ZA200304588B - Herbicide-safener combination based on isoxozoline carboxylate safeners. - Google Patents
Herbicide-safener combination based on isoxozoline carboxylate safeners. Download PDFInfo
- Publication number
- ZA200304588B ZA200304588B ZA200304588A ZA200304588A ZA200304588B ZA 200304588 B ZA200304588 B ZA 200304588B ZA 200304588 A ZA200304588 A ZA 200304588A ZA 200304588 A ZA200304588 A ZA 200304588A ZA 200304588 B ZA200304588 B ZA 200304588B
- Authority
- ZA
- South Africa
- Prior art keywords
- alkyl
- safener
- herbicide
- alkoxy
- phenyl
- Prior art date
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- 150000007942 carboxylates Chemical class 0.000 title 1
- 239000004009 herbicide Substances 0.000 claims description 87
- 230000002363 herbicidal effect Effects 0.000 claims description 65
- 241000196324 Embryophyta Species 0.000 claims description 48
- 150000001875 compounds Chemical class 0.000 claims description 37
- 239000000203 mixture Substances 0.000 claims description 33
- -1 cyano, nitro, amino Chemical group 0.000 claims description 32
- 125000000217 alkyl group Chemical group 0.000 claims description 26
- 125000003545 alkoxy group Chemical group 0.000 claims description 22
- 150000003254 radicals Chemical class 0.000 claims description 21
- 244000038559 crop plants Species 0.000 claims description 20
- 150000003839 salts Chemical class 0.000 claims description 19
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 17
- 238000009472 formulation Methods 0.000 claims description 16
- 229910052736 halogen Inorganic materials 0.000 claims description 15
- 150000002367 halogens Chemical class 0.000 claims description 15
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 13
- 125000001188 haloalkyl group Chemical group 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 229910052739 hydrogen Inorganic materials 0.000 claims description 11
- 239000001257 hydrogen Substances 0.000 claims description 11
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 10
- 125000003282 alkyl amino group Chemical group 0.000 claims description 9
- 229930195733 hydrocarbon Natural products 0.000 claims description 9
- IRJQWZWMQCVOLA-DNTJNYDQSA-N 2-[(e)-n-[(3,5-difluorophenyl)carbamoylamino]-c-methylcarbonimidoyl]pyridine-3-carboxylic acid Chemical compound N=1C=CC=C(C(O)=O)C=1C(/C)=N/NC(=O)NC1=CC(F)=CC(F)=C1 IRJQWZWMQCVOLA-DNTJNYDQSA-N 0.000 claims description 8
- 239000004215 Carbon black (E152) Substances 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
- 239000004480 active ingredient Substances 0.000 claims description 8
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims description 8
- MWKVXOJATACCCH-UHFFFAOYSA-N isoxadifen-ethyl Chemical compound C1C(C(=O)OCC)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 MWKVXOJATACCCH-UHFFFAOYSA-N 0.000 claims description 8
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 7
- 150000002148 esters Chemical class 0.000 claims description 7
- 239000005504 Dicamba Substances 0.000 claims description 6
- MEFQWPUMEMWTJP-UHFFFAOYSA-N fluroxypyr Chemical compound NC1=C(Cl)C(F)=NC(OCC(O)=O)=C1Cl MEFQWPUMEMWTJP-UHFFFAOYSA-N 0.000 claims description 6
- ITGSCCPVERXFGN-UHFFFAOYSA-N isoxadifen Chemical compound C1C(C(=O)O)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 ITGSCCPVERXFGN-UHFFFAOYSA-N 0.000 claims description 6
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 claims description 6
- QZXATCCPQKOEIH-UHFFFAOYSA-N Florasulam Chemical compound N=1N2C(OC)=NC=C(F)C2=NC=1S(=O)(=O)NC1=C(F)C=CC=C1F QZXATCCPQKOEIH-UHFFFAOYSA-N 0.000 claims description 5
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims description 5
- 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 claims description 5
- FOXFZRUHNHCZPX-UHFFFAOYSA-N metribuzin Chemical compound CSC1=NN=C(C(C)(C)C)C(=O)N1N FOXFZRUHNHCZPX-UHFFFAOYSA-N 0.000 claims description 5
- JLYFCTQDENRSOL-UHFFFAOYSA-N 2-chloro-N-(2,4-dimethylthiophen-3-yl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound COCC(C)N(C(=O)CCl)C=1C(C)=CSC=1C JLYFCTQDENRSOL-UHFFFAOYSA-N 0.000 claims description 4
- 239000005492 Carfentrazone-ethyl Substances 0.000 claims description 4
- 239000005529 Florasulam Substances 0.000 claims description 4
- 239000005531 Flufenacet Substances 0.000 claims description 4
- 239000005558 Fluroxypyr Substances 0.000 claims description 4
- 239000005583 Metribuzin Substances 0.000 claims description 4
- 239000005627 Triclopyr Substances 0.000 claims description 4
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 4
- 125000005092 alkenyloxycarbonyl group Chemical group 0.000 claims description 4
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 4
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 4
- 125000004414 alkyl thio group Chemical group 0.000 claims description 4
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 4
- JLYFCTQDENRSOL-VIFPVBQESA-N dimethenamid-P Chemical compound COC[C@H](C)N(C(=O)CCl)C=1C(C)=CSC=1C JLYFCTQDENRSOL-VIFPVBQESA-N 0.000 claims description 4
- 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 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- 159000000000 sodium salts Chemical class 0.000 claims description 4
- DLFVBJFMPXGRIB-UHFFFAOYSA-N thioacetamide Natural products CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims description 4
- YWBFPKPWMSWWEA-UHFFFAOYSA-O triazolopyrimidine Chemical class BrC1=CC=CC(C=2N=C3N=CN[N+]3=C(NCC=3C=CN=CC=3)C=2)=C1 YWBFPKPWMSWWEA-UHFFFAOYSA-O 0.000 claims description 4
- 229910014585 C2-Ce Inorganic materials 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- DHQGPOIWDYSZML-UHFFFAOYSA-N 2-chloro-n-(2,4-diethylthiophen-3-yl)-n-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CSC(CC)=C1N(C(C)COC)C(=O)CCl DHQGPOIWDYSZML-UHFFFAOYSA-N 0.000 claims description 2
- VONWPEXRCLHKRJ-UHFFFAOYSA-N 2-chloro-n-phenylacetamide Chemical class ClCC(=O)NC1=CC=CC=C1 VONWPEXRCLHKRJ-UHFFFAOYSA-N 0.000 claims description 2
- 231100000674 Phytotoxicity Toxicity 0.000 claims description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 150000004702 methyl esters Chemical class 0.000 claims description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
- 125000006678 phenoxycarbonyl group Chemical group 0.000 claims description 2
- 229940124530 sulfonamide Drugs 0.000 claims 1
- 240000008042 Zea mays Species 0.000 description 22
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 21
- 230000006378 damage Effects 0.000 description 20
- 239000002689 soil Substances 0.000 description 19
- 239000000575 pesticide Substances 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 240000007594 Oryza sativa Species 0.000 description 12
- 235000007164 Oryza sativa Nutrition 0.000 description 12
- 230000000694 effects Effects 0.000 description 12
- 235000009566 rice Nutrition 0.000 description 12
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 10
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 10
- 235000005822 corn Nutrition 0.000 description 10
- 235000009973 maize Nutrition 0.000 description 10
- 240000005979 Hordeum vulgare Species 0.000 description 9
- 235000007340 Hordeum vulgare Nutrition 0.000 description 9
- 208000027418 Wounds and injury Diseases 0.000 description 9
- 208000014674 injury Diseases 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- 241000209140 Triticum Species 0.000 description 8
- 235000021307 Triticum Nutrition 0.000 description 8
- 235000013339 cereals Nutrition 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 239000004562 water dispersible granule Substances 0.000 description 7
- 239000011575 calcium Substances 0.000 description 6
- 239000004495 emulsifiable concentrate Substances 0.000 description 6
- 239000000729 antidote Substances 0.000 description 5
- 239000003995 emulsifying agent Substances 0.000 description 5
- 239000008187 granular material Substances 0.000 description 5
- 238000000227 grinding Methods 0.000 description 5
- 239000002917 insecticide Substances 0.000 description 5
- WVQBLGZPHOPPFO-LBPRGKRZSA-N (S)-metolachlor Chemical compound CCC1=CC=CC(C)=C1N([C@@H](C)COC)C(=O)CCl WVQBLGZPHOPPFO-LBPRGKRZSA-N 0.000 description 4
- 235000006008 Brassica napus var napus Nutrition 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 244000299507 Gossypium hirsutum Species 0.000 description 4
- 239000005617 S-Metolachlor Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 125000003342 alkenyl group Chemical group 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 239000003112 inhibitor Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 229920000151 polyglycol Polymers 0.000 description 4
- 239000010695 polyglycol Substances 0.000 description 4
- 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
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 3
- 244000068988 Glycine max Species 0.000 description 3
- 235000010469 Glycine max Nutrition 0.000 description 3
- 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 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 235000021536 Sugar beet Nutrition 0.000 description 3
- 125000000304 alkynyl group Chemical group 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
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- 230000012010 growth Effects 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 239000003621 irrigation water Substances 0.000 description 3
- 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 3
- 231100001184 nonphytotoxic Toxicity 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
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- CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical class O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 description 2
- ZYDBNGULYNHMSF-UHFFFAOYSA-N 4,5-dihydro-1,2-oxazole-3-carboxylic acid Chemical compound OC(=O)C1=NOCC1 ZYDBNGULYNHMSF-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
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- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
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- DHQGPOIWDYSZML-JTQLQIEISA-N 2-chloro-n-(2,4-diethylthiophen-3-yl)-n-[(2s)-1-methoxypropan-2-yl]acetamide Chemical compound CCC1=CSC(CC)=C1N([C@@H](C)COC)C(=O)CCl DHQGPOIWDYSZML-JTQLQIEISA-N 0.000 description 1
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- NGBMMSDIZNGAOK-UHFFFAOYSA-N 2h-triazolo[4,5-d]pyrimidine-5-sulfonamide Chemical class NS(=O)(=O)C1=NC=C2NN=NC2=N1 NGBMMSDIZNGAOK-UHFFFAOYSA-N 0.000 description 1
- FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical compound COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 1
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- WEQPBCSPRXFQQS-UHFFFAOYSA-N 4,5-dihydro-1,2-oxazole Chemical compound C1CC=NO1 WEQPBCSPRXFQQS-UHFFFAOYSA-N 0.000 description 1
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- HRBKVYFZANMGRE-UHFFFAOYSA-N chlorpyrifos-methyl Chemical compound COP(=S)(OC)OC1=NC(Cl)=C(Cl)C=C1Cl HRBKVYFZANMGRE-UHFFFAOYSA-N 0.000 description 1
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- IBBMAWULFFBRKK-UHFFFAOYSA-N picolinamide Chemical class NC(=O)C1=CC=CC=N1 IBBMAWULFFBRKK-UHFFFAOYSA-N 0.000 description 1
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- PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-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
- 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
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
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| EP01102222 | 2001-01-31 |
Publications (1)
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|---|---|
| ZA200304588B true ZA200304588B (en) | 2004-07-19 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200304588A ZA200304588B (en) | 2001-01-31 | 2003-06-12 | Herbicide-safener combination based on isoxozoline carboxylate safeners. |
Country Status (17)
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|---|---|
| US (2) | US20040106518A1 (pl) |
| EP (1) | EP1365649B1 (pl) |
| JP (1) | JP4476547B2 (pl) |
| CN (1) | CN1243474C (pl) |
| AT (1) | ATE357139T1 (pl) |
| AU (1) | AU2002242701B2 (pl) |
| BR (1) | BR0206799B1 (pl) |
| CA (1) | CA2435761C (pl) |
| DE (1) | DE60218986T2 (pl) |
| ES (1) | ES2280508T3 (pl) |
| HU (1) | HUP0303981A3 (pl) |
| MX (1) | MXPA03006879A (pl) |
| PL (2) | PL207109B1 (pl) |
| RU (1) | RU2351132C2 (pl) |
| UA (1) | UA77407C2 (pl) |
| WO (1) | WO2002060255A2 (pl) |
| ZA (1) | ZA200304588B (pl) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003103394A2 (en) | 2002-06-08 | 2003-12-18 | Bayer Cropscience Gmbh | Combinations of herbicidal aromatic carboxylic acids and safeners |
| DE102004035137A1 (de) * | 2004-07-20 | 2006-02-16 | Bayer Cropscience Gmbh | Wirkstoffe zur Steigerung der Pathogenabwehr in Pflanzen und Methoden zu ihrer Auffindung |
| WO2006065815A1 (en) * | 2004-12-14 | 2006-06-22 | Bayer Cropscience Lp | Methods for increasing maize yields |
| GB0505645D0 (en) * | 2005-03-18 | 2005-04-27 | Syngenta Participations Ag | Herbicidal composition |
| WO2008092615A2 (en) * | 2007-01-29 | 2008-08-07 | Syngenta Participations Ag | Herbicidal composition |
| WO2009089165A2 (en) * | 2008-01-07 | 2009-07-16 | Auburn University | Combinations of herbicides and safeners |
| AU2009212525B2 (en) * | 2008-02-05 | 2012-06-21 | Arysta Lifescience North America, Llc | Solid formulation of low melting active compound |
| EP2092825A1 (de) | 2008-02-21 | 2009-08-26 | Bayer CropScience Aktiengesellschaft | Herbizid-Kombinationen enthaltend ein Herbizid der Klasse der Diamino-s-triazine |
| BR112012016866A2 (pt) * | 2010-01-07 | 2015-09-01 | Dow Agrosciences Llc | Tiazolo[5,4-d]pirimidinas e seu uso como agroquímicos. |
| ME03323B (me) | 2012-02-06 | 2019-10-20 | Merial Inc | Paraziticidne oralne veterinarske kompozicije koje sadrže sistemski djelujuća aktivna sredstva, metodi i primjene istih |
| JP6088637B2 (ja) | 2012-04-04 | 2017-03-01 | インターベット インターナショナル ベー． フェー． | イソオキサゾリン化合物のための固形経口医薬組成物 |
| UA117810C2 (uk) | 2012-05-24 | 2018-10-10 | Байєр Кропсайєнс Акцієнгезелльшафт | Гербіцидні композиції, які містять n-(тетразол-5-іл)арилкарбоксаміди |
| UA118765C2 (uk) | 2013-08-09 | 2019-03-11 | Байєр Кропсайєнс Акцієнгезелльшафт | Третинні гербіцидні комбінації, що містять дві сульфонілсечовини |
| KR20160077073A (ko) | 2013-10-25 | 2016-07-01 | 바이엘 크롭사이언스 악티엔게젤샤프트 | N-(1,3,4-옥사디아졸-2-일)-아릴 카르복실산 아미드를 함유하는 제초제 조성물 |
| US20190116791A1 (en) * | 2016-03-15 | 2019-04-25 | Fmc Corporation | Use of safeners with ppo inhibitor herbicides |
| CN105941444A (zh) * | 2016-05-20 | 2016-09-21 | 潍坊中农联合化工有限公司 | 氟吡草腙与麦草畏复配除草剂 |
| RU2726431C1 (ru) * | 2019-06-06 | 2020-07-14 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Кубанский государственный аграрный университет имени И.Т. Трубилина" | (4,6-Диметилтриазоло-[1,5-a]пиримидил-2-сульфанил)-2-трифторацетанилид в качестве регулятора роста кукурузы |
| CN114554847A (zh) * | 2019-09-27 | 2022-05-27 | 阿肯色大学董事会 | 保护水稻免受第15组除草剂的伤害 |
| BR102020019865A2 (pt) * | 2020-09-28 | 2022-04-12 | Upl Do Brasil Industria E Comercio De Insumos Agropecuarios S.A. | Combinações de herbicidas triazinona com fitoprotetores |
Family Cites Families (12)
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| ES2149764T3 (es) * | 1991-04-15 | 2000-11-16 | Aventis Cropscience Gmbh | Agentes protectores de plantas que contienen isoxazolinas o isotiazolinas, nuevas isoxazolinas e isotiazolinas y procedimiento para su preparacion. |
| DE4331448A1 (de) * | 1993-09-16 | 1995-03-23 | Hoechst Schering Agrevo Gmbh | Substituierte Isoxazoline, Verfahren zu deren Herstellung, diese enthaltende Mittel und deren Verwendung als Safener |
| DE19638233A1 (de) * | 1996-09-19 | 1998-03-26 | Hoechst Schering Agrevo Gmbh | Kombinationen aus Sulfonylharnstoff-Herbiziden und Safenern |
| DE19832017A1 (de) * | 1998-07-16 | 2000-01-27 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel mit substituierten Phenylsulfonylharnstoffen zur Unkrautbekämpfung in Reis |
| ATE294501T1 (de) * | 1998-07-16 | 2005-05-15 | Bayer Cropscience Gmbh | Herbizide mittel |
| WO2000008932A1 (de) * | 1998-08-13 | 2000-02-24 | Aventis Cropscience Gmbh | Herbizide mittel mit acylierten aminophenylsulfonylharnstoffen |
| DE19853827A1 (de) * | 1998-11-21 | 2000-05-25 | Aventis Cropscience Gmbh | Kombinationen aus Herbiziden und Safenern |
| HU230234B1 (hu) * | 1999-09-08 | 2015-10-28 | Aventis Cropscience Uk Ltd. | Új herbicid készítmények |
| BR0014670A (pt) * | 1999-09-30 | 2002-06-18 | Bayer Ag | Herbicidas seletivos na base de n-aril-triazolin(ti)onas |
| DE19947918A1 (de) * | 1999-10-06 | 2001-04-12 | Bayer Ag | Selektive Herbizide auf Basis von Pyrimidin-Derivaten |
| CZ20021693A3 (cs) * | 1999-11-17 | 2002-08-14 | Bayer Aktiengesellschaft | Selektivní herbicidy na bázi 2,6-disubstituovaných derivátů pyridinů a jejich pouľití |
| DE19955662B4 (de) * | 1999-11-19 | 2011-03-31 | Arysta LifeScience North America, | Herbizide auf Basis von Carbamoyltriazolinon |
-
2002
- 2002-01-31 AU AU2002242701A patent/AU2002242701B2/en not_active Expired
- 2002-01-31 JP JP2002560461A patent/JP4476547B2/ja not_active Expired - Lifetime
- 2002-01-31 UA UA2003088107A patent/UA77407C2/uk unknown
- 2002-01-31 DE DE60218986T patent/DE60218986T2/de not_active Expired - Lifetime
- 2002-01-31 WO PCT/EP2002/001002 patent/WO2002060255A2/en active IP Right Grant
- 2002-01-31 MX MXPA03006879A patent/MXPA03006879A/es active IP Right Grant
- 2002-01-31 CA CA2435761A patent/CA2435761C/en not_active Expired - Lifetime
- 2002-01-31 EP EP02708323A patent/EP1365649B1/en not_active Expired - Lifetime
- 2002-01-31 PL PL366801A patent/PL207109B1/pl unknown
- 2002-01-31 BR BRPI0206799-4A patent/BR0206799B1/pt active IP Right Grant
- 2002-01-31 US US10/470,509 patent/US20040106518A1/en not_active Abandoned
- 2002-01-31 RU RU2003126585/04A patent/RU2351132C2/ru active
- 2002-01-31 ES ES02708323T patent/ES2280508T3/es not_active Expired - Lifetime
- 2002-01-31 PL PL388370A patent/PL208071B1/pl unknown
- 2002-01-31 AT AT02708323T patent/ATE357139T1/de not_active IP Right Cessation
- 2002-01-31 CN CN02803476.7A patent/CN1243474C/zh not_active Expired - Lifetime
- 2002-01-31 HU HU0303981A patent/HUP0303981A3/hu unknown
-
2003
- 2003-06-12 ZA ZA200304588A patent/ZA200304588B/en unknown
-
2005
- 2005-03-29 US US11/093,658 patent/US7098169B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| BR0206799B1 (pt) | 2013-05-28 |
| CN1484491A (zh) | 2004-03-24 |
| US20040106518A1 (en) | 2004-06-03 |
| UA77407C2 (en) | 2006-12-15 |
| EP1365649B1 (en) | 2007-03-21 |
| MXPA03006879A (es) | 2003-11-13 |
| WO2002060255A3 (en) | 2003-01-09 |
| HUP0303981A2 (hu) | 2004-03-29 |
| ES2280508T3 (es) | 2007-09-16 |
| CN1243474C (zh) | 2006-03-01 |
| ATE357139T1 (de) | 2007-04-15 |
| EP1365649A2 (en) | 2003-12-03 |
| CA2435761A1 (en) | 2002-08-08 |
| PL207109B1 (pl) | 2010-11-30 |
| HUP0303981A3 (en) | 2012-10-29 |
| RU2351132C2 (ru) | 2009-04-10 |
| JP4476547B2 (ja) | 2010-06-09 |
| US7098169B2 (en) | 2006-08-29 |
| BR0206799A (pt) | 2004-02-03 |
| RU2003126585A (ru) | 2005-02-27 |
| CA2435761C (en) | 2011-08-30 |
| DE60218986T2 (de) | 2007-12-13 |
| JP2004517154A (ja) | 2004-06-10 |
| WO2002060255A2 (en) | 2002-08-08 |
| DE60218986D1 (de) | 2007-05-03 |
| PL208071B1 (pl) | 2011-03-31 |
| AU2002242701B2 (en) | 2008-04-03 |
| US20050170963A1 (en) | 2005-08-04 |
| PL366801A1 (pl) | 2005-02-07 |
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