CS235958B2 - Herbicide agent - Google Patents
Herbicide agent Download PDFInfo
- Publication number
- CS235958B2 CS235958B2 CS825939A CS593982A CS235958B2 CS 235958 B2 CS235958 B2 CS 235958B2 CS 825939 A CS825939 A CS 825939A CS 593982 A CS593982 A CS 593982A CS 235958 B2 CS235958 B2 CS 235958B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- stabilizing agent
- agent
- composition
- weight
- halogen
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title claims description 6
- 239000000203 mixture Substances 0.000 claims description 56
- 239000003381 stabilizer Substances 0.000 claims description 31
- 239000000725 suspension Substances 0.000 claims description 18
- 230000002363 herbicidal effect Effects 0.000 claims description 14
- 239000007900 aqueous suspension Substances 0.000 claims description 13
- 239000002270 dispersing agent Substances 0.000 claims description 13
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 11
- -1 alkyl radical Chemical class 0.000 claims description 10
- 125000005843 halogen group Chemical group 0.000 claims description 10
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 7
- 239000002245 particle Substances 0.000 claims description 7
- 239000007787 solid Substances 0.000 claims description 7
- 239000000460 chlorine Substances 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 5
- 229910052794 bromium Inorganic materials 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 3
- 239000013543 active substance Substances 0.000 claims description 3
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- WZKSXHQDXQKIQJ-UHFFFAOYSA-N F[C](F)F Chemical compound F[C](F)F WZKSXHQDXQKIQJ-UHFFFAOYSA-N 0.000 claims description 2
- 150000003254 radicals Chemical class 0.000 claims description 2
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims 3
- 150000002367 halogens Chemical class 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 239000003153 chemical reaction reagent Substances 0.000 claims 1
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 claims 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 1
- CCGPUGMWYLICGL-UHFFFAOYSA-N Neburon Chemical compound CCCCN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 CCGPUGMWYLICGL-UHFFFAOYSA-N 0.000 description 18
- 241000589634 Xanthomonas Species 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 239000003755 preservative agent Substances 0.000 description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 8
- 239000002562 thickening agent Substances 0.000 description 8
- 230000002335 preservative effect Effects 0.000 description 7
- 239000000080 wetting agent Substances 0.000 description 7
- 239000002518 antifoaming agent Substances 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000006185 dispersion Substances 0.000 description 5
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Natural products O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 5
- 238000003860 storage Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 239000000427 antigen Substances 0.000 description 4
- 102000036639 antigens Human genes 0.000 description 4
- 108091007433 antigens Proteins 0.000 description 4
- 239000004202 carbamide Substances 0.000 description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 3
- 229920001222 biopolymer Polymers 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- IQHSSYROJYPFDV-UHFFFAOYSA-N 2-bromo-1,3-dichloro-5-(trifluoromethyl)benzene Chemical group FC(F)(F)C1=CC(Cl)=C(Br)C(Cl)=C1 IQHSSYROJYPFDV-UHFFFAOYSA-N 0.000 description 2
- XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical group CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 description 2
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 241000321050 Xanthomonas campestris pv. incanae Species 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 238000000855 fermentation Methods 0.000 description 2
- 230000004151 fermentation Effects 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- PUIYMUZLKQOUOZ-UHFFFAOYSA-N isoproturon Chemical compound CC(C)C1=CC=C(NC(=O)N(C)C)C=C1 PUIYMUZLKQOUOZ-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- BMLIZLVNXIYGCK-UHFFFAOYSA-N monuron Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C=C1 BMLIZLVNXIYGCK-UHFFFAOYSA-N 0.000 description 2
- WUFSRLQSIDFFMT-UHFFFAOYSA-N oxirane;phosphoric acid Chemical compound C1CO1.OP(O)(O)=O WUFSRLQSIDFFMT-UHFFFAOYSA-N 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920002545 silicone oil Polymers 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- QTERLAXNZRFFMZ-UHFFFAOYSA-N 1,1-dimethyl-3-(4-methylphenyl)urea Chemical compound CN(C)C(=O)NC1=CC=C(C)C=C1 QTERLAXNZRFFMZ-UHFFFAOYSA-N 0.000 description 1
- BZQYHZYTUBMDPQ-UHFFFAOYSA-N 3-(3-bromophenyl)-1,1-dimethylurea Chemical compound CN(C)C(=O)NC1=CC=CC(Br)=C1 BZQYHZYTUBMDPQ-UHFFFAOYSA-N 0.000 description 1
- IGLUDRFAKOZADW-UHFFFAOYSA-N 3-(3-chloro-4-methylphenyl)-1-ethyl-1-methylurea Chemical compound CCN(C)C(=O)NC1=CC=C(C)C(Cl)=C1 IGLUDRFAKOZADW-UHFFFAOYSA-N 0.000 description 1
- GSNZNZUNAJCHDO-UHFFFAOYSA-N 3-(4-bromophenyl)-1,1-dimethylurea Chemical compound CN(C)C(=O)NC1=CC=C(Br)C=C1 GSNZNZUNAJCHDO-UHFFFAOYSA-N 0.000 description 1
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 241000697872 Bactria Species 0.000 description 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 240000001307 Myosotis scorpioides Species 0.000 description 1
- MGJKQDOBUOMPEZ-UHFFFAOYSA-N N,N'-dimethylurea Chemical compound CNC(=O)NC MGJKQDOBUOMPEZ-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 241001517672 Xanthomonas axonopodis pv. begoniae Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 1
- 230000003254 anti-foaming effect Effects 0.000 description 1
- 239000002519 antifouling agent Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000031018 biological processes and functions Effects 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- JXCGFZXSOMJFOA-UHFFFAOYSA-N chlorotoluron Chemical compound CN(C)C(=O)NC1=CC=C(C)C(Cl)=C1 JXCGFZXSOMJFOA-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical class OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229930182830 galactose Natural products 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 229920000140 heteropolymer Polymers 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 229920001477 hydrophilic polymer Polymers 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 229940094522 laponite Drugs 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical compound [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003871 sulfonates 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
- 239000012929 tonicity agent Substances 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229940082509 xanthan gum Drugs 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<
- A01N47/30—Derivatives containing the group >N—CO—N aryl or >N—CS—N—aryl
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Zoology (AREA)
- Dentistry (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- Toxicology (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Detergent Compositions (AREA)
- Peptides Or Proteins (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8115574A FR2510870A1 (fr) | 1981-08-10 | 1981-08-10 | Suspensions aqueuses concentrees a base de neburon |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CS235958B2 true CS235958B2 (en) | 1985-05-15 |
Family
ID=9261400
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS825939A CS235958B2 (en) | 1981-08-10 | 1982-08-10 | Herbicide agent |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US4678503A (pt) |
| EP (1) | EP0073727B1 (pt) |
| JP (1) | JPS5841806A (pt) |
| AT (1) | ATE10153T1 (pt) |
| AU (1) | AU564458B2 (pt) |
| BG (1) | BG41994A3 (pt) |
| CS (1) | CS235958B2 (pt) |
| DE (1) | DE3261200D1 (pt) |
| ES (1) | ES8306003A1 (pt) |
| FR (1) | FR2510870A1 (pt) |
| HU (1) | HU189168B (pt) |
| PL (1) | PL134307B1 (pt) |
| PT (1) | PT75401B (pt) |
| ZA (1) | ZA825760B (pt) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH652391A5 (de) * | 1982-01-15 | 1985-11-15 | Sandoz Ag | Harnstoff-derivate. |
| DE3573368D1 (en) * | 1984-04-27 | 1989-11-09 | Ciba Geigy Ag | Herbicidal compositions |
| US5624884A (en) * | 1986-05-23 | 1997-04-29 | American Cyanamid Company | Aqueous suspension concentrate compositions of pendimethalin |
| US4875929A (en) * | 1986-05-23 | 1989-10-24 | American Cyanamid Company | Aqueous suspension concentrate compositions |
| US5679619A (en) * | 1986-05-23 | 1997-10-21 | American Cyanamid Company | Aqueous suspension concentrate compositions of pendimethalin |
| JPH01175901A (ja) * | 1987-12-31 | 1989-07-12 | Nippon Nohyaku Co Ltd | 白蟻防除用乳剤 |
| FR2630885B1 (fr) * | 1988-05-09 | 1991-03-01 | Rhone Poulenc Agrochimie | Emulsion pesticide huile dans l'eau, procede de mise en oeuvre |
| US5206021A (en) * | 1988-05-09 | 1993-04-27 | Rhone-Poulenc Ag Company | Stabilized oil-in-water emulsions or suspoemulsions containing pesticidal substances in both oil and water phases |
| US5254344A (en) * | 1988-05-09 | 1993-10-19 | Rhone-Poulenc Inc. | Oil-in-water pesticidal emulsion, process for application |
| US5731266A (en) * | 1993-03-17 | 1998-03-24 | Ciba-Geigy Corporation | Herbicidal compositions comprising diamino-1,3,5-triazine and chloroacetanilide herbicides and a surfactant system |
| DE19543097A1 (de) * | 1995-11-18 | 1997-05-22 | Riedel De Haen Ag | Algizide Kombinationsprodukte für die Konservierung von technischen Materialien |
| EP1623756A1 (en) * | 2000-06-12 | 2006-02-08 | Kureha Corporation | Microcapsule suspension liquid and process for production thereof |
| BRPI1013788B1 (pt) * | 2009-06-26 | 2021-02-02 | Solenis Technologies Cayman, L.P | uso de monoclorouréia para tratar águas industriais |
| CN110938019B (zh) * | 2019-12-10 | 2022-06-24 | 江苏快达农化股份有限公司 | 连续化合成异丙隆方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3399991A (en) * | 1964-05-05 | 1968-09-03 | Du Pont | Freeze-resistant pesticidal composition |
| FR2183625A1 (en) * | 1972-05-09 | 1973-12-21 | Pepro | N-4-isopropylphenyl-N',N'-dimethylurea herbicide - having synergistic action with mixts of neburon or linuron, esp for cereals |
| US3948636A (en) * | 1972-11-09 | 1976-04-06 | Diamond Shamrock Corporation | Flowable aqueous composition of water-insoluble pesticide |
-
1981
- 1981-08-10 FR FR8115574A patent/FR2510870A1/fr active Granted
-
1982
- 1982-07-27 BG BG057558A patent/BG41994A3/xx unknown
- 1982-08-06 PL PL1982237811A patent/PL134307B1/pl unknown
- 1982-08-06 EP EP82420112A patent/EP0073727B1/fr not_active Expired
- 1982-08-06 JP JP57137149A patent/JPS5841806A/ja active Pending
- 1982-08-06 DE DE8282420112T patent/DE3261200D1/de not_active Expired
- 1982-08-06 AT AT82420112T patent/ATE10153T1/de not_active IP Right Cessation
- 1982-08-09 HU HU822559A patent/HU189168B/hu unknown
- 1982-08-09 ZA ZA825760A patent/ZA825760B/xx unknown
- 1982-08-09 AU AU86970/82A patent/AU564458B2/en not_active Ceased
- 1982-08-09 ES ES514846A patent/ES8306003A1/es not_active Expired
- 1982-08-09 PT PT75401A patent/PT75401B/pt unknown
- 1982-08-10 CS CS825939A patent/CS235958B2/cs unknown
- 1982-08-12 US US06/407,464 patent/US4678503A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| PL134307B1 (en) | 1985-08-31 |
| HU189168B (en) | 1986-06-30 |
| BG41994A3 (en) | 1987-09-15 |
| ATE10153T1 (de) | 1984-11-15 |
| FR2510870B1 (pt) | 1983-11-18 |
| DE3261200D1 (en) | 1984-12-13 |
| EP0073727A1 (fr) | 1983-03-09 |
| AU8697082A (en) | 1983-02-17 |
| PL237811A1 (en) | 1983-07-04 |
| ZA825760B (en) | 1983-06-29 |
| JPS5841806A (ja) | 1983-03-11 |
| AU564458B2 (en) | 1987-08-13 |
| FR2510870A1 (fr) | 1983-02-11 |
| ES514846A0 (es) | 1983-05-01 |
| PT75401B (fr) | 1985-11-15 |
| ES8306003A1 (es) | 1983-05-01 |
| PT75401A (fr) | 1982-09-01 |
| EP0073727B1 (fr) | 1984-11-07 |
| US4678503A (en) | 1987-07-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CS235958B2 (en) | Herbicide agent | |
| US6045816A (en) | Water-based microemulsion of a pyrethroid | |
| DE2355882C3 (pt) | ||
| US3060084A (en) | Improved homogeneous, readily dispersed, pesticidal concentrate | |
| US5684025A (en) | Liquid formulations of 1,2-benzisothiazolin-3-one | |
| EP0088049B1 (de) | Herbizide Mischungen | |
| DD256822A5 (de) | Waessrige suspensionskonzentrazusammensetzung und methode fuer deren herstellung | |
| JPS5980321A (ja) | 水性微小乳剤及びその調製方法 | |
| EP0679333A2 (en) | Non-sensitizing biocide composition | |
| HU199063B (en) | Liquide herbicide suspensive concentrate | |
| SK17432002A3 (sk) | Kvapalná suspenzia mikrokapsúl a postup na jej výrobu | |
| JPH0217104A (ja) | グリホセイト、シマジン及びジウロンを含む組成物 | |
| US4188202A (en) | Composition | |
| DD276023A5 (de) | Verfahren zur herstellung einer waessrigen suspensionskonzentratzusammensetzung von pendimethalin | |
| DE69215702T2 (de) | Herbizide, emulgierbare Konzentrate von Imidazolinon- und Dinitroanilinherbizid-Zusammensetzungen | |
| PT86039B (pt) | Preparacao de composicoes contendo glifosato | |
| CA1186217A (en) | Aqueous pesticide concentrates | |
| CA1185522A (en) | Baits for ants, process for their preparation and their use | |
| CH646070A5 (de) | Chemische praeparate mit stabilem schwebevermoegen und verfahren zur herstellung derselben. | |
| US4390451A (en) | Concentrated aqueous metal aldonate and/or ammonium aldonate composition | |
| US4305750A (en) | Herbicides based on pyridazones | |
| JPS61126001A (ja) | 水性懸濁状殺生剤組成物およびその製造法 | |
| JP2652000B2 (ja) | 農芸化学において特に有用なホスフェート化ポリアルコキシル化トリスチリルフェノール誘導体を含有する流体状濃厚処方物 | |
| PL109495B1 (en) | Herbicide | |
| BR112018073649B1 (pt) | Formulação agroquímica, e, processo para preparar uma formulação agroquímica |