ES2430813T3 - Formulación acuosa de N-(cianofenil)pirazolcarboxamida - Google Patents
Formulación acuosa de N-(cianofenil)pirazolcarboxamida Download PDFInfo
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- ES2430813T3 ES2430813T3 ES10752511T ES10752511T ES2430813T3 ES 2430813 T3 ES2430813 T3 ES 2430813T3 ES 10752511 T ES10752511 T ES 10752511T ES 10752511 T ES10752511 T ES 10752511T ES 2430813 T3 ES2430813 T3 ES 2430813T3
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- 239000013011 aqueous formulation Substances 0.000 title description 2
- LIRTYGUPQDVSLQ-UHFFFAOYSA-N n-(2-cyanophenyl)-1h-pyrazole-5-carboxamide Chemical compound C=1C=NNC=1C(=O)NC1=CC=CC=C1C#N LIRTYGUPQDVSLQ-UHFFFAOYSA-N 0.000 title description 2
- 239000000203 mixture Substances 0.000 claims abstract description 377
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 107
- 239000007788 liquid Substances 0.000 claims abstract description 44
- 239000004546 suspension concentrate Substances 0.000 claims abstract description 36
- 150000001875 compounds Chemical class 0.000 claims abstract description 27
- 230000000749 insecticidal effect Effects 0.000 claims abstract description 17
- DVBUIBGJRQBEDP-UHFFFAOYSA-N cyantraniliprole Chemical compound CNC(=O)C1=CC(C#N)=CC(C)=C1NC(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl DVBUIBGJRQBEDP-UHFFFAOYSA-N 0.000 claims abstract description 16
- 229920005682 EO-PO block copolymer Polymers 0.000 claims abstract description 10
- -1 acrinatrine Chemical compound 0.000 claims description 125
- 229920001983 poloxamer Polymers 0.000 claims description 88
- 241000607479 Yersinia pestis Species 0.000 claims description 56
- 241000238631 Hexapoda Species 0.000 claims description 53
- 239000002917 insecticide Substances 0.000 claims description 27
- 230000002441 reversible effect Effects 0.000 claims description 24
- 229920001987 poloxamine Polymers 0.000 claims description 20
- 239000013543 active substance Substances 0.000 claims description 16
- 241000193388 Bacillus thuringiensis Species 0.000 claims description 10
- 229940097012 bacillus thuringiensis Drugs 0.000 claims description 10
- 239000005950 Oxamyl Substances 0.000 claims description 9
- KZAUOCCYDRDERY-UHFFFAOYSA-N oxamyl Chemical compound CNC(=O)ON=C(SC)C(=O)N(C)C KZAUOCCYDRDERY-UHFFFAOYSA-N 0.000 claims description 9
- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Aalpha Natural products C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 claims description 7
- 239000005660 Abamectin Substances 0.000 claims description 6
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- HMIBKHHNXANVHR-UHFFFAOYSA-N Fenothiocarb Chemical compound CN(C)C(=O)SCCCCOC1=CC=CC=C1 HMIBKHHNXANVHR-UHFFFAOYSA-N 0.000 claims description 3
- VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 claims description 3
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- VEHPJKVTJQSSKL-UHFFFAOYSA-N azadirachtin Natural products O1C2(C)C(C3(C=COC3O3)O)CC3C21C1(C)C(O)C(OCC2(OC(C)=O)C(CC3OC(=O)C(C)=CC)OC(C)=O)C2C32COC(C(=O)OC)(O)C12 VEHPJKVTJQSSKL-UHFFFAOYSA-N 0.000 claims description 3
- FTNJWQUOZFUQQJ-NDAWSKJSSA-N azadirachtin A Chemical compound C([C@@H]([C@]1(C=CO[C@H]1O1)O)[C@]2(C)O3)[C@H]1[C@]23[C@]1(C)[C@H](O)[C@H](OC[C@@]2([C@@H](C[C@@H]3OC(=O)C(\C)=C\C)OC(C)=O)C(=O)OC)[C@@H]2[C@]32CO[C@@](C(=O)OC)(O)[C@@H]12 FTNJWQUOZFUQQJ-NDAWSKJSSA-N 0.000 claims description 3
- FTNJWQUOZFUQQJ-IRYYUVNJSA-N azadirachtin A Natural products C([C@@H]([C@]1(C=CO[C@H]1O1)O)[C@]2(C)O3)[C@H]1[C@]23[C@]1(C)[C@H](O)[C@H](OC[C@@]2([C@@H](C[C@@H]3OC(=O)C(\C)=C/C)OC(C)=O)C(=O)OC)[C@@H]2[C@]32CO[C@@](C(=O)OC)(O)[C@@H]12 FTNJWQUOZFUQQJ-IRYYUVNJSA-N 0.000 claims description 3
- CJJOSEISRRTUQB-UHFFFAOYSA-N azinphos-methyl Chemical group C1=CC=C2C(=O)N(CSP(=S)(OC)OC)N=NC2=C1 CJJOSEISRRTUQB-UHFFFAOYSA-N 0.000 claims description 3
- PRLVTUNWOQKEAI-VKAVYKQESA-N buprofezin Chemical compound O=C1N(C(C)C)\C(=N\C(C)(C)C)SCN1C1=CC=CC=C1 PRLVTUNWOQKEAI-VKAVYKQESA-N 0.000 claims description 3
- IRUJZVNXZWPBMU-UHFFFAOYSA-N cartap Chemical compound NC(=O)SCC(N(C)C)CSC(N)=O IRUJZVNXZWPBMU-UHFFFAOYSA-N 0.000 claims description 3
- SBPBAQFWLVIOKP-UHFFFAOYSA-N chlorpyrifos Chemical compound CCOP(=S)(OCC)OC1=NC(Cl)=C(Cl)C=C1Cl SBPBAQFWLVIOKP-UHFFFAOYSA-N 0.000 claims description 3
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- NGPMUTDCEIKKFM-UHFFFAOYSA-N dieldrin Natural products CC1=C(Cl)C2(Cl)C3C4CC(C5OC45)C3C1(Cl)C2(Cl)Cl NGPMUTDCEIKKFM-UHFFFAOYSA-N 0.000 claims description 3
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- RDYMFSUJUZBWLH-SVWSLYAFSA-N endosulfan Chemical compound C([C@@H]12)OS(=O)OC[C@@H]1[C@]1(Cl)C(Cl)=C(Cl)[C@@]2(Cl)C1(Cl)Cl RDYMFSUJUZBWLH-SVWSLYAFSA-N 0.000 claims description 3
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- CKVMAPHTVCTEMM-ALPQRHTBSA-N milbemycin oxime Chemical compound O1[C@H](C)[C@@H](C)CC[C@@]11O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)C(=N/O)/[C@H]3OC\2)O)C[C@H]4C1.C1C[C@H](C)[C@@H](CC)O[C@@]21O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/1[C@]3([C@H](C(=O)O4)C=C(C)C(=N/O)/[C@H]3OC\1)O)C[C@H]4C2 CKVMAPHTVCTEMM-ALPQRHTBSA-N 0.000 claims description 3
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- 229960002715 nicotine Drugs 0.000 claims description 3
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- NJPPVKZQTLUDBO-UHFFFAOYSA-N novaluron Chemical compound C1=C(Cl)C(OC(F)(F)C(OC(F)(F)F)F)=CC=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F NJPPVKZQTLUDBO-UHFFFAOYSA-N 0.000 claims description 3
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 claims description 3
- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 claims description 3
- AEHJMNVBLRLZKK-UHFFFAOYSA-N pyridalyl Chemical group N1=CC(C(F)(F)F)=CC=C1OCCCOC1=C(Cl)C=C(OCC=C(Cl)Cl)C=C1Cl AEHJMNVBLRLZKK-UHFFFAOYSA-N 0.000 claims description 3
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- ZOCSXAVNDGMNBV-UHFFFAOYSA-N 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile Chemical compound NC1=C(S(=O)C(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl ZOCSXAVNDGMNBV-UHFFFAOYSA-N 0.000 claims description 2
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- JUVIOZPCNVVQFO-UHFFFAOYSA-N rotenone Natural products O1C2=C3CC(C(C)=C)OC3=CC=C2C(=O)C2C1COC1=C2C=C(OC)C(OC)=C1 JUVIOZPCNVVQFO-UHFFFAOYSA-N 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 229920005552 sodium lignosulfonate Polymers 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- DTDSAWVUFPGDMX-UHFFFAOYSA-N spirodiclofen Chemical compound CCC(C)(C)C(=O)OC1=C(C=2C(=CC(Cl)=CC=2)Cl)C(=O)OC11CCCCC1 DTDSAWVUFPGDMX-UHFFFAOYSA-N 0.000 description 1
- CLSVJBIHYWPGQY-GGYDESQDSA-N spirotetramat Chemical compound CCOC(=O)OC1=C(C=2C(=CC=C(C)C=2)C)C(=O)N[C@@]11CC[C@H](OC)CC1 CLSVJBIHYWPGQY-GGYDESQDSA-N 0.000 description 1
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 description 1
- 235000020354 squash Nutrition 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 229910052572 stoneware Inorganic materials 0.000 description 1
- 235000021012 strawberries Nutrition 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- JXHJNEJVUNHLKO-UHFFFAOYSA-N sulprofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(SC)C=C1 JXHJNEJVUNHLKO-UHFFFAOYSA-N 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- ROZUQUDEWZIBHV-UHFFFAOYSA-N tecloftalam Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(=O)NC1=CC=CC(Cl)=C1Cl ROZUQUDEWZIBHV-UHFFFAOYSA-N 0.000 description 1
- CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- UBCKGWBNUIFUST-YHYXMXQVSA-N tetrachlorvinphos Chemical compound COP(=O)(OC)O\C(=C/Cl)C1=CC(Cl)=C(Cl)C=C1Cl UBCKGWBNUIFUST-YHYXMXQVSA-N 0.000 description 1
- LITQZINTSYBKIU-UHFFFAOYSA-F tetracopper;hexahydroxide;sulfate Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[O-]S([O-])(=O)=O LITQZINTSYBKIU-UHFFFAOYSA-F 0.000 description 1
- 239000004308 thiabendazole Substances 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- 235000010296 thiabendazole Nutrition 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 description 1
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
- UGCNRZFAUBJVPT-UHFFFAOYSA-N tricyclohexyltin;hydrate Chemical compound O.C1CCCCC1[Sn](C1CCCCC1)C1CCCCC1 UGCNRZFAUBJVPT-UHFFFAOYSA-N 0.000 description 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 description 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- NRHFWOJROOQKBK-UHFFFAOYSA-N triphenyltin;hydrate Chemical compound O.C1=CC=CC=C1[Sn](C=1C=CC=CC=1)C1=CC=CC=C1 NRHFWOJROOQKBK-UHFFFAOYSA-N 0.000 description 1
- 241000701447 unidentified baculovirus Species 0.000 description 1
- JARYYMUOCXVXNK-IMTORBKUSA-N validamycin Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-IMTORBKUSA-N 0.000 description 1
- DBXFMOWZRXXBRN-LWKPJOBUSA-N valifenalate Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)NC(CC(=O)OC)C1=CC=C(Cl)C=C1 DBXFMOWZRXXBRN-LWKPJOBUSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 239000007966 viscous suspension Substances 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
- FJBGIXKIXPUXBY-UHFFFAOYSA-N {2-[3-(4-chlorophenyl)propyl]-2,4,4-trimethyl-1,3-oxazolidin-3-yl}(imidazol-1-yl)methanone Chemical compound C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1 FJBGIXKIXPUXBY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
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)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US23990209P | 2009-09-04 | 2009-09-04 | |
| US239902P | 2009-09-04 | ||
| PCT/US2010/047797 WO2011028993A1 (en) | 2009-09-04 | 2010-09-03 | N-(cyanophenyl)pyrazolecarboxamide aqueous formulation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2430813T3 true ES2430813T3 (es) | 2013-11-21 |
Family
ID=43064477
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES10752511T Active ES2430813T3 (es) | 2009-09-04 | 2010-09-03 | Formulación acuosa de N-(cianofenil)pirazolcarboxamida |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US20120156262A1 (enExample) |
| EP (1) | EP2473050B1 (enExample) |
| JP (1) | JP5785549B2 (enExample) |
| CN (1) | CN102595901B (enExample) |
| AR (1) | AR078325A1 (enExample) |
| BR (1) | BR112012004564B1 (enExample) |
| ES (1) | ES2430813T3 (enExample) |
| IL (1) | IL218335A (enExample) |
| IN (1) | IN2012DN01867A (enExample) |
| MA (1) | MA33646B1 (enExample) |
| MX (1) | MX2012002722A (enExample) |
| PL (1) | PL2473050T3 (enExample) |
| PT (1) | PT2473050E (enExample) |
| TW (1) | TWI501726B (enExample) |
| WO (1) | WO2011028993A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2022119797A3 (en) * | 2020-12-02 | 2022-10-27 | Valent U.S.A. Llc | An aqueous composition of epyrifenacil, flumioxazin and pyroxasulfone |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR036872A1 (es) | 2001-08-13 | 2004-10-13 | Du Pont | Compuesto de antranilamida, composicion que lo comprende y metodo para controlar una plaga de invertebrados |
| TWI325302B (en) | 2001-08-13 | 2010-06-01 | Du Pont | Benzoxazinone compounds |
| TWI283164B (en) | 2001-09-21 | 2007-07-01 | Du Pont | Anthranilamide arthropodicide treatment |
| KR100921594B1 (ko) | 2003-01-28 | 2009-10-14 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 시아노 안트라닐아미드 살충제 |
| TWI324908B (en) * | 2006-01-05 | 2010-05-21 | Du Pont | Liquid formulations of carboxamide arthropodicides |
| TWI547238B (zh) * | 2009-09-04 | 2016-09-01 | 杜邦股份有限公司 | 用於塗覆繁殖體之鄰胺苯甲酸二醯胺組合物 |
| WO2012153735A1 (ja) * | 2011-05-10 | 2012-11-15 | 日本曹達株式会社 | 液状殺虫剤組成物 |
| CN102405929A (zh) * | 2011-11-20 | 2012-04-11 | 广东中迅农科股份有限公司 | 含有氰虫酰胺和氟氯氰菊酯的农药组合物 |
| US9204644B2 (en) | 2011-12-19 | 2015-12-08 | E I Du Pont De Nemours And Company | Nanoparticles compositions containing polymers and anthranilic acid diamide insecticides for propagule coating |
| CN103190422B (zh) * | 2013-05-04 | 2017-12-05 | 青岛奥迪斯生物科技有限公司 | 一种含有甲氧虫酰肼与灭多威的杀虫组合物 |
| CN103283747B (zh) * | 2013-05-20 | 2017-12-01 | 青岛奥迪斯生物科技有限公司 | 一种含有苯磺隆与啶磺草胺的除草组合物 |
| CN103636610A (zh) * | 2013-10-30 | 2014-03-19 | 广东中迅农科股份有限公司 | 甲氧虫酰肼和溴氰虫酰胺杀虫组合物 |
| CN113660861B (zh) * | 2019-04-10 | 2025-06-03 | 先正达农作物保护股份公司 | 杀有害生物组合物 |
| AU2021213071A1 (en) * | 2020-01-27 | 2022-08-18 | Sumitomo Chemical Company, Limited | An aqueous insecticidal composition and methods of use thereof |
| MX2023006523A (es) * | 2020-12-02 | 2023-06-23 | Valent Usa Llc | Una composicion acuosa de epirifenacil, mesotriona y piroxasulfona. |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2674619A (en) | 1953-10-19 | 1954-04-06 | Wyandotte Chemicals Corp | Polyoxyalkylene compounds |
| US4411692A (en) * | 1981-03-26 | 1983-10-25 | Monsanto Company | Flowable herbicides |
| JPS601101A (ja) * | 1983-06-15 | 1985-01-07 | Yuukou Yakuhin Kogyo Kk | 水性懸濁農薬製剤 |
| US4875929A (en) * | 1986-05-23 | 1989-10-24 | American Cyanamid Company | Aqueous suspension concentrate compositions |
| JP2761902B2 (ja) * | 1988-10-19 | 1998-06-04 | 東邦化学工業株式会社 | 保存安定性の良好な水中油型懸濁状農薬組成物 |
| US5496845A (en) * | 1994-05-25 | 1996-03-05 | American Cyanamid Co. | Suspension concentrate compositions of arylpyrrole insecticidal and acaricidal agents |
| AU2097600A (en) * | 1998-12-17 | 2000-07-03 | Syngenta Participations Ag | Pesticidal aqueous suspension concentrates |
| US20030073583A1 (en) | 2001-10-09 | 2003-04-17 | Kostka Stanley J. | Wetting of water repellent soil by low HLB EO/PO block copolymers and enhancing solubility of same |
| KR100921594B1 (ko) * | 2003-01-28 | 2009-10-14 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 시아노 안트라닐아미드 살충제 |
| AU2005213943B2 (en) * | 2004-02-24 | 2010-06-24 | Sumitomo Chemical Company, Limited | Insecticide compositions |
| AU2005259394A1 (en) * | 2004-07-06 | 2006-01-12 | Basf Aktiengesellschaft | Liquid pesticide compositions |
| MY140912A (en) * | 2004-07-26 | 2010-01-29 | Du Pont | Mixtures of anthranilamide invertebrate pest control agents |
| TWI363756B (en) | 2004-12-07 | 2012-05-11 | Du Pont | Method for preparing n-phenylpyrazole-1-carboxamides |
| AU2006237147B2 (en) * | 2005-04-20 | 2011-04-07 | Syngenta Participations Ag | Cyano anthranilamide insecticides |
| US7534324B2 (en) | 2005-06-24 | 2009-05-19 | Hercules Incorporated | Felt and equipment surface conditioner |
| NZ573758A (en) * | 2006-07-05 | 2012-01-12 | Aventis Agriculture | 1-Phenyl-3-cyano-pyrazole derivatives and pesticidal formulations containing them |
| TWI484910B (zh) * | 2006-12-01 | 2015-05-21 | Du Pont | 甲醯胺殺節肢動物劑之液體調配物 |
| CA2685081A1 (en) * | 2007-06-27 | 2008-12-31 | E.I. Du Pont De Nemours And Company | Solid formulations of carboxamide arthropodicides |
-
2010
- 2010-08-09 TW TW099126508A patent/TWI501726B/zh not_active IP Right Cessation
- 2010-09-03 MX MX2012002722A patent/MX2012002722A/es active IP Right Grant
- 2010-09-03 US US13/392,103 patent/US20120156262A1/en not_active Abandoned
- 2010-09-03 IN IN1867DEN2012 patent/IN2012DN01867A/en unknown
- 2010-09-03 PT PT107525115T patent/PT2473050E/pt unknown
- 2010-09-03 AR ARP100103244A patent/AR078325A1/es active IP Right Grant
- 2010-09-03 ES ES10752511T patent/ES2430813T3/es active Active
- 2010-09-03 PL PL10752511T patent/PL2473050T3/pl unknown
- 2010-09-03 EP EP10752511.5A patent/EP2473050B1/en active Active
- 2010-09-03 BR BR112012004564-4A patent/BR112012004564B1/pt active IP Right Grant
- 2010-09-03 JP JP2012528083A patent/JP5785549B2/ja active Active
- 2010-09-03 WO PCT/US2010/047797 patent/WO2011028993A1/en not_active Ceased
- 2010-09-03 CN CN201080049481.5A patent/CN102595901B/zh active Active
-
2012
- 2012-02-27 IL IL218335A patent/IL218335A/en not_active IP Right Cessation
- 2012-04-02 MA MA34741A patent/MA33646B1/fr unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2022119797A3 (en) * | 2020-12-02 | 2022-10-27 | Valent U.S.A. Llc | An aqueous composition of epyrifenacil, flumioxazin and pyroxasulfone |
| US12369587B2 (en) | 2020-12-02 | 2025-07-29 | Valent U.S.A., Llc | Aqueous composition of epyrifenacil, flumioxazin and pyroxasulfone |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2473050B1 (en) | 2013-07-24 |
| IL218335A0 (en) | 2012-04-30 |
| JP5785549B2 (ja) | 2015-09-30 |
| TWI501726B (zh) | 2015-10-01 |
| TW201125490A (en) | 2011-08-01 |
| CN102595901B (zh) | 2014-04-16 |
| US20120156262A1 (en) | 2012-06-21 |
| EP2473050A1 (en) | 2012-07-11 |
| MA33646B1 (fr) | 2012-10-01 |
| AR078325A1 (es) | 2011-11-02 |
| IL218335A (en) | 2014-11-30 |
| IN2012DN01867A (enExample) | 2015-08-21 |
| BR112012004564A2 (pt) | 2020-02-04 |
| PL2473050T3 (pl) | 2013-12-31 |
| MX2012002722A (es) | 2012-04-11 |
| PT2473050E (pt) | 2013-10-16 |
| CN102595901A (zh) | 2012-07-18 |
| WO2011028993A1 (en) | 2011-03-10 |
| BR112012004564B1 (pt) | 2020-12-08 |
| JP2013503900A (ja) | 2013-02-04 |
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