UA80145C2 - Cyclohexanedionoxyme herbicide-safener combination and use thereof - Google Patents

Cyclohexanedionoxyme herbicide-safener combination and use thereof Download PDF

Info

Publication number: UA80145C2
Authority: UA; Ukraine
Prior art keywords: herbicide; alkyl; compounds; antidote; plants
Prior art date: 2002-07-18

Application number

UAA200501487A

Other languages

English (en)

Ukrainian (uk)

Inventor

Erwin Hacker

Hermann Bieringer

Hans Filipp Huff

Original Assignee

Bayer Cropscience Gmbh

Priority date (The priority date 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 date listed.)

2002-07-18

Filing date

2003-07-07

Publication date

2007-08-27

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=29762654&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=UA80145(C2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

2003-07-07 Application filed by Bayer Cropscience Gmbh filed Critical Bayer Cropscience Gmbh

2007-08-27 Publication of UA80145C2 publication Critical patent/UA80145C2/uk

Links

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
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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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235000021307 Triticum Nutrition 0.000 description 14
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239000000843 powder Substances 0.000 description 10
241000894007 species Species 0.000 description 10
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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
150000003254 radicals Chemical class 0.000 description 6
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239000004562 water dispersible granule Substances 0.000 description 6
244000068988 Glycine max Species 0.000 description 5
235000010469 Glycine max Nutrition 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
150000004665 fatty acids Chemical class 0.000 description 3
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
229920002451 polyvinyl alcohol Polymers 0.000 description 3
239000002689 soil Substances 0.000 description 3
239000007787 solid Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
239000000600 sorbitol Substances 0.000 description 3
238000001228 spectrum Methods 0.000 description 3
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125000001424 substituent group Chemical group 0.000 description 3
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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244000062793 Sorghum vulgare Species 0.000 description 2
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
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238000009835 boiling Methods 0.000 description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
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150000001735 carboxylic acids Chemical class 0.000 description 2
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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
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239000010949 copper Substances 0.000 description 2
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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150000002085 enols Chemical class 0.000 description 2
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150000002191 fatty alcohols Chemical class 0.000 description 2
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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
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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
239000000417 fungicide Substances 0.000 description 2
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239000012535 impurity Substances 0.000 description 2
239000003112 inhibitor 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
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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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125000005913 (C3-C6) cycloalkyl group Chemical group 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)

UAA200501487A 2002-07-18 2003-07-07 Cyclohexanedionoxyme herbicide-safener combination and use thereof UA80145C2 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
EP02016006A EP1382247A1 (fr)	2002-07-18	2002-07-18	Associations d'herbicides d'oximes de cyclohexanedione et de phytoprotecteurs
PCT/EP2003/007251 WO2004008854A1 (fr)	2002-07-18	2003-07-07	Combinaisons d'herbicides et de phytoprotecteurs cyclohexanedione oxime

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 (fr)
EP (2)	EP1382247A1 (fr)
JP (1)	JP2005533124A (fr)
CN (1)	CN100334948C (fr)
AR (1)	AR040584A1 (fr)
AT (1)	ATE319308T1 (fr)
AU (1)	AU2003249966B2 (fr)
BR (1)	BR0312741B1 (fr)
CA (1)	CA2493382C (fr)
DE (1)	DE60303951T2 (fr)
EA (1)	EA007734B1 (fr)
ES (1)	ES2258231T3 (fr)
MA (1)	MA27259A1 (fr)
MX (1)	MXPA05000752A (fr)
NZ (1)	NZ537723A (fr)
PL (1)	PL208076B1 (fr)
UA (1)	UA80145C2 (fr)
WO (1)	WO2004008854A1 (fr)
ZA (1)	ZA200410132B (fr)

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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
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EP2078089B1 (fr)	2006-10-31	2016-05-04	E. I. du Pont de Nemours and Company	Événement de soja dp-305423-1, leurs compositions et leurs procédés d'identification et/ou de détection
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
KR20170036112A (ko) *	2008-11-24	2017-03-31	다우 아그로사이언시즈 엘엘씨	직파 및 이앙 논벼에서의 6-(삼치환된 페닐)-4-아미노-2-피리딘카르복실레이트 제초제 피해 완화 방법
GB201013009D0 (en) *	2010-08-02	2010-09-15	Syngenta Participations Ag	Agricultural method
WO2012021797A1 (fr)	2010-08-13	2012-02-16	Pioneer Hi-Bred International, Inc.	Procédés et compositions pour cibler des séquences d'intérêt pour le chloroplaste
CA2810180C (fr)	2010-11-24	2015-07-28	Pioneer Hi-Bred International, Inc.	Evenement dp-073496-4 de brassica gat et compositions et procedes pour l'identifier et/ou le detecter
WO2012071039A1 (fr)	2010-11-24	2012-05-31	Pioner Hi-Bred International, Inc.	Événement dp-061061-7 de brassica gat et compositions et procédés pour l'identifier et/ou le détecter
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
CA2876426A1 (fr)	2012-06-15	2013-12-19	E. I. Du Pont De Nemours And Company	Methodes et compositions impliquant des variants d'als a preference pour les substrats natifs
CN105008541A (zh)	2012-12-21	2015-10-28	先锋国际良种公司	用于生长素类似物缀合的组合物和方法
WO2014159306A1 (fr)	2013-03-13	2014-10-02	Pioneer Hi-Bred International, Inc.	Application de glyphosate pour désherbage d'une brassicée
CA2905595A1 (fr)	2013-03-14	2014-09-25	Pioneer Hi-Bred International, Inc.	Compositions ayant une activite de dicamba decarboxylase et procedes d'utilisation
AU2014236162A1 (en)	2013-03-14	2015-09-17	Arzeda Corp.	Compositions having dicamba decarboxylase activity and methods of use
WO2014172551A1 (fr)	2013-04-17	2014-10-23	Sepro Corporation	Compositions et procédés herbicides
US11026423B2 (en)	2013-04-17	2021-06-08	Sepro Corporation	Herbicidal compositions and methods
WO2015055448A1 (fr) *	2013-10-17	2015-04-23	Basf Se	Composition herbicide contenant des inhibiteurs de l'acc
CA2927180A1 (fr)	2013-10-18	2015-04-23	Pioneer Hi-Bred International, Inc.	Sequences de glyphosate-n-acetyltransferase (glyat) et leurs procedes d'utilisation
AU2015228653B2 (en) *	2014-03-11	2018-01-18	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

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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
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CA1218379A (fr)	1980-11-25	1987-02-24	Tatao Luo	Derives de substitution herbicides de 2-(1-oxyamino)- alcoylidene)-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
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2002
- 2002-07-18 EP EP02016006A patent/EP1382247A1/fr not_active Withdrawn
2003
- 2003-07-07 CA CA2493382A patent/CA2493382C/fr not_active Expired - Lifetime
- 2003-07-07 MX MXPA05000752A patent/MXPA05000752A/es active IP Right Grant
- 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 ES ES03764947T patent/ES2258231T3/es not_active Expired - Lifetime
- 2003-07-07 NZ NZ537723A patent/NZ537723A/en not_active IP Right Cessation
- 2003-07-07 DE DE60303951T patent/DE60303951T2/de not_active Expired - Lifetime
- 2003-07-07 JP JP2004522415A patent/JP2005533124A/ja not_active Abandoned
- 2003-07-07 WO PCT/EP2003/007251 patent/WO2004008854A1/fr not_active Ceased
- 2003-07-07 EA EA200500110A patent/EA007734B1/ru not_active IP Right Cessation
- 2003-07-07 AU AU2003249966A patent/AU2003249966B2/en not_active Ceased
- 2003-07-07 UA UAA200501487A patent/UA80145C2/uk unknown
- 2003-07-07 PL PL373463A patent/PL208076B1/pl not_active IP Right Cessation
- 2003-07-07 CN CNB038169568A patent/CN100334948C/zh not_active Expired - Lifetime
- 2003-07-07 EP EP03764947A patent/EP1538901B1/fr not_active Expired - Lifetime
- 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
CA2493382C (fr)	2012-05-15
MXPA05000752A (es)	2005-04-19
CA2493382A1 (fr)	2004-01-29
BR0312741B1 (pt)	2014-03-11
ATE319308T1 (de)	2006-03-15
EA007734B1 (ru)	2006-12-29
EP1538901A1 (fr)	2005-06-15
PL373463A1 (en)	2005-08-22
ES2258231T3 (es)	2006-08-16
EP1382247A1 (fr)	2004-01-21
DE60303951D1 (de)	2006-05-04
CN100334948C (zh)	2007-09-05
NZ537723A (en)	2006-09-29
US7060657B2 (en)	2006-06-13
US20040018940A1 (en)	2004-01-29
EP1538901B1 (fr)	2006-03-08
PL208076B1 (pl)	2011-03-31
ZA200410132B (en)	2006-07-26
AR040584A1 (es)	2005-04-13
MA27259A1 (fr)	2005-03-01
DE60303951T2 (de)	2006-09-28
CN1668192A (zh)	2005-09-14
JP2005533124A (ja)	2005-11-04
EA200500110A1 (ru)	2005-08-25
AU2003249966B2 (en)	2009-05-28
WO2004008854A1 (fr)	2004-01-29
AU2003249966A1 (en)	2004-02-09
BR0312741A (pt)	2005-04-26

Publication	Publication Date	Title
UA80145C2 (en)	2007-08-27	Cyclohexanedionoxyme herbicide-safener combination and use thereof
RU2342834C2 (ru)	2009-01-10	Комбинации арилоксифеноксипропионатов и средств защиты культур и их применение для повышения подавления сорной растительности
HUP0402105A2 (hu)	2005-02-28	Herbicid hatóanyagot és széfenert tartalmazó kombinációk
CN108697084B (zh)	2021-06-25	协同性除草组合物和控制不期望植物生长的方法
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TWI738710B (zh)	2021-09-11	協同性除草組合物
JPH06128106A (ja)	1994-05-10	除草剤組成物
EA009211B1 (ru)	2007-12-28	Синергические гербицидные средства, содержащие гербициды из группы бензоилпиразолов
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WO2023110491A1 (fr)	2023-06-22	Procédé de régulation de la végétation indésirable dans un environnement aquatique
TW201626893A (zh)	2016-08-01	除草組合物及控制植株生長的方法
JP2021070631A (ja)	2021-05-06	除草組成物
JPH09143006A (ja)	1997-06-03	除草剤の薬害軽減方法
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AU2006268972A1 (en)	2007-01-18	Cultigen-compatible herbicidal agents containing herbicides and acylsulfamoylbenzamide safeners