UA72761C2 - Compositions and method of eliminating plant growth or controlling thereof - Google Patents
Compositions and method of eliminating plant growth or controlling thereof Download PDFInfo
- Publication number
- UA72761C2 UA72761C2 UA2001118000A UA2001118000A UA72761C2 UA 72761 C2 UA72761 C2 UA 72761C2 UA 2001118000 A UA2001118000 A UA 2001118000A UA 2001118000 A UA2001118000 A UA 2001118000A UA 72761 C2 UA72761 C2 UA 72761C2
- Authority
- UA
- Ukraine
- Prior art keywords
- composition
- glyphosate
- herbicide
- amine
- compositions
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 530
- 238000000034 method Methods 0.000 title claims abstract description 75
- 230000008635 plant growth Effects 0.000 title claims description 8
- 239000004094 surface-active agent Substances 0.000 claims abstract description 276
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims abstract description 231
- 239000005562 Glyphosate Substances 0.000 claims abstract description 227
- 229940097068 glyphosate Drugs 0.000 claims abstract description 227
- 238000011282 treatment Methods 0.000 claims abstract description 155
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 143
- 150000001412 amines Chemical class 0.000 claims abstract description 124
- 239000004009 herbicide Substances 0.000 claims abstract description 101
- 239000012141 concentrate Substances 0.000 claims abstract description 94
- 125000000129 anionic group Chemical group 0.000 claims abstract description 85
- 150000005215 alkyl ethers Chemical class 0.000 claims abstract description 72
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 49
- 239000001257 hydrogen Substances 0.000 claims abstract description 43
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 43
- 239000002253 acid Substances 0.000 claims abstract description 35
- 150000002431 hydrogen Chemical group 0.000 claims abstract description 23
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 19
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 17
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 13
- 208000024891 symptom Diseases 0.000 claims abstract description 11
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 9
- 231100000674 Phytotoxicity Toxicity 0.000 claims abstract description 8
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 5
- 239000000126 substance Substances 0.000 claims description 143
- -1 polyoxyethylene chains Polymers 0.000 claims description 113
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 65
- 125000006353 oxyethylene group Chemical group 0.000 claims description 65
- 239000013543 active substance Substances 0.000 claims description 51
- 125000005907 alkyl ester group Chemical group 0.000 claims description 46
- 150000003839 salts Chemical class 0.000 claims description 44
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 36
- 239000005590 Oxyfluorfen Substances 0.000 claims description 25
- OQMBBFQZGJFLBU-UHFFFAOYSA-N Oxyfluorfen Chemical compound C1=C([N+]([O-])=O)C(OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 OQMBBFQZGJFLBU-UHFFFAOYSA-N 0.000 claims description 25
- 125000000217 alkyl group Chemical group 0.000 claims description 25
- JJWLVOIRVHMVIS-UHFFFAOYSA-O isopropylaminium Chemical compound CC(C)[NH3+] JJWLVOIRVHMVIS-UHFFFAOYSA-O 0.000 claims description 24
- 239000007787 solid Substances 0.000 claims description 22
- 239000007788 liquid Substances 0.000 claims description 19
- 125000002091 cationic group Chemical group 0.000 claims description 16
- 150000003973 alkyl amines Chemical class 0.000 claims description 13
- IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical group CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 claims description 12
- 239000005561 Glufosinate Substances 0.000 claims description 12
- 125000003277 amino group Chemical group 0.000 claims description 12
- 230000002209 hydrophobic effect Effects 0.000 claims description 11
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 10
- 150000001450 anions Chemical class 0.000 claims description 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 239000005492 Carfentrazone-ethyl Substances 0.000 claims description 5
- 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 claims description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 4
- 125000003342 alkenyl group Chemical group 0.000 claims description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- CONWAEURSVPLRM-UHFFFAOYSA-N lactofen Chemical compound C1=C([N+]([O-])=O)C(C(=O)OC(C)C(=O)OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 CONWAEURSVPLRM-UHFFFAOYSA-N 0.000 claims description 4
- 229910052700 potassium Inorganic materials 0.000 claims description 4
- 239000011591 potassium Substances 0.000 claims description 4
- 229910052708 sodium Inorganic materials 0.000 claims description 4
- 239000011734 sodium Substances 0.000 claims description 4
- 125000002723 alicyclic group Chemical group 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- FOUWCSDKDDHKQP-UHFFFAOYSA-N flumioxazin Chemical compound FC1=CC=2OCC(=O)N(CC#C)C=2C=C1N(C1=O)C(=O)C2=C1CCCC2 FOUWCSDKDDHKQP-UHFFFAOYSA-N 0.000 claims description 3
- BGZZWXTVIYUUEY-UHFFFAOYSA-N fomesafen Chemical compound C1=C([N+]([O-])=O)C(C(=O)NS(=O)(=O)C)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 BGZZWXTVIYUUEY-UHFFFAOYSA-N 0.000 claims description 3
- 125000000743 hydrocarbylene group Chemical group 0.000 claims description 3
- 229920001451 polypropylene glycol Polymers 0.000 claims description 3
- IRECWLYBCAZIJM-UHFFFAOYSA-N Flumiclorac pentyl Chemical group C1=C(Cl)C(OCC(=O)OCCCCC)=CC(N2C(C3=C(CCCC3)C2=O)=O)=C1F IRECWLYBCAZIJM-UHFFFAOYSA-N 0.000 claims description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 2
- IPPAUTOBDWNELX-UHFFFAOYSA-N (2-ethoxy-2-oxoethyl) 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate Chemical group C1=C([N+]([O-])=O)C(C(=O)OCC(=O)OCC)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 IPPAUTOBDWNELX-UHFFFAOYSA-N 0.000 claims 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims 1
- 238000012876 topography Methods 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 abstract description 3
- 125000000204 (C2-C4) acyl group Chemical group 0.000 abstract 1
- 241000196324 Embryophyta Species 0.000 description 142
- 235000008504 concentrate Nutrition 0.000 description 71
- 241000894007 species Species 0.000 description 34
- 230000000052 comparative effect Effects 0.000 description 31
- 239000000945 filler Substances 0.000 description 26
- 239000004615 ingredient Substances 0.000 description 26
- 238000010561 standard procedure Methods 0.000 description 26
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 25
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 23
- 230000001965 increasing effect Effects 0.000 description 23
- 239000000787 lecithin Substances 0.000 description 23
- 229940067606 lecithin Drugs 0.000 description 23
- 235000010445 lecithin Nutrition 0.000 description 23
- 238000002156 mixing Methods 0.000 description 20
- 238000012360 testing method Methods 0.000 description 20
- 230000005764 inhibitory process Effects 0.000 description 16
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 15
- 239000003921 oil Substances 0.000 description 15
- 244000058871 Echinochloa crus-galli Species 0.000 description 14
- 235000008247 Echinochloa frumentacea Nutrition 0.000 description 14
- 230000004071 biological effect Effects 0.000 description 14
- 235000019198 oils Nutrition 0.000 description 14
- QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 description 13
- 230000008485 antagonism Effects 0.000 description 13
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- 150000003863 ammonium salts Chemical class 0.000 description 12
- 230000009044 synergistic interaction Effects 0.000 description 12
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 11
- 239000000377 silicon dioxide Substances 0.000 description 11
- 238000003756 stirring Methods 0.000 description 11
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- 239000007864 aqueous solution Substances 0.000 description 9
- 230000000875 corresponding effect Effects 0.000 description 9
- 235000012239 silicon dioxide Nutrition 0.000 description 9
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 8
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 8
- 235000011130 ammonium sulphate Nutrition 0.000 description 8
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- PZNPLUBHRSSFHT-RRHRGVEJSA-N 1-hexadecanoyl-2-octadecanoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCCCC(=O)O[C@@H](COP([O-])(=O)OCC[N+](C)(C)C)COC(=O)CCCCCCCCCCCCCCC PZNPLUBHRSSFHT-RRHRGVEJSA-N 0.000 description 6
- PDYXIVPKOMYDOK-UHFFFAOYSA-N Glyphosate-monoammonium Chemical class [NH4+].OC(=O)CNCP(O)([O-])=O PDYXIVPKOMYDOK-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 230000009471 action Effects 0.000 description 6
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- 239000002609 medium Substances 0.000 description 6
- 238000012545 processing Methods 0.000 description 6
- 239000000523 sample Substances 0.000 description 6
- 239000002689 soil Substances 0.000 description 6
- 239000008347 soybean phospholipid Substances 0.000 description 6
- 238000003860 storage Methods 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 239000011230 binding agent Substances 0.000 description 5
- 238000005516 engineering process Methods 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 239000005645 nematicide Substances 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- 239000003760 tallow Substances 0.000 description 5
- 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 4
- 241001290610 Abildgaardia Species 0.000 description 4
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 4
- 244000062793 Sorghum vulgare Species 0.000 description 4
- 240000003864 Ulex europaeus Species 0.000 description 4
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- 150000007513 acids Chemical class 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 230000003993 interaction Effects 0.000 description 4
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- 238000003973 irrigation Methods 0.000 description 4
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical class CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 125000001117 oleyl 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])=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])[H] 0.000 description 4
- 125000000913 palmityl 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])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
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- 239000005648 plant growth regulator Substances 0.000 description 4
- 230000004044 response Effects 0.000 description 4
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 4
- 125000004079 stearyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- VDZOOKBUILJEDG-UHFFFAOYSA-M tetrabutylammonium hydroxide Chemical compound [OH-].CCCC[N+](CCCC)(CCCC)CCCC VDZOOKBUILJEDG-UHFFFAOYSA-M 0.000 description 4
- CLQMBPJKHLGMQK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)nicotinic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=CC=C1C(O)=O CLQMBPJKHLGMQK-UHFFFAOYSA-N 0.000 description 3
- 235000014698 Brassica juncea var multisecta Nutrition 0.000 description 3
- 241000287828 Gallus gallus Species 0.000 description 3
- 238000005481 NMR spectroscopy Methods 0.000 description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
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- 238000011161 development Methods 0.000 description 3
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- 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 2
- 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 2
- ZBMRKNMTMPPMMK-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid;azane Chemical class [NH4+].CP(O)(=O)CCC(N)C([O-])=O ZBMRKNMTMPPMMK-UHFFFAOYSA-N 0.000 description 2
- ICIDSZQHPUZUHC-UHFFFAOYSA-N 2-octadecoxyethanol Chemical compound CCCCCCCCCCCCCCCCCCOCCO ICIDSZQHPUZUHC-UHFFFAOYSA-N 0.000 description 2
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- OMOVVBIIQSXZSZ-UHFFFAOYSA-N [6-(4-acetyloxy-5,9a-dimethyl-2,7-dioxo-4,5a,6,9-tetrahydro-3h-pyrano[3,4-b]oxepin-5-yl)-5-formyloxy-3-(furan-3-yl)-3a-methyl-7-methylidene-1a,2,3,4,5,6-hexahydroindeno[1,7a-b]oxiren-4-yl] 2-hydroxy-3-methylpentanoate Chemical compound CC12C(OC(=O)C(O)C(C)CC)C(OC=O)C(C3(C)C(CC(=O)OC4(C)COC(=O)CC43)OC(C)=O)C(=C)C32OC3CC1C=1C=COC=1 OMOVVBIIQSXZSZ-UHFFFAOYSA-N 0.000 description 2
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- NQLVQOSNDJXLKG-UHFFFAOYSA-N prosulfocarb Chemical compound CCCN(CCC)C(=O)SCC1=CC=CC=C1 NQLVQOSNDJXLKG-UHFFFAOYSA-N 0.000 description 1
- 238000001472 pulsed field gradient Methods 0.000 description 1
- FFSSWMQPCJRCRV-UHFFFAOYSA-N quinclorac Chemical compound ClC1=CN=C2C(C(=O)O)=C(Cl)C=CC2=C1 FFSSWMQPCJRCRV-UHFFFAOYSA-N 0.000 description 1
- BACHBFVBHLGWSL-JTQLQIEISA-N rac-diclofop methyl Natural products C1=CC(O[C@@H](C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-JTQLQIEISA-N 0.000 description 1
- 238000013102 re-test Methods 0.000 description 1
- 230000010076 replication Effects 0.000 description 1
- 230000033458 reproduction Effects 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 229940010735 steareth-12 Drugs 0.000 description 1
- 229940080728 steareth-30 Drugs 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- RJKCKKDSSSRYCB-UHFFFAOYSA-N tebutam Chemical compound CC(C)(C)C(=O)N(C(C)C)CC1=CC=CC=C1 RJKCKKDSSSRYCB-UHFFFAOYSA-N 0.000 description 1
- BCQMBFHBDZVHKU-UHFFFAOYSA-N terbumeton Chemical compound CCNC1=NC(NC(C)(C)C)=NC(OC)=N1 BCQMBFHBDZVHKU-UHFFFAOYSA-N 0.000 description 1
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
- FZXISNSWEXTPMF-UHFFFAOYSA-N terbutylazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C)=N1 FZXISNSWEXTPMF-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 229910052716 thallium Inorganic materials 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- SRVJKTDHMYAMHA-WUXMJOGZSA-N thioacetazone Chemical compound CC(=O)NC1=CC=C(\C=N\NC(N)=S)C=C1 SRVJKTDHMYAMHA-WUXMJOGZSA-N 0.000 description 1
- 229960003231 thioacetazone Drugs 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 230000005945 translocation 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
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000000080 wetting agent Substances 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
- 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
- A01N25/30—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 characterised by the surfactants
-
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
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 |
|---|---|---|---|
| US13075699P | 1999-04-23 | 1999-04-23 | |
| PCT/US2000/008763 WO2000064256A1 (en) | 1999-04-23 | 2000-04-03 | Enhanced herbicide compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA72761C2 true UA72761C2 (en) | 2005-04-15 |
Family
ID=22446174
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UA2001117999A UA72760C2 (en) | 1999-04-23 | 2000-03-04 | Method to treat plant foliage |
| UA2001118000A UA72761C2 (en) | 1999-04-23 | 2000-03-04 | Compositions and method of eliminating plant growth or controlling thereof |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UA2001117999A UA72760C2 (en) | 1999-04-23 | 2000-03-04 | Method to treat plant foliage |
Country Status (26)
| Country | Link |
|---|---|
| EP (2) | EP1173059B1 (pl) |
| JP (2) | JP5030332B2 (pl) |
| KR (2) | KR20020008393A (pl) |
| CN (2) | CN1356869A (pl) |
| AR (3) | AR023557A1 (pl) |
| AT (2) | ATE276657T1 (pl) |
| AU (3) | AU4192100A (pl) |
| BR (2) | BR0010657B1 (pl) |
| CA (2) | CA2369636C (pl) |
| CO (1) | CO5241274A1 (pl) |
| CZ (2) | CZ20013764A3 (pl) |
| DE (2) | DE60023872T2 (pl) |
| DK (1) | DK1173059T3 (pl) |
| EA (2) | EA200101123A1 (pl) |
| ES (2) | ES2251998T3 (pl) |
| GT (1) | GT200000047A (pl) |
| HU (2) | HUP0201106A3 (pl) |
| MX (2) | MXPA01010763A (pl) |
| MY (2) | MY130215A (pl) |
| NZ (2) | NZ514816A (pl) |
| PH (2) | PH12000000990B1 (pl) |
| PL (2) | PL201290B1 (pl) |
| SK (2) | SK15002001A3 (pl) |
| UA (2) | UA72760C2 (pl) |
| WO (3) | WO2000064258A1 (pl) |
| ZA (2) | ZA200108684B (pl) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1192707C (zh) | 1999-10-26 | 2005-03-16 | 陶氏益农有限责任公司 | 除草剂的浓悬浮剂 |
| MY158895A (en) | 2000-05-19 | 2016-11-30 | Monsanto Technology Llc | Potassium glyphosate formulations |
| DE10063960A1 (de) * | 2000-12-20 | 2002-06-27 | Aventis Cropscience Gmbh | Herbizide Mittel |
| MXPA03010265A (es) * | 2001-05-08 | 2004-03-10 | Monsanto Europe Sa | Composiciones de glifosato y su uso. |
| DK1464221T3 (da) * | 2001-12-19 | 2011-06-14 | Nihon Nohyaku Co Ltd | Herbicid sammensætning og fremgangsmåde til anvendelse deraf |
| WO2004028254A1 (ja) * | 2002-09-30 | 2004-04-08 | Nihon Green & Garden Corporation | 除草用混合液剤 |
| US20050026781A1 (en) | 2003-04-22 | 2005-02-03 | Monsanto Technology Llc | Herbicidal compositions containing glyphosate and a pyridine analog |
| BRPI0413266B8 (pt) * | 2003-08-04 | 2022-06-28 | Dow Agrosciences Llc | Composição de concentrado herbicida de alta potência, e método para controle de vegetação indesejável |
| US20050101488A1 (en) * | 2003-10-21 | 2005-05-12 | Sumitomo Chemical Company, Limited | Herbicidal composition |
| WO2005087007A1 (en) | 2004-03-10 | 2005-09-22 | Monsanto Technology Llc | Herbicidal compositions containing n-phosphonomethyl glycine and an auxin herbicide |
| CA2472806A1 (en) | 2004-05-18 | 2005-11-18 | Petro-Canada | Compositions and methods for treating turf insect pests and diseases such as fungal infestations |
| JP2006056784A (ja) * | 2004-08-17 | 2006-03-02 | Sankyo Agro Kk | 安定化された水性除草剤組成物 |
| WO2006034459A1 (en) | 2004-09-23 | 2006-03-30 | Akzo Nobel N.V. | Alkoxylated alkylamines / alkyl ether amines with peaked distribution |
| JP2006117650A (ja) * | 2004-09-27 | 2006-05-11 | Kao Corp | 除草剤組成物 |
| MY148811A (en) * | 2004-09-27 | 2013-05-31 | Kao Corp | Herbicide composition, herbicide-enhancer and enhancing method |
| TWI451842B (zh) | 2005-07-04 | 2014-09-11 | Sumitomo Chemical Co | 殺蟲劑組成物 |
| CN101511175A (zh) * | 2006-03-23 | 2009-08-19 | 阿克佐诺贝尔股份有限公司 | 具有峰值分布的烷氧基化烷基胺或烷氧基化烷基醚胺 |
| US9357768B2 (en) | 2006-10-05 | 2016-06-07 | Suncor Energy Inc. | Herbicidal composition with increased herbicidal efficacy |
| EP2094083B1 (en) | 2006-12-06 | 2014-07-23 | Akzo Nobel N.V. | Alkylamidopropyl dialkylamine surfactants as adjuvants |
| US9012365B2 (en) | 2006-12-06 | 2015-04-21 | Akzo Nobel N.V. | Compatibility agents for herbicidal formulations comprising 2,4-(Dichlorophenoxy) acetic acid salts |
| WO2009004044A1 (en) * | 2007-07-05 | 2009-01-08 | Akzo Nobel N.V. | Alkoxylated asymmetric alkylamine surfactants as adjuvants |
| JP5596678B2 (ja) | 2008-06-26 | 2014-09-24 | サンコー エナジー インコーポレーテッド | 顔料を含む改善された芝草用殺菌製剤 |
| EP2425716B1 (en) | 2008-08-19 | 2016-05-04 | Akzo Nobel N.V. | Thickening glyphosate formulations |
| EP2266394A1 (en) | 2009-06-17 | 2010-12-29 | Cognis IP Management GmbH | Non-aqueous agricultural compositions |
| CN103338642A (zh) | 2010-09-09 | 2013-10-02 | 桑科能源股份有限公司 | 协同作用的石蜡油和啶酰菌胺杀真菌剂 |
| US9451773B2 (en) | 2011-06-03 | 2016-09-27 | Suncor Energy Inc. | Paraffinic oil-in-water emulsions for controlling infection of crop plants by fungal pathogens |
| UY34416A (es) | 2011-10-26 | 2013-01-03 | Monsanto Technology Llc | ?sales de herbicidas de ácido carboxílico? |
| ES2698505T3 (es) * | 2012-03-23 | 2019-02-05 | Dow Agrosciences Llc | Concentrados acuosos de herbicidas que contienen ésteres alquílicos de ácidos grasos, amidas de ácidos grasos o ésteres de ácidos grasos triglicéridos y métodos de uso |
| KR101367258B1 (ko) * | 2012-04-17 | 2014-02-27 | 인바이오 주식회사 | 속효성과 지효성을 동시에 갖는 제초제 |
| WO2013181738A1 (en) | 2012-06-04 | 2013-12-12 | Suncor Energy Inc. | Formulations containing paraffinic oil and anti-settling agent |
| US10736322B2 (en) | 2012-06-04 | 2020-08-11 | Monsanto Technology Llc | Aqueous concentrated herbicidal compositions containing glyphosate salts and dicamba salts |
| US10285404B2 (en) | 2013-02-27 | 2019-05-14 | Monsanto Technology Llc | Glyphosate composition for dicamba tank mixtures with improved volatility |
| EP3821709A4 (en) * | 2018-07-05 | 2022-04-13 | Kao Corporation | HERBICIDE COMPOSITION |
| JP7321761B2 (ja) | 2018-07-05 | 2023-08-07 | 花王株式会社 | 除草剤組成物 |
| BR112021014592A2 (pt) | 2019-01-25 | 2021-10-05 | Suncor Energy Inc. | Compostos fotosensibilizadores, métodos de fabricação e aplicação em plantas |
| AU2020222515B2 (en) | 2019-02-15 | 2025-10-09 | Nutrien Ag Solutions (Canada) Inc. | The use of protoporphyrin IX derivatives to improve the health of plants |
| CN112998002A (zh) * | 2021-03-06 | 2021-06-22 | 通辽市农业科学研究院 | 一种荞麦田的除草方法 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU3148384A (en) * | 1983-10-28 | 1985-05-02 | Chevron Research Company | Glyphosate type herbicide plus oxyfluorfen |
| US5206021A (en) | 1988-05-09 | 1993-04-27 | Rhone-Poulenc Ag Company | Stabilized oil-in-water emulsions or suspoemulsions containing pesticidal substances in both oil and water phases |
| AU609628B2 (en) | 1988-06-14 | 1991-05-02 | Monsanto Company | Improved herbicide formulations container silicone surfactant and their uses |
| EP0448538B1 (en) | 1990-03-15 | 1997-01-02 | Monsanto Company | Improved glyphosate formulations |
| GB2267825B (en) * | 1992-05-26 | 1995-08-30 | Dowelanco | Herbicidal aqueous-based microemulsion compositions |
| ES2050643T1 (es) * | 1992-08-24 | 1994-06-01 | Monsanto Co | Composiciones herbicidas. |
| EP0617894B1 (en) * | 1993-04-02 | 1998-12-16 | Monsanto Europe S.A./N.V. | Liquid concentrated herbicidal glyphosate compositions |
| GB9412722D0 (en) * | 1994-06-24 | 1994-08-17 | Zeneca Ltd | Herbicidal composition |
| JP3799669B2 (ja) * | 1996-07-29 | 2006-07-19 | 日産化学工業株式会社 | 除草剤組成物 |
| US5821195A (en) * | 1996-08-16 | 1998-10-13 | Monsanto Company | Sequential application method for enhancing glyphosate herbicidal effectiveness with reduced antagonism |
| ATE348518T1 (de) * | 1996-10-25 | 2007-01-15 | Monsanto Technology Llc | Zusammensetzung und verfahren zur behandlung von pflanzen mit exogenen chemikalien |
-
2000
- 2000-03-04 UA UA2001117999A patent/UA72760C2/uk unknown
- 2000-03-04 UA UA2001118000A patent/UA72761C2/uk unknown
- 2000-04-03 BR BRPI0010657-7A patent/BR0010657B1/pt active IP Right Grant
- 2000-04-03 KR KR1020017013524A patent/KR20020008393A/ko not_active Withdrawn
- 2000-04-03 DE DE60023872T patent/DE60023872T2/de not_active Expired - Lifetime
- 2000-04-03 EP EP00928138A patent/EP1173059B1/en not_active Expired - Lifetime
- 2000-04-03 ES ES00928138T patent/ES2251998T3/es not_active Expired - Lifetime
- 2000-04-03 HU HU0201106A patent/HUP0201106A3/hu unknown
- 2000-04-03 AT AT00925888T patent/ATE276657T1/de not_active IP Right Cessation
- 2000-04-03 WO PCT/US2000/008907 patent/WO2000064258A1/en not_active Ceased
- 2000-04-03 JP JP2000613261A patent/JP5030332B2/ja not_active Expired - Lifetime
- 2000-04-03 EP EP00925888A patent/EP1202623B1/en not_active Expired - Lifetime
- 2000-04-03 NZ NZ514816A patent/NZ514816A/en not_active IP Right Cessation
- 2000-04-03 DE DE60014105T patent/DE60014105T2/de not_active Expired - Lifetime
- 2000-04-03 EA EA200101123A patent/EA200101123A1/ru unknown
- 2000-04-03 WO PCT/US2000/008843 patent/WO2000064257A1/en not_active Ceased
- 2000-04-03 DK DK00928138T patent/DK1173059T3/da active
- 2000-04-03 WO PCT/US2000/008763 patent/WO2000064256A1/en not_active Ceased
- 2000-04-03 BR BR0010656-9A patent/BR0010656A/pt not_active Application Discontinuation
- 2000-04-03 KR KR1020017013525A patent/KR20020008844A/ko not_active Withdrawn
- 2000-04-03 ES ES00925888T patent/ES2228507T3/es not_active Expired - Lifetime
- 2000-04-03 CZ CZ20013764A patent/CZ20013764A3/cs unknown
- 2000-04-03 SK SK1500-2001A patent/SK15002001A3/sk unknown
- 2000-04-03 CN CN00809186A patent/CN1356869A/zh active Pending
- 2000-04-03 CZ CZ20013765A patent/CZ20013765A3/cs unknown
- 2000-04-03 JP JP2000613259A patent/JP2002542266A/ja active Pending
- 2000-04-03 PL PL351838A patent/PL201290B1/pl unknown
- 2000-04-03 EA EA200101120A patent/EA200101120A1/ru unknown
- 2000-04-03 AT AT00928138T patent/ATE308880T1/de not_active IP Right Cessation
- 2000-04-03 CA CA002369636A patent/CA2369636C/en not_active Expired - Lifetime
- 2000-04-03 SK SK1502-2001A patent/SK15022001A3/sk unknown
- 2000-04-03 NZ NZ514817A patent/NZ514817A/en not_active IP Right Cessation
- 2000-04-03 HU HU0201138A patent/HUP0201138A3/hu unknown
- 2000-04-03 CA CA002369738A patent/CA2369738C/en not_active Expired - Lifetime
- 2000-04-03 AU AU41921/00A patent/AU4192100A/en not_active Abandoned
- 2000-04-03 CN CN00809194A patent/CN1356870A/zh active Pending
- 2000-04-03 AU AU44510/00A patent/AU776036B2/en not_active Expired
- 2000-04-03 PL PL351840A patent/PL199160B1/pl unknown
- 2000-04-03 AU AU46418/00A patent/AU776887B2/en not_active Expired
- 2000-04-18 GT GT200000047A patent/GT200000047A/es unknown
- 2000-04-19 AR ARP000101857A patent/AR023557A1/es active IP Right Grant
- 2000-04-19 AR ARP000101859A patent/AR023559A1/es unknown
- 2000-04-19 PH PH12000000990A patent/PH12000000990B1/en unknown
- 2000-04-19 CO CO00029094A patent/CO5241274A1/es not_active Application Discontinuation
- 2000-04-19 AR ARP000101858A patent/AR023558A1/es active IP Right Grant
- 2000-04-19 PH PH12000000991A patent/PH12000000991B1/en unknown
- 2000-04-21 MY MYPI20001701A patent/MY130215A/en unknown
- 2000-04-21 MY MYPI20001703A patent/MY126950A/en unknown
-
2001
- 2001-10-22 ZA ZA200108684A patent/ZA200108684B/xx unknown
- 2001-10-22 ZA ZA200108687A patent/ZA200108687B/xx unknown
- 2001-10-23 MX MXPA01010763 patent/MXPA01010763A/es active IP Right Grant
- 2001-10-23 MX MXPA01010762 patent/MXPA01010762A/es active IP Right Grant
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