ZA200410132B - Combinations of cyclohexanedione oxime herbicides and safeners - Google Patents

Combinations of cyclohexanedione oxime herbicides and safeners Download PDF

Info

Publication number: ZA200410132B
Authority: ZA; South Africa
Prior art keywords: herbicide; alkyl; hydrogen; safener combination; safener
Prior art date: 2002-07-18

Application number

ZA200410132A

Other languages

English (en)

Inventor

Erwin Hacker

Hermann Bieringer

Hans P 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

2004-12-15

Publication date

2006-07-26

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=ZA200410132(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

2004-12-15 Application filed by Bayer Cropscience Gmbh filed Critical Bayer Cropscience Gmbh

2006-07-26 Publication of ZA200410132B publication Critical patent/ZA200410132B/en

Links

239000004009 herbicide Substances 0.000 title claims description 30
IEGRLEZDTRNPRH-UHFFFAOYSA-N 2-hydroxyiminocyclohexan-1-one Chemical compound ON=C1CCCCC1=O IEGRLEZDTRNPRH-UHFFFAOYSA-N 0.000 title claims description 13
230000002363 herbicidal effect Effects 0.000 claims description 23
229910052739 hydrogen Inorganic materials 0.000 claims description 23
239000001257 hydrogen Substances 0.000 claims description 23
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 21
150000003839 salts Chemical class 0.000 claims description 21
241000196324 Embryophyta Species 0.000 claims description 20
150000001875 compounds Chemical class 0.000 claims description 19
244000038559 crop plants Species 0.000 claims description 13
GGWHBJGBERXSLL-NBVRZTHBSA-N chembl113137 Chemical compound C1C(=O)C(C(=N/OCC)/CCC)=C(O)CC1C1CSCCC1 GGWHBJGBERXSLL-NBVRZTHBSA-N 0.000 claims description 8
150000004696 coordination complex Chemical class 0.000 claims description 8
230000000694 effects Effects 0.000 claims description 8
239000000203 mixture Substances 0.000 claims description 8
239000005497 Clethodim Substances 0.000 claims description 5
239000005501 Cycloxydim Substances 0.000 claims description 5
238000000034 method Methods 0.000 claims description 5
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 description 4
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 description 3
CSPPKDPQLUUTND-NBVRZTHBSA-N Sethoxydim Chemical compound CCO\N=C(/CCC)C1=C(O)CC(CC(C)SCC)CC1=O CSPPKDPQLUUTND-NBVRZTHBSA-N 0.000 claims description 3
239000005624 Tralkoxydim Substances 0.000 claims description 3
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 claims description 3
229910052801 chlorine Inorganic materials 0.000 claims description 3
230000000885 phytotoxic effect Effects 0.000 claims description 3
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 claims description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
229910052731 fluorine Inorganic materials 0.000 claims description 2
229910052736 halogen Inorganic materials 0.000 claims description 2
150000002367 halogens Chemical class 0.000 claims 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 claims 2
229910014585 C2-Ce Inorganic materials 0.000 claims 2
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 claims 2
231100000208 phytotoxic Toxicity 0.000 claims 2
238000009472 formulation Methods 0.000 claims 1
-1 alkali metal salts Chemical class 0.000 description 9
229910052751 metal Inorganic materials 0.000 description 6
239000002184 metal Substances 0.000 description 6
IOYNQIMAUDJVEI-BMVIKAAMSA-N Tepraloxydim Chemical compound C1C(=O)C(C(=N/OC\C=C\Cl)/CC)=C(O)CC1C1CCOCC1 IOYNQIMAUDJVEI-BMVIKAAMSA-N 0.000 description 4
150000001768 cations Chemical class 0.000 description 4
230000006378 damage Effects 0.000 description 4
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
240000008042 Zea mays Species 0.000 description 3
235000002017 Zea mays subsp mays Nutrition 0.000 description 3
150000003863 ammonium salts Chemical class 0.000 description 3
SILSDTWXNBZOGF-KUZBFYBWSA-N chembl111058 Chemical compound CCSC(C)CC1CC(O)=C(\C(CC)=N\OC\C=C\Cl)C(=O)C1 SILSDTWXNBZOGF-KUZBFYBWSA-N 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
150000003460 sulfonic acids Chemical class 0.000 description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
244000068988 Glycine max Species 0.000 description 2
235000010469 Glycine max Nutrition 0.000 description 2
240000005979 Hordeum vulgare Species 0.000 description 2
235000007340 Hordeum vulgare Nutrition 0.000 description 2
240000007594 Oryza sativa Species 0.000 description 2
235000007164 Oryza sativa Nutrition 0.000 description 2
235000021307 Triticum Nutrition 0.000 description 2
244000098338 Triticum aestivum Species 0.000 description 2
208000027418 Wounds and injury Diseases 0.000 description 2
235000005824 Zea mays ssp. parviglumis Nutrition 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
150000001412 amines Chemical class 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
150000001735 carboxylic acids Chemical class 0.000 description 2
235000005822 corn Nutrition 0.000 description 2
125000001188 haloalkyl group Chemical group 0.000 description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
208000014674 injury Diseases 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
150000002923 oximes Chemical class 0.000 description 2
239000000575 pesticide Substances 0.000 description 2
159000000001 potassium salts Chemical class 0.000 description 2
KRQUFUKTQHISJB-UHFFFAOYSA-N profoxydim Chemical compound OC=1CC(C2CSCCC2)CC(=O)C=1C(CCC)=NOCC(C)OC1=CC=C(Cl)C=C1 KRQUFUKTQHISJB-UHFFFAOYSA-N 0.000 description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
235000009566 rice Nutrition 0.000 description 2
159000000000 sodium salts Chemical class 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 description 1
125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 1
CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical class O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 description 1
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
240000002791 Brassica napus Species 0.000 description 1
235000006008 Brassica napus var napus Nutrition 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
239000005561 Glufosinate Substances 0.000 description 1
239000005562 Glyphosate Substances 0.000 description 1
244000299507 Gossypium hirsutum Species 0.000 description 1
235000003222 Helianthus annuus Nutrition 0.000 description 1
244000020551 Helianthus annuus Species 0.000 description 1
235000004431 Linum usitatissimum Nutrition 0.000 description 1
240000006240 Linum usitatissimum Species 0.000 description 1
240000004658 Medicago sativa Species 0.000 description 1
235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 1
244000061176 Nicotiana tabacum Species 0.000 description 1
235000002637 Nicotiana tabacum Nutrition 0.000 description 1
231100000674 Phytotoxicity Toxicity 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
235000021536 Sugar beet Nutrition 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
241001148683 Zostera marina Species 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
125000003282 alkyl amino group Chemical group 0.000 description 1
239000004411 aluminium Substances 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
239000005557 antagonist Substances 0.000 description 1
239000000729 antidote Substances 0.000 description 1
229940075522 antidotes Drugs 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
239000002738 chelating agent Substances 0.000 description 1
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 1
125000002587 enol group Chemical group 0.000 description 1
XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 1
229940097068 glyphosate Drugs 0.000 description 1
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000003815 herbicide antidote Substances 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
235000009973 maize Nutrition 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
DNXIASIHZYFFRO-UHFFFAOYSA-N pyrazoline Chemical compound C1CN=NC1 DNXIASIHZYFFRO-UHFFFAOYSA-N 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
241000894007 species Species 0.000 description 1
239000000126 substance Substances 0.000 description 1
235000011149 sulphuric acid Nutrition 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
239000010936 titanium Substances 0.000 description 1
229910052719 titanium Inorganic materials 0.000 description 1
230000009261 transgenic effect Effects 0.000 description 1
238000011282 treatment Methods 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 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
- 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)

ZA200410132A 2002-07-18 2004-12-15 Combinations of cyclohexanedione oxime herbicides and safeners ZA200410132B (en)

Applications Claiming Priority (1)

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

Publications (1)

Publication Number	Publication Date
ZA200410132B true ZA200410132B (en)	2006-07-26

Family

ID=29762654

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ZA200410132A ZA200410132B (en)	2002-07-18	2004-12-15	Combinations of cyclohexanedione oxime herbicides and safeners

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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* Cited by examiner, † Cited by third party
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EP1475370B1 (fr) *	2002-02-15	2009-08-05	Mitsui Chemicals, Inc.	Derive d'azole optiquement actif et procede de production de celui-ci
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 (fr) *	2005-10-28	2007-05-03	Valent U.S.A. Corporation	Compositions herbicides
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
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
WO2009089165A2 (fr) *	2008-01-07	2009-07-16	Auburn University	Combinaisons d'herbicides et de phytoprotecteurs
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
BRPI0921004B1 (pt) *	2008-11-24	2017-02-14	Dow Agrosciences Llc	composição para proteção de arroz com casca semeado e transplantado direto dos efeitos prejudiciais de um herbicida 6-(fenil trisubstituído 1)-4-amino-piridinacarboxilato, e método para proteção do referido arroz
GB201013009D0 (en) *	2010-08-02	2010-09-15	Syngenta Participations Ag	Agricultural method
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2003
- 2003-07-07 CN CNB038169568A patent/CN100334948C/zh not_active Expired - Lifetime
- 2003-07-07 AU AU2003249966A patent/AU2003249966B2/en not_active Ceased
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- 2003-07-07 PL PL373463A patent/PL208076B1/pl not_active IP Right Cessation
- 2003-07-07 NZ NZ537723A patent/NZ537723A/en not_active IP Right Cessation
- 2003-07-07 CA CA2493382A patent/CA2493382C/fr not_active Expired - Lifetime
- 2003-07-07 BR BRPI0312741-9A patent/BR0312741B1/pt active IP Right Grant
- 2003-07-07 DE DE60303951T patent/DE60303951T2/de not_active Expired - Lifetime
- 2003-07-07 EP EP03764947A patent/EP1538901B1/fr not_active Expired - Lifetime
- 2003-07-07 EA EA200500110A patent/EA007734B1/ru not_active IP Right Cessation
- 2003-07-07 JP JP2004522415A patent/JP2005533124A/ja not_active Abandoned
- 2003-07-07 AT AT03764947T patent/ATE319308T1/de not_active IP Right Cessation
- 2003-07-07 UA UAA200501487A patent/UA80145C2/uk unknown
- 2003-07-07 WO PCT/EP2003/007251 patent/WO2004008854A1/fr not_active Ceased
- 2003-07-07 MX MXPA05000752A patent/MXPA05000752A/es 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
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2005
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Also Published As

Publication number	Publication date
AR040584A1 (es)	2005-04-13
BR0312741B1 (pt)	2014-03-11
JP2005533124A (ja)	2005-11-04
US7060657B2 (en)	2006-06-13
PL373463A1 (en)	2005-08-22
NZ537723A (en)	2006-09-29
ES2258231T3 (es)	2006-08-16
UA80145C2 (en)	2007-08-27
ATE319308T1 (de)	2006-03-15
CA2493382A1 (fr)	2004-01-29
EP1382247A1 (fr)	2004-01-21
CN1668192A (zh)	2005-09-14
EP1538901B1 (fr)	2006-03-08
WO2004008854A1 (fr)	2004-01-29
DE60303951D1 (de)	2006-05-04
EA007734B1 (ru)	2006-12-29
DE60303951T2 (de)	2006-09-28
EA200500110A1 (ru)	2005-08-25
PL208076B1 (pl)	2011-03-31
AU2003249966B2 (en)	2009-05-28
MA27259A1 (fr)	2005-03-01
EP1538901A1 (fr)	2005-06-15
MXPA05000752A (es)	2005-04-19
CN100334948C (zh)	2007-09-05
BR0312741A (pt)	2005-04-26
US20040018940A1 (en)	2004-01-29
CA2493382C (fr)	2012-05-15
AU2003249966A1 (en)	2004-02-09

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