ZA200005053B - Synergistic herbicidal agents based on leaf herbicides containing phosphorus, imidazolinones and hormone weed-killers. - Google Patents
Synergistic herbicidal agents based on leaf herbicides containing phosphorus, imidazolinones and hormone weed-killers. Download PDFInfo
- Publication number
- ZA200005053B ZA200005053B ZA200005053A ZA200005053A ZA200005053B ZA 200005053 B ZA200005053 B ZA 200005053B ZA 200005053 A ZA200005053 A ZA 200005053A ZA 200005053 A ZA200005053 A ZA 200005053A ZA 200005053 B ZA200005053 B ZA 200005053B
- Authority
- ZA
- South Africa
- Prior art keywords
- herbicides
- salts
- esters
- glufosinate
- group
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title claims description 67
- CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical class O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 title claims description 9
- 230000002195 synergetic effect Effects 0.000 title claims description 8
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 title claims description 3
- 239000011574 phosphorus Substances 0.000 title claims 2
- 229910052698 phosphorus Inorganic materials 0.000 title claims 2
- 239000005556 hormone Substances 0.000 title 1
- 229940088597 hormone Drugs 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims description 37
- 239000000203 mixture Substances 0.000 claims description 36
- 150000003839 salts Chemical class 0.000 claims description 32
- 230000002363 herbicidal effect Effects 0.000 claims description 30
- 150000002148 esters Chemical class 0.000 claims description 21
- 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 claims description 14
- 239000005562 Glyphosate Substances 0.000 claims description 13
- 238000009472 formulation Methods 0.000 claims description 12
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims description 9
- 229940097068 glyphosate Drugs 0.000 claims description 8
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 claims description 6
- CLQMBPJKHLGMQK-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)nicotinic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=CC=C1C(O)=O CLQMBPJKHLGMQK-UHFFFAOYSA-N 0.000 claims description 6
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 claims description 6
- RUCAXVJJQQJZGU-UHFFFAOYSA-M hydron;2-(phosphonatomethylamino)acetate;trimethylsulfanium Chemical compound C[S+](C)C.OP(O)(=O)CNCC([O-])=O RUCAXVJJQQJZGU-UHFFFAOYSA-M 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 239000005574 MCPA Substances 0.000 claims description 5
- GINJFDRNADDBIN-FXQIFTODSA-N bilanafos Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCP(C)(O)=O GINJFDRNADDBIN-FXQIFTODSA-N 0.000 claims description 5
- XZIDTOHMJBOSOX-UHFFFAOYSA-N 2,3,6-TBA Chemical compound OC(=O)C1=C(Cl)C=CC(Cl)=C1Cl XZIDTOHMJBOSOX-UHFFFAOYSA-N 0.000 claims description 4
- YIVXMZJTEQBPQO-UHFFFAOYSA-N 2,4-DB Chemical compound OC(=O)CCCOC1=CC=C(Cl)C=C1Cl YIVXMZJTEQBPQO-UHFFFAOYSA-N 0.000 claims description 4
- 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 claims description 4
- LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 claims description 4
- 239000005575 MCPB Substances 0.000 claims description 4
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 claims description 4
- IAJOBQBIJHVGMQ-BYPYZUCNSA-N glufosinate-P Chemical compound CP(O)(=O)CC[C@H](N)C(O)=O IAJOBQBIJHVGMQ-BYPYZUCNSA-N 0.000 claims description 4
- WNTGYJSOUMFZEP-SSDOTTSWSA-N (R)-mecoprop Chemical compound OC(=O)[C@@H](C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-SSDOTTSWSA-N 0.000 claims description 3
- 239000002794 2,4-DB Substances 0.000 claims description 3
- MZHCENGPTKEIGP-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-UHFFFAOYSA-N 0.000 claims description 3
- KFEFNHNXZQYTEW-UHFFFAOYSA-N 2-(4-isopropyl-4-methyl-5-oxo-4,5-dihydro-1H-imidazol-2-yl)-4-methylbenzoic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=CC(C)=CC=C1C(O)=O KFEFNHNXZQYTEW-UHFFFAOYSA-N 0.000 claims description 3
- 239000005504 Dicamba Substances 0.000 claims description 3
- XVOKUMIPKHGGTN-UHFFFAOYSA-N Imazethapyr Chemical compound OC(=O)C1=CC(CC)=CN=C1C1=NC(C)(C(C)C)C(=O)N1 XVOKUMIPKHGGTN-UHFFFAOYSA-N 0.000 claims description 3
- 101150039283 MCPB gene Proteins 0.000 claims description 3
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims description 3
- MZHCENGPTKEIGP-RXMQYKEDSA-N (R)-dichlorprop Chemical compound OC(=O)[C@@H](C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-RXMQYKEDSA-N 0.000 claims description 2
- 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 claims description 2
- CABMTIJINOIHOD-UHFFFAOYSA-N 2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]quinoline-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC2=CC=CC=C2C=C1C(O)=O CABMTIJINOIHOD-UHFFFAOYSA-N 0.000 claims description 2
- 239000005505 Dichlorprop-P Substances 0.000 claims description 2
- 239000005566 Imazamox Substances 0.000 claims description 2
- 239000005981 Imazaquin Substances 0.000 claims description 2
- 239000005576 Mecoprop-P Substances 0.000 claims description 2
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 2
- RTWIRLHWLMNVCC-WQYNNSOESA-M sodium (2S)-2-[[(2S)-2-[[(2S)-2-amino-4-[hydroxy(methyl)phosphoryl]butanoyl]amino]propanoyl]amino]propanoate Chemical compound [Na+].[O-]C(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCP(C)(O)=O RTWIRLHWLMNVCC-WQYNNSOESA-M 0.000 claims description 2
- YWICANUUQPYHOW-UHFFFAOYSA-M sodium;2-(phosphonomethylamino)acetate Chemical compound [Na+].OP(O)(=O)CNCC([O-])=O YWICANUUQPYHOW-UHFFFAOYSA-M 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims 1
- RFOHRSIAXQACDB-UHFFFAOYSA-M sodium;2-(2,4-dichlorophenoxy)acetate Chemical compound [Na+].[O-]C(=O)COC1=CC=C(Cl)C=C1Cl RFOHRSIAXQACDB-UHFFFAOYSA-M 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 20
- 239000005561 Glufosinate Substances 0.000 description 10
- 230000000694 effects Effects 0.000 description 10
- -1 ether sulfates Chemical class 0.000 description 5
- 239000002689 soil Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000003995 emulsifying agent Substances 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 239000000575 pesticide Substances 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 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
- 239000013543 active substance Substances 0.000 description 3
- 239000004495 emulsifiable concentrate Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 150000002191 fatty alcohols Chemical class 0.000 description 3
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- 241001253168 Asystasia Species 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 241000209504 Poaceae Species 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
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- 150000002170 ethers Chemical class 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
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- 230000002349 favourable effect Effects 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- 239000002563 ionic surfactant Substances 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 125000005328 phosphinyl group Chemical group [PH2](=O)* 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
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- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 1
- ZBMRKNMTMPPMMK-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid;azane Chemical compound [NH4+].CP(O)(=O)CCC(N)C([O-])=O ZBMRKNMTMPPMMK-UHFFFAOYSA-N 0.000 description 1
- PVSGXWMWNRGTKE-UHFFFAOYSA-N 5-methyl-2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]pyridine-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=C(C)C=C1C(O)=O PVSGXWMWNRGTKE-UHFFFAOYSA-N 0.000 description 1
- 244000296912 Ageratum conyzoides Species 0.000 description 1
- 235000004405 Ageratum conyzoides Nutrition 0.000 description 1
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- 244000099147 Ananas comosus Species 0.000 description 1
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- 244000049532 Axonopus compressus Species 0.000 description 1
- 241000339490 Brachyachne Species 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
- 241000132536 Cirsium Species 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- 241001655719 Clidemia Species 0.000 description 1
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- 101100377706 Escherichia phage T5 A2.2 gene Proteins 0.000 description 1
- PDYXIVPKOMYDOK-UHFFFAOYSA-N Glyphosate-monoammonium Chemical compound [NH4+].OC(=O)CNCP(O)([O-])=O PDYXIVPKOMYDOK-UHFFFAOYSA-N 0.000 description 1
- 241000219146 Gossypium Species 0.000 description 1
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- 241000069499 Ottochloa Species 0.000 description 1
- 241000069501 Ottochloa nodosa Species 0.000 description 1
- 241000209117 Panicum Species 0.000 description 1
- 244000236458 Panicum colonum Species 0.000 description 1
- 235000015225 Panicum colonum Nutrition 0.000 description 1
- 235000006443 Panicum miliaceum subsp. miliaceum Nutrition 0.000 description 1
- 235000009037 Panicum miliaceum subsp. ruderale Nutrition 0.000 description 1
- 241001330453 Paspalum Species 0.000 description 1
- 241000209046 Pennisetum Species 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 241000219053 Rumex Species 0.000 description 1
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- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
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- 239000000654 additive Substances 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
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- 150000001412 amines Chemical class 0.000 description 1
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- 238000009835 boiling Methods 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
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- 235000013399 edible fruits Nutrition 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002194 fatty esters Chemical class 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
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- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical class CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
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- 229920000570 polyether Polymers 0.000 description 1
- 229920001522 polyglycol ester Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 229920005552 sodium lignosulfonate Polymers 0.000 description 1
- KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 1
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- YRYSAWZMIRQUBO-UHFFFAOYSA-N trimethylsulfoxonium Chemical compound C[S+](C)(C)=O YRYSAWZMIRQUBO-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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (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)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19815820A DE19815820A1 (de) | 1998-04-08 | 1998-04-08 | Synergistische herbizide Mittel auf Basis von phosphorhaltigen Blattherbiziden, Imidazolinonen und Wuchsstoffherbiziden |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200005053B true ZA200005053B (en) | 2001-11-27 |
Family
ID=7864040
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200005053A ZA200005053B (en) | 1998-04-08 | 2000-09-21 | Synergistic herbicidal agents based on leaf herbicides containing phosphorus, imidazolinones and hormone weed-killers. |
Country Status (23)
Country | Link |
---|---|
US (1) | US6436874B1 (fr) |
EP (1) | EP1069826B1 (fr) |
JP (1) | JP4563580B2 (fr) |
KR (1) | KR100738764B1 (fr) |
CN (1) | CN1119079C (fr) |
AP (1) | AP1064A (fr) |
AR (1) | AR016459A1 (fr) |
AU (1) | AU763130B2 (fr) |
BR (1) | BR9909464A (fr) |
CA (1) | CA2327732C (fr) |
CO (1) | CO5050302A1 (fr) |
DE (2) | DE19815820A1 (fr) |
ES (1) | ES2193697T3 (fr) |
ID (1) | ID28939A (fr) |
IL (1) | IL138835A (fr) |
MY (1) | MY123468A (fr) |
NZ (1) | NZ507379A (fr) |
OA (1) | OA12190A (fr) |
PT (1) | PT1069826E (fr) |
TR (1) | TR200002903T2 (fr) |
TW (1) | TW490289B (fr) |
WO (1) | WO1999052367A1 (fr) |
ZA (1) | ZA200005053B (fr) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19836684A1 (de) * | 1998-08-13 | 2000-02-17 | Hoechst Schering Agrevo Gmbh | Herbizide Mittel für tolerante oder resistente Reiskulturen |
ES2215886T3 (es) * | 2000-03-27 | 2004-10-16 | Basf Aktiengesellschaft | Metodo y composiciones herbicidas sinergicos. |
BRPI0508542B1 (pt) * | 2004-03-10 | 2014-09-16 | Monsanto Technology Llc | Composições de concentrado herbicida compreendendo glifosato e herbicida auxina |
RU2372777C2 (ru) * | 2004-03-12 | 2009-11-20 | Фмк Корпорейшн | Композиции глифосата |
AU2013201552B2 (en) * | 2007-06-29 | 2015-01-15 | Corteva Agriscience Llc | Synergistic herbicidal composition containing a substituted phenoxy alkanoic acid derivative and a glyphosate derivative |
ES2412258T3 (es) * | 2007-06-29 | 2013-07-10 | Dow Agrosciences Llc | Composición herbicida sinérgica que contiene un derivado de ácido fenoxi alcanoico sustituido y un derivado de glifosato. |
ES2588369T3 (es) * | 2011-04-27 | 2016-11-02 | Dow Agrosciences Llc | Método para mitigar las malas hierbas en un campo de plantas de algodón |
UY39627A (es) | 2011-10-26 | 2022-03-31 | Monsanto Technology Llc | Sales de herbicidas de ácido carboxílico |
AR091268A1 (es) | 2012-06-04 | 2015-01-21 | Monsanto Technology Llc | Composiciones herbicidas concentradas acuosas que contienen sales de glifosato y sales de dicamba |
CA3120042C (fr) | 2012-11-05 | 2024-02-27 | Monsanto Technology Llc | Compositions herbicides a faible volatilite comprenant un herbicide de type auxine et un acide monocarboxylique ou un monocarboxylate de celui-ci |
TR201815726T4 (tr) | 2013-02-27 | 2018-11-21 | Monsanto Technology Llc | Geliştirilmiş bir uçuculuğa sahip glifosat ve dikamba tank karışımlar. |
US10492490B2 (en) * | 2015-03-06 | 2019-12-03 | Board Of Trustees Of Michigan State University | Adjuvant compositions and related methods for reducing herbicide volatility |
BR122023020914A2 (pt) | 2017-08-09 | 2024-01-09 | Basf Se | Uso de uma mistura herbicida, mistura pesticida, composição pesticida e método para controlar a vegetação indesejável |
AU2018314499A1 (en) | 2017-08-09 | 2020-02-13 | Basf Se | Herbicidal mixtures comprising L-glufosinate and their use in canola cultures |
EP3440939A1 (fr) | 2017-08-09 | 2019-02-13 | Basf Se | Mélanges herbicides comprenant du l-glufosinate |
WO2019030088A1 (fr) | 2017-08-09 | 2019-02-14 | Basf Se | Mélanges herbicides comprenant du l-glufosinate et leur utilisation dans des cultures céréalières |
WO2019030090A1 (fr) | 2017-08-09 | 2019-02-14 | Basf Se | Mélanges herbicides comprenant du l-glufosinate et leur utilisation dans des cultures de riz |
BR112020002666A2 (pt) | 2017-08-09 | 2020-07-28 | Basf Se | uso de mistura de herbicidas, mistura de pesticidas, composição pesticida e método de controle da vegetação |
WO2019030089A1 (fr) | 2017-08-09 | 2019-02-14 | Basf Se | Mélanges herbicides comprenant du l-glufosinate ou son sel et au moins un inhibiteur de als |
WO2019030103A1 (fr) * | 2017-08-09 | 2019-02-14 | Basf Se | Mélanges herbicides comprenant du l-glufosinate ou son sel et au moins un herbicide auxinique |
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JPS5839127B2 (ja) * | 1978-03-09 | 1983-08-27 | 明治製菓株式会社 | 除草剤組成物 |
JPS59484B2 (ja) * | 1978-03-30 | 1984-01-07 | 明治製菓株式会社 | 除草剤組成物 |
JPS5492627A (en) * | 1977-12-28 | 1979-07-23 | Meiji Seika Kaisha Ltd | Herbicidal composition |
GB2011416B (en) * | 1977-12-28 | 1982-10-20 | Meiji Seika Kaisha | Herbicidal compositions |
HU182980B (en) * | 1979-12-28 | 1984-03-28 | Nitrokemia Ipartelepek | Concentrates and spray solutions containing n-bracket-phosphono-methyl-bracket closed-glycine |
EP0252237B1 (fr) * | 1986-05-09 | 1991-07-03 | Hoechst Aktiengesellschaft | Agents herbicides |
JPS6341407A (ja) * | 1986-08-08 | 1988-02-22 | 明治製菓株式会社 | 除草剤組成物 |
NZ231897A (en) * | 1988-12-30 | 1992-09-25 | Monsanto Co | Dry water-soluble granular composition comprising glyphosate and a liquid surfactant |
FR2644036B1 (fr) * | 1989-03-07 | 1992-01-17 | Rhone Poulenc Agrochimie | Combine herbicide constitue d'un emballage polymere hydrosoluble et d'un herbicide contenant de la n-phosphonomethylglycine |
FR2648316A1 (fr) | 1989-06-20 | 1990-12-21 | Rhone Poulenc Agrochimie | Compositions herbicides a base de n-phosphonomethylglycine et leur utilisation |
US5525578A (en) * | 1989-11-21 | 1996-06-11 | Hoechst Aktiengesellschaft | Herbicidal agents containing imidazole herbicide and ether sulfate surfactants |
DE3938564A1 (de) | 1989-11-21 | 1991-05-23 | Hoechst Ag | Herbizide mittel |
EP0568635B1 (fr) * | 1991-01-24 | 1997-03-19 | Monsanto Company | Formulations ameliorees a base de glyphosate |
DE59310333D1 (de) | 1992-05-15 | 2003-04-17 | Bayer Cropscience Gmbh | Synergistisch wirksame Herbizidkombinationen |
US5481258A (en) * | 1993-08-11 | 1996-01-02 | Glenayre Electronics, Inc. | Method and apparatus for coordinating clocks in a simulcast network |
DE4432888A1 (de) * | 1994-09-15 | 1996-03-21 | Bayer Ag | Verwendung von Aryluracilen im semi- und nicht-selektiven Bereich der Unkrautbekämpfung |
US5696024A (en) * | 1995-06-06 | 1997-12-09 | American Cyanmid | Herbicidal water soluble granular compositions |
-
1998
- 1998-04-08 DE DE19815820A patent/DE19815820A1/de not_active Withdrawn
-
1999
- 1999-03-30 DE DE59904334T patent/DE59904334D1/de not_active Expired - Lifetime
- 1999-03-30 IL IL13883599A patent/IL138835A/xx not_active IP Right Cessation
- 1999-03-30 AP APAP/P/2000/001976A patent/AP1064A/en active
- 1999-03-30 KR KR1020007011187A patent/KR100738764B1/ko not_active IP Right Cessation
- 1999-03-30 ES ES99917925T patent/ES2193697T3/es not_active Expired - Lifetime
- 1999-03-30 NZ NZ507379A patent/NZ507379A/en unknown
- 1999-03-30 TR TR2000/02903T patent/TR200002903T2/xx unknown
- 1999-03-30 PT PT99917925T patent/PT1069826E/pt unknown
- 1999-03-30 EP EP99917925A patent/EP1069826B1/fr not_active Expired - Lifetime
- 1999-03-30 US US09/647,830 patent/US6436874B1/en not_active Expired - Fee Related
- 1999-03-30 OA OA00000276A patent/OA12190A/fr unknown
- 1999-03-30 AU AU36030/99A patent/AU763130B2/en not_active Ceased
- 1999-03-30 CN CN99804590A patent/CN1119079C/zh not_active Expired - Fee Related
- 1999-03-30 CA CA002327732A patent/CA2327732C/fr not_active Expired - Fee Related
- 1999-03-30 WO PCT/EP1999/002187 patent/WO1999052367A1/fr active IP Right Grant
- 1999-03-30 BR BR9909464-9A patent/BR9909464A/pt not_active Application Discontinuation
- 1999-03-30 ID IDW20002008A patent/ID28939A/id unknown
- 1999-03-30 JP JP2000542989A patent/JP4563580B2/ja not_active Expired - Fee Related
- 1999-04-06 CO CO99019908A patent/CO5050302A1/es unknown
- 1999-04-06 AR ARP990101557A patent/AR016459A1/es active IP Right Grant
- 1999-04-07 MY MYPI99001334A patent/MY123468A/en unknown
- 1999-04-08 TW TW088105612A patent/TW490289B/zh not_active IP Right Cessation
-
2000
- 2000-09-21 ZA ZA200005053A patent/ZA200005053B/en unknown
Also Published As
Publication number | Publication date |
---|---|
KR20010052242A (ko) | 2001-06-25 |
ES2193697T3 (es) | 2003-11-01 |
US6436874B1 (en) | 2002-08-20 |
EP1069826A1 (fr) | 2001-01-24 |
TR200002903T2 (tr) | 2000-12-21 |
JP2002511394A (ja) | 2002-04-16 |
EP1069826B1 (fr) | 2003-02-19 |
BR9909464A (pt) | 2000-12-12 |
CA2327732C (fr) | 2008-03-25 |
CN1119079C (zh) | 2003-08-27 |
PT1069826E (pt) | 2003-06-30 |
KR100738764B1 (ko) | 2007-07-12 |
AP1064A (en) | 2002-04-26 |
AP2000001976A0 (en) | 2000-12-31 |
NZ507379A (en) | 2003-10-31 |
IL138835A0 (en) | 2001-10-31 |
AU3603099A (en) | 1999-11-01 |
CO5050302A1 (es) | 2001-06-27 |
JP4563580B2 (ja) | 2010-10-13 |
OA12190A (en) | 2006-05-09 |
WO1999052367A1 (fr) | 1999-10-21 |
MY123468A (en) | 2006-05-31 |
CA2327732A1 (fr) | 1999-10-21 |
ID28939A (id) | 2001-07-19 |
AR016459A1 (es) | 2001-07-04 |
CN1295436A (zh) | 2001-05-16 |
TW490289B (en) | 2002-06-11 |
DE59904334D1 (de) | 2003-03-27 |
IL138835A (en) | 2005-08-31 |
AU763130B2 (en) | 2003-07-17 |
DE19815820A1 (de) | 1999-10-14 |
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