AR093828A1 - Mezclas activas como plaguicidas, que comprenden compuestos de antranilamida - Google Patents
Mezclas activas como plaguicidas, que comprenden compuestos de antranilamidaInfo
- Publication number
- AR093828A1 AR093828A1 ARP130103520A ARP130103520A AR093828A1 AR 093828 A1 AR093828 A1 AR 093828A1 AR P130103520 A ARP130103520 A AR P130103520A AR P130103520 A ARP130103520 A AR P130103520A AR 093828 A1 AR093828 A1 AR 093828A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkoxy
- alkyl
- group
- radicals
- partially
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title abstract 3
- 239000000575 pesticide Substances 0.000 title abstract 3
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 13
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 13
- 125000001424 substituent group Chemical group 0.000 abstract 11
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 8
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 7
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 7
- 229910052736 halogen Inorganic materials 0.000 abstract 7
- 150000002367 halogens Chemical group 0.000 abstract 7
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 6
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 6
- 125000001931 aliphatic group Chemical group 0.000 abstract 6
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 6
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 5
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 239000001257 hydrogen Substances 0.000 abstract 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 5
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 4
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 4
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 4
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 4
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 4
- 125000004076 pyridyl group Chemical group 0.000 abstract 4
- 229910052717 sulfur Inorganic materials 0.000 abstract 4
- 125000004450 alkenylene group Chemical group 0.000 abstract 3
- 125000002947 alkylene group Chemical group 0.000 abstract 3
- 125000004419 alkynylene group Chemical group 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 3
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 2
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 2
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 2
- 125000004970 halomethyl group Chemical group 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 1
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 1
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 1
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 1
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 1
- 125000004793 2,2,2-trifluoroethoxy group Chemical group FC(CO*)(F)F 0.000 abstract 1
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- 241000233866 Fungi Species 0.000 abstract 1
- 241000238631 Hexapoda Species 0.000 abstract 1
- 206010061217 Infestation Diseases 0.000 abstract 1
- 241000244206 Nematoda Species 0.000 abstract 1
- 241000607479 Yersinia pestis Species 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- -1 anthranilamide compound Chemical class 0.000 abstract 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- 125000001246 bromo group Chemical group Br* 0.000 abstract 1
- 239000000460 chlorine Chemical group 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 abstract 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 abstract 1
- 125000004785 fluoromethoxy group Chemical group [H]C([H])(F)O* 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- PXBFMLJZNCDSMP-UHFFFAOYSA-N ortho-aminobenzoylamine Natural products NC(=O)C1=CC=CC=C1N PXBFMLJZNCDSMP-UHFFFAOYSA-N 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/50—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids the nitrogen atom being doubly bound to the carbon skeleton
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/20—N-Aryl derivatives thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
También métodos y el uso de estas mezclas para combatir y controlar insectos, acáridos o nematodos y hongos dañinos en las plantas, y para proteger estas plantas contra la infestación por plagas, en especial, también para proteger el material de propagación vegetal, como las semillas. Reivindicación 1: Mezclas plaguicidas caracterizadas porque comprenden como compuestos activos i) al menos un compuesto de antranilamida activo como plaguicida de la fórmula (1), en donde R¹ se selecciona del grupo que consiste en halógeno, metilo y halometilo; R² se selecciona del grupo que consiste en hidrógeno, halógeno, halometilo y ciano; R³ se selecciona de hidrógeno, alquilo C₁₋₆, haloalquilo C₁₋₆, alquenilo C₂₋₆, haloalquenilo C₂₋₆, alquinilo C₂₋₆, haloalquinilo C₂₋₆, cicloalquilo C₃₋₈, halocicloalquilo C₃₋₈, alcoxi C₁₋₄-alquilo C₁₋₄, haloalcoxi C₁₋₄-alquilo C₁₋₄; C(=O)Rᵃ, C(=O)ORᵇ y C(=O)NRᶜRᵈ; R⁴ es hidrógeno o halógeno; R⁵, R⁶ se seleccionan, independientemente entre sí, del grupo que consiste en hidrógeno, alquilo C₁₋₁₀, cicloalquilo C₃₋₈, alquenilo C₂₋₁₀, alquinilo C₂₋₁₀, en donde los radicales alifáticos y cicloalifáticos antes mencionados se pueden sustituir con 1 a 10 sustituyentes Rᵉ, y fenilo, que es no sustituido o tiene de 1 a 5 sustituyentes Rᶠ; o R⁵ y R⁶ juntos representan cadenas de alquileno C₂₋₇, alquenileno C₂₋₇ o alquinileno C₆₋₉ que forman, junto con el átomo de azufre al que están unidas, un anillo saturado, parcialmente insaturado o totalmente insaturado de 3, 4, 5, 6, 7, 8, 9 ó 10 miembros, en donde de 1 a 4 de los grupos CH₂ en la cadena de alquileno C₂₋₇, de 1 a 4 de cualquiera de los grupos CH₂ o CH en la cadena de alquenileno C₂₋₇, o de 1 a 4 de cualquiera de los grupos CH₂ en la cadena de alquinileno C₆₋₉ se pueden reemplazar por 1 a 4 grupos seleccionados independientemente del grupo que consiste en C=O, C=S, O, S, N, NO, SO, SO₂ y NH, y en donde los átomos de carbono y/o nitrógeno en las cadenas de alquileno C₂₋₇, alquenileno C₂₋₇ o alquinileno C₆₋₉ se pueden sustituir con 1 a 5 sustituyentes seleccionados independientemente del grupo que consiste en halógeno, ciano, alquilo C₁₋₆, haloalquilo C₁₋₆, alcoxi C₁₋₆, haloalcoxi C₁₋₆, alquiltio C₁₋₆, haloalquiltio C₁₋₆, cicloalquilo C₃₋₈, halocicloalquilo C₃₋₈, alquenilo C₂₋₆, haloalquenilo C₂₋₆, alquinilo C₂₋₆ y haloalquinilo C₂₋₆; estos sustituyentes son idénticos o diferentes entre sí si hay más de un sustituyente presente; R⁷ se selecciona del grupo que consiste en bromo, cloro, difluorometilo, trifluorometilo, nitro, ciano, OCH₃, OCHF₂, OCH₂F, OCH₂CF₃, S(O)ₙCH₃ y S(=O)ₙCF₃; Rᵃ se selecciona del grupo que consiste en alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₈, alcoxi C₁₋₆, alquiltio C₁₋₆, alquilsulfinilo C₁₋₆, alquilsulfonilo C₁₋₆, en donde uno o más grupos CH₂ de los radicales antes mencionados se pueden reemplazar por un grupo C=O, y/o las porciones alifáticas y cicloalifáticas de los radicales antes mencionados pueden ser no sustituidas, parcial o totalmente halogenadas y/o pueden tener 1 ó 2 sustituyentes seleccionados de alcoxi C₁₋₄; fenilo, bencilo, piridilo y fenoxi, en donde los cuatro últimos radicales pueden ser no sustituidos, parcial o totalmente halogenados y/o pueden tener 1, 2 ó 3 sustituyentes seleccionados de alquilo C₁₋₆, haloalquilo C₁₋₆, alcoxi C₁₋₆, haloalcoxi C₁₋₆, (alcoxi C₁₋₆)carbonilo, alquilamino C₁₋₆ y di-(alquil C₁₋₆)amino; Rᵇ se selecciona del grupo que consiste en alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₈, alcoxi C₁₋₆, alquiltio C₁₋₆, alquilsulfinilo C₁₋₆, alquilsulfonilo C₁₋₆, en donde uno o más grupos CH₂ de los radicales antes mencionados se pueden reemplazar por un grupo C=O, y/o las porciones alifáticas y cicloalifáticas de los radicales antes mencionados pueden ser no sustituidas, parcial o totalmente halogenadas y/o pueden tener 1 ó 2 sustituyentes seleccionados de alcoxi C₁₋₄; fenilo, bencilo, piridilo y fenoxi, en donde los cuatro últimos radicales pueden ser no sustituidos, parcial o totalmente halogenados y/o pueden tener 1, 2 ó 3 sustituyentes seleccionados de alquilo C₁₋₆, haloalquilo C₁₋₆, alcoxi C₁₋₆, haloalcoxi C₁₋₆ y (alcoxi C₁₋₆)carbonilo; Rᶜ, Rᵈ se seleccionan, independientemente entre sí e independientemente de cada caso, del grupo que consiste en hidrógeno, ciano, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₈, en donde uno o más grupos CH₂ de los radicales antes mencionados se pueden reemplazar por un grupo C=O, y/o las porciones alifáticas y cicloalifáticas de los radicales antes mencionados pueden ser no sustituidas, parcial o totalmente halogenadas y/o pueden tener 1 ó 2 radicales seleccionados de alcoxi C₁₋₄; alcoxi C₁₋₆, haloalcoxi C₁₋₆, alquiltio C₁₋₆, alquilsulfinilo C₁₋₆, alquilsulfonilo C₁₋₆, haloalquiltio C₁₋₆, fenilo, bencilo, piridilo y fenoxi, en donde los cuatro últimos radicales mencionados pueden ser no sustituidos, parcial o totalmente halogenados y/o pueden tener 1, 2 ó 3 sustituyentes seleccionados de alquilo C₁₋₆, haloalquilo C₁₋₆, alcoxi C₁₋₆, haloalcoxi C₁₋₆ y (alcoxi C₁₋₆)carbonilo; o Rᶜ y Rᵈ, junto con el átomo de nitrógeno al que están unidos, pueden formar un anillo heterocíclico saturado, parcialmente insaturado o totalmente insaturado de 3, 4, 5, 6 o 7 miembros, que también puede contener 1 ó 2 heteroátomos o grupos de heteroátomos adicionales seleccionados de N, O, S, NO, SO y SO₂, como miembros del anillo, en donde el anillo heterocíclico se puede sustituir opcionalmente con halógeno, haloalquilo C₁₋₄, alcoxi C₁₋₄ o haloalcoxi C₁₋₄; Rᵉ se selecciona independientemente del grupo que consiste en halógeno, ciano, nitro, -OH, -SH, -SCN, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₈, en donde uno o más grupos CH₂ de los radicales antes mencionados se pueden reemplazar por un grupo C=O, y/o las porciones alifáticas y cicloalifáticas de los radicales antes mencionados pueden ser no sustituidas, pueden ser parcial o totalmente halogenadas y/o pueden tener 1 ó 2 radicales seleccionados de alcoxi C₁₋₄; alcoxi C₁₋₆, haloalcoxi C₁₋₆, alquiltio C₁₋₆, alquilsulfinilo C₁₋₆, alquilsulfonilo C₁₋₆, haloalquiltio C₁₋₆, -ORᵃ, -NRᶜRᵈ, -S(O)ₙRᵃ, -S(O)ₙNRᶜRᵈ, -C(=O)Rᵃ, -C(=O)NRᶜRᵈ, -C(=O)ORᵇ, -C(=S)Rᵃ, -C(=S)NRᶜRᵈ, -C(=S)ORᵇ, -C(=S)SRᵇ, -C(=NRᶜ)Rᵇ, -C(=NRᶜ)NRᶜRᵈ, fenilo, bencilo, piridilo y fenoxi, en donde los cuatro últimos radicales mencionados pueden ser no sustituidos, parcial o totalmente halogenados y/o pueden tener 1, 2 ó 3 sustituyentes seleccionados de alquilo C₁₋₆, haloalquilo C₁₋₆, alcoxi C₁₋₆ y haloalcoxi C₁₋₆; o dos radicales vecinos Rᵉ forman juntos un grupo =O, =CH(alquilo C₁₋₄), =C(alquil C₁₋₄)alquilo C₁₋₄, =N(alquilo C₁₋₆) o =NO(alquilo C₁₋₆); Rᶠ se selecciona independientemente del grupo que consiste en halógeno, ciano, nitro, -OH, -SH, -SCN, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₈, en donde uno o más grupos CH₂ de los radicales antes mencionados se pueden reemplazar por un grupo C=O, y/o las porciones alifáticas y cicloalifáticas de los radicales antes mencionados pueden ser no sustituidas, pueden ser parcial o totalmente halogenadas y/o pueden tener 1 ó 2 radicales seleccionados de alcoxi C₁₋₄; alcoxi C₁₋₆, haloal
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261708061P | 2012-10-01 | 2012-10-01 | |
| US201361763974P | 2013-02-13 | 2013-02-13 | |
| US201361847587P | 2013-07-18 | 2013-07-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR093828A1 true AR093828A1 (es) | 2015-06-24 |
Family
ID=49328505
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP130103520A AR093828A1 (es) | 2012-10-01 | 2013-09-27 | Mezclas activas como plaguicidas, que comprenden compuestos de antranilamida |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US20150250173A1 (es) |
| EP (1) | EP2903442A1 (es) |
| JP (1) | JP2015530414A (es) |
| KR (1) | KR20150067269A (es) |
| CN (1) | CN104768377A (es) |
| AR (1) | AR093828A1 (es) |
| AU (1) | AU2013326645A1 (es) |
| BR (1) | BR112015005094A2 (es) |
| CR (1) | CR20150222A (es) |
| MX (1) | MX2015004169A (es) |
| WO (1) | WO2014053405A1 (es) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2782910B1 (en) | 2011-11-21 | 2016-02-03 | Basf Se | Process for preparing n-substituted 1h-pyrazole-5-carboxylate compounds and derivatives thereof |
| US20150250174A1 (en) * | 2012-10-01 | 2015-09-10 | Basf Se | Use of n-thio-anthranilamide compounds on cultivated plants |
| MX2015004168A (es) * | 2012-10-01 | 2015-09-25 | Basf Se | Uso de compuestos de antranilamida en metodos de aplicacion en el suelo y de tratamiento de semillas. |
| CN104902756B (zh) | 2012-11-22 | 2018-11-27 | 巴斯夫公司 | 农药混合物 |
| CA2894264C (en) * | 2012-12-20 | 2023-03-07 | BASF Agro B.V. | Compositions comprising a triazole compound |
| WO2014108286A1 (en) | 2013-01-09 | 2014-07-17 | Basf Se | Process for the preparation of substituted oxiranes and triazoles |
| WO2014128188A1 (en) | 2013-02-20 | 2014-08-28 | Basf Se | Anthranilamide compounds, their mixtures and the use thereof as pesticides |
| US20160046572A1 (en) * | 2013-03-28 | 2016-02-18 | Basf Se | Process for Preparing Sulfimines and Their in-situ Conversion into N-(1-Amino-Benzoyl)-Sulfimines |
| CA2916777A1 (en) | 2013-07-08 | 2015-01-15 | BASF Agro B.V. | Compositions comprising a triazole compound and a biopesticide |
| US20150272132A1 (en) * | 2014-03-30 | 2015-10-01 | Pieter W. Booysen | Neem oil granule with nutrients |
| EP3160229A1 (en) | 2014-06-25 | 2017-05-03 | BASF Agro B.V. | Pesticidal compositions |
| WO2016034353A1 (en) * | 2014-09-03 | 2016-03-10 | Basf Se | Pesticidally active mixtures |
| PL3214937T3 (pl) | 2014-11-07 | 2024-10-14 | Basf Se | Mieszaniny szkodnikobójcze |
| PL3240403T3 (pl) | 2014-12-29 | 2020-03-31 | Fmc Corporation | Kompozycje mikrobiologiczne i sposoby zastosowania w celu sprzyjania wzrostowi roślin i leczeniu chorób roślin |
| CN105340974B (zh) * | 2015-10-30 | 2018-01-09 | 湖北省生物农药工程研究中心 | 一种生物拌种剂及应用 |
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| TWI528899B (zh) | 2010-12-29 | 2016-04-11 | 杜邦股份有限公司 | 中離子性殺蟲劑 |
| BR112013024609B1 (pt) | 2011-03-31 | 2018-11-27 | Novozymes Biologicals, Inc. | composição, e, método para intensificar o crescimento da planta |
| WO2013003977A1 (zh) | 2011-07-01 | 2013-01-10 | 合肥星宇化学有限责任公司 | 2,5-二取代-3-硝亚胺基-1,2,4-三唑啉类化合物及其制备方法与其作为杀虫剂的应用 |
| ES2558166T3 (es) * | 2011-08-12 | 2016-02-02 | Basf Se | Compuestos de N-tio-antranilamida y su uso como pesticidas |
| US20140179519A1 (en) * | 2011-08-12 | 2014-06-26 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
| WO2013024008A1 (en) * | 2011-08-12 | 2013-02-21 | Basf Se | Aniline type compounds |
| WO2013050317A1 (en) | 2011-10-03 | 2013-04-11 | Syngenta Limited | Polymorphs of an isoxazoline derivative |
| TWI577286B (zh) | 2011-10-13 | 2017-04-11 | 杜邦股份有限公司 | 殺線蟲磺醯胺之固體形態 |
| EP2793885A1 (en) * | 2011-12-21 | 2014-10-29 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
| WO2013113789A1 (en) * | 2012-02-02 | 2013-08-08 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
| CN102613183A (zh) | 2012-03-07 | 2012-08-01 | 中化蓝天集团有限公司 | 一种杀虫剂 |
-
2013
- 2013-09-27 AU AU2013326645A patent/AU2013326645A1/en not_active Abandoned
- 2013-09-27 EP EP13774629.3A patent/EP2903442A1/en not_active Withdrawn
- 2013-09-27 US US14/432,044 patent/US20150250173A1/en not_active Abandoned
- 2013-09-27 WO PCT/EP2013/070160 patent/WO2014053405A1/en not_active Ceased
- 2013-09-27 KR KR1020157011488A patent/KR20150067269A/ko not_active Withdrawn
- 2013-09-27 CN CN201380051204.1A patent/CN104768377A/zh active Pending
- 2013-09-27 MX MX2015004169A patent/MX2015004169A/es unknown
- 2013-09-27 AR ARP130103520A patent/AR093828A1/es unknown
- 2013-09-27 JP JP2015533602A patent/JP2015530414A/ja not_active Withdrawn
- 2013-09-27 BR BR112015005094A patent/BR112015005094A2/pt not_active IP Right Cessation
-
2015
- 2015-04-29 CR CR20150222A patent/CR20150222A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP2015530414A (ja) | 2015-10-15 |
| MX2015004169A (es) | 2015-10-22 |
| CR20150222A (es) | 2015-09-16 |
| WO2014053405A1 (en) | 2014-04-10 |
| KR20150067269A (ko) | 2015-06-17 |
| EP2903442A1 (en) | 2015-08-12 |
| AU2013326645A1 (en) | 2015-04-23 |
| BR112015005094A2 (pt) | 2017-07-04 |
| CN104768377A (zh) | 2015-07-08 |
| US20150250173A1 (en) | 2015-09-10 |
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