ES2337300T3 - Formulacion sin disolvente de ester butoxietilico de tricolor. - Google Patents
Formulacion sin disolvente de ester butoxietilico de tricolor. Download PDFInfo
- Publication number
- ES2337300T3 ES2337300T3 ES06837962T ES06837962T ES2337300T3 ES 2337300 T3 ES2337300 T3 ES 2337300T3 ES 06837962 T ES06837962 T ES 06837962T ES 06837962 T ES06837962 T ES 06837962T ES 2337300 T3 ES2337300 T3 ES 2337300T3
- Authority
- ES
- Spain
- Prior art keywords
- percent
- weight
- ester
- triclopyr
- herbicide
- 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.)
- Active
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 47
- 238000009472 formulation Methods 0.000 title description 7
- 150000002148 esters Chemical class 0.000 title description 6
- 239000002904 solvent Substances 0.000 title description 2
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 26
- 239000004094 surface-active agent Substances 0.000 claims abstract description 15
- IVDRCZNHVGQBHZ-UHFFFAOYSA-N 2-butoxyethyl 2-(3,5,6-trichloropyridin-2-yl)oxyacetate Chemical group CCCCOCCOC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl IVDRCZNHVGQBHZ-UHFFFAOYSA-N 0.000 claims abstract description 10
- 150000003839 salts Chemical class 0.000 claims abstract description 9
- 150000002191 fatty alcohols Chemical class 0.000 claims abstract description 8
- 239000004009 herbicide Substances 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 10
- 239000005558 Fluroxypyr Substances 0.000 claims description 2
- 239000005595 Picloram Substances 0.000 claims description 2
- 238000010790 dilution Methods 0.000 claims description 2
- 239000012895 dilution Substances 0.000 claims description 2
- MEFQWPUMEMWTJP-UHFFFAOYSA-N fluroxypyr Chemical compound NC1=C(Cl)C(F)=NC(OCC(O)=O)=C1Cl MEFQWPUMEMWTJP-UHFFFAOYSA-N 0.000 claims description 2
- NQQVFXUMIDALNH-UHFFFAOYSA-N picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 claims description 2
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 claims 1
- 229920005682 EO-PO block copolymer Polymers 0.000 abstract description 2
- -1 ethyl triclopyr Chemical compound 0.000 description 17
- 241000196324 Embryophyta Species 0.000 description 15
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 8
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 8
- 239000000975 dye Substances 0.000 description 8
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 7
- 239000005627 Triclopyr Substances 0.000 description 6
- 229920001400 block copolymer Polymers 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 238000011282 treatment Methods 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 241000894007 species Species 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 159000000007 calcium salts Chemical class 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- 238000012423 maintenance Methods 0.000 description 2
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000003209 petroleum derivative Substances 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 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
- RBSXHDIPCIWOMG-UHFFFAOYSA-N 1-(4,6-dimethoxypyrimidin-2-yl)-3-(2-ethylsulfonylimidazo[1,2-a]pyridin-3-yl)sulfonylurea Chemical compound CCS(=O)(=O)C=1N=C2C=CC=CN2C=1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 RBSXHDIPCIWOMG-UHFFFAOYSA-N 0.000 description 1
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 1
- XUYKQQDSTGNPFV-UHFFFAOYSA-N 1-oxidooxiran-1-ium Chemical compound [O-][O+]1CC1 XUYKQQDSTGNPFV-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
- CABMTIJINOIHOD-UHFFFAOYSA-N 2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]quinoline-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC2=CC=CC=C2C=C1C(O)=O CABMTIJINOIHOD-UHFFFAOYSA-N 0.000 description 1
- NQQBTWVFKDDVIB-UHFFFAOYSA-N 2-aminoethanol;3,6-dichloropyridine-2-carboxylic acid Chemical compound NCCO.OC(=O)C1=NC(Cl)=CC=C1Cl NQQBTWVFKDDVIB-UHFFFAOYSA-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
- JWUJQDFVADABEY-UHFFFAOYSA-N 2-methyltetrahydrofuran Chemical compound CC1CCCO1 JWUJQDFVADABEY-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
- NGZWZIAGFHOSDS-UHFFFAOYSA-N 6-methylheptyl 4-amino-3,5,6-trichloropyridine-2-carboxylate Chemical compound CC(C)CCCCCOC(=O)C1=NC(Cl)=C(Cl)C(N)=C1Cl NGZWZIAGFHOSDS-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000005492 Carfentrazone-ethyl Substances 0.000 description 1
- WMLPCIHUFDKWJU-UHFFFAOYSA-N Cinosulfuron Chemical compound COCCOC1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(OC)=NC(OC)=N1 WMLPCIHUFDKWJU-UHFFFAOYSA-N 0.000 description 1
- 241000218631 Coniferophyta Species 0.000 description 1
- OFSLKOLYLQSJPB-UHFFFAOYSA-N Cyclosulfamuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)NC=2C(=CC=CC=2)C(=O)C2CC2)=N1 OFSLKOLYLQSJPB-UHFFFAOYSA-N 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
- QNXAVFXEJCPCJO-UHFFFAOYSA-N Diclosulam Chemical compound N=1N2C(OCC)=NC(F)=CC2=NC=1S(=O)(=O)NC1=C(Cl)C=CC=C1Cl QNXAVFXEJCPCJO-UHFFFAOYSA-N 0.000 description 1
- 239000005507 Diflufenican Substances 0.000 description 1
- 239000005510 Diuron Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000005562 Glyphosate Substances 0.000 description 1
- 239000005566 Imazamox Substances 0.000 description 1
- 239000005981 Imazaquin 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
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 244000007853 Sarothamnus scoparius Species 0.000 description 1
- 235000010495 Sarothamnus scoparius Nutrition 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
- 239000005619 Sulfosulfuron Substances 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
- 239000005626 Tribenuron Substances 0.000 description 1
- 206010047531 Visual acuity reduced Diseases 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- RQVYBGPQFYCBGX-UHFFFAOYSA-N ametryn Chemical compound CCNC1=NC(NC(C)C)=NC(SC)=N1 RQVYBGPQFYCBGX-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000005557 antagonist Substances 0.000 description 1
- VGPYEHKOIGNJKV-UHFFFAOYSA-N asulam Chemical compound COC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 VGPYEHKOIGNJKV-UHFFFAOYSA-N 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
- JEDYYFXHPAIBGR-UHFFFAOYSA-N butafenacil Chemical compound O=C1N(C)C(C(F)(F)F)=CC(=O)N1C1=CC=C(Cl)C(C(=O)OC(C)(C)C(=O)OCC=C)=C1 JEDYYFXHPAIBGR-UHFFFAOYSA-N 0.000 description 1
- 125000006226 butoxyethyl group Chemical group 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 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
- HCWYXKWQOMTBKY-UHFFFAOYSA-N calcium;dodecyl benzenesulfonate Chemical compound [Ca].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 HCWYXKWQOMTBKY-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- JXCGFZXSOMJFOA-UHFFFAOYSA-N chlorotoluron Chemical compound CN(C)C(=O)NC1=CC=C(C)C(Cl)=C1 JXCGFZXSOMJFOA-UHFFFAOYSA-N 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000008021 deposition Effects 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
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 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
- 229940071161 dodecylbenzenesulfonate Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 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
- JBTWLSYIZRCDFO-UHFFFAOYSA-N ethyl methyl carbonate Chemical compound CCOC(=O)OC JBTWLSYIZRCDFO-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
- 239000000295 fuel oil Substances 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
- 235000008216 herbs Nutrition 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 239000000463 material 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
- GLBLPMUBLHYFCW-UHFFFAOYSA-N n-(5,7-dimethoxy-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)-2-methoxy-4-(trifluoromethyl)pyridine-3-sulfonamide Chemical compound N1=C2N=C(OC)C=C(OC)N2N=C1NS(=O)(=O)C1=C(OC)N=CC=C1C(F)(F)F GLBLPMUBLHYFCW-UHFFFAOYSA-N 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-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
- 239000010452 phosphate Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 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
- 239000000600 sorbitol Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance 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
- 239000013589 supplement Substances 0.000 description 1
- 230000009885 systemic effect Effects 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
- 229940087291 tridecyl alcohol Drugs 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
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US77341706P | 2006-02-15 | 2006-02-15 | |
| US773417P | 2006-02-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2337300T3 true ES2337300T3 (es) | 2010-04-22 |
Family
ID=37831491
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES06837962T Active ES2337300T3 (es) | 2006-02-15 | 2006-11-17 | Formulacion sin disolvente de ester butoxietilico de tricolor. |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US7488702B2 (enExample) |
| EP (1) | EP1983829B8 (enExample) |
| JP (1) | JP5225866B2 (enExample) |
| KR (1) | KR101375958B1 (enExample) |
| CN (1) | CN101304657B (enExample) |
| AU (1) | AU2006338192B2 (enExample) |
| BR (1) | BRPI0621351B8 (enExample) |
| CA (1) | CA2630847C (enExample) |
| CR (1) | CR10159A (enExample) |
| DE (1) | DE602006011790D1 (enExample) |
| ES (1) | ES2337300T3 (enExample) |
| MY (1) | MY177114A (enExample) |
| NZ (1) | NZ567245A (enExample) |
| RU (1) | RU2413414C2 (enExample) |
| WO (1) | WO2007094836A1 (enExample) |
| ZA (1) | ZA200804632B (enExample) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2337300T3 (es) | 2006-02-15 | 2010-04-22 | Dow Agrosciences Llc | Formulacion sin disolvente de ester butoxietilico de tricolor. |
| MY158318A (en) * | 2007-08-30 | 2016-09-30 | Dow Agrosciences Llc | Stable emulsion formulation hindering interaction across the water-oil interface |
| AR069011A1 (es) * | 2007-10-24 | 2009-12-23 | Dow Agrosciences Llc | Formulaciones herbicidas libres de solvente aromaticas de ester de fluroxipir meptilo con esteres c₄₋₈ de triclopir, 2,4-d o mcpa |
| US20090155142A1 (en) * | 2007-12-12 | 2009-06-18 | Bauer John E | Molecular sieve and catalyst incorporating the sieve |
| AR071339A1 (es) * | 2008-02-05 | 2010-06-16 | Arysta Lifescience North Ameri | Formulacion solida de compuesto activo de baja fusion |
| HUE028192T2 (en) * | 2008-10-29 | 2016-12-28 | Dow Agrosciences Llc | Concentrates of stable, emulsifiable, first herbicide carboxylic acid salt and second herbicide carboxylic acid ester |
| JP2012073978A (ja) * | 2010-09-30 | 2012-04-12 | Hitachi Ltd | サーバ装置の筐体構造 |
| MX377775B (es) | 2012-09-13 | 2025-03-11 | Corteva Agriscience Llc | Composiciones herbicidas que contienen aminopiralid y triclopir. |
| US9603363B2 (en) | 2012-12-21 | 2017-03-28 | Dow Agrosciences Llc | Weed control from applications of aminopyralid, triclopyr, and an organosilicone surfactant |
| CN105377030B (zh) | 2013-07-31 | 2018-01-19 | 阿克佐诺贝尔化学国际公司 | 无溶剂的液体烷基苯磺酸盐组合物及其在农业化学配制剂中的用途 |
| CN107926955B (zh) * | 2017-04-25 | 2021-03-09 | 湖南比德生化科技股份有限公司 | 一种含绿草定酯与毒莠定的混合乳油 |
| BR112021014078A2 (pt) | 2019-01-18 | 2021-09-21 | Sbm Developpment Sas | Misturas e composições herbicidas sinérgicas compreendendo triclopir e adjuvantes éster de fosfato |
| AU2021266078B2 (en) * | 2020-04-30 | 2024-08-15 | Evonik Operations Gmbh | Use of polyethers as carriers for active ingredients |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU612347B2 (en) * | 1987-02-24 | 1991-07-11 | Rhone-Poulenc Agrochimie | Herbicidal composition and method |
| US5834006A (en) | 1990-04-05 | 1998-11-10 | Dow Agrosciences Llc | Latex-based agricultural compositions |
| US5466659A (en) * | 1993-01-15 | 1995-11-14 | Dowelanco | Triclopyr butoxyethyl ester compositions comprising vegetable oil esters as carriers |
| CA2120375A1 (en) | 1993-04-02 | 1994-10-03 | John Klier | A laundry pretreater having enhanced oily soil removal |
| GB9315501D0 (en) | 1993-07-27 | 1993-09-08 | Ici Plc | Surfactant compositions |
| GB9414318D0 (en) | 1994-07-15 | 1994-09-07 | Dowelanco Ltd | Preparation of aqueous emulsions |
| IT1275167B (it) | 1995-02-23 | 1997-07-30 | Isagro Spa | Adiuvanti per fungicidi sistemici composizioni fungicide che li contengono e loro impiego |
| GB9505204D0 (en) | 1995-03-15 | 1995-05-03 | Dowelanco | Mixed herbicidal compositions |
| DE50102537D1 (de) * | 2000-03-13 | 2004-07-15 | Basf Ag | Agrotechnische formulierung |
| DE10035930A1 (de) | 2000-07-21 | 2002-01-31 | Clariant Gmbh | Feinemulsionen |
| AU2004100006A4 (en) | 2003-01-06 | 2004-03-11 | Nufarm Australia Limited | Herbicidal composition |
| CN1764374B (zh) * | 2003-03-26 | 2010-09-22 | 拜尔作物科学股份公司 | 芳族羟基化合物用作安全剂的用途 |
| NZ543037A (en) | 2003-04-22 | 2009-10-30 | Monsanto Technology Llc | Herbicidal compositions containing glyphosate and a pyridine analog |
| JP4377612B2 (ja) * | 2003-05-21 | 2009-12-02 | 日本曹達株式会社 | つる性植物の生育抑制用塗料及びつる性植物の生育抑制方法 |
| ES2337300T3 (es) | 2006-02-15 | 2010-04-22 | Dow Agrosciences Llc | Formulacion sin disolvente de ester butoxietilico de tricolor. |
-
2006
- 2006-11-17 ES ES06837962T patent/ES2337300T3/es active Active
- 2006-11-17 CN CN2006800421362A patent/CN101304657B/zh active Active
- 2006-11-17 BR BRPI0621351A patent/BRPI0621351B8/pt active IP Right Grant
- 2006-11-17 EP EP06837962A patent/EP1983829B8/en active Active
- 2006-11-17 AU AU2006338192A patent/AU2006338192B2/en active Active
- 2006-11-17 DE DE602006011790T patent/DE602006011790D1/de active Active
- 2006-11-17 CA CA2630847A patent/CA2630847C/en active Active
- 2006-11-17 NZ NZ567245A patent/NZ567245A/en not_active IP Right Cessation
- 2006-11-17 KR KR1020087019933A patent/KR101375958B1/ko not_active Expired - Fee Related
- 2006-11-17 WO PCT/US2006/044751 patent/WO2007094836A1/en not_active Ceased
- 2006-11-17 RU RU2008136885/21A patent/RU2413414C2/ru not_active IP Right Cessation
- 2006-11-17 JP JP2008555225A patent/JP5225866B2/ja active Active
- 2006-11-17 US US11/601,231 patent/US7488702B2/en active Active
- 2006-11-17 MY MYPI20064526A patent/MY177114A/en unknown
-
2008
- 2008-05-28 ZA ZA2008/04632A patent/ZA200804632B/en unknown
- 2008-07-17 CR CR10159A patent/CR10159A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU2006338192A1 (en) | 2007-08-23 |
| NZ567245A (en) | 2010-07-30 |
| US7488702B2 (en) | 2009-02-10 |
| CR10159A (es) | 2008-10-29 |
| CA2630847A1 (en) | 2007-08-23 |
| RU2413414C2 (ru) | 2011-03-10 |
| US20070191229A1 (en) | 2007-08-16 |
| EP1983829B1 (en) | 2010-01-13 |
| JP2009526843A (ja) | 2009-07-23 |
| CN101304657A (zh) | 2008-11-12 |
| EP1983829A1 (en) | 2008-10-29 |
| BRPI0621351B8 (pt) | 2022-06-28 |
| KR20080093053A (ko) | 2008-10-17 |
| CN101304657B (zh) | 2011-08-31 |
| DE602006011790D1 (de) | 2010-03-04 |
| AU2006338192B2 (en) | 2012-03-22 |
| BRPI0621351B1 (pt) | 2015-02-24 |
| CA2630847C (en) | 2013-09-10 |
| RU2008136885A (ru) | 2010-03-20 |
| MY177114A (en) | 2020-09-07 |
| JP5225866B2 (ja) | 2013-07-03 |
| WO2007094836A1 (en) | 2007-08-23 |
| KR101375958B1 (ko) | 2014-03-18 |
| ZA200804632B (en) | 2009-12-30 |
| EP1983829B8 (en) | 2010-03-17 |
| BRPI0621351A2 (pt) | 2011-12-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES3053856T3 (en) | Non-aqueous solution of plant growth regulators and semipolar organic solvent | |
| US9839218B2 (en) | Pesticidal composition | |
| ES2559441T3 (es) | Composición herbicida sinérgica que contiene aminopiralid y ácido 2,4-diclorofenoxiacético | |
| AU2011253539B2 (en) | Use of compositions comprising triclopyr butoxyethyl ester for the control of woody plants | |
| RU2413414C2 (ru) | Композиция бутоксиэтилового эфира триклопира, не содержащая растворитель | |
| ES2639198T5 (es) | Composición herbicida sinérgica que contiene penoxsulam y pendimetalina | |
| ES2639226T3 (es) | Sal de ácido isetiónico que contiene nitrógeno en formulaciones agrícolas estables | |
| Gous et al. | The evaluation of aerially applied triclopyr mixtures for the control of dense infestations of wilding Pinus contorta in New Zealand | |
| CA2767922C (en) | Cocoalkylpolyamine alkoxylates as agents for high strength herbicide compositions | |
| MX2008010135A (en) | Solventless formulation of triclopyr butoxyethyl ester | |
| WO2026037843A1 (en) | Use of a solvent composition in agrochemical formulations and corresponding agrochemical formulations | |
| AU2012205427B2 (en) | Growth inhibition of cotton with penoxsulam | |
| OA21042A (en) | An agrochemical composition. | |
| MXPA06010398A (en) | Herbicidal compositions containing n-phosphonomethyl glycine and an auxin herbicide |