UA80145C2 - Cyclohexanedionoxyme herbicide-safener combination and use thereof - Google Patents
Cyclohexanedionoxyme herbicide-safener combination and use thereof Download PDFInfo
- Publication number
- UA80145C2 UA80145C2 UAA200501487A UA2005001487A UA80145C2 UA 80145 C2 UA80145 C2 UA 80145C2 UA A200501487 A UAA200501487 A UA A200501487A UA 2005001487 A UA2005001487 A UA 2005001487A UA 80145 C2 UA80145 C2 UA 80145C2
- Authority
- UA
- Ukraine
- Prior art keywords
- herbicide
- alkyl
- compounds
- antidote
- plants
- Prior art date
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- 150000001875 compounds Chemical class 0.000 claims abstract description 74
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 47
- 150000003839 salts Chemical class 0.000 claims abstract description 31
- IEGRLEZDTRNPRH-UHFFFAOYSA-N 2-hydroxyiminocyclohexan-1-one Chemical compound ON=C1CCCCC1=O IEGRLEZDTRNPRH-UHFFFAOYSA-N 0.000 claims abstract description 15
- GGWHBJGBERXSLL-NBVRZTHBSA-N chembl113137 Chemical compound C1C(=O)C(C(=N/OCC)/CCC)=C(O)CC1C1CSCCC1 GGWHBJGBERXSLL-NBVRZTHBSA-N 0.000 claims abstract description 10
- 150000004696 coordination complex Chemical class 0.000 claims abstract description 9
- KRQUFUKTQHISJB-YYADALCUSA-N 2-[(E)-N-[2-(4-chlorophenoxy)propoxy]-C-propylcarbonimidoyl]-3-hydroxy-5-(thian-3-yl)cyclohex-2-en-1-one Chemical compound CCC\C(=N/OCC(C)OC1=CC=C(Cl)C=C1)C1=C(O)CC(CC1=O)C1CCCSC1 KRQUFUKTQHISJB-YYADALCUSA-N 0.000 claims abstract description 5
- 244000045561 useful plants Species 0.000 claims abstract description 5
- ZOGDSYNXUXQGHF-XIEYBQDHSA-N Butroxydim Chemical compound CCCC(=O)C1=C(C)C=C(C)C(C2CC(=O)C(\C(CC)=N\OCC)=C(O)C2)=C1C ZOGDSYNXUXQGHF-XIEYBQDHSA-N 0.000 claims abstract description 3
- 241000196324 Embryophyta Species 0.000 claims description 80
- 239000004009 herbicide Substances 0.000 claims description 74
- 239000000203 mixture Substances 0.000 claims description 57
- 238000011282 treatment Methods 0.000 claims description 26
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 23
- 238000009472 formulation Methods 0.000 claims description 23
- 229910052739 hydrogen Inorganic materials 0.000 claims description 23
- 239000001257 hydrogen Substances 0.000 claims description 23
- 239000000126 substance Substances 0.000 claims description 15
- 239000000729 antidote Substances 0.000 claims description 13
- 230000000694 effects Effects 0.000 claims description 10
- 238000009331 sowing Methods 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 230000000885 phytotoxic effect Effects 0.000 claims description 4
- 241000592344 Spermatophyta Species 0.000 claims description 3
- 229940075522 antidotes Drugs 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 231100000208 phytotoxic Toxicity 0.000 claims description 3
- 239000005497 Clethodim Substances 0.000 abstract description 4
- SILSDTWXNBZOGF-JWGBMQLESA-N clethodim Chemical compound CCSC(C)CC1CC(O)=C(C(CC)=NOC\C=C\Cl)C(=O)C1 SILSDTWXNBZOGF-JWGBMQLESA-N 0.000 abstract description 4
- CSPPKDPQLUUTND-NBVRZTHBSA-N Sethoxydim Chemical compound CCO\N=C(/CCC)C1=C(O)CC(CC(C)SCC)CC1=O CSPPKDPQLUUTND-NBVRZTHBSA-N 0.000 abstract description 2
- 239000005624 Tralkoxydim Substances 0.000 abstract description 2
- DQFPEYARZIQXRM-LTGZKZEYSA-N tralkoxydim Chemical compound C1C(=O)C(C(/CC)=N/OCC)=C(O)CC1C1=C(C)C=C(C)C=C1C DQFPEYARZIQXRM-LTGZKZEYSA-N 0.000 abstract description 2
- IOYNQIMAUDJVEI-ZFNPBRLTSA-N 2-[N-[(E)-3-chloroprop-2-enoxy]-C-ethylcarbonimidoyl]-3-hydroxy-5-(oxan-4-yl)cyclohex-2-en-1-one Chemical compound C1C(=O)C(C(=NOC\C=C\Cl)CC)=C(O)CC1C1CCOCC1 IOYNQIMAUDJVEI-ZFNPBRLTSA-N 0.000 abstract 1
- 239000005501 Cycloxydim Substances 0.000 abstract 1
- PNCNFDRSHBFIDM-WOJGMQOQSA-N chembl111617 Chemical compound C=CCO\N=C(/CCC)C1=C(O)C(C(=O)OC)C(C)(C)CC1=O PNCNFDRSHBFIDM-WOJGMQOQSA-N 0.000 abstract 1
- -1 alkali metal salts Chemical class 0.000 description 30
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- 240000005979 Hordeum vulgare Species 0.000 description 13
- 235000007340 Hordeum vulgare Nutrition 0.000 description 13
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- 239000000843 powder Substances 0.000 description 10
- 241000894007 species Species 0.000 description 10
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- 239000000839 emulsion Substances 0.000 description 9
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- 229910052751 metal Chemical class 0.000 description 7
- 239000002184 metal Chemical class 0.000 description 7
- 239000000575 pesticide Substances 0.000 description 7
- 230000001681 protective effect Effects 0.000 description 7
- 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 description 6
- 240000007594 Oryza sativa Species 0.000 description 6
- 235000007164 Oryza sativa Nutrition 0.000 description 6
- OPGCOAPTHCZZIW-UHFFFAOYSA-N diethyl 1-(2,4-dichlorophenyl)-5-methyl-4h-pyrazole-3,5-dicarboxylate Chemical group CCOC(=O)C1(C)CC(C(=O)OCC)=NN1C1=CC=C(Cl)C=C1Cl OPGCOAPTHCZZIW-UHFFFAOYSA-N 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
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- 235000009566 rice Nutrition 0.000 description 6
- 239000004562 water dispersible granule Substances 0.000 description 6
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- 235000010469 Glycine max Nutrition 0.000 description 5
- 240000008042 Zea mays Species 0.000 description 5
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- 239000004480 active ingredient Substances 0.000 description 5
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- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 150000001768 cations Chemical class 0.000 description 4
- 235000005822 corn Nutrition 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- PQKBPHSEKWERTG-LLVKDONJSA-N ethyl (2r)-2-[4-[(6-chloro-1,3-benzoxazol-2-yl)oxy]phenoxy]propanoate Chemical group C1=CC(O[C@H](C)C(=O)OCC)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 PQKBPHSEKWERTG-LLVKDONJSA-N 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 150000004702 methyl esters Chemical class 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 230000009261 transgenic effect Effects 0.000 description 4
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 3
- 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 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 150000003863 ammonium salts Chemical class 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
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- 229910052731 fluorine Inorganic materials 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 230000012010 growth Effects 0.000 description 3
- 125000001188 haloalkyl group Chemical group 0.000 description 3
- 229920001522 polyglycol ester Polymers 0.000 description 3
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- 239000002689 soil Substances 0.000 description 3
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- 239000002904 solvent Substances 0.000 description 3
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- 239000000080 wetting agent Substances 0.000 description 3
- HZKBYBNLTLVSPX-UHFFFAOYSA-N 6-[(6,6-dimethyl-5,7-dihydropyrrolo[2,1-c][1,2,4]thiadiazol-3-ylidene)amino]-7-fluoro-4-prop-2-ynyl-1,4-benzoxazin-3-one Chemical compound C#CCN1C(=O)COC(C=C2F)=C1C=C2N=C1SN=C2CC(C)(C)CN21 HZKBYBNLTLVSPX-UHFFFAOYSA-N 0.000 description 2
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 2
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 229910020637 Co-Cu Inorganic materials 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- DQZCVNGCTZLGAQ-UHFFFAOYSA-N Cycluron Chemical compound CN(C)C(=O)NC1CCCCCCC1 DQZCVNGCTZLGAQ-UHFFFAOYSA-N 0.000 description 2
- 241000219146 Gossypium Species 0.000 description 2
- 241000208818 Helianthus Species 0.000 description 2
- 235000003222 Helianthus annuus Nutrition 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 235000007238 Secale cereale Nutrition 0.000 description 2
- 244000082988 Secale cereale Species 0.000 description 2
- 244000061456 Solanum tuberosum Species 0.000 description 2
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- 235000021536 Sugar beet Nutrition 0.000 description 2
- PNRAZZZISDRWMV-UHFFFAOYSA-N Terbucarb Chemical compound CNC(=O)OC1=C(C(C)(C)C)C=C(C)C=C1C(C)(C)C PNRAZZZISDRWMV-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000000304 alkynyl group Chemical group 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
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- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- WYKYKTKDBLFHCY-UHFFFAOYSA-N chloridazon Chemical compound O=C1C(Cl)=C(N)C=NN1C1=CC=CC=C1 WYKYKTKDBLFHCY-UHFFFAOYSA-N 0.000 description 2
- KIEDNEWSYUYDSN-UHFFFAOYSA-N clomazone Chemical compound O=C1C(C)(C)CON1CC1=CC=CC=C1Cl KIEDNEWSYUYDSN-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
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- MZZBPDKVEFVLFF-UHFFFAOYSA-N cyanazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C#N)=N1 MZZBPDKVEFVLFF-UHFFFAOYSA-N 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
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- 239000000945 filler Substances 0.000 description 2
- IANUJLZYFUDJIH-UHFFFAOYSA-N flufenacet Chemical compound C=1C=C(F)C=CC=1N(C(C)C)C(=O)COC1=NN=C(C(F)(F)F)S1 IANUJLZYFUDJIH-UHFFFAOYSA-N 0.000 description 2
- 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 description 2
- OQZCSNDVOWYALR-UHFFFAOYSA-N flurochloridone Chemical compound FC(F)(F)C1=CC=CC(N2C(C(Cl)C(CCl)C2)=O)=C1 OQZCSNDVOWYALR-UHFFFAOYSA-N 0.000 description 2
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- 239000012535 impurity Substances 0.000 description 2
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- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 2
- 239000000546 pharmaceutical excipient Substances 0.000 description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 2
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- 159000000001 potassium salts Chemical class 0.000 description 2
- 235000012015 potatoes Nutrition 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
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- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
- GXEKYRXVRROBEV-FBXFSONDSA-N (1r,2s,3r,4s)-7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid Chemical compound C1C[C@@H]2[C@@H](C(O)=O)[C@@H](C(=O)O)[C@H]1O2 GXEKYRXVRROBEV-FBXFSONDSA-N 0.000 description 1
- HTBQOINACZOEPC-UHFFFAOYSA-N (2,4-dichlorophenyl)-(1-methyl-5-phenylmethoxypyrazol-4-yl)methanone Chemical compound C=1C=CC=CC=1COC=1N(C)N=CC=1C(=O)C1=CC=C(Cl)C=C1Cl HTBQOINACZOEPC-UHFFFAOYSA-N 0.000 description 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 1
- 125000006530 (C4-C6) alkyl group Chemical group 0.000 description 1
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- XUHGTGGPZFJRMF-UHFFFAOYSA-N 1,3-dihydropyrazole-2-carboxylic acid Chemical compound OC(=O)N1CC=CN1 XUHGTGGPZFJRMF-UHFFFAOYSA-N 0.000 description 1
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- 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
- BXKKQFGRMSOANI-UHFFFAOYSA-N 1-methoxy-3-[4-[(2-methoxy-2,4,4-trimethyl-3h-chromen-7-yl)oxy]phenyl]-1-methylurea Chemical compound C1=CC(NC(=O)N(C)OC)=CC=C1OC1=CC=C2C(C)(C)CC(C)(OC)OC2=C1 BXKKQFGRMSOANI-UHFFFAOYSA-N 0.000 description 1
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- BDQWWOHKFDSADC-UHFFFAOYSA-N 2-(2,4-dichloro-3-methylphenoxy)-n-phenylpropanamide Chemical compound C=1C=CC=CC=1NC(=O)C(C)OC1=CC=C(Cl)C(C)=C1Cl BDQWWOHKFDSADC-UHFFFAOYSA-N 0.000 description 1
- WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 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
- GOCUAJYOYBLQRH-UHFFFAOYSA-N 2-(4-{[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=NC=C(C(F)(F)F)C=C1Cl GOCUAJYOYBLQRH-UHFFFAOYSA-N 0.000 description 1
- YUVKUEAFAVKILW-UHFFFAOYSA-N 2-(4-{[5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(C(F)(F)F)C=N1 YUVKUEAFAVKILW-UHFFFAOYSA-N 0.000 description 1
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- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
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- 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
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- 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
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
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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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/50—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids the nitrogen atom being doubly bound to the carbon skeleton
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen
- A01N35/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen containing a carbon-to-nitrogen double bond
-
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
- A01N43/16—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom
-
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
- A01N43/18—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with sulfur as the ring hetero atom
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (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)
- Pest Control & Pesticides (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP02016006A EP1382247A1 (en) | 2002-07-18 | 2002-07-18 | Combinations of cyclohexanedione oxime herbicides and safeners |
| PCT/EP2003/007251 WO2004008854A1 (en) | 2002-07-18 | 2003-07-07 | Combinations of cyclohexanedione oxime herbicides and safeners |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA80145C2 true UA80145C2 (en) | 2007-08-27 |
Family
ID=29762654
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UAA200501487A UA80145C2 (en) | 2002-07-18 | 2003-07-07 | Cyclohexanedionoxyme herbicide-safener combination and use thereof |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US7060657B2 (pl) |
| EP (2) | EP1382247A1 (pl) |
| JP (1) | JP2005533124A (pl) |
| CN (1) | CN100334948C (pl) |
| AR (1) | AR040584A1 (pl) |
| AT (1) | ATE319308T1 (pl) |
| AU (1) | AU2003249966B2 (pl) |
| BR (1) | BR0312741B1 (pl) |
| CA (1) | CA2493382C (pl) |
| DE (1) | DE60303951T2 (pl) |
| EA (1) | EA007734B1 (pl) |
| ES (1) | ES2258231T3 (pl) |
| MA (1) | MA27259A1 (pl) |
| MX (1) | MXPA05000752A (pl) |
| NZ (1) | NZ537723A (pl) |
| PL (1) | PL208076B1 (pl) |
| UA (1) | UA80145C2 (pl) |
| WO (1) | WO2004008854A1 (pl) |
| ZA (1) | ZA200410132B (pl) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2003211498A1 (en) * | 2002-02-15 | 2003-09-04 | Mitsui Chemicals, Inc. | Optically active azole derivative and process for producing the same |
| US7651977B2 (en) * | 2004-10-28 | 2010-01-26 | Valent U.S.A. Corporation | Herbicidal compositions |
| US20060199738A1 (en) * | 2005-03-04 | 2006-09-07 | Sumitomo Chemical Company, Limited | Herbicidal composition |
| DE102005014944A1 (de) * | 2005-04-01 | 2006-10-05 | Bayer Cropscience Gmbh | Synergistische kulturpflanzenverträgliche herbizide Mittel enthaltend Herbizide aus der Gruppe der Benzoylpyrazole |
| WO2007050090A1 (en) * | 2005-10-28 | 2007-05-03 | Valent U.S.A. Corporation | Herbicidal compositions |
| DE102005057250A1 (de) * | 2005-11-29 | 2007-06-06 | Bayer Cropscience Gmbh | Wirkstoffe zur Steigerung der Stressabwehr in Pflanzen gegenüber abiotischem Stress und Methoden zu ihrer Auffindung |
| US7951995B2 (en) | 2006-06-28 | 2011-05-31 | Pioneer Hi-Bred International, Inc. | Soybean event 3560.4.3.5 and compositions and methods for the identification and detection thereof |
| EP3067425A1 (en) | 2006-10-31 | 2016-09-14 | E. I. du Pont de Nemours and Company | Soybean event dp-305423-1 and constructs for the generation thereof |
| US20090215625A1 (en) * | 2008-01-07 | 2009-08-27 | Auburn University | Combinations of Herbicides and Safeners |
| CN101401572B (zh) * | 2008-09-05 | 2011-12-21 | 河北科技大学 | 稀禾啶的环糊精或其亲水衍生物包合物及其制备方法 |
| WO2010059671A2 (en) * | 2008-11-24 | 2010-05-27 | Dow Agrosciences Llc | Safening 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide injury on direct seeded and transplanted paddy rice |
| GB201013009D0 (en) * | 2010-08-02 | 2010-09-15 | Syngenta Participations Ag | Agricultural method |
| WO2012021785A1 (en) | 2010-08-13 | 2012-02-16 | Pioneer Hi-Bred International, Inc. | Compositions and methods comprising sequences having hydroxyphenylpyruvate dioxygenase (hppd) activity |
| CA2818918A1 (en) | 2010-11-24 | 2012-05-31 | Pioneer Hi-Bred International, Inc. | Brassica gat event dp-061061-7 and compositions and methods for the identification and/or detection thereof |
| AU2010364322C1 (en) | 2010-11-24 | 2013-09-19 | E. I. Du Pont De Nemours And Company | Brassica GAT event DP-073496-4 and compositions and methods for the identification and/or detection thereof |
| TWI667347B (zh) | 2010-12-15 | 2019-08-01 | 瑞士商先正達合夥公司 | 大豆品種ｓｙｈｔ０ｈ２及偵測其之組合物及方法 |
| WO2013188291A2 (en) | 2012-06-15 | 2013-12-19 | E. I. Du Pont De Nemours And Company | Methods and compositions involving als variants with native substrate preference |
| WO2014100525A2 (en) | 2012-12-21 | 2014-06-26 | Pioneer Hi-Bred International, Inc. | Compositions and methods for auxin-analog conjugation |
| CA2905743C (en) | 2013-03-13 | 2021-09-28 | Pioneer Hi-Bred International, Inc. | Glyphosate application for weed control in brassica |
| AU2014236162A1 (en) | 2013-03-14 | 2015-09-17 | Arzeda Corp. | Compositions having dicamba decarboxylase activity and methods of use |
| WO2014153234A1 (en) | 2013-03-14 | 2014-09-25 | Pioneer Hi-Bred International, Inc. | Compositions having dicamba decarboxylase activity and methods of use |
| US11026423B2 (en) | 2013-04-17 | 2021-06-08 | Sepro Corporation | Herbicidal compositions and methods |
| WO2014172551A1 (en) | 2013-04-17 | 2014-10-23 | Sepro Corporation | Herbicidal compositions and methods |
| EP3187049B1 (en) * | 2013-10-17 | 2019-08-07 | Basf Se | Herbicidal composition comprising the acc inhibitor cycloxydim |
| WO2015057600A1 (en) | 2013-10-18 | 2015-04-23 | E. I. Du Pont De Nemours And Company | Glyphosate-n-acetyltransferase (glyat) sequences and methods of use |
| EP4136975A1 (fr) * | 2014-03-11 | 2023-02-22 | Arysta Lifescience | Herbicide composition |
| RU2634048C1 (ru) * | 2016-05-05 | 2017-10-23 | Федеральное государственное бюджетное научное учреждение "Всероссийский научно-исследовательский институт биологической защиты растений" | Способ защиты вегетирующих растений сахарной свёклы от негативного воздействия гербицидов |
| CN109645013A (zh) * | 2019-02-21 | 2019-04-19 | 上海祥霖农业技术有限公司 | 一种除草组合物及其应用、除草剂 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6026778B2 (ja) | 1976-02-05 | 1985-06-25 | 日本曹達株式会社 | オキシム誘導体の製造方法 |
| JPS52112945A (en) | 1976-03-16 | 1977-09-21 | Fujitec Co Ltd | Device for controlling elevator |
| AU503917B1 (en) | 1977-05-23 | 1979-09-27 | Nippon Soda Co., Ltd. | Cyclohexane-1, 3-dione derivatives |
| CA1218379A (en) | 1980-11-25 | 1987-02-24 | Tatao Luo | Herbicidal substituted 2-(1-oxyamino)-alkylidene)- cyclohexane-1,3-diones |
| DE3121355A1 (de) | 1981-05-29 | 1982-12-16 | Basf Ag, 6700 Ludwigshafen | Cyclohexandionderivate, verfahren zu ihrer herstellung und diese enthaltende herbizide |
| DE3939503A1 (de) * | 1989-11-30 | 1991-06-06 | Hoechst Ag | Neue pyrazoline zum schutz von kulturpflanzen gegenueber herbiziden |
| ES2058983T3 (es) | 1990-05-09 | 1994-11-01 | Basf Ag | Ciclohexenonoximeteres, procedimiento para su obtencion y su empleo como herbicidas. |
| DE19638233A1 (de) * | 1996-09-19 | 1998-03-26 | Hoechst Schering Agrevo Gmbh | Kombinationen aus Sulfonylharnstoff-Herbiziden und Safenern |
| GB9717321D0 (en) * | 1997-08-15 | 1997-10-22 | Zeneca Ltd | Herbicidal composition |
| WO1999057982A1 (en) * | 1998-05-14 | 1999-11-18 | E.I. Du Pont De Nemours And Company | Crop-safened herbicidal mixtures |
-
2002
- 2002-07-18 EP EP02016006A patent/EP1382247A1/en not_active Withdrawn
-
2003
- 2003-07-07 EP EP03764947A patent/EP1538901B1/en not_active Expired - Lifetime
- 2003-07-07 PL PL373463A patent/PL208076B1/pl not_active IP Right Cessation
- 2003-07-07 BR BRPI0312741-9A patent/BR0312741B1/pt active IP Right Grant
- 2003-07-07 AT AT03764947T patent/ATE319308T1/de not_active IP Right Cessation
- 2003-07-07 EA EA200500110A patent/EA007734B1/ru not_active IP Right Cessation
- 2003-07-07 UA UAA200501487A patent/UA80145C2/uk unknown
- 2003-07-07 NZ NZ537723A patent/NZ537723A/en not_active IP Right Cessation
- 2003-07-07 CN CNB038169568A patent/CN100334948C/zh not_active Expired - Lifetime
- 2003-07-07 MX MXPA05000752A patent/MXPA05000752A/es active IP Right Grant
- 2003-07-07 ES ES03764947T patent/ES2258231T3/es not_active Expired - Lifetime
- 2003-07-07 CA CA2493382A patent/CA2493382C/en not_active Expired - Lifetime
- 2003-07-07 JP JP2004522415A patent/JP2005533124A/ja not_active Abandoned
- 2003-07-07 DE DE60303951T patent/DE60303951T2/de not_active Expired - Lifetime
- 2003-07-07 AU AU2003249966A patent/AU2003249966B2/en not_active Ceased
- 2003-07-07 WO PCT/EP2003/007251 patent/WO2004008854A1/en active IP Right Grant
- 2003-07-16 AR AR20030102556A patent/AR040584A1/es active IP Right Grant
- 2003-07-16 US US10/621,236 patent/US7060657B2/en not_active Expired - Lifetime
-
2004
- 2004-12-15 ZA ZA200410132A patent/ZA200410132B/en unknown
-
2005
- 2005-01-05 MA MA28034A patent/MA27259A1/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| MA27259A1 (fr) | 2005-03-01 |
| NZ537723A (en) | 2006-09-29 |
| WO2004008854A1 (en) | 2004-01-29 |
| ES2258231T3 (es) | 2006-08-16 |
| EP1382247A1 (en) | 2004-01-21 |
| AU2003249966B2 (en) | 2009-05-28 |
| EP1538901A1 (en) | 2005-06-15 |
| ZA200410132B (en) | 2006-07-26 |
| MXPA05000752A (es) | 2005-04-19 |
| DE60303951D1 (de) | 2006-05-04 |
| AR040584A1 (es) | 2005-04-13 |
| BR0312741B1 (pt) | 2014-03-11 |
| CA2493382A1 (en) | 2004-01-29 |
| EP1538901B1 (en) | 2006-03-08 |
| CA2493382C (en) | 2012-05-15 |
| PL208076B1 (pl) | 2011-03-31 |
| JP2005533124A (ja) | 2005-11-04 |
| PL373463A1 (pl) | 2005-08-22 |
| BR0312741A (pt) | 2005-04-26 |
| US7060657B2 (en) | 2006-06-13 |
| CN100334948C (zh) | 2007-09-05 |
| US20040018940A1 (en) | 2004-01-29 |
| EA007734B1 (ru) | 2006-12-29 |
| EA200500110A1 (ru) | 2005-08-25 |
| DE60303951T2 (de) | 2006-09-28 |
| CN1668192A (zh) | 2005-09-14 |
| AU2003249966A1 (en) | 2004-02-09 |
| ATE319308T1 (de) | 2006-03-15 |
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