JP5416111B2 - 高強度の低温安定なフルロキシピルメプチルエステルの除草製剤 - Google Patents
高強度の低温安定なフルロキシピルメプチルエステルの除草製剤 Download PDFInfo
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- JP5416111B2 JP5416111B2 JP2010521914A JP2010521914A JP5416111B2 JP 5416111 B2 JP5416111 B2 JP 5416111B2 JP 2010521914 A JP2010521914 A JP 2010521914A JP 2010521914 A JP2010521914 A JP 2010521914A JP 5416111 B2 JP5416111 B2 JP 5416111B2
- Authority
- JP
- Japan
- Prior art keywords
- fluroxypyrmeptyl
- ester
- high strength
- formulation
- low temperature
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000000203 mixture Substances 0.000 title claims abstract description 51
- 238000009472 formulation Methods 0.000 title claims abstract description 34
- -1 fluroxypyrmeptyl ester Chemical class 0.000 title claims abstract description 23
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 17
- 239000002904 solvent Substances 0.000 claims abstract description 15
- 239000004094 surface-active agent Substances 0.000 claims description 11
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 150000002148 esters Chemical class 0.000 claims description 4
- AASPBTJOWALDEO-UHFFFAOYSA-N 1-morpholin-4-ylpentan-1-one Chemical compound CCCCC(=O)N1CCOCC1 AASPBTJOWALDEO-UHFFFAOYSA-N 0.000 claims description 2
- DIVMORBOGQJESX-UHFFFAOYSA-N 1-morpholin-4-ylundecan-1-one Chemical compound CCCCCCCCCCC(=O)N1CCOCC1 DIVMORBOGQJESX-UHFFFAOYSA-N 0.000 claims description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Natural products C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 abstract description 2
- 239000000975 dye Substances 0.000 description 7
- 239000004009 herbicide Substances 0.000 description 6
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 239000005558 Fluroxypyr Substances 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000005022 packaging material Substances 0.000 description 3
- 239000005496 Chlorsulfuron Substances 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Chemical class 0.000 description 2
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- VJYIFXVZLXQVHO-UHFFFAOYSA-N chlorsulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)Cl)=N1 VJYIFXVZLXQVHO-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- MEFQWPUMEMWTJP-UHFFFAOYSA-N fluroxypyr Chemical compound NC1=C(Cl)C(F)=NC(OCC(O)=O)=C1Cl MEFQWPUMEMWTJP-UHFFFAOYSA-N 0.000 description 2
- 229920001903 high density polyethylene Polymers 0.000 description 2
- 239000004700 high-density polyethylene Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- OLZQTUCTGLHFTQ-UHFFFAOYSA-N octan-2-yl 2-(4-amino-3,5-dichloro-6-fluoropyridin-2-yl)oxyacetate Chemical group CCCCCCC(C)OC(=O)COC1=NC(F)=C(Cl)C(N)=C1Cl OLZQTUCTGLHFTQ-UHFFFAOYSA-N 0.000 description 2
- 239000008194 pharmaceutical composition Substances 0.000 description 2
- 229920001223 polyethylene glycol Chemical class 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- MZHCENGPTKEIGP-RXMQYKEDSA-N (R)-dichlorprop Chemical compound OC(=O)[C@@H](C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-RXMQYKEDSA-N 0.000 description 1
- TVFWYUWNQVRQRG-UHFFFAOYSA-N 2,3,4-tris(2-phenylethenyl)phenol Chemical class C=1C=CC=CC=1C=CC1=C(C=CC=2C=CC=CC=2)C(O)=CC=C1C=CC1=CC=CC=C1 TVFWYUWNQVRQRG-UHFFFAOYSA-N 0.000 description 1
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 1
- NUPJIGQFXCQJBK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-5-(methoxymethyl)nicotinic acid Chemical compound OC(=O)C1=CC(COC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 NUPJIGQFXCQJBK-UHFFFAOYSA-N 0.000 description 1
- IRJQWZWMQCVOLA-ZBKNUEDVSA-N 2-[(z)-n-[(3,5-difluorophenyl)carbamoylamino]-c-methylcarbonimidoyl]pyridine-3-carboxylic acid Chemical compound N=1C=CC=C(C(O)=O)C=1C(/C)=N\NC(=O)NC1=CC(F)=CC(F)=C1 IRJQWZWMQCVOLA-ZBKNUEDVSA-N 0.000 description 1
- SVOAUHHKPGKPQK-UHFFFAOYSA-N 2-chloro-9-hydroxyfluorene-9-carboxylic acid Chemical compound C1=C(Cl)C=C2C(C(=O)O)(O)C3=CC=CC=C3C2=C1 SVOAUHHKPGKPQK-UHFFFAOYSA-N 0.000 description 1
- XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 description 1
- PVSGXWMWNRGTKE-UHFFFAOYSA-N 5-methyl-2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]pyridine-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=C(C)C=C1C(O)=O PVSGXWMWNRGTKE-UHFFFAOYSA-N 0.000 description 1
- 239000005492 Carfentrazone-ethyl Substances 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- 239000005504 Dicamba Substances 0.000 description 1
- 239000005505 Dichlorprop-P Substances 0.000 description 1
- 239000005507 Diflufenican Substances 0.000 description 1
- 239000005510 Diuron Substances 0.000 description 1
- 229920005682 EO-PO block copolymer Polymers 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 239000005562 Glyphosate Substances 0.000 description 1
- CAWXEEYDBZRFPE-UHFFFAOYSA-N Hexazinone Chemical compound O=C1N(C)C(N(C)C)=NC(=O)N1C1CCCCC1 CAWXEEYDBZRFPE-UHFFFAOYSA-N 0.000 description 1
- 239000005566 Imazamox Substances 0.000 description 1
- 239000005567 Imazosulfuron Substances 0.000 description 1
- NAGRVUXEKKZNHT-UHFFFAOYSA-N Imazosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2N3C=CC=CC3=NC=2Cl)=N1 NAGRVUXEKKZNHT-UHFFFAOYSA-N 0.000 description 1
- 239000005574 MCPA Substances 0.000 description 1
- 239000005584 Metsulfuron-methyl Substances 0.000 description 1
- 239000005595 Picloram Substances 0.000 description 1
- CNILNQMBAHKMFS-UHFFFAOYSA-M Pyrithiobac-sodium Chemical compound [Na+].COC1=CC(OC)=NC(SC=2C(=C(Cl)C=CC=2)C([O-])=O)=N1 CNILNQMBAHKMFS-UHFFFAOYSA-M 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- FHNINJWBTRXEBC-UHFFFAOYSA-N Sudan III Chemical compound OC1=CC=C2C=CC=CC2=C1N=NC(C=C1)=CC=C1N=NC1=CC=CC=C1 FHNINJWBTRXEBC-UHFFFAOYSA-N 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- HBPDKDSFLXWOAE-UHFFFAOYSA-N Tebuthiuron Chemical compound CNC(=O)N(C)C1=NN=C(C(C)(C)C)S1 HBPDKDSFLXWOAE-UHFFFAOYSA-N 0.000 description 1
- NBQCNZYJJMBDKY-UHFFFAOYSA-N Terbacil Chemical compound CC=1NC(=O)N(C(C)(C)C)C(=O)C=1Cl NBQCNZYJJMBDKY-UHFFFAOYSA-N 0.000 description 1
- YIJZJEYQBAAWRJ-UHFFFAOYSA-N Thiazopyr Chemical compound N1=C(C(F)F)C(C(=O)OC)=C(CC(C)C)C(C=2SCCN=2)=C1C(F)(F)F YIJZJEYQBAAWRJ-UHFFFAOYSA-N 0.000 description 1
- 239000005626 Tribenuron Substances 0.000 description 1
- 239000005627 Triclopyr Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- WYEHFWKAOXOVJD-UHFFFAOYSA-N diflufenican Chemical compound FC1=CC(F)=CC=C1NC(=O)C1=CC=CN=C1OC1=CC=CC(C(F)(F)F)=C1 WYEHFWKAOXOVJD-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- 229940043264 dodecyl sulfate Drugs 0.000 description 1
- DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- MLKCGVHIFJBRCD-UHFFFAOYSA-N ethyl 2-chloro-3-{2-chloro-5-[4-(difluoromethyl)-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-4-fluorophenyl}propanoate Chemical group C1=C(Cl)C(CC(Cl)C(=O)OCC)=CC(N2C(N(C(F)F)C(C)=N2)=O)=C1F MLKCGVHIFJBRCD-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000013020 final formulation Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 1
- 229940097068 glyphosate Drugs 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- RSMUVYRMZCOLBH-UHFFFAOYSA-N metsulfuron methyl Chemical group COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(C)=NC(OC)=N1 RSMUVYRMZCOLBH-UHFFFAOYSA-N 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- NQQVFXUMIDALNH-UHFFFAOYSA-N picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- TVRGPOFMYCMNRB-UHFFFAOYSA-N quinizarine green ss Chemical compound C1=CC(C)=CC=C1NC(C=1C(=O)C2=CC=CC=C2C(=O)C=11)=CC=C1NC1=CC=C(C)C=C1 TVRGPOFMYCMNRB-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- FZMKKCQHDROFNI-UHFFFAOYSA-N sulfometuron Chemical compound CC1=CC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 FZMKKCQHDROFNI-UHFFFAOYSA-N 0.000 description 1
- LOQQVLXUKHKNIA-UHFFFAOYSA-N thifensulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C2=C(SC=C2)C(O)=O)=N1 LOQQVLXUKHKNIA-UHFFFAOYSA-N 0.000 description 1
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
- BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
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)
Description
本発明は、フルロキシピルエステルの除草製剤に関する。さらに詳細には、本発明は、低温で液体のままであるフルロキシピルメプチルエステルの高強度製剤に関する。
高強度フルロキシピルメプチルエステル製剤の調製
443g/LのJeffsol AG1730(Huntsman Corporation;N−ペンタノイルモルホリンからN−ウンデカノイルモルホリンまでのN−アルカノイルモルホリン混合物)、78.5g/LのTensiofix N9811HF(OmniChem nv、独占所有権のある、陰イオン−非イオン性ブレンド)および78.5 g/Lのエトキシル化トリスチリルフェノール中に、室温で撹拌しながら、480g/Lの工業用フルロキシピルメプチルエステルを溶解することにより、333gae/Lのフルロキシピルメプチルエステルを含む高強度の製剤を調製した。
高強度フルロキシピルメプチルエステル製剤の低温保存安定性
実施例1の製剤を冷却し、結晶化点が0℃より低いと判定した。結晶種を入れた製剤試料は、−10℃で4週間より長期間結晶化しなかった。
Claims (2)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US96573707P | 2007-08-22 | 2007-08-22 | |
US60/965,737 | 2007-08-22 | ||
PCT/US2008/072203 WO2009025987A1 (en) | 2007-08-22 | 2008-08-05 | High-strength, low-temperature stable herbicidal formulations of fluroxypyr meptyl ester |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2010536859A JP2010536859A (ja) | 2010-12-02 |
JP5416111B2 true JP5416111B2 (ja) | 2014-02-12 |
Family
ID=39811667
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2010521914A Active JP5416111B2 (ja) | 2007-08-22 | 2008-08-05 | 高強度の低温安定なフルロキシピルメプチルエステルの除草製剤 |
Country Status (12)
Country | Link |
---|---|
US (1) | US20090054239A1 (ja) |
EP (1) | EP2154964B1 (ja) |
JP (1) | JP5416111B2 (ja) |
CN (1) | CN101784189B (ja) |
AT (1) | ATE505953T1 (ja) |
AU (1) | AU2008289325B2 (ja) |
BR (1) | BRPI0813975B8 (ja) |
CA (1) | CA2689551C (ja) |
DE (1) | DE602008006389D1 (ja) |
PL (1) | PL2154964T3 (ja) |
RU (1) | RU2472341C2 (ja) |
WO (1) | WO2009025987A1 (ja) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8044059B2 (en) * | 2008-02-26 | 2011-10-25 | Dow Agrosciences Llc | Stable emulsifiable concentrate formulation |
ES2691386T3 (es) * | 2009-10-28 | 2018-11-27 | Dow Agrosciences Llc | Composición herbicida sinérgica que contiene fluroxipir y halosulfurón-metilo |
CA2785654C (en) * | 2009-12-29 | 2018-02-27 | Syngenta Participations Ag | Pesticidal composition |
AU2011257348B2 (en) * | 2010-05-27 | 2014-02-27 | Akzo Nobel Chemicals International B.V. | Agricultural formulations with acyl morpholines and polar aprotic co-solvents |
CN101999357A (zh) * | 2010-12-17 | 2011-04-06 | 上海生农生化制品有限公司 | 一种除草剂组合物及其用途 |
RU2606800C2 (ru) * | 2011-11-24 | 2017-01-10 | Акцо Нобель Кемикалз Интернэшнл Б.В. | Сельскохозяйственные составы с амидами и ацилморфолинами |
US20140329683A1 (en) * | 2011-11-24 | 2014-11-06 | Akzo Nobel Chemicals International B.V. | Agricultural formulations with aromatic solvents and acyl morpholines |
CN103120182A (zh) * | 2012-12-26 | 2013-05-29 | 广西三晶化工科技有限公司 | 含草甘膦、氯氟吡氧乙酸异辛酯和唑草酮的除草剂组合物 |
CN103109848A (zh) * | 2012-12-28 | 2013-05-22 | 广西壮族自治区化工研究院 | 一种含有草甘膦的除草组合物 |
EP4307890A1 (en) | 2021-03-17 | 2024-01-24 | Globachem NV | Herbicidal compositions of fluroxypyr |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5283229A (en) * | 1989-12-11 | 1994-02-01 | Isp Investments Inc. | Delivery system for agricultural chemicals |
US5374603A (en) * | 1993-04-23 | 1994-12-20 | Dowelanco | Agricultural formulations comprising fluroxypyr esters which are liquid at 25° C. |
EP0970611A3 (en) * | 1994-12-22 | 2000-04-12 | Monsanto Company | Herbicidal compositions |
AR032844A1 (es) * | 2001-02-26 | 2003-11-26 | Syngenta Participations Ag | Composicion herbicida |
US6825151B2 (en) * | 2002-01-30 | 2004-11-30 | Nufarm Americas Inc. | Liquid herbicidal compositions and use thereof in a granular herbicide |
EP2031966B1 (en) * | 2006-05-26 | 2018-08-22 | Huntsman Petrochemical LLC | Low odor, low volatility solvent for agricultural chemicals |
MY141272A (en) * | 2006-06-29 | 2010-04-16 | Dow Agrosciences Llc | High-strength, low-temperature stable herbicidal formulations of fluroxypyr esters |
-
2008
- 2008-08-05 DE DE602008006389T patent/DE602008006389D1/de active Active
- 2008-08-05 CA CA2689551A patent/CA2689551C/en active Active
- 2008-08-05 AT AT08797179T patent/ATE505953T1/de not_active IP Right Cessation
- 2008-08-05 PL PL08797179T patent/PL2154964T3/pl unknown
- 2008-08-05 JP JP2010521914A patent/JP5416111B2/ja active Active
- 2008-08-05 RU RU2010110603/13A patent/RU2472341C2/ru active
- 2008-08-05 AU AU2008289325A patent/AU2008289325B2/en active Active
- 2008-08-05 WO PCT/US2008/072203 patent/WO2009025987A1/en active Application Filing
- 2008-08-05 CN CN2008801039406A patent/CN101784189B/zh active Active
- 2008-08-05 EP EP08797179A patent/EP2154964B1/en active Active
- 2008-08-05 BR BRPI0813975A patent/BRPI0813975B8/pt active IP Right Grant
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AU2008289325B2 (en) | 2014-04-03 |
EP2154964B1 (en) | 2011-04-20 |
WO2009025987A1 (en) | 2009-02-26 |
CN101784189B (zh) | 2013-05-08 |
BRPI0813975B1 (pt) | 2016-05-17 |
ATE505953T1 (de) | 2011-05-15 |
RU2472341C2 (ru) | 2013-01-20 |
CA2689551C (en) | 2015-10-06 |
DE602008006389D1 (de) | 2011-06-01 |
JP2010536859A (ja) | 2010-12-02 |
BRPI0813975A2 (pt) | 2015-01-06 |
PL2154964T3 (pl) | 2011-09-30 |
AU2008289325A1 (en) | 2009-02-26 |
RU2010110603A (ru) | 2011-09-27 |
CN101784189A (zh) | 2010-07-21 |
US20090054239A1 (en) | 2009-02-26 |
BRPI0813975B8 (pt) | 2022-06-28 |
CA2689551A1 (en) | 2009-02-26 |
EP2154964A1 (en) | 2010-02-24 |
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