CS147192A3 - Aqueous herbicidal composition based on sulfonyl urea derivatives - Google Patents
Aqueous herbicidal composition based on sulfonyl urea derivatives Download PDFInfo
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- CS147192A3 CS147192A3 CS921471A CS147192A CS147192A3 CS 147192 A3 CS147192 A3 CS 147192A3 CS 921471 A CS921471 A CS 921471A CS 147192 A CS147192 A CS 147192A CS 147192 A3 CS147192 A3 CS 147192A3
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- Czechoslovakia
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- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 title claims abstract description 12
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 7
- 239000000203 mixture Substances 0.000 title claims description 20
- 229920002125 Sokalan® Polymers 0.000 claims abstract description 11
- 239000004584 polyacrylic acid Substances 0.000 claims abstract description 9
- 238000000034 method Methods 0.000 claims abstract description 5
- 238000002360 preparation method Methods 0.000 claims abstract description 5
- -1 antifoams Substances 0.000 claims description 24
- 150000001875 compounds Chemical class 0.000 claims description 10
- 239000003666 Amidosulfuron Substances 0.000 claims description 9
- CTTHWASMBLQOFR-UHFFFAOYSA-N Amidosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)N(C)S(C)(=O)=O)=N1 CTTHWASMBLQOFR-UHFFFAOYSA-N 0.000 claims description 9
- 229940100389 Sulfonylurea Drugs 0.000 claims description 7
- 239000002270 dispersing agent Substances 0.000 claims description 5
- 239000002562 thickening agent Substances 0.000 claims description 5
- 239000003755 preservative agent Substances 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 3
- 239000007798 antifreeze agent Substances 0.000 claims description 3
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 claims description 3
- 229940071161 dodecylbenzenesulfonate Drugs 0.000 claims description 3
- 230000008635 plant growth Effects 0.000 claims description 3
- 239000000725 suspension Substances 0.000 claims description 3
- KRTNITDCKAVIFI-UHFFFAOYSA-N tridecyl benzenesulfonate Chemical compound CCCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 KRTNITDCKAVIFI-UHFFFAOYSA-N 0.000 claims description 3
- 239000000080 wetting agent Substances 0.000 claims description 3
- 239000012752 auxiliary agent Substances 0.000 claims description 2
- 238000009736 wetting Methods 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims 3
- 239000002671 adjuvant Substances 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 claims 1
- 239000004009 herbicide Substances 0.000 claims 1
- 239000004548 suspo-emulsion Substances 0.000 claims 1
- 239000013543 active substance Substances 0.000 abstract description 6
- 239000007900 aqueous suspension Substances 0.000 abstract description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 26
- 125000000217 alkyl group Chemical group 0.000 description 11
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- 125000003545 alkoxy group Chemical group 0.000 description 7
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- 125000005843 halogen group Chemical group 0.000 description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 6
- PUIYMUZLKQOUOZ-UHFFFAOYSA-N isoproturon Chemical compound CC(C)C1=CC=C(NC(=O)N(C)C)C=C1 PUIYMUZLKQOUOZ-UHFFFAOYSA-N 0.000 description 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 5
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- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
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- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
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- 230000007062 hydrolysis Effects 0.000 description 2
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
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- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
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- 125000001424 substituent group Chemical group 0.000 description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
- 239000004563 wettable powder Substances 0.000 description 2
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 description 1
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- FCAKZZMVXCLLHM-UHFFFAOYSA-N 1,1-dimethyl-3-[3-(1,1,2,2-tetrafluoroethoxy)phenyl]urea Chemical compound CN(C)C(=O)NC1=CC=CC(OC(F)(F)C(F)F)=C1 FCAKZZMVXCLLHM-UHFFFAOYSA-N 0.000 description 1
- AZUYLZMQTIKGSC-UHFFFAOYSA-N 1-[6-[4-(5-chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methylindazol-5-yl)pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl]prop-2-en-1-one Chemical compound ClC=1C(=C2C=NNC2=CC=1C)C=1C(=NN(C=1C)C1CC2(CN(C2)C(C=C)=O)C1)C=1C=C2C=NN(C2=CC=1)C AZUYLZMQTIKGSC-UHFFFAOYSA-N 0.000 description 1
- VMFDZAIIYSKZDE-UHFFFAOYSA-N 1h-pyrazol-5-ylsulfonylurea Chemical compound NC(=O)NS(=O)(=O)C=1C=CNN=1 VMFDZAIIYSKZDE-UHFFFAOYSA-N 0.000 description 1
- QQGRFMIMXPWKPM-UHFFFAOYSA-N 2,3,4-tributylphenol Chemical compound CCCCC1=CC=C(O)C(CCCC)=C1CCCC QQGRFMIMXPWKPM-UHFFFAOYSA-N 0.000 description 1
- WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 description 1
- OOLBCHYXZDXLDS-UHFFFAOYSA-N 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(Cl)C=C1Cl OOLBCHYXZDXLDS-UHFFFAOYSA-N 0.000 description 1
- WUZNHSBFPPFULJ-UHFFFAOYSA-N 2-[[4-chloro-6-(cyclopropylamino)-1,3,5-triazin-2-yl]amino]-2-methylpropanenitrile Chemical compound N#CC(C)(C)NC1=NC(Cl)=NC(NC2CC2)=N1 WUZNHSBFPPFULJ-UHFFFAOYSA-N 0.000 description 1
- WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 description 1
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 description 1
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- NLYNUTMZTCLNOO-UHFFFAOYSA-N Chlorbromuron Chemical compound CON(C)C(=O)NC1=CC=C(Br)C(Cl)=C1 NLYNUTMZTCLNOO-UHFFFAOYSA-N 0.000 description 1
- HCRWJJJUKUVORR-UHFFFAOYSA-N Desmetryn Chemical compound CNC1=NC(NC(C)C)=NC(SC)=N1 HCRWJJJUKUVORR-UHFFFAOYSA-N 0.000 description 1
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- NPWMZOGDXOFZIN-UHFFFAOYSA-N Dipropetryn Chemical compound CCSC1=NC(NC(C)C)=NC(NC(C)C)=N1 NPWMZOGDXOFZIN-UHFFFAOYSA-N 0.000 description 1
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- 238000003801 milling Methods 0.000 description 1
- BMLIZLVNXIYGCK-UHFFFAOYSA-N monuron Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C=C1 BMLIZLVNXIYGCK-UHFFFAOYSA-N 0.000 description 1
- ZBJVLWIYKOAYQH-UHFFFAOYSA-N naphthalen-2-yl 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=C(C=CC=C2)C2=C1 ZBJVLWIYKOAYQH-UHFFFAOYSA-N 0.000 description 1
- XITQUSLLOSKDTB-UHFFFAOYSA-N nitrofen Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C(Cl)C=C1Cl XITQUSLLOSKDTB-UHFFFAOYSA-N 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 description 1
- CHIFOSRWCNZCFN-UHFFFAOYSA-N pendimethalin Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical class OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 1
- ONJQDTZCDSESIW-UHFFFAOYSA-N polidocanol Chemical compound CCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO ONJQDTZCDSESIW-UHFFFAOYSA-N 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- ISEUFVQQFVOBCY-UHFFFAOYSA-N prometon Chemical compound COC1=NC(NC(C)C)=NC(NC(C)C)=N1 ISEUFVQQFVOBCY-UHFFFAOYSA-N 0.000 description 1
- AAEVYOVXGOFMJO-UHFFFAOYSA-N prometryn Chemical compound CSC1=NC(NC(C)C)=NC(NC(C)C)=N1 AAEVYOVXGOFMJO-UHFFFAOYSA-N 0.000 description 1
- MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 description 1
- WJNRPILHGGKWCK-UHFFFAOYSA-N propazine Chemical compound CC(C)NC1=NC(Cl)=NC(NC(C)C)=N1 WJNRPILHGGKWCK-UHFFFAOYSA-N 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- MEFOUWRMVYJCQC-UHFFFAOYSA-N rimsulfuron Chemical compound CCS(=O)(=O)C1=CC=CN=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 MEFOUWRMVYJCQC-UHFFFAOYSA-N 0.000 description 1
- MGLWZSOBALDPEK-UHFFFAOYSA-N simetryn Chemical compound CCNC1=NC(NCC)=NC(SC)=N1 MGLWZSOBALDPEK-UHFFFAOYSA-N 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
- AHTPATJNIAFOLR-UHFFFAOYSA-N thifensulfuron-methyl Chemical group S1C=CC(S(=O)(=O)NC(=O)NC=2N=C(OC)N=C(C)N=2)=C1C(=O)OC AHTPATJNIAFOLR-UHFFFAOYSA-N 0.000 description 1
- KLPPUPBECAHKEF-UHFFFAOYSA-N thiophen-2-ylsulfonylurea Chemical compound NC(=O)NS(=O)(=O)C1=CC=CS1 KLPPUPBECAHKEF-UHFFFAOYSA-N 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- SBXWFLISHPUINY-UHFFFAOYSA-N triphenyltin Chemical compound C1=CC=CC=C1[Sn](C=1C=CC=CC=1)C1=CC=CC=C1 SBXWFLISHPUINY-UHFFFAOYSA-N 0.000 description 1
- 238000001238 wet grinding Methods 0.000 description 1
- 229920001285 xanthan gum Polymers 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
- 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
- A01N25/02—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 containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Dispersion Chemistry (AREA)
- Toxicology (AREA)
- Chemical & Material Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4116441 | 1991-05-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS147192A3 true CS147192A3 (en) | 1992-12-16 |
Family
ID=6432039
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS921471A CS147192A3 (en) | 1991-05-18 | 1992-05-15 | Aqueous herbicidal composition based on sulfonyl urea derivatives |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US5573998A (ja) |
| EP (1) | EP0514768B1 (ja) |
| JP (1) | JP3482218B2 (ja) |
| AT (1) | ATE142423T1 (ja) |
| AU (1) | AU661687B2 (ja) |
| CA (1) | CA2068824C (ja) |
| CS (1) | CS147192A3 (ja) |
| DE (1) | DE59207084D1 (ja) |
| DK (1) | DK0514768T3 (ja) |
| ES (1) | ES2092592T3 (ja) |
| GR (1) | GR3021207T3 (ja) |
| ZA (1) | ZA923543B (ja) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU3243093A (en) * | 1991-12-20 | 1993-07-28 | E.I. Du Pont De Nemours And Company | Stabilized gelled-paste formulations of sulfonylureas and an injection system for their application |
| DE4313093C2 (de) * | 1993-04-22 | 1996-01-11 | Stefes Pflanzenschutz Gmbh | Metamitron enthaltende Suspensionskonzentrate auf Basis von Wasser als einzigen Trägerstoff |
| DE4433653A1 (de) | 1994-09-21 | 1996-03-28 | Hoechst Schering Agrevo Gmbh | Thixotrope wäßrige Pflanzenschutzmittel-Suspensionen |
| US5635447A (en) * | 1996-03-22 | 1997-06-03 | Donlar Corporation | Polyorganic acids and their analogues to enhance herbicide effectiveness |
| JP3270819B2 (ja) * | 1997-02-13 | 2002-04-02 | 北興化学工業株式会社 | 湛水下水田の直接散布用水性懸濁製剤 |
| JP3270825B2 (ja) * | 1997-02-14 | 2002-04-02 | 北興化学工業株式会社 | 湛水下水田の直接散布用水性懸濁製剤 |
| DE19951427A1 (de) * | 1999-10-26 | 2001-05-17 | Aventis Cropscience Gmbh | Nichtwässrige oder wasserarme Suspensionskonzentrate von Wirkstoffmischungen für den Pflanzenschutz |
| DE10020671A1 (de) * | 2000-04-27 | 2001-11-08 | Aventis Cropscience Gmbh | Flüssige Formulierungen |
| DE10022990A1 (de) * | 2000-05-11 | 2001-11-22 | Aventis Cropscience Gmbh | Kombination von Pflanzenschutzmitteln mit Wasserstoffbrücken bildenden Polymeren |
| BRPI0308777B1 (pt) * | 2002-03-29 | 2015-10-13 | Kumiai Chemical Industry Co | composição agroquímica granular e composição agroquímica granular mista |
| HRP20020884A2 (en) * | 2002-11-11 | 2005-06-30 | Unbehend Ljiljana | Method for preparing dough without applying external energy |
| DE10334301A1 (de) | 2003-07-28 | 2005-03-03 | Bayer Cropscience Gmbh | Flüssige Formulierung |
| DE102004011007A1 (de) | 2004-03-06 | 2005-09-22 | Bayer Cropscience Ag | Suspensionskonzentrate auf Ölbasis |
| RS51063B (sr) * | 2005-06-04 | 2010-10-31 | Bayer Cropscience Ag. | Koncentrat uljne suspenzije |
| PL1893017T3 (pl) * | 2005-06-10 | 2014-10-31 | Bayer Ip Gmbh | Suspoemulsje olej w wodzie zawierające skuteczne wobec roślin hydroksybenzonitryle |
| JP5137348B2 (ja) * | 2005-08-10 | 2013-02-06 | 石原産業株式会社 | 水性懸濁状除草組成物 |
| US7824367B2 (en) * | 2005-08-17 | 2010-11-02 | Merit Medical Systems, Inc. | Drainage catheter with locking hub |
| DE102005048539A1 (de) * | 2005-10-11 | 2007-04-12 | Bayer Cropscience Ag | Suspensionskonzentrate auf Ölbasis |
| WO2007079573A1 (en) * | 2006-01-13 | 2007-07-19 | U-Putt Inc. | Golf putter with laser |
| BRPI0708368A2 (pt) | 2006-03-02 | 2011-05-24 | Ishihara Sangyo Kaisha | composição herbicida sólida |
| JP5049601B2 (ja) * | 2006-03-02 | 2012-10-17 | 石原産業株式会社 | 固形除草組成物 |
| WO2007112834A2 (de) | 2006-03-29 | 2007-10-11 | Bayer Cropscience Ag | Herbizide mittel als dispersionen enthaltend diflufenican und flurtamone |
| EP1886565A1 (de) | 2006-03-29 | 2008-02-13 | Bayer CropScience AG | Wässrige Dispersionen enthaltend Diflufenican und Flurtamone |
| EP2180785A2 (de) * | 2007-07-06 | 2010-05-05 | Basf Se | Verwendung von homo- und copolymeren zur stabilisierung von wirkstoffformulierungen |
| EP2326169B1 (en) * | 2008-05-28 | 2016-07-27 | GAT Microencapsulation GmbH | Suspension concentrates in oil of sulfonylureas and combinations with fluroxypyr or other agrochemicals |
| EA025265B1 (ru) | 2012-05-25 | 2016-12-30 | Байер Кропсайенс Аг | Химическая стабилизация йодосульфурон-метил натриевой соли с помощью гидроксистеаратов |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4225337A (en) * | 1978-10-27 | 1980-09-30 | E. I. Du Pont De Nemours And Company | Herbicidal sulfonamides |
| US4483781A (en) * | 1983-09-02 | 1984-11-20 | The Procter & Gamble Company | Magnesium salts of peroxycarboxylic acids |
| BR8401507A (pt) * | 1983-04-04 | 1984-11-13 | Du Pont | Composicao aquosa estabilizada |
| DE3324802A1 (de) * | 1983-07-09 | 1985-01-17 | Hoechst Ag, 6230 Frankfurt | Neue n-alkoxy- und n- alkylsulfonylaminosulfonylharnstoffe, und neue (pyrimido) triazino-thiadiazinoxide als vorprodukte |
| DE3573368D1 (en) * | 1984-04-27 | 1989-11-09 | Ciba Geigy Ag | Herbicidal compositions |
| WO1988002598A1 (en) * | 1986-10-10 | 1988-04-21 | E.I. Du Pont De Nemours And Company | Herbicidal mixtures |
| FR2617167B1 (fr) * | 1987-06-25 | 1989-11-24 | Rhone Poulenc Agrochimie | Herbicides de type sulfonyluree, leur preparation, les compositions les contenant et leur utilisation |
| DE3736959A1 (de) * | 1987-10-31 | 1989-05-18 | Hoechst Ag | Heterocyclisch substituierte n-sultam-sulfonamide, verfahren zu ihrer herstellung und ihre verwendung als herbizide und pflanzenwachstumsregulatoren |
| US4959095A (en) * | 1987-11-25 | 1990-09-25 | E. I. Du Pont De Nemours And Company | Herbicidal O-carbomethoxysulfonylurea |
| JPH05500507A (ja) * | 1989-09-21 | 1993-02-04 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 非水性懸濁液の安定化 |
-
1992
- 1992-05-14 ES ES92108144T patent/ES2092592T3/es not_active Expired - Lifetime
- 1992-05-14 DE DE59207084T patent/DE59207084D1/de not_active Expired - Fee Related
- 1992-05-14 EP EP92108144A patent/EP0514768B1/de not_active Expired - Lifetime
- 1992-05-14 DK DK92108144.4T patent/DK0514768T3/da active
- 1992-05-14 AT AT92108144T patent/ATE142423T1/de not_active IP Right Cessation
- 1992-05-15 JP JP12391192A patent/JP3482218B2/ja not_active Expired - Fee Related
- 1992-05-15 CA CA002068824A patent/CA2068824C/en not_active Expired - Fee Related
- 1992-05-15 CS CS921471A patent/CS147192A3/cs unknown
- 1992-05-15 AU AU16261/92A patent/AU661687B2/en not_active Ceased
- 1992-05-15 ZA ZA923543A patent/ZA923543B/xx unknown
-
1995
- 1995-05-25 US US08/450,372 patent/US5573998A/en not_active Expired - Lifetime
-
1996
- 1996-08-05 US US08/692,254 patent/US5707926A/en not_active Expired - Lifetime
- 1996-09-30 GR GR960402563T patent/GR3021207T3/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA2068824C (en) | 2002-12-24 |
| DE59207084D1 (de) | 1996-10-17 |
| JPH06219913A (ja) | 1994-08-09 |
| JP3482218B2 (ja) | 2003-12-22 |
| EP0514768A1 (de) | 1992-11-25 |
| ES2092592T3 (es) | 1996-12-01 |
| AU1626192A (en) | 1992-12-03 |
| ATE142423T1 (de) | 1996-09-15 |
| DK0514768T3 (ja) | 1997-02-17 |
| CA2068824A1 (en) | 1992-11-19 |
| GR3021207T3 (en) | 1996-12-31 |
| ZA923543B (en) | 1992-12-30 |
| AU661687B2 (en) | 1995-08-03 |
| EP0514768B1 (de) | 1996-09-11 |
| US5707926A (en) | 1998-01-13 |
| US5573998A (en) | 1996-11-12 |
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