперсии, предназначенной для уничтожения микроорганизмов, полученной указанным способом. Технический результат - получение стабильной дисперсии 1,2-бензотиазолин-3-она с малым размером частиц. 2 н. и 9 з.п. ф-лы, 20 пр.

ПЕСТИЦИДНЫЕ КОМПОЗИЦИИ И СВЯЗАННЫЕ С НИМИ СПОСОБЫ

Изобретение относится к сельскому хозяйству. Соединение формулы два или тригде:(a) Arпредставляет собой (1) фуранил, фенил, пиридазинил, пиридил, пиримидинил, тиенил или (2) замещенный фуранил, замещенный фенил, замещенный пиридазинил, замещенный пиридил, замещенный пиримидинил, или замещенный тиенил или другие заместители, перечисленные в описании. Изобретение позволяет повысить эффективность борьбы с вредителями. 5 н. и 22 з.п. ф-лы, 5 табл.

ИНГИБИРОВАНИЕ ОБРАЗОВАНИЯ БИОГЕННОГО СУЛЬФИДА ПОСРЕДСТВОМ КОМБИНАЦИИ БИОЦИДА И МЕТАБОЛИЧЕСКОГО ИНГИБИТОРА

Изобретение относится к биотехнологии. В частности изобретение относится к композиции для эффективного ингибирования продукции сульфида сульфатвосстанавливающими бактериями (SRB), причем указанная композиция включает комбинацию: (а) компонента биоцида, способного непосредственно уничтожать первую порцию SRB, где указанный компонент биоцида присутствует в комбинации в первой концентрации, которая меньше, чем примерно 90% минимальной ингибирующей концентрации (MIC) компонента биоцида; и (b) компонента метаболического ингибитора, способного ингибировать рост второй порции SRB без прямого уничтожения второй порции SRB, где указанный компонент метаболического ингибитора присутствует в комбинации во второй концентрации, которая меньше, чем примерно 90% минимальной ингибирующей концентрации (MIC) компонента метаболического ингибитора, где комбинация проявляет синергетический эффект в ингибировании продукции сульфида SRB в сравнении с каждым компонентом в отдельности. Обработка SRB и биоцидом, ...

СИНЕРГЕТИЧЕСКАЯ БОРЬБА С СОРНЯКАМИ ПУТЕМ НАНЕСЕНИЯ ФЕНОКССУЛАМА И БЕНЗОБИЦИКЛОНА ИЛИ КЛОМАЗОНА И БЕНЗОБИЦИКЛОНА

Изобретение относится к сельскому хозяйству. Гербицидная композиция содержит синергетически гербицидно эффективное количество (а) фенокссулама или его сельскохозяйственно приемлемой соли или кломазона или его сельскохозяйственно приемлемой соли и (b) бензобициклона или его сельскохозяйственно приемлемой соли, в которой, если (а) представляет собой фенокссулам или его сельскохозяйственно приемлемую соль, гербицидная смесь состоит из (а) фенокссулама или его сельскохозяйственно приемлемой соли и (b) бензобициклона или его сельскохозяйственно приемлемой соли. Изобретение позволяет повысить эффективность борьбы с сорняками. 2 н. и 22 з.п. ф-лы, 2 табл.

ГЕРБИЦИДНАЯ КОМБИНАЦИЯ

Изобретение относится к сельскому хозяйству, в частности к контролю нежелательной растительности. Синергетическая гербицидная смесь для контроля сорняков в сельскохозяйственных культурах содержит: (a) амикарбазон; (b) по меньшей мере ингибитор фотосистемы II, выбранный из атразина, диурона, аметрина, и (c) по меньшей мере третий гербицид, выбранный из изоксафлютола, кломазона, сульфентразона, мезотриона, S-метолахлора, где указанная смесь выбрана из: (i) смеси амикарбазона, изоксафлютола и атразина; (iv) смеси амикарбазона, кломазона и диурона; (vii) смеси амикарбазона, S-метолахлора и атразина; (viii) смеси амикарбазона, сульфентразона и диурона; и (х) смеси амикарбазона, мезотриона и аметрина. Синергическую гербицидную смесь применяют в композиции для контроля нежелательной растительности. Предлагаемая синергическая гербицидная смесь и композиция на её основе обеспечивают эффективную борьбу с широким спектром сорной растительности, способствуют управлению устойчивостью к гербицидам, снижению ...

СИНЕРГЕТИЧЕСКАЯ КОМБИНАЦИЯ, ВКЛЮЧАЮЩАЯ ГЛИФОСАТ И ОДНО ИЗ СЛЕДУЮЩИХ СОЕДИНЕНИЙ: ДХОИТ ИЛИ ОИТ ИЛИ ББИТ

Группа изобретений относится к синергетической противомикробной композиции, включающей цинковую соль глифосата и 4,5-дихлор-2-н-октил-4-изотиазолин-3-он, и предназначена для обеспечения контроля уровня грибов и водорослей. Также группа изобретений обеспечивает способ подавления роста или контроля роста микроорганизмов в строительном материале при добавлении указанной синергетической противомикробной композиции, композицию для покрытия, содержащую указанную синергетическую противомикробную композицию, и сухую пленку, полученную из указанной композиции для покрытия. Использование группы изобретений позволяет повысить эффективность подавления роста микроорганизмов, обеспечить более точный контроль роста микроорганизмов, не оказывая при этом влияния на здоровье и/или окружающее среду. 12 н.п. ф-лы, 7 таб.

МИКРОКАПСУЛЫ С АЦЕТИЛЕНКАРБАМИД-ПОЛИМОЧЕВИННЫМИ ПОЛИМЕРАМИ И ИХ КОМПОЗИЦИИ ДЛЯ РЕГУЛИРОВАННОГО ВЫСВОБОЖДЕНИЯ

Настоящее изобретение относится к микрокапсулам, используемым в агрохимических композициях, в составе какого-либо типа композиции, приемлемого для применения в сельском хозяйстве, а также для микрокапсуляции фармацевтических или медицинских соединений, замедлителей горения, материалов фазового превращения, термореактивных материалов, чернил, катализаторов. Микрокапсулы заключают материал с растворимостью в воде ниже 750 мг/л при 20°С, причем стенка микрокапсул сформирована посредством реакции межфазовой полимеризации материалов, формирующих стенку: (а) алифатический изоцианат(ы), и (b) ароматический изоцианат(ы), и (с) соединение(ия) формулы (I), ацетиленкарбамидные производные, ! ! где R1, R3, R5, R7 представляют собой, независимо друг от друга, метил, этил, n-пропил, изопропил, n-бутил, изобутил, втор-бутилен, трет-бутил; R2, R4, R6, R8 представляют собой, независимо друг от друга, водород, метил, этил, n-пропил, изопропил, n-бутил, изобутил, втор.-бутил, трет.-бутил; R9, R10 представляют ...

СПОСОБ ПОЛУЧЕНИЯ 1,2-БЕНЗИЗОТИАЗОЛИН-3-ОНОВ(ВАРИАНТЫ)

Изобретение относится к способу получения 2-алкилбензизотиазолинов, который включает взаимодействие бисамида формулы 2 в воде или в содержащей воду органической жидкости с бисульфитом или с выделяющим бисульфит агентом с образованием соли Бунте и превращение соли Бунте в щелочных условиях в 2-алкил-БИТ. R представляет собой алкил. Предпочтительными R-заместителями являются бутил, гексил, 2-этилбутил, 2-этилгексил или циклоалкил. Технический результат - увеличение выхода N-алкил-БИТ. 3 с. и 7 з.п. ф-лы.

СПОСОБ БОРЬБЫ С РОСТОМ СОРНЯКОВ, ГЕРБИЦИДНАЯ КОМПОЗИЦИЯ И ПРОДУКТ

Способ борьбы с ростом сорняков включает применение к локусу в качестве активного компонента а) производного 4-бензоилизоксазола формулы I, где R - Н или -CO2R3, R1 - циклопропил; R2 - галоген, -S(O)pMe и C1-6-галогеналкил; n = 2 или 3; p = 0 или 2; R3 - C1-4-алкил; и б) триазиновый гербицид, выбранный из атразина, цианазина или метрибузина, при массовом соотношении (а) : (б) = 2:1-1:1000. Предпочтительным является объединенное использование (а) и (б) для подавления травянистых сорняков в посевах кукурузы. 3 с. и 13 з.п. ф-лы, 8 ил., 20 табл.

ПРОИЗВОДНОЕ 4-БЕНЗОИЛИЗОКСАЗОЛА ИЛИ ЕГО ПРИЕМЛЕМАЯ ДЛЯ СЕЛЬСКОГО ХОЗЯЙСТВА СОЛЬ, ГЕРБИЦИДНАЯ КОМПОЗИЦИЯ И СПОСОБ БОРЬБЫ С СОРНЯКАМИ

Изобретение относится к новым производным 4-бензоилизоксазола формулы I, где R - водород или -CO2R4; R1 - C3-6-циклоалкил; R2 - галоген, н-алкил, возможно замещенный одним и более атомов галогена, или -OR5, -S(O)pR6; R3 - -S(O)qR7; X - -(CR9R10)t-; n = 0, 1 и 2; когда n больше 1, группы R2 могут быть одинаковыми или различными; R4, R5 и R6 -н-алкил; R7-н-алкил, возможно замещенный одним или большим числом атомов водорода, C3-C6-алкенил с прямой цепью или фенил; R9 и R10 - водород или C1-C6-алкил с прямой цепью; p и q = 0, 1 или 2; t - целое число от 1 до 4, когда t > 1, группы -CR9R10 могут быть одинаковыми или различными; или их приемлемые для сельского хозяйства соли. Соединения формулы I демонстрируют гербицидную активность против двудольных и однодольных сорняков при применении до и после появления всходов. 3 с. и 7 з.п. ф-лы. 9 табл.

ПРОИЗВОДНЫЕ БЕНЗИМИДАЗОЛА И ИХ СОЛИ, ОБРАЗОВАННЫЕ ПРИСОЕДИНЕНИЕМ КИСЛОТ, СПОСОБ ИХ ПОЛУЧЕНИЯ И МИКРОБИЦИДНОЕ СРЕДСТВО НА ИХ ОСНОВЕ

Производные бензимидазола общей фрмулы I, где Х1 - Х4 и R1 имеют указанные в формуле изобретения значения, и их соли. Указанные соединения получают взаимодействием соединения указанной в формуле изобретения формулы II с соединением формулы Гал-Y-R1. производные бензимидазола общей формулы I обладают микробицидной активностью. 3 с.п.ф-лы, 4 табл.

ЦИКЛИЧЕСКИЕ АМИДЫ ИЛИ ИХ СЕЛЬСКОХОЗЯЙСТВЕННО ПРИГОДНЫЕ СОЛИ, ФУНГИЦИДНАЯ КОМПОЗИЦИЯ, СПОСОБ БОРЬБЫ С БОЛЕЗНЯМИ РАСТЕНИЙ, ВЫЗВАННЫМИ ФИТОПАТОГЕННЫМИ ГРИБАМИ

Изобретение относится к циклическим амидам , замещенным в α-положении различными арильными группами, их сельскохозяйственно пригодным солям и составам на их основе, и их использованию в качестве фунгицидов системного или избирательного действия. Указанные соединения представлены общей формулой I (значение радикалов см. в формуле изобретения). 3 с. и 8 з.п.ф-лы, 33 табл.

ПРОИЗВОДНЫЕ 5-АРИЛИЗОКСАЗОЛА, СПОСОБЫ ИХ ПОЛУЧЕНИЯ, ГЕРБИЦИДНАЯ КОМПОЗИЦИЯ И СПОСОБ ПОДАВЛЕНИЯ СОРНЯКОВ В ЛОКУСЕ

Использование: в сельском хозяйстве в качестве гербицидов. Сущность: продукт-производные 5-арилизоксазола ф-лы 1 с определенными значениями радикалов. Получение соединений 1 ведут тремя способами. Гербицидная композиция, содержащая эффективное количество соединений ф-лы 1 и целевые добавки и способ подавления сорняков в локусе с использованием в качестве гербицида соединений ф-лы 1: 6 с. п. ф-лы, 5 з. п. ф-лы, 5 табл.

Изоксазолиновые композиции и их применение в провилактике или лечении паразитарных инвазий животных

Группа изобретений относится к ветеринарии. Предложено применение фармацевтической композиции, содержащей флураланер, или его соль, или его сольват и фармацевтически приемлемый носитель, содержащий моноэтиловый эфир диэтиленгликоля и полисорбатное поверхностно-активное вещество, для получения лекарственного средства для введения через питьевую воду для профилактики или лечения паразитарных инвазий животных. Также предложена лечебная питьевая вода и способ получения лечебной питьевой воды. Группа изобретений обеспечивает профилактику и лечение паразитарных инвазий у домашней птицы. 3 н. и 33 з.п. ф-лы, 5 табл., 5 пр.

СОЕДИНЕНИЕ МАЛОНОНИТРИЛА В КАЧЕСТВЕ ПЕСТИЦИДОВ

... 1. Соединение малононитрила, представленное формулой(I) где любой из X1, X2, X3 и X4 представляет собой CR100, (где R100 представляет собой группу, представленную формулой где R1 представляет собой C1-C5 алкил, необязательно замещенный одним или несколькими галогенами, C2-C5 алкенил, необязательно замещенный одним или несколькими галогенами, C2-C5 алкинил, необязательно замещенный одним или несколькими галогенами, или водород, R2 представляет собой C1-C5 алкил, необязательно замещенный одним или несколькими галогенами, C1-C5 алкокси, необязательно замещенный одним или несколькими галогенами, C2-C5 алкенил, необязательно замещенный одним или несколькими галогенами, C2-C5 алкинил, необязательно замещенный одним или несколькими галогенами, циано или водород, каждый из R3 и R4 представляет собой C1-C5 алкил, необязательно замещенный одним или несколькими галогенами, C2-C5 алкенил, необязательно замещенный одним или несколькими галогенами, C2-C5 алкинил, необязательно замещенный одним или несколькими ...

СПОСОБ БОРЬБЫ С ВРЕДНЫМИ РАСТЕНИЯМИ В КУЛЬТУРАХ ПОЛЕЗНЫХ РАСТЕНИЙ

... 1. Способ борьбы с вредными растениями в культурах полезных растений, в котором на вредные растения, культурные растения, семена растений или площади, на которых произрастают растения, наносят со смещением во времени А) эффективное количество одного или нескольких гербицидов формулы (I) где символы и индексы имеют следующие значения: R - водород или (С1-С4)-алкоксикарбонил; R1 - водород, (С1-С4)-алкил, (С2-С4)-алкенил, (С2-С4)-алкинил, (С3-С8)-циклоалкил, (С3-С8)-циклоалкенил, (С1-С4)-алкил-(С3-С8 )-циклоалкил, (С3-С7)-галоидциклоалкил, (С1-С4)-алкилтио-(С3-С8)-циклоалкил, (С1-С8)-галоидалкил или (С2-С8)-галоидалкенил, преимущественно (С3-С7)-циклоалкил, (C1-C4)-алкил-(С3-С7)-циклоалкил; R2 - одинаковые или разные галоиды, нитро, циано, (С1-С4)-алкил, (С2-С4)-алкенил, (С2-С4)-алкинил, (С1-С4 )-галоидалкил, (С2-С4)-галоидалкенил, (С2-С4)-галоидалкинил, (С1-С4)-алкокси-(С1-С4)-алкил, (С1-С4)-алкилтио, (C1-C4)-алкилсульфинил, (С1-С4)-алкилсульфонил, (С1-С4)-алкокси-(С1-С4)-алкокси, (С1-С4) ...

ГЕРБИЦИДНАЯ КОМПОЗИЦИЯ

... 1. Гербицидная композиция, содержащая, в качестве активных ингредиентов, (а) никосульфурон или его соль, b) тербутилазин или его соль и (с) соединение С (соединение С представляет собой по меньшей мере одно гербицидное соединение, выбранное из группы, состоящей из группы С1 и группы С2 или его соли; группа С1 представляет собой по меньшей мере один ингибитор 4-гидроксифенилпируватдиоксигеназы, выбранный из группы, состоящей из сулкотриона, бициклопирона, мезотриона, топрамезона и их солей; и группа С2 представляет собой по меньшей мере один ингибитор биосинтеза жирной кислоты с очень длинной цепью, выбранный из группы, состоящей из диметенамида-П, флуфенацета и их солей).2. Гербицидная композиция по п. 1, где отношение в смеси (а) к (b) составляет от 1:0,5 до 1:800 по массе, и отношение в смеси (а) к (с) равно от 1:0,03 до 1:800 по массе.3. Гербицидная композиция по п. 1, где (с) представляет собой по меньшей мере один ингибитор 4-гидроксифенилпируватдиоксигеназы, выбранный из группы, состоящей ...

СРЕДСТВА НА ОСНОВЕ ГЕТЕРОЦИКЛИЧЕСКОГО ДИАМИДА ДЛЯ СРЕДСТВА НА ОСНОВЕ ГЕТЕРОЦИКЛИЧЕСКОГО ДИАМИДА ДЛЯ БОРЬБЫ С БЕСПОЗВОНОЧНЫМИ ВРЕДИТЕЛЯМИ БОРЬБЫ С БЕСПОЗВОНОЧНЫМИ ВРЕДИТЕЛЯМИ

... 1. Соединение формулы I, его N-оксид или приемлемая соль где A и B обозначают независимо O или S; каждый J обозначает независимо фенильное кольцо, нафтильную кольцевую систему, 5- или 6-членное гетероароматическое кольцо или ароматическую 8-, 9- или 10-членную конденсированную гетеробициклическую кольцевую систему, где каждое кольцо или кольцевая система необязательно замещены 1-4 R5; K обозначает, вместе с двумя соседними связующими атомами углерода, 5- или 6-членное гетероароматическое кольцо, необязательно замещенное 1-3 R4; n равно 1-3; R1 обозначает H; или C1-C6алкил, C2-C6алкенил, C2 -C6алкинил или C3-C6циклоалкил, каждый из которых необязательно замещен одним или несколькими заместителями, выбранными из группы, включающей галоген, CN, NO2, гидрокси, C1 -C4алкокси, C1-C4алкилтио, C1-C4алкилсульфинил, C1-C4алкилсульфонил, C2-C4алкоксикарбонил, C1-C4алкиламино, C2-C8диалкиламино и C3-C6циклоалкиламино, или R1 обозначает C2-C6 алкилкарбонил, C2-C6алкоксикарбонил, C2- C6алкиламинокарбонил ...

ГЕРБИЦИДНОЕ СРЕДСТВО, СОДЕРЖАЩЕЕ БЕНЗОИЛПИРАЗОЛЫ И ЗАЩИТНЫЕ СРЕДСТВА

... 1. Гербицидное средство, содержащее А) гербицидно- активное количество одного или нескольких соединений формулы (I) символы и индексы в которой означают: R1 является алкилом с 1-6 атомами углерода, R2 является водородом или алкилом с 1-6 атомами углерода, R3 является водородом, галогеном, алкилом с 1-6 атомами углерода, галогеналкилом с 1-6 атомами углерода, алкокси с 1-6 атомами углерода, галогеналкокси с 1-6 атомами углерода, алкилтио с 1-6 атомами углерод, алкилсульфинил с 1-6 атомами углерода, алкилсульфонил с 1-6 атомами углерода, R4, R5, R6 являются водородом, алкилом с 1-6 атомами углерода, R7 является алкилом с 1-6 атомами углерода, а является 0, 1 или 2, и В) антидото -активное количество одного или нескольких соединений формулы (II) или (III) в которых R8, R9, R10 независимо друг от друга означают водород или алкил с 1-4 атомами углерода, включая стереоизомеры и приемлемые в сельском хозяйстве соли. 2. Гербицидное средство по п.1, символы и индексы в котором означают: R1 является ...

ПРОИЗВОДНЫЕ ИЗОКСАЗОЛИНА В КАЧЕСТВЕ ПРОТИВОПАРАЗИТАРНЫХ АГЕНТОВ

... 1. Соединение формулы (1),гдеА представляет собой фенил, нафтил или гетероарил, где указанный гетероарил содержит от 1 до 4 гетероатомов, каждый из которых независимо выбран из N, О и S;каждый из R, Rи Rнезависимо представляет собой водород, галоген, гидроксил, циано, нитро, C-Салкил, C-Сгалогеналкил, C-Салкокси, С-СалкилС-Сциклоалкил, C-Сгалогеналкокси, -C(O)NH, -SFили -S(O)R;Rпредставляет собой галоген, циано, C-Салкил, C-Сгалогеналкил, нитро, гидроксил, -C(O)NRR, С-Салкенил, С-Салкинил, -S(O)R или -OR;Rпредставляет собой водород, галоген, гидроксил, циано, C-Салкил, C-Сгалогеналкил, С-СалкилС-Сциклоалкил, -C(O)NH, нитро, -SC(O)R, -C(O)NRR, С-СалкилNRR, -NRNRR, -NROR, -ONRR, N, -NHR, -OR или -S(O)R;Rпредставляет собой водород, C-Салкил, C-СалкилС-Сциклоалкил, -C(O)R, -C(S)R, -C(O)NRR, -C(O)C(O)NRR, -S(O)R, -S(O)NRR, -C(NR)R, -C(NR)NRR, С-Салкилфенил, С-Салкилгетероарил или С-Салкилгетероцикл;Rпредставляет собой водород, C-Салкил, С-Салкенил, С-СалкилС-Сциклоалкил, С-Салкилфенил, С-Салкилгетероарил ...

ГЕРБИЦИДНЫЕ КОМПОЗИЦИИ, СОДЕРЖАЩИЕ ИЗОКСАБЕН И АМИНОПИРАЛИД

ГЕРБИЦИДНЫЕ КОМПОЗИЦИИ НА ОСНОВЕ КАРБАМОИЛТРИАЗОЛИНОНА И СПОСОБЫ ИХ ПРИМЕНЕНИЯ

ХИТООЛИГОСАХАРИДЫ И СПОСОБЫ ИХ ПРИМЕНЕНИЯ ДЛЯ УСИЛЕНИЯ РОСТА РАСТЕНИЙ

Изобретение относится к сельскому хозяйству. Композиция для усиления роста растения содержит сельскохозяйственно подходящий носитель и хитоолигосахарид (ХО), представленный формулой:,в которой Rозначает водород или метил; Rозначает водород или метил; Rозначает водород, ацетил или карбамоил; Rозначает водород, ацетил или карбамоил; Rозначает водород, ацетил или карбамоил; Rозначает водород, арабинозил, фукозил, ацетил, сульфат, 3--S-2--MeFuc, 2--MeFuc и 4--AcFuc; Rозначает водород, маннозил или глицерин; Rозначает водород, метил или -CHOH; Rозначает водород, арабинозил или фукозил; Rозначает водород, ацетил или фукозил; и n равно 0, 1, 2 или 3. Указанный ХО присутствует в концентрации, подходящей для усиления роста растения, когда семена растения, обработанные указанной композицией, высаживают и выращивают в почве. 3 н. и 17 з.п. ф-лы, 31 ил., 3 табл., 20 пр.

ГЕРБИЦИДНАЯ КОМПОЗИЦИЯ

СПОСОБ СТАБИЛИЗАЦИИ БАКТЕРИАЛЬНОГО СОДЕРЖИМОГО ВОДНОГО ИЗМЕЛЬЧЕННОГО ПРИРОДНОГО КАРБОНАТА КАЛЬЦИЯ, И/ИЛИ ОСАЖДЕННОГО КАРБОНАТА КАЛЬЦИЯ, И/ИЛИ ПРОРЕАГИРОВАВШИХ НА ПОВЕРХНОСТИ СОДЕРЖАЩИХ КАРБОНАТ КАЛЬЦИЯ МИНЕРАЛЬНЫХ ПРЕПАРАТОВ

Изобретение относится к биоцидам. Осуществляют стабилизацию водного минерального препарата, включающую стадии:(a) добавления, по крайней мере, одного содержащего альдегид, и/или выделяющего альдегид, и/или фенольного, и/или изотиазолинового биоцида к указанному водному минеральному препарату. Указанный минерал содержит, по крайней мере, один из: измельченного природного карбоната кальция, осажденного карбоната кальция, доломита, прореагировавшего на поверхности карбоната кальция, глины, талька, TiO, каолина, каолинитовой глины, кальцинированной каолинитовой глины, сульфата кальция, кварца, аттапульгита, монтмориллонита, диатомовой земли, тонкоизмельченной двуокиси кремния, оксида алюминия, гидроксида алюминия, силикатов, таких как силикат алюминия, пемза и сепиолит, или их смесей. Осуществляют стадию (b), которая может быть одновременной и/или отдельной от стадии (a), путем добавления, по крайней мере, одного соединения линейного или циклического диамина или триамина к указанному водному ...

СИНЕРГИЧЕСКИЕ ФУНГИЦИДНЫЕ КОМПОЗИЦИИ

ПРИМЕНЕНИЕ КОМБИНАЦИЙ, СОДЕРЖАЩИХ ИНДУКТОРЫ ЗАЩИТНЫХ СИЛ ОРГАНИЗМА И СРЕДСТВА БИОЛОГИЧЕСКОЙ БОРЬБЫ, ДЛЯ БОРЬБЫ С БАКТЕРИАЛЬНЫМИ ВРЕДНЫМИ ОРГАНИЗМАМИ В ПОЛЕЗНЫХ РАСТЕНИЯХ

ФУНГИЦИДНЫЕ ПИРАЗОЛЫ

ЗАМЕЩЕННЫЕ ЦИКЛИЧЕСКИЕ АМИДЫ В КАЧЕСТВЕ ГЕРБИЦИДОВ

СИНЕРГЕТИЧЕСКАЯ КОМБИНАЦИЯ ФЛУМЕТСУЛАМА ИЛИ ДИКЛОЗУЛАМА И ИЗОТИАЗОЛОНОВ

... 1. Синергетическая противомикробная композиция, включающая (а) флуметсулам и (b) биоцид на основе изотиазолона, выбранный из группы, включающей 4,5-дихлор-2-н-октил-4-изотиазолин-3-он, 2-н-октил-4-изотиазолин-3-он и N-н-бутил-1,2-бензизотиазолин-3-он, где массовое соотношение флуметсулама и 4,5-дихлор-2-н-октил-4-изотиазолин-3-она составляет от 15:1 до 1:15, массовое соотношение флуметсулама и 2-н-октил-4-изотиазолин-3-она составляет от 7:1 до 1:5 и массовое соотношение флуметсулама и N-н-бутил-1,2-бензизотиазолин-3-она составляет от 15:1 до 1:15.2. Композиция по п.1, в которой биоцидом на основе изотиазолона является 4,5-дихлор-2-н-октил-4-изотиазолин-3-он, и массовое соотношение флуметсулама и 4,5-дихлор-2-н-октил-4-изотиазолин-3-она составляет от 10:1 до 1:10.3. Композиция по п.1, в которой биоцидом на основе изотиазолона является 2-н-октил-4-изотиазолин-3-он, и массовое соотношение флуметсулама и 2-н-октил-4-изотиазолин-3-она составляет от 5:1 до 1:3.4. Композиция по п.1, в которой ...

СТАБИЛИЗИРОВАННАЯ ПРОТИВОМИКРОБНАЯ КОМПОЗИЦИЯ

... 1. Противомикробная композиция, включающая:(а) 2-25 мас.% 2,2-дибром-3-нитрилопропионамида,(б) 2-30 мас.% воды,(в) 5-30 мас.% алифатического соединения, содержащего от 2 до 6 гидроксильных групп, и(г) 20-70 мас.% этиленгликоля.2. Композиция по п.1, в которой алифатическое соединение, содержащее от 2 до 6 гидроксильных групп, выбирают из алифатического соединения, содержащего от 3 до 6 гидроксильных групп и от трех до шести атомов углерода.3. Композиция по п.2, дополнительно включающая 0,1-6 мас.% смеси 5-хлор-2-метил-4-изотиазолин-3-она и 2-метил-4-изотиазолин-3-она.4. Композиция по п.3, включающая 7-25 мас.% воды и 8-22 мас.% 2,2-дибром-3-нитрилопропионамида.5. Композиция по п.4, в которой массовое соотношение 5-хлор-2-метил-4-изотиазолин-3-она и 2-метил-4-изотиазолин-3-ону составляет от 4:1 до 1:1.6. Композиция по п.2, дополнительно включающая 1-20 мас.% 2-бром-2-нитро-1,3-пропандиола.7. Композиция по п.6, включающая 5-18 мас.% воды.8. Композиция по п.2, дополнительно включающая 4-12 ...

ГЕРБИЦИДНЫЕ КОМПОЗИЦИИ, СОДЕРЖАЩИЕ 4-АМИНО-3-ХЛОР-5-ФТОР-6-(4-ХЛОР-2-ФТОР-3-МЕТОКСИФЕНИЛ)ПИРИДИН-2-КАРБОНОВУЮ КИСЛОТУ ИЛИ ЕЕ ПРОИЗВОДНОЕ И ФУНГИЦИДЫ

АГРОХИМИЧЕСКАЯ КОМПОЗИЦИЯ, СПОСОБ ЕЕ ПОЛУЧЕНИЯ И ПРИМЕНЕНИЯ

СОСТАВ ИЗОКСАЗОЛИНА ДЛЯ МЕСТНОГО И НАРУЖНОГО ПРИМЕНЕНИЯ

4-АМИНО-6-(ГЕТЕРОЦИКЛИЛ)ПИКОЛИНАТЫ И 6-АМИНО-2-(ГЕТЕРОЦИКЛИЛ)ПИРИМИДИН-4-КАРБОКСИЛАТЫ И ИХ ПРИМЕНЕНИЕ В КАЧЕСТВЕ ГЕРБИЦИДОВ

УЛУЧШЕННЫЙ ГЕРБИЦИДНЫЙ СОСТАВ

... 1. Состав капсульной суспензии, содержащий микроинкапсулированный пендиметалин, содержащий гербицидно эффективное количество пендиметалина, являющегося инкапсулированным при помощи полимерной стенки, при этом указанная полимерная стенка является образованной in situ путем реакции межфазной полимеризации, происходящей между второй фазой и первой фазой, диспергированной во второй фазе, причем по меньшей мере одна из указанных первой и второй фаз характеризуется тем, что содержит заранее заданное количество по меньшей мере одной соли органической кислоты и щелочного или щелочно-земельного металла; и гербицидно эффективное количество кломазона.2. Состав капсульной суспензии по п. 1, где указанное гербицидно эффективное количество кломазона является совместно инкапсулированным с пендиметалином внутри микрокапсул.3. Состав капсульной суспензии по п. 1, где указанное гербицидно эффективное количество кломазона является инкапсулированным отдельно и смешанным с гербицидно эффективным количеством ...

БИОЦИДНЫЕ КОМПОЗИЦИИ И СПОСОБЫ ПРИМЕНЕНИЯ

... 1. Композиция, включающая: гидроксиметил-замещенное фосфорсодержащее соединение, выбранное из группы, включающей соль тетракис(гидроксиметил)фосфония, соль C-Салкил- или С-Салкенил-трис(гидроксиметил)фосфония, и трис(гидроксиметил)фосфин, и соединение изотиазолинона, выбранное из 1,2-бензизотиазолин-3-она, 2-метил-1,2-бензизотиазолин-3-она и их смесей.2. Композиция по п. 1, где соединением изотиазолинона является 1,2-бензизотиазолин-3-он и массовое соотношение гидроксиметил-замещенного фосфорсодержащего соединения и 1,2-бензизотиазолин-3-она составляет от 8:1 до 1:8.3. Композиция по п. 1, где соединением изотиазолинона является 2-метил-1,2-бензизотиазолин-3-он и массовое соотношение гидроксиметил-замещенного фосфорсодержащего соединения и 2-метил-1,2-бензизотиазолин-3-она составляет от 10000:1 до 5000:1.4. Композиция по любому из пп. 1-3, где гидроксиметил-замещенным фосфорсодержащим соединением является сульфат тетракис(гидроксиметил)фосфония.5. Способ контроля микроорганизмов в водной ...

НОВЫЕ ПИРИДАЗИНОНОВЫЕ ГЕРБИЦИДЫ

ГЕРБИЦИДНОЕ СРЕДСТВО, СОДЕРЖАЩЕЕ БЕНЗОИЛЦИКЛОГЕКСАНДИОН И ЗАЩИТНОЕ СРЕДСТВО

Описывается гербицидное средство, содержащее А) гербицидно действующее количество соединения формулы (I), где R1 означает галоид или (С1-С4)-алкилсульфонил, R2 означает (С1-С4)-галоидалкокси-(С1-С4)-алкил, (C1-С4)-алкокси-(С1-С4)-алкокси-(С1-С4)-алкокси-(С1-С4)-алкил, (С3-С6)-циклоалкил-(С1-С4)-алкокси, тетрагидрофуран-2-ил-метокси-(С1-С4)-алкил или 4,5-дигидроизоксазол-3-ил-группу, замещенную радикалом из ряда, включающего цианометил, этоксиметил или метоксиметил, и В) защитно (антидотно) действующее количество соединения из рядов от а) до е). Технический результат - гербицидное средство позволяет существенно снизить повреждения, вызываемые гербицидом у культурных растений. 5 з.п. ф-лы, 8 табл.

ИНГИБИРОВАНИЕ ОБРАЗОВАНИЯ БИОГЕННОГО СУЛЬФИДА ПОСРЕДСТВОМ КОМБИНАЦИИ БИОЦИДА И МЕТАБОЛИЧЕСКОГО ИНГИБИТОРА

... 1. Способ ингибирования продукции сульфида восстанавливающими сульфат бактериями (SRB), причем указанный способ включает стадии: (а) контакта SRB с первой концентрацией биоцидного компонента, где первая концентрация составляет менее, чем примерно 90% от минимальной ингибирующей концентрации (MIC) биоцидного компонента; и (b) контакта SRB со второй концентрацией компонента метаболического ингибитора, где указанная вторая концентрация составляет менее, чем примерно 90% от MIC компонента метаболического ингибитора. 2. Способ по п.1, где по меньшей мере одна из указанных первой и второй концентраций составляет менее, чем примерно 50% от ее MIC. 3. Способ по п.1, где указанные первая и вторая концентрации меньше, чем примерно 75% от их соответствующих MIC. 4. Способ по п.1, где по меньшей мере одна из указанной первой и второй концентраций составляет менее, чем примерно 25% от ее MIC. 5. Способ по п.4, где указанные первая и вторая концентрации меньше, чем примерно 50% от их соответствующих ...

КОМПОЗИЦИИ ДЛЯ БОРЬБЫ С ФИТОПАТОГЕННЫМИ МИКРООРГАНИЗМАМИ И СПОСОБЫ БОРЬБЫ С ФИТОПАТОГЕННЫМИ МИКРООРГАНИЗМАМИ С ИСПОЛЬЗОВАНИЕМ ДАННЫХ КОМПОЗИЦИЙ

... 1. Композиция для борьбы с фитопатогенными микроорганизмами, которая включает (a) эффективное количество, по меньшей мере, одного соединения изоксазола, представляющего собой дезинфектант по отношению к фитопатогенным микроорганизмам, и (b) эффективное количество, по меньшей мере, одного соединения имидазола, представленного формулой (I): где R представляет собой алкильную группу, имеющую от 1 до 6 атомов углерода, или алкоксильную группу, имеющую от 1 до 6 атомов углерода; и n равно целому числу от 1 до 5. 2. Композиция по п.1, где массовое отношение соединения изоксазола к соединению имидазола находится в диапазоне от 1:300 до 300:1. 3. Композиция по п.1, где соединение изоксазола представляет собой гимексазол. 4. Композиция по п.1, где соединение имидазола представляет собой 4-хлор-2-циано-1-диметилсульфамоил-5-(4-метилфенил)имидазол. 5. Способ борьбы с фитопатогенными микроорганизмами, который включает нанесение композиции для борьбы с фитопатогенными микроорганизмами по п.1 на фитопатогенные ...

ПРОИЗВОДНЫЕ ИЗОТИАЗОЛА И ПИРАЗОЛА В КАЧЕСТВЕ ФУНГИЦИДОВ

... 1. Соединение формулы I ! ! в которой: ! Х обозначает S, N или NR5, Y обозначает N или NR5 при условии, что один, но не оба, Х или Y обозначает N; ! R1 и R3 независимо обозначают водород или необязательно замещенный алкил, алкенил, алкинил, гетероциклил, триалкилсилил, арилалкил, арилоксиалкил, арилтиоалкил, арил или гетероарил при условии, что они не оба обозначают водород; ! R2 обозначает необязательно замещенный алкил, алкенил, алкинил, гетероциклил, арилалкил, арил или гетероарил; ! R4 обозначает водород или группу, которая в биологических условиях может быть отщеплена с образованием гидроксигруппы в этом положении; ! R5 обозначает водород или необязательно замещенный алкил, алкенил, алкинил, гетероциклил, триалкилсилил, арилалкил, арилоксиалкил, арилтиоалкил, арил или гетероарил; ! или его соль или N-оксид. ! 2. Соединение по п.1, в котором Х обозначает S, Y обозначает N. ! 3. Соединение по п.1, в котором Х обозначает NR5, Y обозначает N. ! 4. Соединение по п.1, в котором Х обозначает ...

ИНСЕКТИЦИДНЫЕ ПРОИЗВОДНЫЕ АРИЛИЗОКСАЗОЛИНА

... 1. Производное арилизоксазолина, представленное формулой: ! ! в которой A представляет собой C или N; ! R представляет собой алкил или галоалкил; ! X, которые могут быть одинаковыми или разными, представляют собой галоген, галоалкил, нитрогруппу, алкил, алкоксигруппу, цианогруппу, галоалкоксигруппу, алкилсульфинил, алкилсульфенил, алкилсульфонил, галоалкилсульфинил, галоалкилсульфенил, галоалкилсульфонил, аминогруппу, ациламиногруппу, алкоксикарбониламиногруппу, галоалкилкарбониламиногруппу, галоалкоксикарбониламиногруппу, алкилсульфониламиногруппу, галоалкилсульфониламиногруппу, гидроксигруппу или меркаптогруппу; ! Y, которые могут быть одинаковыми или разными, представляют собой галоген, галоалкил, нитрогруппу, алкил, алкоксигруппу, цианогруппу, галоалкоксигруппу, алкилсульфинил, алкилсульфенил, алкилсульфонил, галоалкилсульфинил, галоалкилсульфенил, галоалкилсульфонил, гидроксигруппу, меркаптогруппу, аминогруппу, ациламиногруппу, алкоксикарбониламиногруппу, галоалкилкарбониламиногруппу ...

СПОСОБЫ БОРЬБЫ С ПОЧВЕННЫМИ ВРЕДИТЕЛЯМИ

... 1. Способ борьбы с обитающими в почве вредителями и/или предупреждения их появления в полезных растениях, включающий внесение соединения формулы I в место произрастания полезного растения или обработку его растительного материала для размножения соединением формулы I,где-В-В-В- представляет собой -C=N-O-, -C=N-CH-, -С=СН-O- или -N-CH-CH-;L представляет собой прямую связь или метилен;Аи Апредставляют собой С-Н, или один из Аи Апредставляет собой С-Н, а другой представляет собой N;Xпредставляет собой группу X;Rпредставляет собой С-Салкил, С-Сгалогеналкил или С-Сциклоалкил;Rпредставляет собой хлордифторметил или трифторметил;каждый Rнезависимо представляет собой бром, хлор, фтор или трифторметил;Rпредставляет собой водород, галоген, метил, галогенметил или циано;Rпредставляет собой водород;или Rи Rвместе формируют мостиковую 1,3-бутадиеновую группу;р равно 2 или 3.2. Способ по п. 1, где обитающий в почве вредитель представляет собой кукурузного корневого жука.3. Способ по п. 1, где обитающие ...

ПЕСТИЦИДНЫЕ КОМПОЗИЦИИ И ОТНОСЯЩИЕСЯ К НИМ СПОСОБЫ

... 1. Композиция, содержащая соединение, соответствующее,где(a) A представляет собой или,(b) R1 представляет собой H, F, Cl, Br, I, CN, NO, замещенный или незамещенный C-Cалкил, замещенный или незамещенный C-Cалкенил, замещенный или незамещенный C-Cалкокси, замещенный или незамещенный C-Cалкенилокси, замещенный или незамещенный C-Cциклоалкил, замещенный или незамещенный C-Cциклоалкенил, замещенный или незамещенный C-Cарил, замещенный или незамещенный C-Cгетероциклил, OR9, C(=X1)R9, C(=X1)OR9, C(=X1)N(R9), N(R9), N(R9)C(=X1)R9, S(O)R9, S(O)OR9, S(O)N(R9)или R9S(O)R9,где каждый указанный R1, который является замещенным, содержит один или несколько заместителей, выбранных из F, Cl, Br, I, CN, NO, C-Cалкила, C-Cалкенила, C-Cгалогеналкила, C-Cгалогеналкенила, C-Cгалогеналкилокси, C-Cгалогеналкенилокси, C-Cциклоалкила, C-Cциклоалкенила, C-Cгалогенциклоалкила, C-Cгалогенциклоалкенила, OR9, S(O)OR9, C-Cарила или C-Cгетероциклила (каждый из которых может быть замещенным, необязательно может быть замещенным ...

Состав для уничтожения нежелательных и регулирования роста полезных растений

Mikroemulsionen von 3-Isothiazolonverbindungen

Mikrobizide Mikroemulsion.

NEUE HERBIZIDE ZUSAMMENSETZUNGEN

DIAMID-DERIVATE VON HETEROCYCLISCHEN DICARBONSÄUREN, INSEKTIZIDE FÜR ACKER- UND GARTENBAU UND EIN VERFAHREN ZU IHRER VERWENDUNG

VERFAHREN ZUR STABILISIERUNG VON ISOTHIAZOLINONEN.

3-Anilino-benzisothiazole und diese enthaltende Fungizide.

SYNERGISTISCHE, ANTIMIKROBISCHE BEIMISCHUNGEN, ENTHALTEND 2-BROMO-2-BROMOMETHYLGLUTARONITRIL, VERFAHREN ZUR HEMMUNG MIKROBISCHEN WACHSTUMS UND GEGEN MIKROBISCHES WACHSTUM GESCHUETZTE SUBSTRATE.

Mikrobiozide Zusammensetzungen.

SYNERGISTICHE HERBIZIDE ZUSAMMENSETZUNGEN

Glutarimide.

Hydrochinondiether, ihre Herstellung und ihre Verwendung.

Novel 5-nitrobenzisothiazole-3-sulphides, their preparation, and their use for controlling fungi

The invention relates to 5-nitrobenzisothiazole-3-sulphides of the formula I in which R is as defined in the description. The novel compounds are fungicides.

Chloracetamide, Verfahren zu ihrer Herstellung und diese enthaltende herbizide Mittel

Cyclohexenonverbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses.

Herbizide Tetrahydropyran-2,4-dione.

HERBIZIDE SACCHARINCARBONSÄURE-DERIVATE UND VERFAHREN ZU IHRER HERSTELLUNG

EINE STABILISIERTE ISOTHIAZOLON-ZUSAMMENSETZUNG UND EIN VERFAHREN ZUR STABILISIERUNG VON ISOTHIAZOLON

ARYL- UND HETEROARYL-CYCLOPROPYL OXIMETHERN UND DEREN VERWENDUNG ALS FUNGIZIDE

BIOZIDE ZUSAMMENSETZUNG UND DEREN VERWENDUNG

Acylamino-substituierte Isoxazol- bzw. Isothiazolderivate, Verfahren zu deren Herstellung und ihre Verwendung

Mikrobizide Zusammensetzung

STABLE LIQUID COMPOSITIONS AND THEIR USE

Herbicidal compounds

ISOTHIAZOLONE DERIVATIVES THEIR PREPARATION AND USE AS BIOCIDES

... 1390443 3-lsothiazolone derivatives and their preparation ROHM & HAAS CO 10 May 1972 [12 May 1971] 21941/72 Heading C2C [Also in Division C5] 3-Isothiazolones complexed with metal salts, e.g. complexes of the formula wherein Y is a hydrogen atom, an optionally substituted C 1-18 alkyl group, an optionally substituted C 2-18 alkenyl or alkynyl group, an optionally substituted C 3-12 cycloalkyl group, an optionally substituted aralkyl group of up to 10 carbon atoms, or an optionally substituted aryl group of up to 10 carbon atoms, R is hydrogen, halogen or a C 1-4 alkyl group, R1 is hydrogen, halogen or a C 1-4 alkyl group, or R and R1 can be joined together to complete a benzene ring which may be substituted by one or more halogen atoms, nitro groups, C 1-4 alkyl groups, C 1-4 alkoxy groups or cyano groups, M is a cation or a cationic complex of a metal, X is an anion forming a compound with the cation M, a is 1 or 2 and n is the integer for which the anion X satisfies ...

HETEROCYCLIC COMPOUNDS

DIPHENYL ETHER COMPOUNDS

HETEROCYCLIC COMPOUNDS

New herbicides

Alpha-pyrimidin-5-yl acrylic acid derivatives and methyl 2-(pyrimidin-5-yl)-acetate intermediates

The invention discloses compounds of formula I (I) the use of such compounds for the control of phytopathogens, composition for facilitating such use, and the preparation of the compounds of formula I.

Wood preservative formulations comprising RH-287

A wood preservative composition comprising a synergistic combination of RH-287 and one or more co-biocides. Examples of such co-biocides include, fenpropimorph, cyproconazole, imazalil and propiconazole. The efficacy of potential wood preservative compositions can be tested by a simple test provided herein.

Diphenyl ether compounds

Herbicidal compounds of the general formula I, in which A<1> represents a hydrogen or halogen atom or an alkyl or haloalkyl group, and each of A<2> and A<3> independently represents a hydrogen or halogen atom or an alkyl, haloalkyl, nitro or cyano group; X represents an oxygen atom, R represents a group of formula COZ where Z represents a hydroxy group or an optionally substituted alkyl, alkoxy, aryl or aryloxy group and Y represents a group of formula CR<1> where R<1> represents an optionally substituted aryl group or a group of formula COZ; or X represents an oxygen atom, R represents a hydrogen or halogen atom and Y represents a group of formula CH; or X represents a sulphur atom, Y represents a group of formula CR<1> and R<1> represents a group of formula COZ and R represents a hydrogen atom or an optionally substituted alkyl or aryl group, or a group of formula COZ; or X represents a sulphur atom, Y represents a nitrogen atom and R represents a group of formula COZ; and salts ...

Substituted 2-phenyl-3-methoxypropenoate fungicides

Animal ectoparasite-controlling agent

The present invention provides an animal ectoparasite-controlling agent containing as an active ingredient a hydrazide compound represented by the formula (1) wherein R 3 represents a fluorine atom, a chlorine atom, a bromine atom, a methyl group, an ethyl group or a hydrogen atom, R 5 and R 6 are the same or different each other and each represents a methyl group or a hydrogen atom, R 4 represents a C1-C6 haloalkyl group, which shows excellent controlling effects on animal ectoparasites.

5-aryl isoxazolines for controlling invertebrate pests

Disclosed are compounds of Formula 1, including all geometric and stereoisomers, N-oxides, and salts thereof, wherein A 1 , A 2 and A 3 are independently selected from the group consisting of CR 3 and N; B 1 B 2 and B 3 are independently selected from the group consisting of CR 2 and N; Q is a phenyl ring or a 5- or 6-membered saturated or unsaturated heterocyclic ring, each ring optionally substituted with one or more substituents independently selected from halogen, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 3 -C 6 cycloalkyl, C 3 -C 6 halocycloalkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, C 1 -C 6 alkylthio, C 1 -C 6 haloalkylthio, C 1 -C 6 alkylsulfinyl, C 1 -C 6 haloalkylsulfinyl, C 1 -C 6 alkylsulfonyl, C 1 -C 6 haloalkylsulfonyl, —CN, —NO 2 , —N(R 4 )R 5 , —C(W)N(R4)R 5 , —C(O)OR 5 and R 8 ; or —S(O) 2 N(R 21 )R 22 , —S(O) p R 25 or —S(O)(═NR 28 )R 29 ; and R 1 , R 2 , R 3 , R 4 , R 5 , R 8 , R 21 , R 22 , R 25 , R 28 , R 29 ; p and n are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula 1 and methods for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a compound or a composition' of the invention.

Disinfectant composition comprising a biguanide compound

Disclosed is a method for killing spores from a surface or a material, comprising applying an effective amount of a biocidal composition which comprises one or more biguanide polymers, and one or more further active agents on said surface or material, characterised in that the or each further active agent is, when taken alone, sporicidally inactive. Compositions comprising polymeric biguanides and one or more further biocidal agents and, optionally, a polyorganosiloxane, have been found to be effective as a sporicidal agent and are particularly effective against the spores of C. difficile. The compositions may be used in industry, in domestic applications and are particularly suitable for use in hospital due to their low toxicity. Furthermore, the method may comprise impregnating a fabric to thereby provide long lasting sporicidal activity thereto.

Novel Heterocyclic Compounds as Pesticides

The present invention relates to novel heterocyclic compounds, to processes for preparation thereof and to the use thereof for controlling animal pests, which include arthropods and especially insects.

Synergistic combination of flumetsulam or diclosulam with zinc pyrithione

A synergistic antimicrobial composition containing flumetsulam or diclosulam; and zinc pyrithione.

Stabilized microbicidal composition

A microbicidal composition having at least four components. The first component is 2-25 wt % of 2,2-dibromo-3-nitrilopropionamide. The second component is 2-30 wt % water. The third component is 5-30 wt % of an aliphatic compound having 2-6 hydroxyl groups. The fourth component is 20-70 wt % of a glycol solvent.

Isoxazoline derivatives as insecticides

The present invention relates to compounds formula (I), wherein P is P1, P2, heterocyclyl or heterocyclyl substituted by one to five Z; and wherein A 1 , A 2 , A 3 , A 4 , G 1 , R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 17 , R 18 , R 19 and R 20 are as defined in claim 1 ; or a salt or N-oxide thereof. Furthermore, the present invention relates to processes and intermediates for preparing compounds of formula (I), to insecticidal, acaricidal, nematicidal and molluscicidal compositions comprising the compounds of formula (I) and to methods of using the compounds of formula (I) to control insect, acarine, nematode and mollusc pests.

Method of combating and controlling pests

The use of a compound of formula I wherein the substituents are as defined in claim 1 , or compositions containing them in controlling insects, acarines, nematodes or molluscs.

N- SUBSTITUTED PIPERAZINES

Novel N-alkyl substituted piperazines have been discovered, which are useful as insecticides or fungicides. Such compounds are of Formula (I) 2. A composition according to claim one wherein each of X and Y of said compound of Formula (I) are independently selected from the group consisting of a direct bond , alkyl , and carbonyl.3. A composition according to claim one wherein each of R1 and R2 of said compound of Formula (I) are independently selected from the group consisting of:alkyl;aryl, optionally substituted with cyano, alkoxy, halogen, alkylhalo, alkoxyhalo, carboxylalkyl, carbonylalkyl, benzyloxy, nitro, benzoyl, phenyl, carboxamido, or heteroaryl; andheteroaryl, optionally substituted with aryl, heteroaryl, alkyl, halogen, alkylhalo, alkoxy, cycloalkyl or cyano.4. A method of controlling insects comprising applying to a locus where control is desired an insect-inactivating amount of a composition of .5. A composition according to wherein said compound of Formula (I) is one of the compounds 1 through 334. This application claims the benefit of U.S. Provisional Application No. 60/695,364, filed on Jun. 30, 2005, the entire contents of which is hereby incorporated by reference. Additionally, this application claims the benefit of U.S. Non-provisional application Ser. No. 11/479,772, filed 30 Jun. 2006, the entire contents of which is hereby incorporated by reference. Additionally, this application claims the benefit of U.S. Non-provisional application Ser. No. 12/787,440, filed 26 Jun. 2010, the entire contents of which is hereby incorporated by reference. The present invention relates to novel N-alkyl substituted piperazines and their use as fungicides and insecticides.Various piperazine derivatives have been disclosed in references such as WO 2004/060865, WO 97/26252, WO 01/46166, JP8-26995, JP63-141966, U.S. 2003/0044845, U.S. Pat. No. 6,011,035 and U.S. Pat. No. 6,387,897. However, these references do not disclose the piperazine derivatives of the present ...

Gene sequences and uses thereof in plants

This invention provides transgenic plant cells with recombinant DNA for expression of proteins that are useful for imparting enhanced agronomic trait(s) to transgenic crop plants. This invention also provides transgenic plants and progeny seed comprising the transgenic plant cells where the plants are selected for having an enhanced trait selected from the group of traits consisting of enhanced water use efficiency, enhanced cold tolerance, increased yield, enhanced nitrogen use efficiency, enhanced seed protein and enhanced seed oil. Also disclosed are methods for manufacturing transgenic seed and plants with enhanced traits.

PESTICIDAL MIXTURES CONTAINING ISOXAZOLINE DERIVATIVES AND INSECTICIDE OR NEMATOICIDAL BIOLOGICAL AGENT

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, R, R, R, Rand Rare as defined in claim and one of Yand Yis S, SO or SOand the other is CHand component B is an insecticide or nematicidal biological agent as defined in claim . The present invention also relates to methods of using said mixtures for the control of pests. 2. A pesticidal mixture according to claim 1 , wherein in the compound of formula I L is a direct bond or methylene; one of Yand Yis S and the other is CH; Aand Aare C—H; Ris hydrogen or methyl; Ris trifluoromethyl; Ris 3 claim 1 ,5-dichloro-phenyl; Ris methyl; and Ris hydrogen.3. A pesticidal mixture according to claim 1 , wherein in the compound of formula I L is a direct bond or methylene; one of Yand Yis SO and the other is CH; Aand Aare C—H; Ris hydrogen or methyl; Ris trifluoromethyl; Ris 3 claim 1 ,5-dichloro-phenyl; Ris methyl; and Ris hydrogen.4. A pesticidal mixture according to claim 3 , wherein the molar proportion of the cis SO compounds of formula I compared to the total amount of cis SO and trans SO compounds of formula I is greater than 50%.5. A pesticidal mixture according to claim 1 , wherein in the compound of formula I L is a direct bond or methylene; one of Yand Yis SOand the other is CH; Aand Aare C—H; Ris hydrogen or methyl; Ris trifluoromethyl; Ris 3 claim 1 ,5-dichloro-phenyl; Ris methyl; and Ris hydrogen.6. A pesticidal mixture according to claim 1 , wherein when L is a direct bond Yis CHand Yis S claim 1 , SO or SO claim 1 , and wherein when L is methylene Yis S claim 1 , SO or SOand Yis CH.8. A pesticidal mixture according to claim 1 , wherein component B is a compound selected froma) a pyrethroid selected from the group consisting of permethrin, cypermethrin, fenvalerate, esfenvalerate, deltamethrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin, bifenthrin, fenpropathrin, cyfluthrin, tefluthrin, ethofenprox, ...

Biocidal compositions

The present invention relates to storage-stable biocidal compositions comprising at least one halogen-free isothiazolinone such as in particular 2-methyl-2H-isothiazol-3-one (MIT) and/or 1,2-benzisothiazolin-3-one (BIT) and/or salts thereof, and also stabilizing amounts of copper(II) ions, to a method for preserving technical materials by means of the aforementioned biocidal compositions, and to the technical materials treated therewith. 1. Biocidal compositions comprisingone or more isothiazolinones, where the biocidal compositions, based on their total weight fraction of isothiazolinones, comprise to at least 98.0% those isothiazolinones which are halogen-free and1 to 500 ppm by weight of copper(II) ions, based on the total weight fraction of the isothiazolinone or isothiazolinones in the biocidal composition.2. Biocidal compositions according to claim 1 , characterized in that they comprise two or more isothiazolinones.3. Biocidal compositions according to or claim 1 , characterized in that the isothiazolinones are selected from the group: 2-methyl-2H-isothiazol-3-one; 1 claim 1 ,2-benzisothiazolin-3-one or salts thereof; 2-n-octyl-4-isothiazolin-3-one claim 1 , N-butyl-1 claim 1 ,2-benzisothiazolin-3-one and 2-methyl-4 claim 1 ,5-trimethylene-4-isothiazolin-3-one.4. Biocidal compositions according to one of to claim 1 , characterized in that they comprise claim 1 , as isothiazolinones claim 1 , only 2-methyl-2H-isothiazol-3-one and 1 claim 1 ,2-benzisothiazolin-3-one and/or salts thereof.5. Biocidal compositions according to one of to claim 1 , characterized in that they are liquid.6. Biocidal compositions according to claim 5 , characterized in that they are essentially free from organic solvents.7. Biocidal compositions according to one of to claim 5 , characterized in that they further comprise at least one oxidizing agent which is selected from the group: iodate claim 5 , periodate claim 5 , perchlorate claim 5 , chlorate claim 5 , bromate and organic ...

Use of substituted heterocyclic compounds to control sea lice on fish

The present invention relates to the use of compounds of formula wherein the variables are as defined in the description, in the free form or in salt form, for controlling sea lice on fish.

Process for Producing Imine Compounds for Combating Invertebrate Pests

The present invention relates to a process for producing aromatic carbonyl compounds of formula I and aromatic imine compounds of formula III 145-. (canceled)48. The process as claimed in claim 46 , where Z is Br claim 46 , I or —OSO—R.49. The process as claimed in claim 48 , where Z is Br claim 48 , I or —OSO—R claim 48 , where Ris selected from the group consisting of CH claim 48 , CFand 4-methylphenyl claim 48 , and is preferably Br.50. The process as claimed in claim 46 , where carbon monoxide and hydrogen are used in a molar ratio of from 20:1 to 1:10.51. The process as claimed in claim 50 , where carbon monoxide and hydrogen are used in a molar ratio of from 2:1 to 1:2 and are preferably used in the form of synthesis gas.52. The process as claimed in claim 46 , where the catalyst is a group VIII metal complex.53. The process as claimed in claim 52 , where the metal is selected from the group consisting of Pd claim 52 , Pt claim 52 , Ni claim 52 , Rh claim 52 , Ir and Ru and is preferably Pd.54. The process as claimed in claim 46 , where the catalyst contains a monodentate and/or bidentate ligand.55. The process as claimed in claim 46 , where the catalyst contains a phosphorus-containing ligand.56. The process as claimed in claim 55 , where the phosphorus-containing ligand is a monodentate ligand selected from the group consisting of phosphorus compounds of formula PRRR claim 55 , where{'sup': a', 'b', 'c', 'd', 'e, 'sub': 3', '12', '3', '12', '3', '10', '3', '10', '5', '18', '5', '18, 'claim-text': or', {'sup': a', 'b', 'e, 'sub': 3', '10, 'Rand Rtogether with the phosphorus atom to which they are bound form a 5-, 6-, 7- or 8-membered heterocyclic ring which may be additionally fused to one, two or three C-C-cycloalkyl, heterocyclyl, aryl or hetaryl groups, where the heterocyclic ring and, if present, the fused-on groups may each independently carry one, two, three or four substituents R;'}, {'sup': d', '1', '2', '1', '2', '3+', '−, 'sub': 3', '10', '3', '10', ...

MICROBICIDAL COMPOSITION

The invention relates to a microbicidal composition which comprises a mixture of at least two components, the first component being 2-methyl-3-isothiazolone (MIT) and the second component being at least one active compound selected from the following groups of active compounds: 1. Microbicidal composition which comprises a mixture of at least two components , the first component being 2-methyl-3-isothiazolone and the second component being at least one active compound selected from the following groups of active compounds:a) compounds having activated methylol groupsb) quats or polyquatsc) carbamatesd) organic acidse) aromatic alcohols.2. Composition according to claim 1 , characterized in that the composition comprises one or more different solvents.3. Composition according to one or both of the preceding claims claim 1 , characterized in that water claim 1 , glycols and/or glycol ethers are provided as solvent.4. Composition according to one or more of the preceding claims claim 1 , characterized by a synergistic action of the components present in the mixture.5. Composition according to one or more of the preceding claims claim 1 , characterized by an activity enhancement by the solvent claim 1 , in particular the glycols and/or glycol ethers.6. Composition according to one or more of the preceding claims claim 1 , characterized in that bronopol claim 1 , diazolidinylurea or imidazolidinylurea are provided as compounds having activated methylol groups.7. Composition according to one or more of the preceding claims claim 1 , characterized in that polyaminopropyl biguanide claim 1 , cetrimonium bromide or benzalconium chloride are provided as quats or polyquats.8. Composition according to one or more of the preceding claims claim 1 , characterized in that iodopropynyl butylcarbamate or dithiocarbamate are provided as carbamates.9. Composition according to one or more of the preceding claims claim 1 , characterized in that dehydroacetic acid claim 1 , undecylenic ...

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

This document discloses molecules having the following formula (“Formula One”): 2. A composition according to wherein said molecule said A is A1.3. A composition according to wherein said molecule said A is A2.4. A composition according to wherein said molecule said R1 is H.5. A composition according to wherein said molecule said R2 is H.6. A composition according to wherein said molecule said R3 is selected from H claim 1 , or substituted or unsubstituted C-Calkyl.7. A composition according to wherein said molecule said R3 is selected from H or CH.8. A composition according to wherein said molecule when said A is A1 then A1 is A11.9. A composition according to wherein said molecule when said A is A1 claim 1 , and A1 is A11 claim 1 , then R4 is selected from H claim 1 , or substituted or unsubstituted C-Calkyl claim 1 , or substituted or unsubstituted C-Caryl.10. A composition according to wherein said molecule when said when A is A1 claim 1 , and A1 is A11 then R4 is selected from CH claim 1 , CH(CH) claim 1 , or phenyl.11. A composition according to wherein said molecule when said when A is A1 claim 1 , and A1 is A12 claim 1 , then R4 is CH.12. A composition according to wherein said molecule when said A is A2 then R4 is selected from H claim 1 , substituted or unsubstituted C-Calkyl claim 1 , substituted or unsubstituted C-Calkenyl claim 1 , substituted or unsubstituted C-Ccycloalkyl claim 1 , substituted or unsubstituted C-Caryl claim 1 , wherein each said R4 claim 1 , which is substituted claim 1 , has one or more substituents selected from F claim 1 , Cl claim 1 , Br claim 1 , or I.13. A composition according to wherein said molecule when said A is A2 then R4 is H or C-Calkyl.14. A composition according to wherein said molecule when said A is A2 then R4 is H claim 1 , CH claim 1 , CHCH claim 1 , CH═CH claim 1 , cyclopropyl claim 1 , CHCl claim 1 , CF claim 1 , or phenyl.15. A composition according to wherein said molecule when said A is A2 then R4 is Cl.16. A ...

Lipo-chitooligosaccharide combination compositions for enhanced plant growth and yield

Compositions and methods for enhancing plant growth and crop yield in legumes and non-legumes are described. The compositions include lipo-chitooligosaccharides in combination with chitins/chitosans or in combination with flavonoid compounds or in combination with a herbicide. The method includes applying the compositions to seeds and/or plants either concomitantly or sequentially.

Biocide

Aqueous solutions of the tetramethylammonium salt of 1,2-benzothiazolone stable below 0° C.

Herbicidal Isoxazolo[5,4-B]pyridines

The invention relates to isoxazolo[5,4-b]pyridine compounds of formula I, 116-. (canceled)18. The method as claimed in claim 17 , wherein in formula I{'sup': '1', 'sub': 1', '6', '1', '6, 'Ris hydrogen, halogen, C-C-alkyl, or C-C-haloalkyl.'}19. The method as claimed in claim 17 , wherein in formula I{'sup': '2', 'sub': 1', '6', '1', '6', '1', '6', '3', '6', '3', '6', '2', '6', '2', '6, 'Ris hydrogen, C-C-alkyl, C-C-haloalkyl, C-C-hydroxyalkyl, C-C-cycloalkyl, C-C-halocycloalkyl, C-C-alkenyl, or C-C-alkynyl.'}20. The method as claimed in claim 17 , wherein in formula I{'sup': '1', 'Ris hydrogen;'}{'sup': '2', 'sub': 1', '6', '1', '6', '1', '6', '3', '6', '3', '6', '2', '6', '2', '6, 'Ris hydrogen, C-C-alkyl, C-C-haloalkyl, C-C-hydroxyalkyl, C-C-cycloalkyl, C-C-halocycloalkyl, C-C-alkenyl, or C-C-alkynyl;'}{'sup': 3', '3, 'sub': 1', '6', '1', '6', '3', '6', '1', '6', '3', '6', '1', '6', '3', '6', '3', '6', '1', '4', '3', '6', '1', '6', '1', '6', '1', '4', '1', '4', '1', '4', '1', '4', '3', '6', '2', '6', '2', '6', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4, 'Ris C-C-alkyl, C-C-haloalkyl, C-C-cycloalkyl-C-C-alkyl, C-C-halocycloalkyl-C-C-alkyl, C-C-cycloalkyl, C-C-halocycloalkyl, C-C-alkyl-C-C-cycloalkyl, C-C-alkoxy, C-C-haloalkoxy, or phenyl; wherein the phenyl moieties of Rcan be unsubstituted or substituted with one or more radicals selected from the group consisting of halogen, hydroxy, nitro, cyano, C-C-alkyl, C-C-haloalkyl, C-C-alkoxy-C-C-alkyl, C-C-cycloalkyl, C-C-alkenyl, C-C-alkynyl, C-C-alkoxy, C-C-haloalkoxy, C-C-alkoxycarbonyl, C-C-alkylsulfinyl, C-C-alkylsulfonyl, amino, C-C-alkylamino, N,N-di-(C-C)-alkylamino, heterocyclyl, or phenyl;'}{'sup': 4', '5, 'X is ORor SR.'}21. The method as claimed in claim 17 , wherein in formula I{'sup': '4', 'X is OR;'}{'sup': '4', 'sub': 1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '2', '6', '2', '6', '2', '6, 'Ris hydrogen, C-C-alkyl, C-C-haloalkyl, C-C-cyanoalkyl, C-C- ...

Fungicidal Compositions

The present invention relates to compositions of fungicidally active compounds comprising at least one active compound I selected from 3-difluoromethyl-1-methyl-1H-pyrazole-4-carboxylic acid (3′,4′,5′-trifluoro-biphenyl-2-yl)-amide (fluxapyroxade), bixafen, fluopyram, isopyrazam, sedaxane, penflufen and penthiopyrad and at least one further active component II as defined below. The invention furthermore relates to a method for controlling harmful fungi, wherein the fungi, their habitat or the plant propagation material, the soil, the plants or the materials to be protected against fungal attack are treated with an effective amount of at least one active compound I in combination with at least one active component II or with an effective amount of a composition according to the invention, to a method for protection of plant propagation material, comprising contacting the plant propagation material with an effective amount of at least one active compound I in combination with at least one active component II or with an effective amount of a composition according to the invention, to a method for protecting plants after germination from the attack of foliar phytopathogenic fungi, which comprises treating the plant propagation material from which the plants are to grow with an effective amount of at least one active compound I in combination with at least one active component II or with an effective amount of a composition according to the invention, to the use of the composition according to the invention for controlling harmful fungi, and to plant propagation material comprising the composition. 115-. (canceled)17. The composition as claimed in claim 16 , where active compound I is selected from the group consisting of 3-difluoromethyl-1-methyl-1H-pyrazole-4-carboxylic acid (3′ claim 16 ,4′ claim 16 ,5′-trifluoro-biphenyl-2-yl)-amide (fluxapyroxade) claim 16 , bixafen claim 16 , fluopyram claim 16 , isopyrazam and penthiopyrad.18. The composition as claimed in claim ...

ISOXAZOLINE DERIVATIVES AS PESTICIDES

The invention relates to new isoxazoline compounds of formula 2. The topical formulation of claim 1 , wherein{'sub': m', '5', '1', '2', '3, 'X is S(O), O or NR′ and Xand Xare each independently of the other CR′ or N,'}n is an integer from 0 to 4; m is an integer from 0 to 2;{'sub': 1', '2', '3', '2, 'B, Band Bare each independently selected from the group consisting of CR′ and N;'}{'sub': 2', '2, 'each R′ is independently of the other H or R;'}{'sub': 3', '3, 'each R′ is independently of the other H or R;'}{'sub': 1', '1', '6', '2', '6', '2', '6', '3', '6', '4', '7', '4', '7', '4, 'Ris C-C-alkyl, C-C-alkenyl, C-C-alkynyl, C-C-cycloalkyl, C-C-alkylcycloalkyl or C-C-cycloalkylalkyl, each unsubstituted or substituted with one or more substituents independently selected from R;'}{'sub': 4', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6, 'Ris halogen, C-C-alkyl, C-C-alkoxy, C-C-alkylthio, C-C-alkylsulfinyl, C-C-alkyl-sulfonyl, cyano or nitro;'}{'sub': 2', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '2', '6', '2, 'each Ris independently halogen, C-C-alkyl, C-C-haloalkyl, C-C-alkoxy, C-C-haloalkoxy, C-C-alkylthio, C-C-haloalkylthio, C-C-alkylsulfinyl, C-C-haloalkylsulfinyl, C-C-alkylsulfonyl, C-C-haloalkylsulfonyl, N-mono- or N,N-di-C-C-alkylamino, C-C-alkoxycarbonyl, cyano (—CN) or nitro (—NO);'}{'sub': 3', '1', '6', '1', '6', '3', '6', '3', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '2', '6, 'each Ris independently H, halogen, C-C-alkyl, C-C-haloalkyl, C-C-cycloalkyl, C-C-halocycloalkyl, C-C-alkoxy, C-C-haloalkoxy, C-C-alkylthio, C-C-haloalkylthio, C-Calkyl-sulfinyl, C-C-haloalkylsulfinyl, C-C-alkylsulfonyl, C-C-haloalkylsulfonyl, amino, N-mono- or N,N-di-C-C-alkylamino, C-C-alkoxycarbonyl, cyano or nitro;'}{'sub': 5', '6, 'Z is halogen, a radical Q or a group —C(W)—NRR;'}{'sub': 6', '10', '1', '6', '1', '6', '3', '6', '3', '6', '1', '6', '1', '6', '1', ...

PEST CONTROL COMPOSITION

A pest control composition comprising a hydrazide compound shown by formula (1) below (in the formula, G, M, Q, Q, Q, Q, R, R, R, Rand m have the same meanings described in the specification) and a pyrazole compound shown by formula (2) below (in the formula, X, Xand Xhave the same meanings described in the specification) and a method for controlling pests whereby an effective dose of the hydrazide compound represented by formula (1) and the pyrazole compound represented by formula (II) is applied to a pest or a pest habitat. 2. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , G is a group shown by G-1 claim 1 , Yis an oxygen atom claim 1 , Ris a trifluoromethyl group claim 1 , each of Q claim 1 , Q claim 1 , and Qis a CH group claim 1 , Qis a CRgroup claim 1 , Ris the group defined above claim 1 , (R)is a substituent at 3- and 5-positions claim 1 , m is 2 claim 1 , and Ris a chlorine atom.3. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a hydrogen atom.4. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a hydrogen atom or a methyl group.5. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a halogen atom.6. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a chlorine atom.7. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C2 to C6 alkyl group claim 1 , a C1 to C6 haloalkyl group claim 1 , a C3 to C6 cycloalkyl group claim 1 , or a (C1 to C6 alkoxy) C1 to C6 alkyl group.8. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C2 to C6 alkyl group.9. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C1 to C6 haloalkyl group.10. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C3 ...

PEST CONTROL COMPOSITION

A pest control composition comprising a hydrazide compound shown by formula (1) below (in the formula, G, M, Q, Q, Q, Q, R, R, R, Rand m have the same meanings described in the specification) and etofenprox and a method for controlling pests whereby an effective dose of the hydrazide compound represented by formula (1) and etofenprox is applied to a pest or a pest habitat. 2. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , G is a group shown by G-1 claim 1 , Yis an oxygen atom claim 1 , Ris a trifluoromethyl group claim 1 , each of Q claim 1 , Q claim 1 , and Qis a CH group claim 1 , Qis a CRgroup claim 1 , Ris the group defined above claim 1 , (R)is a substituent at 3- and 5-positions claim 1 , m is 2 claim 1 , and Ris a chlorine atom.3. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a hydrogen atom.4. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a hydrogen atom or a methyl group.5. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a halogen atom.6. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a chlorine atom.7. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C2 to C6 alkyl group claim 1 , a C1 to C6 haloalkyl group claim 1 , a C3 to C6 cycloalkyl group claim 1 , or a (C1 to C6 alkoxy) C1 to C6 alkyl group.8. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C2 to C6 alkyl group.9. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C1 to C6 haloalkyl group.10. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C3 to C6 cycloalkyl group.11. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a (C1 to C6 alkoxy) C1 to C6 alkyl ...

PEST CONTROL COMPOSITION

A pest control composition comprising a hydrazide compound shown by formula (1) below (in the formula, G, M, Q, Q, Q, Q, R, R, R, Rand m have the same meanings described in the specification) and an ester compound shown by formula (2) below (in the formula, X, X, Xand Xhave the same meanings described in the specification) and a method for controlling pests whereby an effective dose of the hydrazide compound represented by formula (1) and the ester compound represented by formula (II) is applied to a pest or a pest habitat. 2. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , G is a group shown by G-1 claim 1 , Yis an oxygen atom claim 1 , Ris a trifluoromethyl group claim 1 , each of Q claim 1 , Q claim 1 , and Qis a CH group claim 1 , Qis a CRgroup claim 1 , Ris the group defined above claim 1 , (R)is a substituent at 3- and 5-positions claim 1 , m is 2 claim 1 , and Ris a chlorine atom.3. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a hydrogen atom.4. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a hydrogen atom or a methyl group.5. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a halogen atom.6. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a chlorine atom.7. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C2 to C6 alkyl group claim 1 , a C1 to C6 haloalkyl group claim 1 , a C3 to C6 cycloalkyl group claim 1 , or a (C1 to C6 alkoxy) C1 to C6 alkyl group.8. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C2 to C6 alkyl group.9. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C1 to C6 haloalkyl group.10. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C3 to ...

PEST CONTROL COMPOSITION

A pest control composition comprising a hydrazide compound shown by formula (1) below (in the formula, G, M, Q, Q, Q, Q, R, R, R, Rand m have the same meanings described in the specification) and dinotefuran, and a method for controlling pests whereby an effective dose of the hydrazide compound represented by formula (1) and dinotefuran is applied to a pest or a pest habitat. 2. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , G is a group shown by G-1 claim 1 , Yis an oxygen atom claim 1 , Ris a trifluoromethyl group claim 1 , each of Q claim 1 , Q claim 1 , and Qis a CH group claim 1 , Qis a CRgroup claim 1 , Ris the group defined above claim 1 , (R)is a substituent at 3- and 5-positions claim 1 , m is 2 claim 1 , and Ris a chlorine atom.3. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a hydrogen atom.4. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a hydrogen atom or a methyl group.5. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a halogen atom.6. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a chlorine atom.7. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C2 to C6 alkyl group claim 1 , a C1 to C6 haloalkyl group claim 1 , a C3 to C6 cycloalkyl group claim 1 , or a (C1 to C6 alkoxy) C1 to C6 alkyl group.8. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C2 to C6 alkyl group.9. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C1 to C6 haloalkyl group.10. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C3 to C6 cycloalkyl group.11. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a (C1 to C6 alkoxy) C1 to C6 ...

PEST CONTROL COMPOSITION

A pest control composition comprising a hydrazide compound shown by formula (1) below (in the formula, G, M, Q, Q, Q, Q, R, R, R, Rand m have the same meanings described in the specification) and an ester compound shown by formula (2) below (in the formula, X, Xand Xhave the same meanings described in the specification) and a method for controlling pests whereby an effective dose of the hydrazide compound represented by formula (1) and the ester compound represented by formula (II) is applied to a pest or a pest habitat. 2. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , G is a group shown by G-1 claim 1 , Yis an oxygen atom claim 1 , Ris a trifluoromethyl group claim 1 , each of Q claim 1 , Q claim 1 , and Qis a CH group claim 1 , Qis a CRgroup claim 1 , Ris the group defined above claim 1 , (R)is a substituent at 3- and 5-positions claim 1 , m is 2 claim 1 , and Ris a chlorine atom.3. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a hydrogen atom.4. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a hydrogen atom or a methyl group.5. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a halogen atom.6. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a chlorine atom.7. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C2 to C6 alkyl group claim 1 , a C1 to C6 haloalkyl group claim 1 , a C3 to C6 cycloalkyl group claim 1 , or a (C1 to C6 alkoxy) C1 to C6 alkyl group.8. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C2 to C6 alkyl group.9. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C1 to C6 haloalkyl group.10. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C3 to C6 ...

SYNERGISTIC PRESERVATIVE COMPOSITIONS

A preservative composition comprising: (a) 1,2-Benzisothiazolin-3-one (BIT); (b) 3-Iodo-2-propynyl carbamate (IPBC); and (c) a mixture of 5-Chloro-2-methyl-4-isothiazolin-3-one (CMIT) and 2-Methyl-4-isothiazolm-3-one (MIT). 1. A preservative composition comprising:(a) 1,2-Benzisothiazolin-3-one (BIT);(b) 3-Iodo-2-propynyl carbamate (IPBC); and(c) a mixture of 5-Chloro-2-methyl-4-isothiazolin-3-one (CMIT) and 2-Methyl-4-isothiazolin-3-one (MIT).2. The composition of wherein said 1 claim 1 ,2-Benzisothiazolin-3-one is present in a total amount of about 1% to 20%.3. The composition of wherein said 3-Iodo-2-propynyl carbamate is present in a total amount of about 0.5% to 30%.4. A composition of wherein said mixture of 5-Chloro-2-methyl-4-isothiazolin-3-one and 2-Methyl-4-isothiazolin-3-one is present in a total amount of about 0.01% to 1.5%.5. The composition of claim I wherein the CMIT and MIT are present at a ratio of about 6:4 to 9:1.6. The composition of comprising about 15% (a) claim 1 , about 2.4% (b) and about 0.4% (c).7. The composition of wherein (c) comprises a 3:1 ratio of CMIT and MIT.8. A method for inhibiting the growth of microorganisms comprising adding a preservative composition in accordance with to a product susceptible to growth of microorganisms wherein said composition is added in an amount sufficient to inhibit said growth. The present application relates to preservative compositions and more particularly, to synergistic preservative compositions containing a mixture of (a) 1,2-Benzisothiazolin-3-one (BIT); (b) 3-Iodo-2-propynyl carbamate (IPBC); and (c) a mixture of 5-Chloro-2-methyl-4-isothiazolin-3-one (CMIT) and 2-Methyl-4-isothiazolin-3-one (MIT).Commercial use products are generally designed to have a substantial shelf life. The products need to be manufactured at one site, transported possibly over a considerable distance to a depot or other storage facility prior to further transport to a point of sale. The product may then spend ...

PEST CONTROL COMPOSITION

A pest control composition comprising a hydrazide compound shown by formula (1) below (in the formula, G, M, Q, Q, Q, Q, R, R, R, Rand m have the same meanings described in the specification) and a neonicotinoid compound selected from the group consisting of imidacloprid, thiacloprid, acetamiprid, nitenpyram, clothianidin, and thiamethoxam, and a method for controlling pests whereby an effective dose of the hydrazide compound represented by formula (1) and a neonicotinoid compound selected from the group consisting of imidacloprid, thiacloprid, acetamiprid, nitenpyram, clothianidin, and thiamethoxam is applied to a pest or a pest habitat. 2. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , G is a group shown by G-1 claim 1 , Yis an oxygen atom claim 1 , Ris a trifluoromethyl group claim 1 , each of Q claim 1 , Q claim 1 , and Qis a CH group claim 1 , Qis a CRgroup claim 1 , Ris the group defined above claim 1 , (R)is a substituent at 3- and 5-positions claim 1 , m is 2 claim 1 , and Ris a chlorine atom.3. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a hydrogen atom.4. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a hydrogen atom or a methyl group.5. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a halogen atom.6. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a chlorine atom.7. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C2 to C6 alkyl group claim 1 , a C1 to C6 haloalkyl group claim 1 , a C3 to C6 cycloalkyl group claim 1 , or a (C1 to C6 alkoxy) C1 to C6 alkyl group.8. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C2 to C6 alkyl group.9. The pest control composition according to claim 1 , wherein in the formula (1) claim 1 , Ris a C1 to C6 ...

CRYSTALLINE FORM OF 4- [5 - [3 -CHLORO-5 - (TRIFLUOROMETHYL) PHENYL] -4, 5 - DIHYDRO - 5 - (TRIFLUOROMETHYL) -3 - ISOXAZOLYL] -N- [2-0X0-2- [ ( 2, 2, 2 - TRIFLUOROETHYL) AMINO] ETHYL] -1- NAPH-THALENECARBOXAMIDE

Disclosed is a solid form of 4-[5-[3-chloro-5-(trifluoromethyl)phenyl]-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-N-[2-oxo-2-[(2,2,2-trifluoroethyl)amino]ethyl]-1-naphthalenecarboxamide (Compound 1). Also disclosed are compositions containing a solid form of Compound 1 and methods for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a solid form of Compound 1 or a composition containing a solid form of Compound 1. 2. A composition comprising the polymorph Form B of and at least one additional component selected from the group consisting of surfactants claim 1 , solid diluents and liquid diluents claim 1 , said composition optionally further comprising at least one additional biologically active compound or agent.3. A composition for protecting an animal from an invertebrate parasitic pest comprising a parasiticidally effective amount of the polymorph Form B of and at least one carrier.4. The composition of in a dosage form for oral administration.5. A method for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of the polymorph Form B of .6. The method of wherein the environment is a plant.7. The method of wherein the environment is an animal. This invention relates to a solid form of 4-[5-[3-chloro-5-(trifluoromethyl)phenyl]-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-N-[2-oxo-2-[(2,2,2-trifluoroethyl)amino]ethyl]-1-naphthalenecarboxamide.The solid state of chemical compounds can be amorphous (i.e. no long-range order in the positions of atoms) or crystalline (i.e. atoms arranged in an orderly repeating pattern). While only one crystal form is known for the solid state of many compounds, polymorphs have been discovered for some compounds. The term “polymorph” refers to a particular crystal form (i.e. structure of crystal lattice) of a chemical compound that can exist in more than one crystal ...

Nitrogen-containing heterocyclic compound and pest control agent

The present invention offers compounds or their salts expressed by formula (I) (in the formula, X indicates an alkyl group, or the like; Y indicates an alkyl group; Z indicates a respectively independent nitro group, or the like; n indicates any integer from 0 to 3; A indicates carbon atom, or the like, and hydrogen atom is bonded thereto in the case where the carbon atom is not substituted with Z; D indicates oxygen atom, or the like; W indicates hydrogen atom, or the like; R 1 and R 2 indicate respectively independent hydrogen atoms, or the like; R 1 and R 2 may be bonded, and may form a heterocycle together with the nitrogen atom between R 1 and R 2 ).

AQUEOUS-MISCIBLE OR AQUEOUS-DISPERSIBLE, VOC-FREE BIOCIDAL COMPOSITIONS FOR THE ENHANCED INHIBITION OF GRAM-NEGATIVE BACTERIAL STRAINS, AND METHOD OF PREPARING THE SAME

Disclosed herein is an aqueous-miscible or aqueous-dispersible biocidal composition of BIT capable of exhibiting substantially enhanced biocidal activity with lesser minimum inhibitory concentration (MIC) level at faster kill rate of gram-negative bacterial strains. The biocidal composition of the present application comprises (i) BIT, (ii) at least one cationic polymer and/or at least one cationic amine surfactant, (iii) optionally one or more sequestering agents, (iv) optionally one or more aromatic aldehydes, and (v) optionally, at least one additive. The composition is volatile organic compounds (VOC) free, heat and cold stable, and has a pH of about 3.0 to about 8.5. Also, disclosed is a process for preparing the aqueous-miscible and aqueous-dispersible compositions and their applications in various fields. 1. An aqueous-miscible or aqueous-dispersible , volatile organic compounds (VOC)-free , heat and cold stable biocidal composition having pH of about 3.0 to about 8.5 capable of exhibiting substantially enhanced biocidal activity via enhanced inhibition of gram-negative bacterial strains comprising:i. 1,2-benzisothiazolin-3-one (BIT);ii. at least one cationic polymer and/or at least one cationic amine surfactant;iii. optionally one or more sequestering agents;iv. optionally one or more aromatic aldehydes; andv. optionally, at least one additive.2. The aqueous-miscible or aqueous-dispersible biocidal composition according to claim 1 , wherein said cationic polymer is selected from the group consisting of homo or copolymers of polyamines claim 1 , polyimines claim 1 , polyalkyleneimines claim 1 , polyethyleneimines claim 1 , polypropyleneimines alone or in combination.3. The aqueous-miscible or aqueous-dispersible biocidal composition according to claim 1 , wherein said cationic amine surfactant is selected from the group consisting of alkanolamines claim 1 , mono-alkyl alkanolamines claim 1 , di-alkyl alkanolamines claim 1 , tri-alkyl alkanolamines claim 1 , ...

CHIMERIC GENE WITH SEVERAL HERBICIDE TOLERANCE GENES, PLANT CELL AND PLANT RESISTANT TO SEVERAL HERBICIDES

Methods for producing plants with multiple herbicide resistance are provided, in which the plants contain at least two basic genes, the first basic gene comprising a coding sequence encoding a mutated HPPD, and the second basic gene encoding an enzyme conferring on plants tolerance to a herbicide. Methods for herbicidal treatment of plants are also provided. 1. A process for producing plants with multiple herbicide tolerance by transgenesis of the plants , comprisinginserting into several cells respectively one of at least two basic genes, the basic genes each containing regulatory elements necessary for its transcription in plants and a coding sequence encoding an enzyme conferring on plants tolerance to a herbicide, wherein said at least two basic genes comprise first and second basic genes, said first basic gene comprising a coding sequence encoding a mutated HPPD and said second basic gene comprising a second coding sequence encoding an enzyme conferring on plants tolerance to a herbicide;regenerating plants from said cells; andcrossing said plants in order to obtain plants with multiple tolerance to field application rates of said herbicides.2. A process for the herbicidal treatment of plants comprising applying at least two herbicides at field application rates to a plant comprising at least two basic genes comprising first and second basic genes , said first basic gene comprising regulatory elements necessary for its transcription in plants and a coding sequence encoding a mutated HPPD , and said second basic gene comprising regulatory elements necessary for its transcription in plants and a second coding sequence encoding an enzyme conferring on plants tolerance to a herbicide.3. The process according to claim 2 , characterized in that three herbicides are applied.4. The process according to claim 2 , characterized in that one of the herbicides is an HPPD inhibitor.5. The process according to claim 2 , characterized in that both herbicides are applied ...

COMPOSITION FOR CONTROLLING HARMFUL ARTHROPODS AND METHOD FOR CONTROLLING HARMFUL ARTHROPODS

A harmful arthropod control composition comprising flonicamid, one or more Delphacidae control compounds selected from Group (A), and one or more rice blast disease control compounds selected from Group (B): 1. A harmful arthropod control composition comprising flonicamid , one or more Delphacidae control compounds selected from Group (A) , and one or more rice blast disease control compounds selected from Group (B):Group (A): a group consisting of clothianidin, imidacloprid, dinotefuran, thiamethoxam, fipronil and pymetrozine.Group (B): a group consisting of isotianil, probenazole, tiadinil, tricyclazole, pyroquilone, thiophanate-methyl, orysastrobin and azoxystrobin.2. The harmful arthropod control composition according to claim 1 , wherein the weight ratio of flonicamid to the Delphacidae control compound is from 100:1 to 1:100.3. The harmful arthropod control composition according to claim 2 , wherein the weight ratio of flonicamid to the rice blast disease control compound is from 10:1 to 1:100.4. A method for controlling a harmful arthropod claim 2 , which comprises applying an effective amount of the harmful arthropod control composition according to any one of to to a plant or an area in which a plant is grown.5. The method for controlling a harmful arthropod according to claim 4 , wherein the plant or the area in which a plant is grown is rice or an area in which rice is grown. The present invention relates to a harmful arthropod control composition and a method for controlling a harmful arthropod.Heretofore, various compounds are known as active ingredients in harmful arthropod control compositions (see, for example, The Pesticide Manual-15th edition (published by BCPC); ISBN 978-1-901396-18-8).The present invention includes the following [1] to [5]:[1] A harmful arthropod control composition comprising flonicamid, one or more Delphacidae control compounds selected from Group (A), and one or more rice blast disease control compounds selected from Group (B ...

INSECTICIDAL COMPOUNDS

A compound of formula (I): 5. A method of controlling insects claim 1 , acarines claim 1 , nematodes or molluscs which comprises applying to a pest claim 1 , to a locus of a pest claim 1 , or to a plant susceptible to attack by a pest an insecticidally claim 1 , acaricidally claim 1 , nematicidally or molluscicidally effective amount of a compound of formula (I) as defined in .6. An insecticidal claim 1 , acaricidal claim 1 , nematicidal or molluscicidal composition comprising an insecticidally claim 1 , acaricidally claim 1 , nematicidally or molluscicidally effective amount of a compound of formula (I) as defined in . The present invention relates to certain tetracyclic derivatives with a sulfur-containing four-membered ring connected to the nitrogen atom of the amide group, to processes and intermediates for preparing these derivatives, to insecticidal, acaricidal, nematicidal and molluscicidal compositions comprising these derivatives and to methods of using these derivatives to control insect, acarine, nematode and mollusc pests.Certain tetracyclic derivatives with a carbon only four-membered ring connected to the nitrogen atom of the amide group are disclosed in, for example, EP 1,731,512 and US 2007/066617 as having insecticidal properties. Certain tetracyclic derivatives with a sulfur-containing four-membered ring connected to the nitrogen atom of the amide group are disclosed in, for example, PCT/EP2008/010701 as having insecticidal properties. The compounds of PCT/EP2008/010701 have been excluded from the present invention.It has now been found that further tetracyclic derivatives with a sulfur-containing four-membered ring connected to the nitrogen atom of the amide group have insecticidal properties.The present invention therefore provides a compound of formula (I)where A is aryl or heteroaryl; B is a saturated or partially unsaturated heterocyclyl; C is aryl or heteroaryl; G is oxygen or sulfur; m is 0, 1, 2, 3, 4 or 5; n is 0, 1, 2, 3, 4 or 5; o is 0, ...

Insecticidal compounds

A compound of formula (I): wherein A 1 , A 2 , A 3 , A 4 , G 1 , G 2 , R 1 , R 2 , R 3 and R 4 are as defined in claim 1 ; or a salt or N-oxide thereof. Furthermore, the present invention relates to processes and intermediates for preparing compounds of formula (I), to insecticidal, acaricidal, nematicidal and molluscicidal compositions comprising them and to methods of using them to combat and control insect, acarine, nematode and mollusc pests.

FUNGICIDAL ACTIVE SUBSTANCE COMBINATIONS

The invention relates to novel fungicidally active compound combinations of 2′-cyano-3,4-dichloroisothiazole-5-carboxanilide and active compounds listed in the disclosure. 2. A composition according to wherein in the active compound combinations the weight ratio of active compound of the formula (I) toactive compound of formula (II) is between 1:0.1 and 1:20,active compound of formula (V) is between 1:0.1 and 1:100,active compound of formula (VI) is between 1:0.1 and 1:100,active compound of formula (VII) is between 1:0.1 and 1:100,active compound of formula (VIII) is between 1:0.1 and 1:100,active compound of formula (IX) is between 1:0.1 and 1:100,active compound of formula (X-a) or (X-b) is between 1:0.1 and 1:100,active compound of formula (XI) is between 1:0.1 and 1:100,active compound of formula (XII) is between 1:0.1 and 1:100, andactive compound of formula (XIV) is between 1:0.1 and 1:100.3. A method for controlling fungi comprising applying an effective amount of an active compound combination according to to the fungi and/or their habitat.5. A process for preparing a fungicidal composition comprising mixing an active compound combination according to with one or more extenders and/or surfactants.6. A fungicidal composition according to wherein component (b) is a compound of formula (V).7. A method for controlling fungi comprising applying an effective amount of an active compound combination according to to the fungi and/or their habitat. This application is a continuation application of U.S. application Ser. No. 12/779,362, filed May 13, 2010 which is a National Stage filing of PCT/EP2004/008072, filed Jul. 20, 2004 which claims priority from German Application Number 103 33 373.8 filed Jul. 23, 2003 the contents of which are incorporated by reference in their entireties.1. Field of InventionThe invention relates to active compound combinations which comprise the known 2′-cyano-3,4-dichloroisothiazole-5-carboxanilide on the one hand and other known ...

FUNGICIDE COMPOSITION COMPRISING A TETRAZOLYLOXIME DERIVATIVE AND A THIAZOLYLPIPERIDINE DERIVATIVE

The present invention relates to a pesticide composition intended for protecting plants, crops or seeds against fungal diseases or insect damages, and the corresponding methods of protection by application of the said composition. More precisely, the subject of the present invention is a pesticide composition based on a tetrazolyloxime derivative and a thiazolylpiperidine derivative, which may further comprise another fungicide and/or an insecticide active substance or compound. 2. A composition according to wherein Rindependently represents a hydrogen atom claim 1 , a halogen atom claim 1 , a substituted or non-substituted C-C-alkyl claim 1 , a substituted or non-substituted C-C-alkoxy.3. A composition according to wherein Rindependently represents a hydrogen atom or a halogen atom.4. A composition according to wherein Y represents a methyl group.5. A composition according to wherein Rand Rindependently represent a hydrogen atom or a halogen atom.6. A composition according to wherein Rindependently represents a hydrogen atom or a halogen atom.7. A composition according to wherein Rrepresents a hydrogen atom or a fluorine.8. A composition according to wherein the tetrazolyloxime derivative of formula (I) is but-3-yn-1-yl {6-[({[(Z)-(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl }carbamate or tert-butyl{6-[{]([(Z)-(1-methyl-1H-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate.9. A composition according to wherein the thiazolylpiperidine derivative of formula (II) is 2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]-1-{4-[4-(5-phenyl-4 claim 1 ,5-dihydro-1 claim 1 ,2-oxazol-3 -yl)-1 claim 1 ,3-thiazol-2]piperidin-1-1-yl}ethanone or1-(4-{4-[5-(2,6-difluorophenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidin-1-yl)-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone.10. A composition according to further comprisingC) a third fungicide compound,in an A/B/C weight ratio ranging from 1,000/1,000/1 to 1/1,000/1 ...

PESTICIDAL MIXTURES INCLUDING ISOXAZOLINE DERIVATIVES

The present invention provides pesticidal mixtures comprising a component A and a component B, wherein component A is an enantiomeric mixture of a compound of formula (I) that is enantiomerically enriched for the S enantiomer wherein the symbol * indicates the chiral centre; wherein A, A, R, R, R, R, Rand p are as defined in claim , and component B is a fungicide as defined in claim . The present invention also relates to methods of using said mixtures for the control of plant pests. 5. A pesticidal mixture according to claim 1 , wherein component A is at least 80% enantiomerically enriched for the S enantiomer.6. A pesticidal mixture according to claim 1 , wherein component A is at least 90% enantiomerically enriched for the S enantiomer.7. A pesticidal mixture according to claim claim 1 , wherein component B is selected from the group consisting ofa strobilurin fungicide including those selected from the group consisting of: Azoxystrobin, Dimoxystrobin, Enestrobin, Fluoxastrobin, Kresoxim-methyl, Metominostrobin, Orysastrobin, Picoxystrobin, Pyraclostrobin, Trifloxystrobin and Coumoxystrobin;an 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, Oxpoconazole, Pefurazoate, Penconazole, Prochloraz, Propiconazole, Prothioconazole, Simeconazole, Tebuconazole, Tetraconazole, Triadimefon, Triadimenol, Triflumizole, Triticonazole, Diclobutrazol, Etaconazole, Furconazole, Furconazole-cis, Thiabendazole and Quinconazole; anda fungicide from the class of succinate dehydrogenase inhibitors including those selected from the group consisting of Isopyrazam, Sedaxane, Bixafen, Penthiopyrad, Fluxapyroxad, Boscalid, Penflufen, Fluopyram, a compound of formula II, a compound of formula III and a compound of formula IV.8. A ...

Pesticidal compositions and processes related thereto

This document discloses molecules having the following formulas (“Formula One” &“Formula Two” and “Formula Three”) The Ar 1 , Het, Ar 2 , R1, R2, R3, R4, and R5 are further described herein.

PESTICIDAL COMPOSITIONS AND PROCESSES RELATED THERETO

This document discloses molecules having the following formulas (“Formula One” & “Formula Two” and “Formula Three”) 2. A molecule according to wherein Aris a substituted phenyl wherein said substituted phenyl has one or more substituents independently selected from C-Chaloalkyl and C-Chaloalkoxy.3. A molecule according to wherein Aris a substituted phenyl wherein said substituted phenyl claim 1 , has one or more substituents independently selected from CF claim 1 , OCF claim 1 , and OCFCF.4. A molecule according to wherein Het is selected from triazolyl claim 1 , imidazolyl claim 1 , or pyrazolyl claim 1 , which can be substituted or unsubstituted.8. A molecule according to wherein Het is a substituted 1 claim 1 ,3-pyrazolyl.10. A molecule according to wherein Aris a phenyl.11. A molecule according to wherein R1 is H or C-Calkyl.12. A molecule according to wherein R1 is H or CH.13. A molecule according to wherein R4 is phenyl claim 1 , C-Calkylphenyl claim 1 , or C-Calkyl-O-phenyl claim 1 , wherein each alkyl and phenyl are optionally substituted with one or more substituents independently selected from F claim 1 , Cl claim 1 , NRR claim 1 , C-Calkyl claim 1 , or C-Calkoxy.14. A molecule according to wherein R5 is unsubstituted.15. A molecule according to wherein Rand Rare independently selected from H and phenyl claim 1 , wherein said phenyl claim 1 , may be optionally substituted with one or more substituents independently selected from F and Cl.16. A molecule according to wherein Het-1 is selected from benzofuranyl claim 1 , benzoisothiazolyl claim 1 , benzoisoxazolyl claim 1 , benzoxazolyl claim 1 , benzothienyl claim 1 , benzothiazolyl cinnolinyl claim 1 , furanyl claim 1 , indazolyl claim 1 , indolyl claim 1 , imidazolyl claim 1 , isoindolyl claim 1 , isoquinolinyl claim 1 , isothiazolyl claim 1 , isoxazolyl claim 1 , oxadiazolyl claim 1 , oxazolinyl claim 1 , oxazolyl claim 1 , phthalazinyl claim 1 , pyrazinyl claim 1 , pyrazolinyl claim 1 , pyrazolyl claim 1 ...

PHOSPHATE-FREE HIGHLY CONCENTRATED AQUEOUS DISPERSION COMPOSITION OF BIOCIDES AND PROCESS FOR PREPARING THE SAME

A phosphate-free, highly-concentrated aqueous dispersion composition comprising at least one biocide, sulfosuccinate based surfactant, block copolymer, suspending agent, and optionally an antifoaming agent and desired additives if any. The composition of the present application is significantly stable against heat, cold, transit, storage and dilution for at least 18 months. The preferred biocides of the dispersion composition are 2-meth-4-isothiazolin-3-one (MIT), 1,2-Benzisothiazolin-3-one (BIT), 5-Chloro-2-methyl-4-isothiazolin-3-one (CMIT), 2-Octyl-4-isothiazolin-3-one (Off) 3-Iodo-2-propynylbutyl carbamate (IPBC), oxyfluorfen, thiabendazole, terbutryn, zinc pyrithione (ZnPy), bronopol, folpet, diiiron, dehydroacetic acid (DHA), dazomet and carbendazim alone or in combination. Also disclosed is a process for preparing the dispersion composition and appropriate applications thereof. 1. A stable , flowable and phosphate-free highly concentrated aqueous dispersion composition comprising:i. about 20.0 wt % to about 60.0 wt % of at least one biocide;ii. about 0.1 wt % to about 10.0 wt % of at least one sulfosuccinate surfactant;iii. about 0.1 wt % to about 5.0 wt % of block copolymer surfactant;iv. about 0.1 wt % to about 5.0 wt % of suspending agent;v. optionally, about 0.1 wt % to about 5.0 wt % of antifoaming agent; andvi. optionally, at least one additive.2. The dispersion composition according to claim 1 , wherein said biocide is selected from the group consisting of 2-methyl-4-isothiazolin-3-one (MIT) claim 1 , 1 claim 1 ,2-Benzisothiazolin-3-one (BIT) claim 1 , 5-Chloro-2-methyl-4-isothiazolin-3-one (CMIT) claim 1 , 2-Octyl-4-isothiazolin-3-one (OIT) 3-iodo-2-propynylbutyl carbamate (IPBC) claim 1 , oxyfluorfen claim 1 , thiabendazole claim 1 , terbutryn claim 1 , zinc pyrithione (ZnPy) claim 1 , bronopol claim 1 , folpet claim 1 , diruon claim 1 , dehydroacetic acid (DHA) claim 1 , dazomet claim 1 , carbendazim alone or in combination.3. The dispersion ...

PESTICIDAL MIXTURES INCLUDING ISOXAZOLINE DERIVATIVES

The present invention provides pesticidal mixtures comprising a component A and a component B, wherein component A is an enantiomeric mixture of a compound of formula I that is enantiomerically enriched for the S enantiomer (Formula I) wherein the symbol * indicates the chiral centre; wherein A, A, R, R, R, R, Rand p are as defined in claim , and component B is a compound as defined in claim . The present invention also relates to methods of using said mixtures for the control of plant pests. 5. A pesticidal mixture according to claim 1 , wherein component A is at least 80% enantiomerically enriched for the S enantiomer.6. A pesticidal mixture according to claim 1 , wherein component A is at least 90% enantiomerically enriched for the S enantiomer.7. A pesticidal mixture according to claim 1 , wherein component B is a compound selected froma macrolide compound including those selected from the group consisting of abamectin, emamectin (e.g. emamectin benzoate), ivermectin, milbemycin, spinosad, azadirachtin and spinetoram;a neonicotinoid compound including those selected from the group consisting of imidacloprid, thiacloprid, acetamiprid, nitenpyram, dinotefuran, thiamethoxam, clothianidin, nithiazine and flonicamid;a pyrethroid compound including those selected from the group consisting of permethrin, cypermethrin, fenvalerate, esfenvalerate, deltamethrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin, bifenthrin, fenpropathrin, cyfluthrin, tefluthrin, ethofenprox, natural pyrethrin, tetramethrin, S-bioallethrin, fenfluthrin, prallethrin and 5-benzyl-3-furylmethyl-(E)-(1R,3S)-2,2-dimethyl-3-(2-oxothiolan-3-ylidenemethyl)cyclopropane carboxylate; anda tetramic acid compound including those selected from the group consisting of spirotetramat and spirodiclofen.8. A pesticidal mixture according to claim 1 , wherein component B is a compound selected from the group consisting of abamectin claim 1 , lambda cyhalothrin claim 1 , spirotetramat claim 1 , and ...

HERBICIDAL COMPOSITION

Many herbicidal compositions have been developed and used, but there are many types of weeds to be controlled, and their development lasts for a long period of time. Accordingly, it has been desired to develop a herbicidal composition having a wider herbicidal spectrum and having a highly active and long-lasting herbicidal activity. The present invention provides a herbicidal composition which comprises as active ingredients (a) at least one herbicidal compound selected from the group consisting of a benzoylpyrazole compound represented by the formula (I): (wherein each of R, R, R, Rand Ris alky, and Ris alkoxyalkoxy), sulcotrione and topramezone, and (b) amicarbazone. 2. The herbicidal composition according to claim 1 , wherein the mixing ratio of (a) the herbicidal compound to (b) amicarbazone is from 1:3 claim 1 ,000 to 1 claim 1 ,000:1 by the weight ratio.3. The herbicidal composition according to claim 1 , wherein (a) the herbicidal compound is at least one herbicidal compound selected from the group consisting of a benzoylpyrazole compound represented by the formula (I) and topramezone.4. The herbicidal composition according to claim 1 , wherein (a) the herbicidal compound is a benzoylpyrazole compound represented by the formula (I).5. The herbicidal composition according to claim 4 , wherein in the formula (I) claim 4 , each of R claim 4 , R claim 4 , R claim 4 , Rand Ris methyl or ethyl claim 4 , and Ris —OCHCHOCH.6. The herbicidal composition according to claim 4 , wherein in the formula (I) claim 4 , each of Rand Ris methyl or ethyl claim 4 , each of R claim 4 , Rand Ris methyl claim 4 , and Ris —OCHCHOCH.7. A method for controlling undesired plants claim 1 , which comprises applying a herbicidally effective amount of (a) the herbicidal compound and a herbicidally effective amount of (b) amicarbazone claim 1 , as defined in claim 1 , to the undesired plants or to a place where they grow.8. The method according to claim 7 , wherein (a) the herbicidal ...

Synergistic pre-emergent and post-emergent weed control compositions and methods of use thereof

Methods and compositions for synergistic pre-emergent and post-emergent weed control are disclosed. In particular, the present disclosure relates to an herbicidal composition comprising at least one pre-emergent herbicide and at least one post-emergent herbicide, wherein the pre-emergent herbicide and the post-emergent herbicide synergistically inhibit pre-emergent and post-emergent development of a weed. The disclosure further relates to herbicidal compositions comprising isoxaben, 2,4-D, mecoprop-P, and dicamba.

MICROBICIDES

The present invention relates to a compound of formula (I): wherein the substituents have the definitions as defined in claim or a salt or a N-oxide thereof, their use and methods for the control and/or prevention of microbial infection, particularly fungal infection, in plants and to processes for the preparation of these compounds. 2. A compounds according to characterized in thatX is S or O;Y is C—H or N;{'sup': '1', 'sub': 1-8', '1-8', '1-8', '1-8', '2-8', '2-8', '1-8', '1-8', '3-8', '3-8', '1-8', '1-8', '7-15', '7-15', '6-10', '6-10', '6-10', '6-10', '6-10', '6-10, 'Ris unsubstituted Calkyl; substituted Calkyl; unsubstituted Calkenyl; substituted Calkenyl; unsubstituted Calkinyl; substituted Calkinyl; unsubstituted Calkoxyalkyl; substituted Calkoxyalkyl; unsubstituted Ccycloalkyl; substituted Ccycloalkyl; unsubstituted Chaloalkyl; substituted Chaloalkyl; unsubstituted Carylalkyl; substituted Carylalkyl; unsubstituted Caryl; substituted Caryl; unsubstituted Caryloxy; substituted Caryloxy; unsubstituted Carylthio; substituted Carylthio; a unsubstituted 5 to 10-membered aromatic heterocycle; or a substituted 5 to 10-membered aromatic heterocycle;'}{'sup': '2', 'sub': 1-8', '1-8', '2-8', '2-8', '2-8', '2-8', '1-8', '1-8', '1-8', '1-8', '3-8', '3-8', '7-15', '7-15', '6-10', '1-8', '6-10', '1-8', '6-10', '1-8', '6-10', '1-8', '6-10', '6-10', '6-10', '6-10', '6-10', '6-10', '1-8', '1-8, 'Ris H; halogen, unsubstituted Calkyl; substituted Calkyl; unsubstituted Calkenyl; substituted Calkenyl; unsubstituted Calkinyl; substituted Calkinyl; unsubstituted Calkoxyalkyl; substituted Calkoxyalkyl; unsubstituted Clhaloalkyl; substituted Chaloalkyl; unsubstituted Ccycloalkyl; substituted Ccycloalkyl; unsubstituted Carylalkyl; substituted Carylalkyl; unsubstituted Caryloxy-Calkyl; substituted Caryloxy-Calkyl; unsubstituted Carylthio-Calkyl; substituted Carylthio-Calkyl; unsubstituted Caryl; substituted Caryl; unsubstituted Caryloxy; substituted Caryloxy; unsubstituted Carylthio; ...

WOOD PRESERVATIVE FORMULATIONS COMPRISING ISOTHIAZOLONES WHICH PROVIDE PROTECTION AGAINST SURFACE STAINING

The present invention provides a wood preservative formulation comprising an isothiazolone, an organic fungicidal timber decay preservative and an unsaturated carboxylic or sulphonic acid, salt or precursor thereof. The formulations of the invention are surprisingly effective at protecting wood and other cellulosic substrates, in particular at providing prolonged protection against in-service surface staining. The invention also provides methods for treating wood and other cellulosic substrates with said formulations. 1. A wood preservative formulation comprising an isothiazolone , an organic fungicidal timber decay preservative and an unsaturated carboxylic or sulphonic acid , salt or precursor thereof.2. The formulation as defined in claim 1 , wherein the unsaturated carboxylic or sulphonic acid claim 1 , salt or precursor thereof is an unsaturated carboxylic or sulphonic acid or alkali metal salt thereof.3. The formulation as defined in claim 1 , wherein the unsaturated carboxylic or sulphonic acid claim 1 , salt or precursor thereof is an unsaturated cyclic carboxylic or sulphonic acid claim 1 , salt or precursor thereof.4. The formulation as defined in claim 3 , wherein the unsaturated carboxylic or sulphonic acid claim 3 , salt or precursor thereof is an aromatic acid claim 3 , salt or precursor thereof.6. The formulation as defined in claim 5 , wherein the aromatic acid or salt thereof is selected from the group consisting of benzoic acid and sodium benzoate.7. The formulation as defined in claim 3 , wherein the cyclic carboxylic or sulphonic acid is a resin acid or salt thereof.8. The formulation as defined in claim 7 , wherein the resin acid or salt thereof is selected from the group consisting of abietic acid claim 7 , sodium abietate claim 7 , pimaric acid and sodium pimarate.9. The formulation as defined in claim 1 , wherein the unsaturated carboxylic or sulphonic acid claim 1 , salt or precursor thereof is a linear unsaturated carboxylic acid claim 1 , ...

Naphthalene Isoxazoline Invertebrate Pest Control Agents

Disclosed are compounds of Formula 1, 2. A compound of wherein{'sup': '4', 'Ris H; and'}{'sup': '5', 'sub': 1', '6', '1', '6', '1', '6', '1', '6', '2', '7', '2', '7, 'Ris C-Calkyl substituted with one substituent independently selected from C-Calkylthio, C-Calkylsulfinyl, C-Calkylsulfonyl, C-Calkylaminocarbonyl and C-Chaloalkylaminocarbonyl.'}3. A compound of wherein{'sup': '1', 'sub': '3', 'Ris Cl, Br or CF;'}{'sup': '2', 'Ris H; and'}{'sup': '3', 'sub': '3', 'Ris H, F, Cl, Br or CF.'}4. A compound of wherein{'sup': '1', 'sub': '3', 'Ris CF.'}5. A compound of wherein{'sup': '3', 'sub': '3', 'Ris Cl, Br or CF.'}6. A compound of wherein{'sup': '5', 'sub': 1', '6', '2', '7', '3', '7, 'Ris C-Calkyl substituted with one C-Calkylaminocarbonyl or C-Chaloalkylaminocarbonyl.'}7. A compound of that is selected from the group consisting of4-[5-[3-chloro-5-(trifluoromethyl)phenyl]-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-N-[2-(methylsulfonyl)ethyl]-1-naphthalenecarboxamide,4-[5-[3-bromo-5-(trifluoromethyl)phenyl]-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-N-[2-(methylsulfonyl)ethyl]-1-naphthalenecarboxamide,4-[5-[3,5-bis(trifluoromethyl)phenyl]-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-N-[2-(methylsulfonyl)ethyl]-1-naphthalenecarboxamide,4-[5-[3-chloro-5-(trifluoromethyl)phenyl]-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-N-[2-(methylamino)-2-oxoethyl]-1-naphthalenecarboxamide,4-[5-[3-chloro-5-(trifluoromethyl)phenyl]-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-N-[2-(ethylamino)-2-oxoethyl]-1-naphthalenecarboxamide,4-[5-[3-chloro-5-(trifluoromethyl)phenyl]-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-N-[2-[(1-methylethyl)amino]-2-oxoethyl]-1-naphthalenecarboxamide,4-[5-[3-chloro-5-(trifluoromethyl)phenyl]-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-N-[2-oxo-2-[(2,2,2-trifluoroethyl)amino]ethyl]-1-naphthalenecarboxamide,4-[5-[3-bromo-5-(trifluoromethyl)phenyl]-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-N-[2-(methylamino)-2-oxoethyl]-1- ...

Spinosyn antifouling compositions, methods of use thereof and articles protected from attachment of biofouling organisms

Disclosed herein are antifouling compositions including at least one spinosyn active material. These compositions provide protection to surfaces coated or impregnated therewith from attachment of various biofouling organisms. Compositions include, for example, paint, varnish, and sealant formulations.

Safener compositions and methods for reducing mycotoxins

Methods, compositions, and uses of herbicide safeners alone, and in combination with fungicides, to reduce mycotoxin accumulation, fungal infection and related disease in agricultural crops, plants and harvested plant material are disclosed.

Herbicidal composition

Provided are technologies for controlling weeds, specifically, a herbicidal composition including as active ingredients isoxaflutole, cyprosulfamide, and one or more compounds selected from Group A has weed control effects, Group A: a group consisting of flumioxazin, sulfentrazone, saflufenacil, oxyfluorfen, fomesafen, and a compound represented by formula (I)

Low Toxicity, Low Odor, Low Volatility Solvent for Agricultural Chemical Formulations

An agricultural chemical composition comprises a solvent having the general formula CO(OR)(R), wherein Ris a linear or branched alkyl group of one to eight carbon atoms and Ris an aromatic group. Active agricultural components are dissolved in the solvent to produce a solution usable for distributing the active components. 1. An agricultural chemical formulation , comprising:between about 5% and about 70% by weight of an agricultural chemical portion comprising one or more compounds of a type selected from the group consisting of pyrethroids, mitose inhibitors, protoporphyrinogen-IX oxidase inhibitors, bleacher herbicides, triazoles, METI compounds, photosynthesis inhibitors, insecticides, nicotinic receptor agonist/antagonist compounds, fungicides, strobilurins, carboxanilides, ALS inhibitors, plant growth regulators, molluscides, nematocides, acaricides, and combinations thereof; and{'sub': a', 'b', 'a', 'b, 'between about 30% and about 80% of an ester portion comprising one or more compounds having the general formula CO(OR)(R), wherein Ris a linear or branched alkyl group of one to eight carbon atoms and Ris an aromatic group.'}2. The agricultural chemical formulation of claim 1 , wherein Rcomprises a benzene ring.3. The agricultural chemical formulation of claim 1 , wherein Ris selected from the group consisting of methyl claim 1 , ethyl claim 1 , propyl claim 1 , butyl claim 1 , pentyl claim 1 , hexyl claim 1 , heptyl claim 1 , octyl claim 1 , and derivatives thereof.4. The agricultural chemical formulation of claim 1 , wherein Ris selected from the group consisting of benzyl claim 1 , xylyl claim 1 , toluyl claim 1 , and derivatives thereof.5. The agricultural chemical formulation of claim 1 , further comprising between about 5% and about 50% of an emulsifier blend.6. The agricultural chemical formulation of claim 1 , wherein the ester is butyl benzoate.7. The agricultural chemical formulation of claim 5 , wherein the agricultural chemical portion comprises a ...

Insecticidal compounds

A compound of formula (I): wherein A 1 , A 2 , A 3 , A 4 , A 5 , G 1 , R 1 , R 2 , R 3 and R 4 are as defined in claim 1 ; or a salt or N-oxide thereof. Furthermore, the present invention relates to processes and intermediates for preparing compounds of formula (I), to insecticidal, acaricidal, nematicidal and molluscicidal compositions comprising them and to methods of using them to combat and control insect, acarine, nematode and mollusc pests.

NOVEL HERBICIDE

Herbicidal composition comprising a pyrandione herbicide and a co-herbicide The present invention relates to a herbicidal composition comprising as active ingredient a mixture of a) a herbicidally effective amount of a compound of formula (I) wherein: Ris methyl, ethyl, n-propyl, halogen, difluoromethoxy, trifluoromethoxy or trifluoromethyl, Ris phenyl or phenyl substituted by C-Calkyl, C-Chaloalkyl, C-Calkoxy, C-Chaloalkoxy or halogen, R, R, Rand R, independently of each other, are hydrogen or C-Calkyl, Y is O, and G is hydrogen, an alkali metal, alkaline earth metal, sulfonium, or ammonium, or G is a latentiating group which is C(O)—Ror C(0)-O—R; and b) a co-herbicide selected from the group consisting of fenoxasulfone, ipfencarbazone, propyrisulfuron, and N-[2-[(4,6-dimethoxy-1,3,5-triazin-2-yl)carbonyl]-6-fluorophenyl]-1,1-difluoro-N-methylmethanesulfonamide. The herbicidal composition is typically for controlling grasses and weeds in crops of useful plants, especially for controlling and/or weeds in crops of rice. 2. A herbicidal composition as claimed in claim 1 , wherein Ris ethyl.3. A herbicidal composition as claimed in claim 1 , wherein Ris phenyl substituted by methyl claim 1 , methoxy claim 1 , or halogen.4. A herbicidal composition as claimed in claim 3 , wherein Ris phenyl substituted by fluorine or chlorine.5. A herbicidal composition as claimed in claim 1 , wherein R claim 1 , R claim 1 , Rand R claim 1 , independently of each other claim 1 , are hydrogen or C-Calkyl.6. A herbicidal composition as claimed in claim 5 , wherein R claim 5 , R claim 5 , Rand Rare methyl.7. A herbicidal composition as claimed in claim 1 , wherein G is hydrogen claim 1 , C(O)—Ror C(O)—O—R; wherein Rand Rare C-Calkyl.8. A herbicidal composition as claimed in claim 7 , wherein G is hydrogen claim 7 , C(O)—Ror C(O)—O—R; wherein Rand Rare methyl claim 7 , ethyl claim 7 , n-propyl claim 7 , isopropyl or t-butyl.9. A herbicidal composition as claimed in claim 8 , wherein G is ...

ISOXAZOLE, ISOTHIAZOLE, FURANE AND THIOPHENE COMPOUNDS AS MICROBICIDES

The present invention relates to a compound of formula I: (I) wherein the substituents have the definitions as defined in claim or a salt or a N-oxide thereof, their use and methods for the control and/or prevention of microbial infection, particularly fungal infection, in plants and to processes for the preparation of these compounds. 2. A compounds according to characterized in thatX is S or O;Y is C—H or N;{'sup': '1', 'sub': 1-8', '1-8', '2-8', '2-8', '2-8', '2-8', '1-8', '1-8', '3-8', '3-8', '1-8', '1-8', '7-15', '7-15', '6-10', '6-10', '6-10', '6-10', '6-10', '6-10, 'Ris unsubstituted Calkyl; substituted Calkyl; unsubstituted Calkenyl; substituted Calkenyl; unsubstituted Calkinyl; substituted Calkinyl; unsubstituted Calkoxyalkyl; substituted Calkoxyalkyl; unsubstituted Ccycloalkyl; substituted Ccycloalkyl; unsubstituted Chaloalkyl; substituted Chaloalkyl; unsubstituted Carylalkyl; substituted Carylalkyl; unsubstituted Caryl; substituted Caryl; unsubstituted Caryloxy; substituted Caryloxy; unsubstituted Carylthio; substituted Carylthio; a unsubstituted 5 to 10-membered aromatic heterocycle; or a substituted 5 to 10-membered aromatic heterocycle;'}{'sup': '2', 'sub': 1-8', '1-8', '2-8', '2-8', '2-8', '2-8', '1-8', '1-8', '1-8', '1-8', '3-8', '3-8', '7-15', '7-15', '6-10', '1-8', '6-10', '1-8', '6-10', '1-8', '6-10', '1-8', '6-10', '6-10', '6-10', '6-10', '6-10', '6-10', '1-8', '1-8, 'Ris H; halogen, unsubstituted Calkyl; substituted Calkyl; unsubstituted Calkenyl; substituted Calkenyl; unsubstituted Calkinyl; substituted Calkinyl; unsubstituted Calkoxyalkyl; substituted Calkoxyalkyl; unsubstituted Chaloalkyl; substituted Chaloalkyl; unsubstituted Ccycloalkyl; substituted Ccycloalkyl; unsubstituted Carylalkyl; substituted Carylalkyl; unsubstituted Caryloxy-Calkyl; substituted Caryloxy-Calkyl; unsubstituted Carylthio-Calkyl; substituted Carylthio-Calkyl; unsubstituted Caryl; substituted Caryl; unsubstituted Caryloxy; substituted Caryloxy; unsubstituted Carylthio; ...

PESTICIDAL MIXTURES COMPRISING ISOXAZOLINE DERIVATIVES

The present invention provides pesticidal mixtures comprising a component A, a component B and a component C, wherein component A is a compound of formula (I) wherein one of Yand Yis S, SO or SOand the other is CH; L is a direct bond or methylene; Aand Aare C—H, or one of Aand Ais C—H and the other is N; Ris hydrogen or methyl; Ris chlorodifluoromethyl or trifluoromethyl; Ris 3,5-dibromo-phenyl, 3,5-dichloro-phenyl, 3,4-dichloro-phenyl, or 3,4,5-trichloro-phenyl; Ris methyl; Ris hydrogen; or Rand Rtogether form a bridging 1,3-butadiene group; component B is a compound selected from Sedaxane, Fludioxonil, Metalaxyl, Mefenoxam, Cyprodinil, Azoxystrobin, Tebuconazole, Difenoconazole, Thiabendazole, Fluopyram, Penflufen, N-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide and Fuxapyroxad; or component B is a compound selected from Tefluthrin, Lambda-cyhalothrin, Abamectin, Spinosad, Spinetoram, Chlorpyrifos, Thiodicarb, Chlorantraniliprole, Cyantraniliprole, spp. such as and , Imidacloprid, Thiacloprid, Acetamiprid, Nitenpyram, Dinotefuran, Thiamethoxam, Clothianidin, Nithiazine, Flonicamid, Fipronil, Pyrifluquinazone, Pymetrozine, Sulfoxaflor and Spirotetramat; and component C is a compound selected from an insecticide, a fungicide and a nematicide, which insecticide is selected from neonicotinoids, carbamates, diamides, spinosyns, phenylpyrazoles, pyrethroids, Pyrifluquinazone, Pymetrozine, Sulfoxaflor and Spirotetramat; which fungicide is selected from Azoxystrobin, Trifloxystrobin, Fluoxastrobin, Cyproconazole, Difenoconazole, Prothioconazole, Tebuconazole, Triticonazole, Fludioxonil, Thiabendazole, Ipconazole, Cyprodinil, Myclobutanil, Metalaxyl, Mefenoxam, Sedaxane, N-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxamide, Fluopyram, Penflufen, Fuxapyroxad, Fluopyram, and Penthiopyrad; which nematicide is selected from ...

NOVEL HETEROCYCLIC COMPOUNDS AS PESTICIDES

The present application relates to novel heterocyclic compounds, to processes for preparation thereof and to the use thereof for controlling animal pests, which also include arthropods and especially insects. 2. A salt claim 1 , tautomeric and/or isomeric form and N-oxides of the compound of formula (I) according to .3. A composition claim 1 , wherein said composition comprises at least one compound of formula (I) according to .4. A method for controlling pests claim 1 , wherein a compound of the formula (I) according to is allowed to act on the pests and/or their habitat.5. A composition claim 2 , wherein said composition comprises at least one compound of formula (I) according to .6. A method for controlling pests claim 2 , wherein a compound of the formula (I) according to is allowed to act on the pests and/or their habitat.7. A method for controlling pests claim 3 , wherein said composition according to is allowed to act on the pests and/or their habitat. The present invention relates to novel heterocyclic compounds, to processes for preparation thereof and to the use thereof for controlling animal pests, which also include arthropods and especially insects.WO 2008/028903 A2, WO 2003/077918 A1 and WO 2003/029210 A2 disclose heterocyclic compounds for which pharmaceutical applications are described.Further heterocycles which may be used in plant protection are described in WO 2009/149858, WO 2010/006713, WO 2011/045240 and WO 2011/045224.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 alone, the search for novel crop protection agents cannot be considered as having been concluded, and there is a ...

FUNGICIDAL AZOCYCLIC AMIDES

Disclosed are compounds of Formula 1, including all stereoisomers, N-oxides, and salts thereof, 6. A compound of wherein:{'sup': 1', '1', '1, 'Z is selected from Z-1, Z-16, Z-18, Z-1 and Z-3.'}7. A compound of wherein:{'sup': 1', '1, 'Z is Z-1, Z-16 or Z-1.'}8. A compound of wherein:{'sup': '12', 'Ris hydrogen.'}9. The compound of which is selected from the group:1-[4-[4-[5-[2-[(2,6-difluorophenoxy)ethyl]-4,5-dihydro-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone,1-[4-[4-[5-[(2,6-difluorophenoxy)methyl]-4,5-dihydro-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone and1-[4-[4-[5-[(2,6-difluoro-4-methoxyphenoxy)methyl]-4,5-dihydro-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone.10. A fungicidal composition comprising (a) a compound of ; and (b) at least one other fungicide.11. A fungicidal composition comprising (a) a compound of ; and (b) at least one additional component selected from the group consisting of surfactants claim 1 , solid diluents and liquid diluents.12. A method for controlling plant diseases caused by fungal plant pathogens comprising applying to the plant or portion thereof claim 1 , or to the plant seed claim 1 , a fungicidally effective amount of a compound of .13. A compound which is selected from the group:1-[4-[4-[4,5-dihydro-5-[2-(2-iodophenoxy)ethyl]-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone,1-[4-[4-[5-[2-[(2,6-difluorophenoxy)ethyl]-4,5-dihydro-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]ethanone,2-[[[4,5-dihydro-3-[2-[1-[2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl]-4-piperidinyl]-4-thiazolyl]-5-isoxazolyl]methoxy]methyl]-1H-isoindole-1,3(2H)-dione,N-[(2,6-difluorophenyl)methyl]-4,5-dihydro-3-[2-[1-[2-[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl]-4-piperidinyl]-4-thiazolyl ...

1-(HETEROCYCLIC CARBONYL) PIPERIDINES

The present invention relates to fungicidal 1-(heterocyclic carbonyl) piperidines and their thiocarbonyl derivatives, their process of preparation and intermediate compounds for their preparation, their use as fungicides, particularly in the form of fungicidal compositions and methods for the control of phytopathogenic fungi of plants using these compounds or their compositions. 3. A compound according to wherein A is selected in the list consisting of A; A; Aand A.4. A compound according to wherein A represents Awherein Rrepresents a substituted or non-substituted C-C-alkyl claim 2 , C-C-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; substituted or non-substituted C-C-alkoxy; Rrepresents a hydrogen atom or a halogen atom and Rrepresents a substituted or non-substituted C-C-alkyl.5. A compound according to wherein A represents Awherein Rrepresents C-C-alkyl claim 2 , C-C-halogenoalkyl comprising up to 3 halogen atoms that can be the same or different; Rrepresents a hydrogen atom; a chlorine atom; or a fluorine atom; and Rrepresents a methyl.6. A compound according to wherein T represents O.7. A compound according to wherein n represents 0 or 1.8. A compound according to wherein Qrepresents a bond or an oxygen atom.9. A compound according to wherein B represents a substituted or non-substituted phenyl ring; a substituted or non-substituted naphthyl ring; a substituted or non-substituted pyridyl ring; a substituted or non-substituted thienyl ring; or a substituted or non-substituted benzothienyl ring.10. A compound according to wherein B represents a substituted or non-substituted phenyl ring11. A compound according to wherein B represents a substituted or non-substituted naphthyl ring.12. A compound according to wherein X independently represents a halogen atom; substituted or non-substituted C-C-alkyl; C-C-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; substituted or non-substituted C-C-alkoxy or ...

FUNGICIDAL N-(2-PHENOXYETHYL)CARBOXAMIDE DERIVATIVES AND THEIR AZA, THIA AND SILA ANALOGUES

The present invention relates to fungicide N-(2-phenoxyethyl)carboxamide derivatives of formula (I), their aza, thia and sila analogues, their process of preparation, their use as fungicides, particularly in the form of fungicidal compositions and methods for the control of phytopathogenic fungi of plants using these compounds or their compositions. Formula (1) wherein A, T, W, X, n and Zto Zrepresent various substituents. 3. A compound according to wherein A is selected in the list consisting of A; A; Aand A.4. A compound according to wherein A represents Aand wherein Rrepresents a C-C-alkyl claim 3 , C-C-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; or C-C-alkoxy; Rrepresents a hydrogen atom or a halogen atom; Rrepresents a C-C-alkyl.5. A compound according to wherein W represents O or S.6. A compound according to wherein n represents 0 claim 1 , 1 or 2.7. A compound according to wherein X independently represents a halogen atom; C-C-alkyl; C-C-halogenoalkyl comprising up to 9 halogen atoms that can be the same or different; tri(C-C-alkyl)silyl; C-Calkoxy or C-C-halogenoalkoxy comprising up to 9 halogen atoms that can be the same or different or wherein two consecutive substituents X together with the phenyl ring form a substituted or non substituted 1 claim 1 ,3-benzodioxolyl; 1 claim 1 ,2 claim 1 ,3 claim 1 ,4-tetrahydro-quinoxalinyl; 3 claim 1 ,4-dihydro-2H-1 claim 1 ,4-benzoxazinyl; 1 claim 1 ,4-benzodioxanyl; indanyl; 2 claim 1 ,3-dihydrobenzofuranyl; or indolinyl.8. A compound according to wherein Zand Zindependently represent a C-C-alkyl.9. A compound according to wherein Zand Zindependently represent a hydrogen atom or a C-C-alkyl.10. A compound according to wherein Zand Zindependently represent a hydrogen atom or a C-C-alkyl.11. A compound according to wherein Zrepresents a C-Ccycloalkyl substituted by up to 10 groups or atoms that can be the same or different and that can be selected in the list consisting of halogen ...

STABLE AND AQUEOUS CONCENTRATED PRESERVATIVE COMPOSITION OF DEHYDROACETIC ACID (DHA) AND METHYLISOTHIAZOLINONE (MIT)

An aqueous, stable, highly-concentrated preservative composition comprising (i) about 5 to 50 wt % of a dehydroacetic acid (DHA) or a salt thereof; (ii) about 1 to 20 wt % of a 2-methyl-4-isothiazolin-3-one (MIT); (iii) about 0.1 to 10 wt % of at least one block copolymer; (iv) optionally, about 0.01 to 5.0 wt % of at least one sulfosuccinate surfactant; (v) optionally, about 0.01 to 5.0 wt % of at least one sequestering agent; and (vi) optionally, about 0.01 to 5.0 wt % of one or more additives. Also disclosed is a process for preparing said preservative composition. 1. An aqueous , stable and highly-concentrated preservative composition comprising:i. about 5 to 50 wt % of a dehydroacetic acid (DHA) or a salt thereof;ii. about 1 to 20 wt % of a 2-methyl-4-isothiazolin-3-one (MIT);iii. about 0.1 to 10 wt % of at least one block copolymer;iv. optionally, about 0.01 to 5.0 wt % of at least one sulfosuccinate surfactant;v. optionally, about 0.01 to 5.0 wt % of at least one sequestering agent; andvi. optionally, about 0.01 to 5.0 wt % of at least one additive2. The preservative composition according to claim 1 , wherein said block copolymer is selected from the group consisting of tetra-functional block copolymer comprising at least one polyethyleneoxide (PEO) and polypropyleneoxide (PPO).3. The preservative composition according to claim 2 , wherein the tetra-functional polyethyleneoxide (PEO) and polypropyleneoxide (PPO) block copolymer has an average molecular weight of from about 1000 to about 100000.4. The preservative composition according to claim 1 , wherein said sulfosuccinate surfactant is selected from the group consisting of sulfosuccinate monoester claim 1 , sulfosuccinate diester claim 1 , monoalkyl sulfosuccinate claim 1 , dialkyl sulfosuccinate or their alkali metal salts.5. The preservative composition according to claim 1 , wherein said sulfosuccinate is selected from the group lauryl sulfosuccinate claim 1 , laureth sulfosuccinate claim 1 , laureth-5 ...

Synergistic Fungicidal Active Substance Combinations

The novel active compound combinations of a carboxamide of the general formula (I) (group 1) 117-. (canceled)19. The active compound combination according to claim 18 , wherein the fungicide is (19-1) acibenzolar-S-methyl.20. The active compound combination according to claim 19 , wherein the ratio of (1-1) penthiopyrad to (19-1) acibenzolar-S-methyl is from 20:1 to 1:100.21. The active compound combination according to claim 18 , wherein the fungicide is (19-2) edifenphos.22. The active compound combination according to claim 21 , wherein the ratio of (1-1) penthiopyrad to (19-2) edifenphos is from 20:1 to 1:100.23. The active compound combination according to claim 18 , wherein the fungicide is (19-3) famoxadone.24. The active compound combination according to claim 23 , wherein the ratio of (1-1) penthiopyrad to (19-3) famoxadone is from 20:1 to 1:100.25. The active compound combination according to claim 18 , wherein the fungicide is (19-4) oxadixyl.26. The active compound combination according to claim 25 , wherein the ratio of (1-1) penthiopyrad to (19-4) oxadixyl is from 20:1 to 1:100.27. The active compound combination according to claim 18 , wherein the fungicide is (19-5) spiroxamine.28. The active compound combination according to claim 27 , wherein the ratio of (1-1) penthiopyrad to (19-5) spiroxamine is from 20:1 to 1:100.29. The active compound combination according to claim 18 , wherein the fungicide is (19-6) dithianon.30. The active compound combination according to claim 29 , wherein the ratio of (1-1) penthiopyrad to (19-6) dithianon is from 20:1 to 1:100.31. The active compound combination according to claim 18 , wherein the fungicide is (19-7) metrafenone.32. The active compound combination according to claim 31 , wherein the ratio of (1-1) penthiopyrad to (19-7) metrafenone is from 20:1 to 1:100.33. The active compound combination according to claim 18 , wherein the fungicide is (19-8) fenamidone.34. The active compound combination according to ...

HERBICIDAL COMPOSITION AND METHOD OF USE THEREOF

The present invention relates to a herbicidal composition comprising topramezone and a pyridine herbicide. The invention also relates to methods of controlling the growth of weeds, and to the use of this composition. 1. A herbicidal composition comprising a herbicidally effective amount of a mixture of topramezone and a pyridine herbicide.2. The composition of claim 1 , wherein the pyridine herbicide is dithiopyr.34-. (canceled)5. The composition of claim 1 , wherein the weight ratio of topramezone to pyridine herbicide is between about 1:10 and about 10:1.6. The composition of claim 5 , wherein the weight ratio of topramezone to pyridine herbicide is between about 1:5 and about 5:1.7. The composition of claim 6 , wherein the weight ratio of topramezone to pyridine herbicide is between about 1:2 and about 2:1.8. A method for controlling or modifying the growth of white clover claim 1 , comprising applying to the locus of the white clover a herbicidally effective amount of a composition according to .9. The method of claim 8 , wherein the white clover is present in turfgrass.10. The method of claim 8 , wherein the composition is applied (i) pre-emergence or (ii) post-emergence.11. The method of claim 8 , wherein the combined amount of topramezone and pyridine herbicide applied to the locus of the weeds is between about 0.005 kg/ha and about 5 kg/ha.12. The method of claim 11 , wherein the combined amount of topramezone and pyridine herbicide applied to the locus of the weeds is between about 0.05 kg/ha and about 2 kg/ha.13. The method of claim 12 , wherein the combined amount of topramezone and pyridine herbicide applied to the locus of the weeds is between about 0.1 kg/ha and about 0.5 kg/ha.14. (canceled) The present invention relates to a herbicidal composition comprising mesotrione and a pyridine herbicide such as dithiopyr or thiazopyr. The invention also relates to a method of controlling the growth of weeds and to the use of this composition.The protection of ...

Herbicidal composition

To provide a technology for controlling weeds and the like. A herbicidal composition containing at least one compound selected from Group A, dicamba or agronomically acceptable salt thereof and isoxadifen-ethyl as active ingredients has a weed control effect: Group A; a group consisting of flumioxazin, sulfentrazone, saflufenacil, oxyfluorfen, fomesafen, and a compound represented by the formula (I);

Topical localized isoxazoline formulation comprising glycofurol

This invention provides topical localized formulations comprising an isoxazoline compound and a pharmaceutically or veterinary acceptable liquid carrier vehicle comprising glycofurol and an improved method for controlling, and preventing parasite infestation in animals.

Synergistic Fungicidal Active Substance Combinations

The novel active compound combinations of a carboxamide of the general formula (I) (group 1) 117-. (canceled)18. An active compound combination comprising (1-1) penthiopyrad , one benzimidazole selected from the group comprising: (10-1) 6-chloro-5-[(3 ,5-dimethylisoxazol-4-yl)sulfonyl]-2 ,2-difluoro-5H-[1 ,3]dioxolo[4 ,5-f]benzimidazole , (10-2) benomyl , (10-3) carbendazim , (10-4) chlorfenazole , (10-5) fuberidazole , and (10-6) thiabendazole , and optionally an extender , a surfactant , or a combination thereof , wherein the ratio of (1-1) penthiopyrad to the benzimidazole is from 10:1 to 1:50 , and wherein said (1-1) penthiopyrad and benzimidazole are present in synergistic amounts.19. The active compound combination according to claim 18 , wherein the benzimidazole is (10-1) 6-chloro-5-[(3 claim 18 ,5-dimethylisoxazol-4-yl)sulfonyl]-2 claim 18 ,2-difluoro-5H-[1 claim 18 ,3]dioxolo[4 claim 18 ,5-f]benzimidazole.20. The active compound combination according to claim 19 , wherein the ratio of (1-1) penthiopyrad to (10-1) 6-chloro-5-[(3 claim 19 ,5-dimethylisoxazol-4-yl)sulfonyl]-2 claim 19 ,2-difluoro-5H-[1 claim 19 ,3]dioxolo[4 claim 19 ,5-f]benzimidazole is from 5:1 to 1:20.21. The active compound combination according to claim 18 , wherein the benzimidazole is (10-2) benomyl.22. The active compound combination according to claim 21 , wherein the ratio of (1-1) penthiopyrad to (10-2) benomyl is from 5:1 to 1:20.23. The active compound combination according to claim 18 , wherein the benzimidazole is (10-3) carbendazim.24. The active compound combination according to claim 23 , wherein the ratio of (1-1) penthiopyrad to (10-3) carbendazim is from 5:1 to 1:20.25. The active compound combination according to claim 18 , wherein the benzimidazole is (10-4) chlorfenazole.26. The active compound combination according to claim 25 , wherein the ratio of (1-1) penthiopyrad to (10-4) chlorfenazole is from 5:1 to 1:20.27. The active compound combination according to claim 18 ...

Synergistic Fungicidal Active Substance Combinations

The novel active compound combinations of a carboxamide of the general formula (I) (group 1) in which R, G, R and A have the meanings given in the description and the active compound groups (2) to (23) listed in the description have very good fungicidal properties.

ISOTHIAZOLINONE BIOCIDES ENHANCED BY ZINC IONS

The present invention relates to an antimicrobial composition comprising an isothiazolinone, such as 1,2-benzisothiazolin-3-one, and a zinc compound selected from zinc salts, zinc oxides, zinc hydroxides or combinations thereof. Useful zinc salts include for example, oxides, sulfates, chlorides, and combinations thereof. In use, the zinc from the zinc compound enhances the antimicrobial activity to the isothiazolin-containing composition. This enhancement permits achieving the desired antimicrobial activity at a lower usage rate than is achieved using the isothiazolinone in the absence of the zinc compound. The antimicrobial composition can also contain co-biocides, such as pyrithiones, including zinc pyrithione or copper pyrithione. 118-. (canceled)19. An antimicrobial composition concentrate comprising:(a) at least one isothiazolin-3-one; and(b) at least one zinc compound selected from the group consisting of zinc salts, zinc oxides, and zinc hydroxides,wherein said isothiazolin-3-one is present in an amount of from about 1% to about 95% w/w based on the total weight of the concentrate,wherein the at least one zinc compound is present in an amount from about 1% to about 50% w/w based on the total weight of the concentrate, andwherein the weight ratio of the isothiazolin-3-one to the zinc compound is from 1:2000 to 100:1.20. The antimicrobial composition concentrate of claim 19 , wherein said isothiazolin-3-one is selected from the group consisting of 1 claim 19 ,2-benzisothiazolin-3-one claim 19 , N-(n-butyl)-1 claim 19 ,2-benzisothiazolin-3-one claim 19 , 4 claim 19 ,5-dichloro-2-n-octyl-4-isothiazolin-3-one claim 19 , 2-methyl-4-isothiazolin-3-one claim 19 , mixtures of 5-chloro-2-methyl-4-isothiazolin-3-one (CIMIT) and 2-methyl-4-isothiazolin-3-one claim 19 , and dithio-2 claim 19 ,2′-bis(benzmethylamide).21. The antimicrobial composition concentrate of claim 20 , wherein said isothiazolin-3-one is 1 claim 20 ,2-benzisothiazolin-3-one.22. The antimicrobial ...

Pesticidal compositions and processes related thereto

This document discloses molecules having the following formula (“Formula One”): and processes related thereto.

Herbicide triazolylpyridine ketones

Triazolylpyridine ketones expressed by the following formula (1) and use thereof as herbicides.

HETEROARYLPIPERIDINE AND -PIPERAZINE DERIVATIVES AS FUNGICIDES

Heteroarylpiperidine and -piperazine derivatives of the formula (I) 2. A compound according to claim 1 , in which {'sup': 3', '4', '3', '4, 'sub': 1', '6', '2', '6', '2', '6', '3', '8', '1', '6', '2', '6', '2', '6', '3', '6', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '1', '6', '1', '4', '1', '6', '1', '6', '1', '6, 'halogen, cyano, hydroxyl, —NRR, —C(═O)NRR, nitro, C-C-alkyl, C-C-alkenyl, C-C-alkynyl, C-C-cycloalkyl, C-C-haloalkyl, C-C-haloalkenyl, C-C-haloalkynyl, C-C-halocycloalkyl, C-C-alkoxy, C-C-haloalkoxy, C-C-alkenyloxy, C-C-alkynyloxy, C-C-alkylthio, C-C-alkylsulphonyl, C-C-haloalkylthio, C-C-haloalkylsulphonyl, C-C-alkoxy-C-C-alkyl, hydroxyl-C-C-alkyl, C-C-alkylcarbonyl, C-C-alkoxycarbonyl, C-C-alkylcarbonyloxy or —C(═O)H, or'}, 'A is phenyl which may contain up to two substituents, where the substituents are each independently selected from the following list substituents on carbon:', {'sup': 3', '4, 'sub': 1', '6', '2', '6', '2', '6', '3', '6', '1', '6', '2', '6', '2', '6', '3', '6', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '1', '6', '1', '6', '1', '6, 'halogen, cyano, hydroxyl, nitro, —NRR, C-C-alkyl, C-C-alkenyl, C-C-alkynyl, C-C-cycloalkyl, C-C-haloalkyl, C-C-haloalkenyl, C-C-haloalkynyl, C-C-halocycloalkyl, C-C-alkoxy, C-C-haloalkoxy, C-C-alkylthio, C-C-alkylsulphonyl, C-C-haloalkylthio, C-C-haloalkylsulphonyl, C-C-alkoxy-C-C-alkyl, hydroxy-C-C-alkyl, C-C-alkylcarbonyl, C-C-alkoxycarbonyl, C-C-alkylcarbonyloxy or phenyl,'}, 'substituents on nitrogen:', {'sub': 1', '6', '2', '6', '2', '6', '1', '6', '2', '6', '2', '6', '3', '10', '1', '6', '1', '6', '1', '4', '1', '4', '1', '6, 'C-C-alkyl, C-C-alkenyl, C-C-alkynyl, C-C-haloalkyl, C-C-haloalkenyl, C-C-haloalkynyl, C-C-cycloalkyl-C-C-alkyl, C-C-haloalkylcarbonyl, phenyl, benzyl, C-C-alkylsulphonyl, C-C-haloalkylsulphonyl, phenylsulphonyl, —C(═O)H, or C-C-alkylcarbonyl.'}], 'A is a heteroaromatic radical ...

Cyanoenamines and their use as fungicides

The present invention relates to cyanoenamine derivatives, their process of preparation, intermediate compounds, their use as fungicide active agents, particularly in the form of fungicide compositions, and methods for the control of phytopathogenic fungi, notably of plants and in material protection, using these compounds or compositions.

ISOXAZOLE DERIVATIVES FOR USE AS FUNGICIDES

The present invention relates to isoxazole compounds of formula (I) having fungicidal activity, to agricultural compositions comprising them, and to the use of said compounds and compositions in agriculture for the control of microbial pests, particularly fungal pests, on plants

Alpha, beta-unsaturated imines

The present application relates to novel alpha, beta-unsaturated imines, to processes for their preparation, to their use for controlling animal pests including arthropods and in particular insects and to their use in the control of vectors. 2. The compound according to claim 1 , where Arepresents —C(R claim 1 ,R)—.3. The compound according to claim 1 , where Arepresents a —C(R claim 1 ,R)— group and where{'sup': 2', '3, 'said C(R,R)— group forms a double bond with the adjacent B position, or'}{'sup': 2', '3', '1', '2', '1', '2, 'sub': 'n', 'said C(R,R)— group is a bridging group which, together with a further bridging group and any B groups, located between these bridging groups, of the C(═C(W,X-Q)-C(═N-Q)-A-[B]-Aring and a corresponding bridge U forms an unsubstituted or substituted cyclic system, or'}{'sup': 2', '3, 'this said C(R,R)— group carries a substituent V.'}4. The compound according to claim 1 , where Ais part of a cyclic system.5. The compound according to claim 1 , where Ais part of a carbocyclic system comprising 6 ring atoms or part of a 5- or 6-membered heterocyclic system.6. The compound according to claim 5 , where Ais part of an aromatic system comprising 6 ring atoms or part of a 5- or 6-membered heteroaromatic system.7. The compound according to claim 1 , where n is 2.11. An insecticidal composition claim 1 , wherein said insecticidal composition comprises at least one compound according to claim 1 , and an extender and/or surfactant.12. A method for protecting transgenic and/or conventional seed and a plant generated therefrom against attack by pests claim 1 , comprising treating the seed with at least one compound according to .13. A compound according claim 1 , capable of being used for controlling pests.14. A compound according to claim 1 , capable of being used for controlling vectors.15. A seed in which a compound according to claim 1 , has been applied to said seed as a constituent of a casing and/or as a further layer and/or further ...

Herbicidal Compositions Comprising Topramezone and Pinoxaden

The present invention relates to herbicidal compositions comprising topramezone and pinoxaden and optionally a herbicide safener compound such as cloquintocet. The present invention also relates to the use of these compositions for controlling undesirable vegetation, in particular in crops. 129-. (canceled)30. A herbicidal composition comprising:a) a herbicide compound A which is selected from topramezone, the salts and esters, carbonates or thiocarbonates thereof;andb) a second herbicide compound B which is pinoxaden.31. The composition as claimed in claim 30 , wherein the weight ratio of the herbicide compound A and the herbicide compound B is from 1:1 to 1:15 claim 30 , wherein the herbicide compound A is calculated as topramezone.32. The composition as claimed in claim 30 , wherein the composition further comprises at least one herbicide safener compound C.33. The composition as claimed in claim 32 , wherein the herbicide safener compound C is selected from the group consisting of benoxacor claim 32 , cloqintocet claim 32 , cyometrinil claim 32 , cyprosulfamide claim 32 , dichlormid claim 32 , dicyclonon claim 32 , dietholate claim 32 , fenchlorazole claim 32 , fenclorim claim 32 , flurazole claim 32 , fluxofenim claim 32 , furilazole claim 32 , isoxadifen claim 32 , mefenpyr claim 32 , mephenate claim 32 , naphthalic anhydride claim 32 , 2 claim 32 ,2 claim 32 ,5-trimethyl-3-(dichloracetyl)-1 claim 32 ,3-oxazolidine claim 32 , 4-(dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane claim 32 , N-(2-methoxybenzoyl)-4-[(methylaminocarbonyl)amino]benzenesulfonamide and oxabetrinil claim 32 , a salt or an agriculturally acceptable derivative thereof.34. The composition as claimed in claim 32 , wherein the herbicide safener compound C is selected from cloquintocet claim 32 , a salt or an ester thereof.35. The composition as claimed in claim 32 , wherein the herbicide safener compound C is selected from the group consisting of mefenpyr claim 32 , isoxadifen and asalt or an ...

THERMO-STABLE, ARSENIC-FREE SYNERGISTIC BIOCIDE CONCENTRATE COMPOSITION FOR POLYMER MATRICES AND PROCESS FOR PREPARING SAME

A thermo-stable, arsenic-free synergistic biocide concentrate composition to afford enhanced antimicrobial properties to a polymer matrix comprising (i) a mixture of trihalomethyl-thio-phthalimide analogue and a second biocide; (ii) an antioxidant; (iii) a carrier; and (iv) optionally, one or more additives. The composition is capable of withstanding high processing temperatures up to about 250° C., substantially without thermal degradation of biocides and discoloration of the polymer matrix employed. 1. A thereto-stable , arsenic-free synergistic biocide concentrate composition to provide enhanced microbicidal properties to a polymer matrix comprising:i. (a) about 2.5 to about 50.0 wt % of trihalomethyl-thio-phthalimide; and (b) about 0.5 to about 25.0 wt % of a second biocide;ii. about 0.5 to 20 wt % of antioxidant;iii. a carrier; andiv. optionally, one or more additives.2. The biocide concentrate composition according to claim 1 , wherein the composition is capable of withstanding high processing temperatures up to about 250° C.3. The biocide concentrate composition according to claim 1 , wherein the composition is free from arsenic claim 1 , salts of arsenic claim 1 , organic derivatives of arsenic and/or inorganic derivatives of arsenic.4. The biocide concentrate composition according to claim 1 , wherein said polymer or polymer matrix is selected from the group comprising a polyolefin claim 1 , a polyacrylate claim 1 , a polyvinyl chloride claim 1 , a polyurethane claim 1 , a polyester claim 1 , a wood-plastic composite claim 1 , a polycarbonate claim 1 , an elastomer claim 1 , a rubber claim 1 , an acrylic claim 1 , a nylon claim 1 , a fluorocarbon claim 1 , a styrenic and mixtures thereof.5. The biocide concentrate composition according to claim 1 , wherein said trihalomethyl-thio-phthalimide is N-[(trichloromethyl)thio]phthalimide.6. The biocide concentrate composition according to claim 1 , wherein said second biocide is selected from the group consisting ...

Chiral3-(benzylsulfinyl)-5,5-dimethyl-4,5-dihydroisoxazole derivatives and 5,5-dimethyl-3-[(1h-pyrazol-4-ylmethyl)sulfinyl]-4,5-dihyddroisoxazole derivatives, method for the production thereof, and use of same as herbicides and plant growth regulators

The invention relates to 3-(benzylsulfinyl)-5,5-dimethyl-4,5-dihydroisoxazole derivatives and 5,5-dimethyl-3-[(1H-pyrazol-4-ylmethyl)sulfinyl]-4,5-dihydroisoxazole derivatives of the formula (I) and their salts 2. The compound of the formula (I) as claimed in wherein{'sup': 1', '5', '9', '10', '9', '10', '9', '10, 'sub': 1', '4', '3', '6', '1', '4', '1', '4', '1', '4', '1', '4', '1', '2', '1', '3', '1', '3', '1', '4', '3', '6', '3', '6', '1', '2', '3', '6', '1', '4', '1', '2', '3', '4', '3', '4', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '3', '4', '2', '4', '6', '1', '4', '6', '1', '4', '2', '4', '2', '4', '1', '6', '3', '6', '1', '6', '1', '6', '1', '6, 'the substituents Rto Rare independently of one another selected from the group consisting of hydrogen, hydroxyl, halogen, cyano, nitro, amino, C(O)OH, (C-C)-alkyl, (C-C)-cycloalkyl, (C-C)-haloalkyl, (C-C)-alkoxy, (C-C)-haloalkoxy, (C-C)-alkoxy-(C-C)-alkyl, (C-C)-alkylcarbonyl, (C-C)-alkylcarbonyloxy, (C-C)-alkoxycarbonyl, (C-C)-cycloalkoxycarbonyl, (C-C)-cycloalkyl-(C-C)-alkoxy, (C-C)-cycloalkoxy, (C-C)-alkoxycarbonyl-(C—O)-alkoxy, (C-C)-alkenyloxy, (C-C)-alkynyloxy, (C-C)-alkylthio, (C-C)-haloalkylthio, (C-C)-alkylsulfinyl, (C-C)-haloalkylsulfinyl, (C-C)-alkylsulfonyl, (C-C)-haloalkylsulfonyl, (C-C)-alkylsulfonyloxy, di-(C-C)-alkylamino, (C-C)-alkenyloxycarbonyl, (C-C)-alkynyloxycarbonyl, C-aryl-(C-C)-alkoxycarbonyl, C-aryl-(C-C)-alkoxy, formyl, (C-C)-alkenyl, (C-C)-alkynyl, phenyl, —C(O)NRR, where Rand Rindependently of one another are selected from the group consisting of hydrogen, (C-C)-alkyl, (C-C)-cycloalkyl, (C-C)-haloalkyl, or where Rand Rtogether form a (C-C)-alkylene group which may contain one oxygen or sulfur atom or one or two amino or (C-C)-alkylamino groups;'} {'sub': 1', '6', '1', '6, 'two substituents ortho to one another together form a (C-C)-alkylene group which may contain one or more oxygen and/or sulfur atoms, where the (C-C)-alkylene group may be mono- or ...

ANTIBACTERIAL RESIN COMPOSITION

An antibacterial resin composition comprising a thermoplastic resin or a thermosetting resin that contains a metal compound represented by the following formula (1), permitting the metal such as silver having antibacterial power to efficiently elute out and the eluted metal to remain stable as metal ions so that excellent antibacterial power can be exhibited using only a decreased amount of an expensive compound containing silver or the like, 2. The antibacterial resin composition according to claim 1 , wherein said metal compound is contained in an amount of 0.01 to 10 parts by weight per 100 parts by weight of said thermoplastic resin or said thermosetting resin.4. The antibacterial resin composition according to claim 3 , wherein said fatty acid metal salt is contained in an amount of 0.001 to 10 parts by weight and said compound represented by the above formula (2) is contained in an amount of 0.001 to 30 parts by weight per 100 parts by weight of said thermoplastic resin or said thermosetting resin.5. An antibacterial resin composition comprising a thermoplastic and/or thermosetting resin blended with a metal-carrying compound carrying at least one kind of metal ions selected from Ag claim 3 , Cu claim 3 , Zn claim 3 , Co and Ni claim 3 , and a compound represented by the above formula (2).6. The antibacterial resin composition according to claim 5 , whereinsaid metal-carrying compound carrying the metal ions is contained in an amount of 0.001 to 10 parts by weight and said compound represented by the formula (2) is contained in an amount of 0.001 to 30 parts by weight per 100 parts by weight of said thermoplastic resin or said thermosetting resin.7. An antibacterial resin formed body obtained by mixing claim 1 , heating and forming the antibacterial resin composition of .8. An antibacterial resin formed body obtained by mixing claim 2 , heating and forming the antibacterial resin composition of .9. An antibacterial resin formed body obtained by mixing claim 3 ...

METHODS OF PEST CONTROL IN SOYBEAN

The present invention provides methods comprising applying to a crop of soybean plants, the locus thereof, or propagation material thereof, a compound a compound of formula III wherein A, A, A and A are independently C—H, or nitrogen and wherein #1 indicates the bond to X and #2 indicates the bond to cycle B; cycle B is selected from B1 to B6 wherein #1 indicates the bond to cycle A, #2 indicates the bond to Rand #3 indicates the bond to cycle C; cycle C is phenyl; Ris chloro, bromo, CFor methyl; Ris chlorodifluoromethyl or trifluoromethyl; each Ris independently bromo, chloro, fluoro or trifluoromethyl; p is 2 or 3; and wherein X is defined in the claims. The methods are preferably for the control of stinkbugs, in particular . 2. (canceled)6. A method according to claim 5 , wherein the method is for controlling and/or preventing infestation of the soybean crop by stinkbugs.7. (canceled)8. A method according to claim 5 , wherein X is P4 claim 5 , P5 or P6.9. A method according to claim 4 , wherein cycle B is cycle B1.11Nezara viridula, PiezodorusAcrosternumEuchistus heros.. A method according to claim 4 , wherein stinkbug is spp. claim 4 , spp claim 4 ,12Euschistus.. A method according to claim 4 , wherein stinkbug is13EuschistusEuschistus heros.. A method according to claim 1 , wherein is14. A method or use according to claim 1 , wherein the compound of formula I or formula II is applied in combination with one or more additional active ingredients selected from neonicotinoids claim 1 , pyrethroids claim 1 , strobilurins claim 1 , triazoles and carboxamides.15. A method according to claim 1 , wherein the compound is applied to the crop by foliar application.16. A method according to claim 1 , wherein the compound of formula I or formula II is applied in combination with an attractant selected from glucose claim 1 , saccharose claim 1 , salt claim 1 , glutamate claim 1 , citric acid claim 1 , soybean oil claim 1 , peanut oil and soybean milk. The present invention ...

N-ALKOXYAMIDES OF 6-(SUBSTITUTED PHENYL)-4-AMINOPICOLINATES AND 2-(SUBSTITUTED PHENYL)-6-AMINO-4-PYRIMIDINECARBOXYLATES AND THEIR USE AS SELECTIVE HERBICIDES FOR CROPS

N-Alkoxyamides of 4-aminopicolinic acids and 6-amino-4-pyrimidinecarboxylates are selective herbicides for corn, canola and sugar beet. This application is a divisional of Ser. No. 12/12,483, filed 25, Feb. 2010; and claims the benefit of U.S. Provisional Application Ser. No. 61/156,088 filed on 27, Feb. 2009.This invention relates to use of certain novel N-alkoxyamides of 6-(substituted phenyl)-4-aminopicolinates and 2-(substituted phenyl)-6-amino-4-pyrimidinecarboxylates as selective herbicides for corn, canola (oilseed rape) and sugar beet and to methods of making the compounds.A number of picolinic acids and their pesticidal properties have been described in the art. U.S. Pat. No. 6,784,137 B2 and U.S. Pat. No. 7,314,849 B2 disclose a genus of 6-aryl-4-aminopicolinic acids and their derivatives and their use as selective herbicides, particularly for rice and cereals such as wheat and barley. WO 2005/063721 A1, WO 2007/082076 A1, U.S. Patent Appl. Publ. 2009/0062125 A1, U.S. Patent Appl. Publ. 2009/0088322 A1, U.S. Patent Appl. Publ. 2007/0197391 A1 and U.S. Pat. No. 7,300,907 B2 disclose certain 2-substituted-6-amino-4-pyrimidinecarboxylic acids and their derivatives and their use as herbicides. It has now been discovered that crop selectivity of certain N-alkoxyamides of 6-(substituted phenyl)-4-aminopicolinates and of 2-(substituted phenyl)-6-amino-4-pyrimidinecarboxylates can be extended to corn, canola and sugar beet.It has now been found that certain N-alkoxyamides of 6-(substituted phenyl)-4-aminopicolinates and of 2-(substituted phenyl)-6-amino-4-pyrimidinecarboxylates are superior herbicides with a broad spectrum of broadleaf weed control and with excellent selectivity to corn, canola and sugar beet. The compounds further possess excellent toxicological or environmental profiles.The invention includes compounds of Formula I:whereinX represents CH, CF, or N;Y represents halogen, C-Calkyl, C-Ccycloalkyl, or phenyl substituted with 1-4 substituents ...

INSECT ODORANT RECEPTOR ANTAGONISTS

Insect repellent compositions are disclosed which are antagonists of insect odorant receptors. These compositions are useful as insect repellents and confusants. These insect repellent compositions may be suitable for topical application. Also disclosed are methods for interfering with the ability of an insect to detect odors. This is accomplished by exposing an insect to an olfactory-disrupting concentration of a compound. 2. (canceled)4. A method according to wherein A is chosen from oxazole claim 3 , thiazole claim 3 , isothiazole claim 3 , oxadiazole claim 3 , thiadiazole claim 3 , isoxazole claim 3 , imidazole claim 3 , pyrazole and triazole.5. (canceled)78-. (canceled)10. (canceled)12. (canceled)1415-. (canceled)1820-. (canceled)22. A method according to claim 21 , wherein:{'sub': '2', 'Z is CH;'}Ar is phenyl optionally substituted with halogen;{'sub': '2', 'Q is CHor C═O;'}{'sub': '2', 'Y is CHor C═O;'}{'sup': '1', 'sub': 1', '10, 'Ris (C-C)hydrocarbon; and'}{'sup': '2', 'sub': 1', '10, 'Ris (C-C)hydrocarbon or phenyl optionally substituted with halogen.'}2531-. (canceled)32. A method according to wherein{'sup': '24', 'D is NRor S;'}{'sup': '24', 'sub': '3', 'Ris H or CH;'}{'sup': '21', 'sub': 1', '10, 'Ris H or (C-C)hydrocarbon; and'}{'sup': 12', '13, 'sub': 1', '10, 'Rand Rare each independently selected from H and (C-C)hydrocarbon.'}3438-. (canceled)4042-. (canceled)43. A method according to wherein the substituents are selected from —N[(C-C)hydrocarbon] claim 39 , halogen claim 39 , cyano and methoxy.4446-. (canceled)4851-. (canceled)52. A method for interfering with the ability of an insect to detect odors claim 39 , the method comprising exposing said insect to an olfactory-disrupting concentration of a compound chosen from the compounds shown in the compound tables of the application.53. An insect repellent composition suitable for topical application comprising a topically acceptable carrier and a compound described in ; ora topically acceptable ...

ISOXAZOLINE DERIVATIVES FOR CONTROLLING INVERTEBRATE PESTS

The invention relates to new isoxazoline compounds of formula 3. A compound of formula (Ia) according to claim 2 , wherein n is an integer of 2 or 3; Ris CF; each Ris independently halogen; X is S or O; Ris H or C-C-alkyl; Ris H; and Ris C-C-alkyl claim 2 , which is unsubstituted or substituted in the alkyl moiety by halogen claim 2 , hydroxy claim 2 , C-C-alkoxy claim 2 , C-C-haloalkoxy claim 2 , C-C-alkylthio claim 2 , C-C-haloalkylthio claim 2 , cyano claim 2 , COOH claim 2 , C-C-alkoxycarbonyl claim 2 , a group —C(O)NRRor a radical Q′; or Ris a radical Q; or Rtogether with Ris a group ═C—NRRor ═C—NR(OR); Ris H or C-C-alkyl; Ris C-C-alkenyl claim 2 , C-C-alkynyl claim 2 , C-C-cycloalkyl claim 2 , or C-C-alkyl which is unsubstituted or substituted by halogen claim 2 , cyano or pyridyl; and Q and Q′ are each 1- claim 2 , 2- or 3-pyrrolyl claim 2 , 1- claim 2 , 2- claim 2 , 4- or 5-imidazolyl claim 2 , 1- or 4-pyrazolyl claim 2 , 2- claim 2 , 4- or 5-thiazolyl claim 2 , 1 claim 2 ,2 claim 2 ,4-triazol-3- or -4-yl claim 2 , 1 claim 2 ,2 claim 2 ,3-triazin-1- or 2-yl claim 2 , 2- 3- or 4-pyridyl claim 2 , 4- or 5-pyrimidinyl claim 2 , thietanyl claim 2 , or tetrahydrofuranyl claim 2 , which is each unsubstituted or substituted by halogen claim 2 , C-C-alkyl claim 2 , C-C-haloalkyl claim 2 , C-C-alkoxy claim 2 , C-C-haloalkoxy claim 2 , cyano claim 2 , nitro claim 2 , or C-C-alkoxycarbonyl.4. A compound of formula (Ia) according to claim 2 , wherein n is an integer of 2 or 3; Ris CF; each Ris independently halogen; X is S or O; Ris H or C-C-alkyl; Ris H; Ris C-C-alkyl claim 2 , which is unsubstituted or are substituted in the alkyl moiety by halogen claim 2 , C-C-alkoxy claim 2 , C-C-alkylthio claim 2 , cyano claim 2 , COOH claim 2 , C-C-alkoxycarbonyl claim 2 , a group —C(O)NRRor a radical Q′; or Ris a radical Q; or Rtogether with Ris a group ═C—N(C-C-alkyl)or ═C—NH(OC-Calkyl); Ris H; Ris C-C-alkynyl claim 2 , C-C-cycloalkyl or C-C-alkyl which is unsubstituted or ...

MICROBICIDAL HETEROCYCLES

Compounds of the formula I Formula (I) wherein the substituents are as defined in claim , are useful as active ingredients, which have microbiocidal activity, in particular fungicidal activity. 2. The compound according to claim 1 , wherein{'sup': 1', '2, 'Gand Gare independently O or S;'}{'sup': '13', 'T is CRor N;'}{'sup': '1', 'Yis N;'}{'sup': 2', '14, 'Yis CRor N;'}{'sup': 15', '16', '12, 'Q is —C(═O)-z, —C(═S)-z, —C(═O)—O-z, —C(═O)—N(R)-z or —C(═S)—N(R)-z, in each case z indicates the bond that is connected to R;'}n is 1 or 2;p is 1;{'sup': 1', '2', '3', '4', '5', '6', '7', '8', '9', '10', '13', '14, 'sub': 1', '4', '1', '4, 'R, R, R, R, R, R, R, R, R, R, Rand Reach independently are hydrogen, halogen, C-Calkyl or C-Chaloalkyl;'}{'sup': 11', '15', '16, 'sub': 1', '4', '1', '4, 'R, Rand Reach independently are hydrogen, C-Calkyl or C-Calkoxy;'}{'sup': 12', '23, 'Ris heteroaryl which can be optionally substituted with 1 to 3 R, or group (a);'}{'sup': 23', '24, 'sub': 1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '2', '1', '4', '1', '4', '1', '4', '1', '4, 'each Rindependently is halogen, hydroxyl, cyano, nitro, C-Calkyl, C-Chaloalkyl, C-Calkoxy, C-Chaloalkoxy, C-Calkylthio, N(R), phenyl, pyridyl, pyrazinyl, pyridazinyl or pyrimidinyl, wherein the phenyl, pyridyl, pyrazinyl, pyridazinyl and pyrimidinyl are optionally substituted with 1 to 3 substituents independently selected from halogen, cyano, C-Calkyl, C-Chaloalkyl, C-Calkoxy and C-Chaloalkoxy; and'}{'sup': '24', 'sub': 1', '4', '1', '4', '1', '4', '1', '4, 'each Rindependently is hydrogen, C-Calkyl, C-Calkylcarbonyl, C-Calkylsulfonyl or C-Chaloalkylsulfonyl;'}q is 1, 2 or 3;e is 1 or 2.3. The compound according to claim 1 , wherein{'sup': '1', 'Gis O;'}{'sup': '2', 'Gis O or S;'}{'sup': '13', 'T is CRor N;'}{'sup': '1', 'Yis N;'}{'sup': 2', '14, 'Yis CRor N;'}{'sup': 15', '12, 'Q is —C(═O)-z, —C(═S)-z, —C(═O)—O-z or —C(═O)—N(R)-z, in each case z indicates the bond that is connected to R;'}n is 1 or 2;p is ...

Compounds useful as modulators of trpm8

The present invention includes compounds useful as modulators of TRPM8, such as compounds of Formula (I) and the subgenus and species thereof; personal products containing those compounds; and the use of those compounds and the personal products, particularly the use of increasing or inducing chemesthetic sensations, such as cooling or cold sensations.

ANTHRANILIC ACID DIAMIDE DERIVATIVE WITH HETERO-AROMATIC AND HETERO-CYCLIC SUBSTITUENTS

The present invention relates to new insecticides of the formula (I) This application is a Continuation Application of U.S. application Ser. No. 13/325,100, filed Dec. 14, 2011, which is a Continuation Application of U.S. application Ser. No. 12/304,630, filed May 20, 2009, which is a§371 National Stage Application of PCT/EP2007/005016, filed Jun. 6, 2007, which claims priority to German Application No. 10 2006 027 336.2, filed Jun. 13, 2006, and German Application No. 10 2006 032 168.5 filed Jul. 12, 2006, the content of all of which are incorporated herein by reference in their entireties.1. Field of the InventionThe present invention relates to new insecticides, to a number of processes for their preparation and to their use as active compounds, more particularly to their use as pest control agents.2. Description of Related ArtIt is already known that certain anthranilamides (e.g. WO 01/70671, WO 03/015519, WO 03/016284, WO 03/015518, WO 03/024222, WO 03/016282, WO 03/016283, WO 03/062226, WO 03/027099, WO 04/027042, WO 04/033468, WO 2004/046129, WO 2004/067528, WO 2005/118552, WO 2005/077934, WO 2005/085234, WO 2006/023783, WO 2006/000336, WO 2006/040113, WO 2006/111341, WO 2007/006670, WO 2007/024833, WO 2007/020877) possess insecticidal properties.The activity of these compounds, though good, is nevertheless found wanting in certain cases.New anthranilamides have now been found, of the formula (I)in whichFinally it has been found that the compounds of the formula (I) according to the invention possess very good insecticidal properties and can be used, not only in crop protection but also in materials protection, for controlling unwanted pests, such as insects.The compounds of the invention may where appropriate take the form of mixtures of different possible isomeric forms, more particularly of stereoisomers, such as, for example, E and Z isomers, threo and erythro isomers, and optical isomers, and also, where appropriate, of tautomers. The E and the Z isomers ...

CROSS-LINKED CYCLIC AMINE COMPOUNDS AND AGENTS FOR PEST CONTROL

Cyclic amine compounds represented by formula (1) 116-. (canceled)19. Cyclic amine compounds according to claim 17 , wherein Cyrepresents a pyridazyl group substituted by halogen claim 17 , nitro claim 17 , or haloalkyl.20. Agents for pest control comprising at least one of the cyclic amine compounds of . The present invention relates to novel cyclic amine compounds and agents for pest control which contain these cyclic amine compounds or the like as active ingredients.Priority is claimed on Japanese Patent Application No. 2005-294126, filed Oct. 6, 2005, Japanese Patent Application No. 2005-294127, filed Oct. 6, 2005, Japanese Patent Application No. 2005-297803, filed Oct. 12, 2005, Japanese Patent Application No. 2005-297804, filed Oct. 12, 2005, Japanese Patent Application No. 2006-016877, filed Jan. 25, 2006, and Japanese Patent Application No. 2006-182314, filed Jun. 30, 2006, the contents of which are incorporated herein by reference.Although many compounds which have insecticidal/acaricidal activities are conventionally known, there are problems such as insufficient effect thereof, limitation of use thereof because of drug resistance problems, occurrence of phytotoxicity or contamination in plant bodies, or strong toxicity against mammalians, fish, or the like.As compounds with backbones similar to those of the compounds of the present invention, compounds represented by the formula below are known.In the formula, X represents —O—, —N(R)—, —S—, or the like and Rrepresents a substituted saturated heterocyclic group or the like. As a representative of such compounds, the compound represented by the formula below is known (refer to Patent document 1).Moreover, the compounds represented by the formula below are known.In the formula, X represents —CH— or the like; Z represents a bonding or the like; Rrepresents an optionally substituted aryl or an optionally substituted heteroaryl; and Rand Rrepresent —(CH)— or the like together. However, when Rand Rrepresent —(CH ...

Active Compound Combinations

The invention relates to active compound combinations, in particular a fungicidal and/or insecticidal composition, comprising Isotianil (-dichloro-N-(-cyanophenyl)--isothiazolecarboxamide) and at least one further insecticide of the anthranilamide group and optionally one further insecticide of the neonicotinoids. Moreover, the invention relates to a method for curatively or preventively controlling the phytopathogenic fungi and/or microorganisms and/or pests 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. 1. (canceled)2. A composition comprising(A) Isotianil;(B) a first insecticidal active compound selected from the group consisting of chlorantraniliprole and 3-bromo-1-(3-chloropyridin-2-yl)-N-[4-cyano-2-methyl-6-(methylcarbamoyl)phenyl]-1H-pyrazole-5-carboxamide; and(C) a second insecticidal active compound which is a neonicotinoid.3. (canceled)4. The composition according to claim 2 , wherein the weight ratio between any two components (A) claim 2 , (B) claim 2 , or (C) claim 2 , independently of each other claim 2 , is 1:1250 to 1250:1.517.-. (canceled)18. The composition according to claim 2 , further comprising adjuvants claim 2 , solvents claim 2 , carriers claim 2 , surfactants claim 2 , or extenders.19. The composition according to claim 2 , wherein the neonicotinoid is selected from the group consisting of imidacloprid claim 2 , acetamiprid claim 2 , clothianidin claim 2 , thiacloprid claim 2 , thiamethoxam claim 2 , imidaclothiz claim 2 , nitenpyram claim 2 , dinotefuran claim 2 , and 1-[(2-chloro-5-thiazolyl)methyl]tetrahydro-3 claim 2 ,5-dimethyl-N-nitro-1 claim 2 ,3 claim 2 ,5-triazin-2(1H)-imine.20. A method for curatively or preventively controlling phytopathogenic fungi claim 2 , microorganisms claim 2 , or pests of plants or crops comprising applying:(A) Isotianil;(B) a first insecticidal active compound selected from the ...

HETEROARYL PIPERIDINE AND HETEROARYL PIPERAZINE DERIVATIVES AS FUNGICIDES

Heteroarylpiperidine and -piperazine derivatives of the formula (I) 3. The compound of formula (I) and/or salt claim 1 , metal complex and/or an N-oxide thereof according to claim 1 , wherein the radical definitions are each as follows:A is phenyl which optionally comprise no more than two substituents, where the substituents are each independently selected from the following list:methyl, ethyl, iodine, chlorine, bromine, fluorine, methoxy, ethoxy, difluoromethyl or trifluoromethyl or 'methyl, ethyl, chlorine, bromine, fluorine or trifluoromethyl.', 'A is pyrazol-1-yl which optionally comprise no more than two substituents, where the substituents are each independently selected from the following list4. The compound of formula (I) and/or salt claim 1 , metal complex and/or an N-oxide thereof according to claim 1 , wherein the radical definitions are each as follows:{'sup': 1', '2', '3', '1, 'G is G, Gor Gand especially G,'}{'sup': 'G1', 'Ris hydrogen.'}6. The compound of the formula (I) and/or salt claim 1 , metal complex and/or an N-oxide thereof according to claim 1 , wherein the radical definitions are each as follows:{'sup': 1', '4', '3', '3, 'Ris phenyl which optionally comprise no more than 3 substituents, where one substituent is selected from Zand any further substituents are selected from the following list: fluorine, chlorine, bromine, iodine, cyano, nitro, hydroxyl, amino, —SH, —C(═O)H, methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1,1-dimethylethyl, 1,2-dimethylethyl, ethenyl, ethynyl, trifluoromethyl, difluoromethyl, trichloromethyl, dichloromethyl, cyclopropyl, methoxy, ethoxy, n-propoxy, 1-methylethoxy, 1,1-dimethylethoxy, methylcarbonyl, ethylcarbonyl, trifluoromethylcarbonyl, methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, 1-methylethoxycarbonyl, 1,1-dimethylethoxycarbonyl, 1-ethenyloxy, 2-propenyloxy, 2-propynyloxy, methylcarbonyloxy, trifluoroalkylcarbonyloxy, chloromethylcarbonyloxy, methylthio, ethylthio, methylsulphonyl, ...

Aminopropenoates as Fungicides

This application claims priority to European Patent Application No. 09173304.8, filed Oct. 16, 2009, and the benefit of U.S. Provisional Application No. 61/253,091, filed Oct. 20, 2009, the disclosure of each of which is incorporated by reference herein in its entirety. 2. A composition claim 1 , comprising at least one aminopropenoate of the formula (I) according to claim 1 , and one or more extenders claim 1 , surfactant claim 1 , or combinations thereof.3. (canceled)4. A method for controlling unwanted microorganisms claim 1 , comprising applying at least one aminopropenoate of the formula (I) according to to the microorganisms claim 1 , their habitat claim 1 , or combinations thereof.5. A process for preparing a composition claim 1 , comprising mixing at least one aminopropenoate of the formula (I) according to with one or more extenders claim 1 , surfactants claim 1 , or combinations thereof.6. A method for controlling unwanted microorganisms on a transgenic plant claim 1 , comprising applying at least one aminopropenoate of the formula (I) according to to the transgenic plant claim 1 , its seed claim 1 , its habitat claim 1 , or combinations thereof.7. The aminopropenoate of the formula (I) according to claim 1 , wherein R represents R.8. The aminopropenoate of the formula (I) according to claim 1 , wherein R represents R.9. The aminopropenoate of the formula (I) according to claim 7 , wherein n represents 0 claim 7 , 1 or 2.10. The aminopropenoate of the formula (I) according to claim 1 , wherein m represents 1 or 2.11. The aminopropenoate of the formula (I) according to claim 1 , wherein Yis S or O.12. The aminopropenoate of the formula (I) according to claim 1 , wherein Yrepresents O or NRwherein Rrepresents hydrogen claim 1 , C-C-alkyl claim 1 , C-C-cycloalkyl claim 1 , C-C-halogenoalkyl comprising up to 9 halogen atoms which can be the same or different claim 1 , C-C-cycloalkyl-C-C-alkyl claim 1 , C-C-alkenyl-C-C-alkyl claim 1 , C-C-alkynyl-C-C-alkyl ...

USE OF N-(TETRAZOL-4-YL)- OR N-(TRIAZOL-3-YL)ARYLCARBOXAMIDES OR THEIR SALTS FOR CONTROLLING UNWANTED PLANTS IN AREAS OF TRANSGENIC CROP PLANTS BEING TOLERANT TO HPPD INHIBITOR HERBICIDES

Use of N-(tetrazol-4-yl)- or N-(triazol-3-yl)arylcarboxamides of formula (I) or salts thereof 2. A N-(tetrazol-4-yl)- or N-(triazol-3-yl)arylcarboxamide of formula (I) and/or a salt thereof claim 1 , capable of being used according to claim 1 , where claim 1 , in formula (I)A is N or CY,B is N or CH,{'sub': 1', '6', '1', '6', '2', '6', '2', '6', '2', '6', '3', '6', '3', '6', '3', '6', '1', '6', '1', '6', '3', '6', '1', '6', '3', '6', '1', '6', '2', 'n', '2', '2', '2', '2', '1', '6', 'n', '1', '6', '1', '6', '1', '6', '2', '1', '6', '2', '1', '6', '2', '1', '6', '2', '1', '6', '2', '2', '1', '6', '1', '6', '2', '1', '6', '1', '6', '1', '6', '1', '6', 'n', '1', '6', '1', '6', '1', '6, 'sup': 1', '1', '1', '2', '2', '1', '1', '1', '2', '1', '1', '2', '1', '1', '2', '1', '1', '1', '1', '1', '1', '1', '2, 'X is nitro, halogen, cyano, thiocyanato, (C-C)-alkyl, halo-(C-C)-alkyl, (C-C)-alkenyl, halo-(C-C)-alkenyl, (C-C)-alkynyl, halo-(C-C)-alkynyl, (C-C)-cycloalkyl, halo-(C-C)-cycloalkyl, (C-C)-alkyl-O—(C-C)-alkyl, (C-C)-cycloalkyl-(C-C)-alkyl, halo-(C-C)-cycloalkyl-(C-C)-alkyl, COR, OR, OCOR, OSOR, S(O)R, SOOR, SON(R), NRSOR, NRCOR, (C-C)-alkyl-S(O)R, (C-C)-alkyl-OR, (C-C)-alkyl-OCOR, (C-C)-alkyl-OSOR, (C-C)-alkyl-COR, (C-C)-alkyl-SOOR, (C-C)-alkyl-CON(R), (C-C)-alkyl-SON(R), (C-C)-alkyl-NRCORor (C-C)-alkyl-NRSOR, (C-C)-alkyl-heteroaryl, (C-C)-alkyl-heterocyclyl, the two last-mentioned radicals being substituted in each case by s halogen, (C-C)-alkyl, halo-(C-C)-alkyl, S(O)—(C-C)-alkyl, (C-C)-alkoxy and/or halo-(C-C)-alkoxy radicals, and where heterocyclyl carries from 0 to 2 oxo groups,'}{'sub': 1', '6', '1', '6', '2', '6', '2', '6', '2', '6', '3', '6', '3', '6', '3', '6', '3', '6', '3', '6', '1', '6', '3', '6', '1', '6', '2', 'n', '2', '2', '2', '2', '2', '1', '6', 'n', '1', '6', '1', '6', '1', '6', '2', '1', '6', '2', '1', '6', '2', '1', '6', '2', '1', '6', '2', '2', '1', '6', '1', '6', '2', '1', '6', '1', '6', '1', '6', '1', '6', '1', '6', '3', '6', 'n', '1', '6', '1', ...

5-FLUORO PYRIMIDINE DERIVATIVES

This present disclosure is related to the field of 5-fluoro pyrimidines and their derivatives and to the use of these compounds as fungicides. 15-. (canceled)7. The compound of claim 6 , wherein Rand Rare taken together to form a 5- or 6-membered saturated or unsaturated ring containing 1-3 heteroatoms wherein each ring may be optionally substituted with 1-3 R.8. The compound of claim 6 , wherein Ris —C(═NR)NRR.9. The compound of claim 6 , wherein Ris hydroxyl or amino.10. The compound of claim 6 , wherein Ris C-Calkenyl optionally substituted with 1-3 R.11. The compound of claim 6 , wherein Ris —(CHR)R claim 6 , or —Si(R).12. The compound of claim 6 , wherein Ris methylene-2-furanyl claim 6 , —CHRC(O)OR claim 6 , or benzyl optionally substituted with 1-3 R.13. The compound of claim 6 , wherein Ris benzothiazoyl claim 6 , quinazolinyl claim 6 , or a 5- or 6-membered saturated or unsaturated ring containing 1-3 heteroatoms wherein each ring may be optionally substituted with 1-3 R.14. The compound of claim 6 , wherein Ris C-Calkenyl claim 6 , 2-benzofuranyl claim 6 , or a 5- or 6-membered saturated or unsaturated ring containing 1-3 heteroatoms wherein each ring may be optionally substituted with 1-3 R.15. The compound of claim 6 , wherein Ris C-Calkenyl claim 6 , benzyl claim 6 , or a 5- or 6-membered saturated or unsaturated ring containing 1-3 heteroatoms wherein each ring may be optionally substituted with 1-3 R.161. The compound of claim claim 6 , wherein Ris benzoyl.17. A composition for the control of a fungal pathogen including the compound of and a phytologically acceptable carrier material.18Venturia inaequalisSeptoria triticiCercospora beticolaCercospora arachidicolaMycosphaerella fijiensis. The composition of wherein the fungal pathogen is Apple Scab () claim 17 , Leaf Blotch of Wheat () claim 17 , Leaf spot of sugarbeets () claim 17 , Leaf Spot of peanut () claim 17 , and Black Sigatoka ().19. A method for the control and prevention of fungal attack on a ...

Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof and clomazone

Provided herein are synergistic herbicidal compositions containing (a) a compound of formula (I): or an agriculturally acceptable salt or ester thereof and (b) clomazone. The compositions and methods provided herein control undesirable vegetation, e.g., in direct-seeded, water-seeded and transplanted rice, cereals, wheat, barley, oats, rye, sorghum, corn/maize, sugarcane, sunflower, oilseed rape, canola, sugar beet, soybean, cotton, pineapple, pastures, grasslands, rangelands, fallowland, turf, tree and vine orchards, aquatics, plantation crops, vegetables, industrial vegetation management (IVM) and rights of way (ROW).

HERBICIDAL COMPOSITIONS COMPRISING 4-AMINO-3-CHLORO-5-FLUORO-6-(4-CHLORO-2-FLUORO-3-METHOXYPHENYL) PYRIDINE-2-CARBOXYLIC ACID OR A DERIVATIVE THEREOF AND 4-HYDROXYPHENYL-PYRUVATE DIOXYGENASE (HPPD) INHIBITORS

Provided herein are synergistic herbicidal compositions containing and methods of controlling undesirable vegetation utilizing (a) a compound of formula (I): 2. The composition of claim 1 , wherein (a) is a Calkyl or benzyl ester of compound (I).3. The composition of claim 2 , wherein (a) is a n-butyl or benzyl ester of compound (I).4. The composition of claim 1 , wherein (a) is the compound of formula (I) claim 1 , which is the carboxylic acid.5. The composition of claim 1 , wherein the (b) is benzobicyclon claim 1 , benzofenap claim 1 , isoxaflutole claim 1 , mesotrione claim 1 , pyrazolynate claim 1 , sulcotrione claim 1 , or tefuryltrione.6. The composition of claim 1 , further comprising a herbicide safener claim 1 , adjunct and/or carrier.7. The composition of claim 5 , wherein the weight ratio of compound of formula (I) or agriculturally acceptable salt or ester thereof to benzobicyclon or agriculturally acceptable salt or ester thereof is from about 1:150 to about 6:1.8. The composition of claim 5 , wherein the weight ratio of compound of formula (I) or agriculturally acceptable salt or ester thereof to benzofenap or agriculturally acceptable salt or ester thereof is from about 1:600 to about 3:19. The composition of claim 5 , wherein the weight ratio of compound of formula (I) or agriculturally acceptable salt or ester thereof to isoxaflutole or agriculturally acceptable salt or ester thereof is from about 1:70 to about 2:1.10. The composition of claim 5 , wherein the weight ratio of the compound of formula (I) or agriculturally acceptable salt or ester thereof to mesotrione or agriculturally acceptable salt or ester thereof is from about 1:115 to about 17:1.11. The composition of claim 5 , wherein the weight ratio of the compound of formula (I) or agriculturally acceptable salt or ester thereof to pyrazolynate or agriculturally acceptable salt or ester thereof is from about 1:229 to about 2:1.12. The composition of claim 5 , wherein the weight ratio of the ...

HERBICIDAL COMPOSITIONS COMPRISING 4-AMINO-3-CHLORO-5-FLUORO-6-(4-CHLORO-2-FLUORO-3-METHOXYPHENYL) PYRIDINE-2-CARBOXYLIC ACID OR A DERIVATIVE THEREOF AND CELLULOSE BIOSYNTHESIS INHIBITOR HERBICIDES

Provided herein are synergistic herbicidal compositions containing and methods for controlling undesirable vegetation utilizing 2. The composition of claim 1 , wherein (b) is indaziflam or isoxaben or an agriculturally acceptable salt thereof.3. The composition of claim 1 , wherein (a) is a Calkyl or benzyl ester of compound (I).4. The composition of claim 1 , wherein (a) is a Calkyl ester of compound (I).5. The composition of claim 1 , wherein (a) is a benzyl ester of compound (I).6. The composition of claim 1 , wherein (a) is the compound of formula (I) claim 1 , which is the carboxylic acid.7. The composition of claim 1 , wherein the ratio of compound (a) and compound (b) are present in proportions that result in synergistic herbicidal activity.8. The composition of claim 1 , further comprising at least one compound selected from the group consisting of agriculturally acceptable claim 1 , herbicide safeners claim 1 , adjuvants claim 1 , and carriers.10. The method of claim 9 , wherein (b) is indaziflam or isoxaben or an agriculturally acceptable salt thereof.11. The method of claim 8 , wherein the undesirable vegetation is controlled in direct-seeded claim 8 , water-seeded and transplanted rice claim 8 , cereals claim 8 , wheat claim 8 , barley claim 8 , oats claim 8 , rye claim 8 , sorghum claim 8 , corn/maize claim 8 , sugarcane claim 8 , sunflower claim 8 , oilseed rape claim 8 , canola claim 8 , sugar beet claim 8 , soybean claim 8 , cotton claim 8 , pineapple claim 8 , pastures claim 8 , grasslands claim 8 , rangelands claim 8 , fallowland claim 8 , turf claim 8 , tree and vine orchards claim 8 , aquatics claim 8 , industrial vegetation management (IVM) or rights of way (ROW).12. The method of claim 9 , wherein the (a) and (b) are applied to water.13. The method of claim 12 , wherein the water is part of a flooded rice paddy.14. The method of claim 9 , wherein the (a) and (b) are applied pre-emergently to the weed or the crop.15. The method of claim 9 , ...

FORMULATIONS OF CLOMAZONE

New formulations of clomazone are provided, as well as new methods for making formulations of clomazone. The new formulations provide improved efficacy, decreased volatility, and/or increased loading of clomazone over the clomazone formulations in the prior art. 1. A formulation comprising clomazone , wherein the formulation exhibits clomazone volatility control of at least 80%.2. The formulation of claim 1 , wherein the formulation comprises multilayered particles comprising:a core comprising clomazone,a first encapsulating layer surrounding the core and comprising a water-insoluble polymer, anda second encapsulating layer surrounding the first encapsulating layer and comprising a water-soluble polymer.3. The formulation of claim 2 , wherein the clomazone is present in an amount of at least 50% by weight of the particle.4. The formulation of wherein the weight ratio of the water-soluble polymer to clomazone is from 1:6 to 1:4.5. The formulation of wherein the water-insoluble polymer is polyurea.6. The formulation of wherein the water-soluble polymer is polyvinyl alcohol.7. An herbicidal composition comprising the formulation of .8. The herbicidal composition of claim 7 , wherein the solid herbicidal composition exhibits clomazone volatility control of at least 80%.10. A liquid composition comprising clomazone and linseed oil.11. The liquid composition of claim 10 , wherein the clomazone is at least partially dissolved in the linseed oil.12. The liquid composition of claim 10 , wherein the liquid composition comprises 80 to 97% by weight of clomazone.13. A microcapsule comprising the liquid composition of claim 10 , wherein the liquid composition is surrounded by a shell comprising a water-insoluble polymer.14. The microcapsule of claim 13 , wherein the polymer shell comprises polyurea.15. An herbicidal composition comprising a plurality of microcapsules of .16. A microcapsule comprising a polyurea shell encapsulating a material comprising clomazone and linseed oil. ...

DISPERSIBLE HERBICIDAL COMPOSITIONS AND METHODS OF USE

Herbicidal dispersible concentrates include an herbicide and substantially water miscible amide-based solvents. Such concentrates may be diluted in water and used in methods to control weeds. 1. A dispersible concentrate comprising:about 0.1% to about 40% by weight of the concentrate of a methylsulfonylphenyl ketone herbicide; andabout 0.6% to about 90% by weight of the concentrate of a water-miscible amide solvent.2. The dispersible concentrate of claim 1 , wherein the water-miscible amide solvent is N-methylpyrrolidone.3. The dispersible concentrate of claim 1 , further comprising an organic co-solvent selected from the group consisting of ethyl lactate claim 1 , ethyl hexyl lactate claim 1 , fatty acid dimethylamide claim 1 , N claim 1 ,N-dimethyloctanamide claim 1 , and N claim 1 ,N-dimethyldecanamide.4. The dispersible concentrate of claim 1 , wherein the methylsulfonylphenyl ketone herbicide comprises one selected from the group consisting of topramezone claim 1 , isoxaflutole claim 1 , mesotrione claim 1 , sulcotrione claim 1 , tembotrione claim 1 , and combinations thereof.5. The dispersible concentrate of claim 1 , wherein the methylsulfonylphenyl ketone herbicide is topramezone.6. The dispersible concentrate of claim 5 , wherein the concentration of topramezone is from about 10% to about 20% by weight of the concentrate.7. The dispersible concentrate of claim 1 , further comprising a surfactant.8. The dispersible concentrate of claim 7 , wherein the surfactant comprises one selected from the group consisting of butyl polyalkylene oxide block copolymers claim 7 , polyalkylene oxide block copolymers claim 7 , tristyrylphenol ethoxylates claim 7 , alkylphenol ethoxylates claim 7 , castor oil ethoxylates claim 7 , acetylenic polydiols claim 7 , organosilicones and mixtures thereof.9. The dispersible concentrate of claim 8 , wherein the surfactant comprises organosilicones.10. The dispersible concentrate of claim 9 , wherein the organosilicones comprise a ...

ISOXAZOLINES FOR CONTROLLING INVERTEBRATE PESTS

Disclosed are compounds of Formula 1, including all geometric and stereoisomers, N-oxides, and salts thereof, 2. A compound of wherein{'sup': 1', '6, 'sub': 1', '3, 'Ris C-Calkyl optionally substituted with one or more substituents independently selected from R;'}{'sup': '2', 'sub': 1', '6', '1', '6, 'each Ris independently H, halogen, C-Chaloalkyl, C-Chaloalkoxy or —CN; and'}{'sup': '3', 'sub': 1', '6', '1', '6', '3', '6, 'each Ris independently H, halogen, C-Calkyl, C-Chaloalkyl, C-Ccycloalkyl,'}{'sub': 3', '6', '1', '6', '1', '6', '2, 'C-Chalocycloalkyl, C-Calkoxy, C-Chaloalkoxy, —CN or —NO.'}3. A compound of wherein{'sup': 1', '2', '3', '2, 'B, Band Bare independently CR;'}W is O;{'sup': '4', 'sub': 1', '6', '2', '7', '2', '7, 'Ris H, C-Calkyl, C-Calkylcarbonyl or C-Calkoxycarbonyl; and'}{'sup': 5', '11', '12', '1', '7, 'sub': 1', '4', '2', '4', '2', '4', '3', '4', '4', '7', '4', '7, 'Ris H, NRRor Q; or C-Calkyl, C-Calkenyl, C-Calkynyl, C-Ccycloalkyl, C-Calkylcycloalkyl or C-Ccycloalkylalkyl, each optionally substituted with one or more substituents independently selected from R.'}4. A compound of wherein{'sup': '1', 'sub': 1', '3, 'Ris C-Calkyl optionally substituted with halogen;'}{'sup': '2', 'sub': 3', '3, 'each Ris independently H, CF, OCF, halogen or —CN;'}{'sup': '3', 'sub': 1', '4', '1', '4', '3', '6', '1', '4, 'each Ris independently H, C-Calkyl, C-Chaloalkyl, C-Ccyclopropyl, C-Calkoxy or —CN; and'}{'sup': 7', '2, 'sub': 1', '4', '1', '4', '1', '4', '1', '4', '1', '4', '2', '4', '2', '4', '2', '5', '2', '5', '2', '5', '2', '5', '2', '2, 'each Ris independently halogen, C-Calkyl, C-Calkoxy, C-Calkylthio, C-Calkylsulfinyl, C-Calkylsulfonyl, C-Calkylcarbonyl, C-Calkoxycarbonyl, C-Calkylaminocarbonyl, C-Chaloalkylcarbonyl, C-Chaloalkoxycarbonyl, C-Chaloalkylaminocarbonyl, —NH, —CN or —NO; or Q.'}5. A compound of wherein{'sup': '4', 'Ris H;'}{'sup': 5', '7, 'sub': 1', '4, 'Ris C-Calkyl optionally substituted with one of more substituents independently ...

Use of 3-Isoxazolidinones as Selective Herbicides in Grass and Brassica Crops

The present invention is directed to the use of at least one 3-isoxazolidone herbicide selected from the group consisting of 2-(2,4-dichlorophenyl)methyl-4,4-dimethyl-3-isoxazolidone and 2-(2,5-dichlorophenyl)methyl-4,4-dimethyl-3-isoxazolidone as a selective herbicide in a grass or crop selected from the group consisting of corn, rice, sorghum, barley, rye, and canola. 1brassica. A method of selectively controlling undesirable vegetation in a grassy monocot or crop selected from the group consisting of corn , rice , sorghum , oil seed rape , barley , rye , and canola comprising applying an herbicidally effective amount of at least one 3-isoxazolidone herbicide selected from the group consisting of 2-(2 ,4-dichlorophenyl)methyl-4 ,4-dimethyl-3-isoxazolidone and 2(2 ,5-dichlorophenyl)methyl-4 ,4-dimethyl-3-isoxazolidone to the locus of such vegetation.2. The method of wherein such herbicide is employed pre-emergently.3. The method of wherein the herbicide is 2-(2 claim 2 ,4-dichlorophenyl)methyl-4 claim 2 ,4-dimethyl-3-isoxazolidone.4. The method of wherein the herbicide is employed at a rate of between about 1 and about 4000 grams of active ingredient/hectare.5. The method of wherein the herbicide is employed at a rate of between about 75 and about 2 claim 4 ,000 grams of active ingredient/hectare.6. The method of wherein the herbicide is employed at a rate of between about 100 and about 1 claim 5 ,500 grams of active ingredient/hectare.7. The method of wherein the crop is a grassy monocot.8. The method of wherein the crop is corn claim 7 , rice claim 7 , sorghum claim 7 , barley or rye.9brassica. The method of wherein the crop is a dicot.10. The method of wherein the crop is canola.11. The method of wherein the herbicide is 2-(2 claim 2 ,5-dichlorophenyl)methyl-4 claim 2 ,4-dimethyl-3-isoxazolidone.12. The method of wherein the herbicide is employed at a rate of between about 1 and about 4000 grams of active ingredient/hectare.13. The method of wherein the ...

NOVEL COMPOUNDS

Compounds of the general formula (I) wherein the substituents are as defined in claim , are useful as fungicides. 2. A compound according to claim 1 , wherein Qis methylthio claim 1 , vinyl claim 1 , ethynyl claim 1 , iodo.3. A compound according to claim 2 , wherein Qis ethynyl.4. A compound according to claim 1 , wherein Qis hydrogen and methyl.5. A compound according to claim 1 , wherein Ris methoxy or methylthio.6. A compound according to claim 5 , wherein Ris methylthio.7. A compound according to claim 1 , wherein Ris hydrogen.8. A compound according to claim 1 , wherein Rand R claim 1 , independently of each other claim 1 , are hydrogen claim 1 , methyl or ethyl.9. A compound according to claim 1 , wherein Ris thiazolyl claim 1 , isothiazolyl claim 1 , isoxazolyl or pyridyl.10. A compound according to claim 9 , wherein Ris Ris isoxazolyl and pyridyl.11. A compound according to claim 1 , wherein Y is oxygen.12. A compound according to claim 1 , wherein Qis methylthio claim 1 , vinyl claim 1 , ethynyl claim 1 , bromo claim 1 , iodo or thienyl; Qis hydrogen claim 1 , methyl claim 1 , fluoro or chloro; Ris ethyl claim 1 , methoxy or methylthio; Ris hydrogen; Ris —CRRR; Rand R claim 1 , independently of each other claim 1 , are hydrogen claim 1 , methyl or ethyl claim 1 , Rand Rtogether with the carbon atom to which they are attached form a cyclopropyl group; and Ris a heteroaryl selected from the group consisting of oxazolyl claim 1 , isoxazolyl claim 1 , benzoxazolyl claim 1 , thiazolyl claim 1 , isothiazolyl and pyridyl claim 1 , which heteroaryls are unsubstituted or substituted by methyl claim 1 , ethyl claim 1 , trifluormethyl claim 1 , hydroxymethyl claim 1 , methoxymethyl claim 1 , methoxy claim 1 , ethoxy claim 1 , phenyl claim 1 , methoxycarbonyl claim 1 , halogen or trimethylsilyl.13. A compound according to claim 1 , wherein Qis methylthio claim 1 , vinyl claim 1 , ethynyl or iodo; Qis hydrogen claim 1 , methyl claim 1 , chloro or fluoro; Ris methylthio ...

Synergistic antimicrobial composition

A synergistic antimicrobial composition containing 3-iodo-2-propynyl-butylcarbamate and fluometuron.

Carbamoyl triazolinone based herbicide combinations and methods of use

The invention relates to herbicidal active compound combinations comprising, carbamoyltriazolinones, and herbicidally active compounds, which combinations are suitable for controlling weeds.