SK416991A3 - Liquid herbicide composition based on water mixed dispersion - Google Patents

Liquid herbicide composition based on water mixed dispersion Download PDF

Info

Publication number: SK416991A3
Authority: SK; Slovakia
Prior art keywords: concentrate; liquid; active; ester; pendimethalin
Prior art date: 1983-01-27

Application number

SK4169-91A

Other languages

English (en)

Slovak (sk)

Inventor

Konrad Albrecht

Gerhard Frisch

Original Assignee

Hoechst Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1983-01-27

Filing date

1991-12-30

Publication date

1994-04-06

1991-12-30 Application filed by Hoechst Ag filed Critical Hoechst Ag

1994-04-06 Publication of SK416991A3 publication Critical patent/SK416991A3/sk

Links

239000000203 mixture Substances 0.000 title claims description 28
239000007788 liquid Substances 0.000 title claims description 10
239000006185 dispersion Substances 0.000 title abstract description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title description 4
230000002363 herbicidal effect Effects 0.000 title description 3
239000004009 herbicide Substances 0.000 title description 2
239000012141 concentrate Substances 0.000 claims abstract description 24
-1 (C1-C12)-alkyl phthalates Chemical class 0.000 claims abstract description 15
238000002844 melting Methods 0.000 claims abstract description 12
230000008018 melting Effects 0.000 claims abstract description 12
239000002904 solvent Substances 0.000 claims abstract description 5
239000004480 active ingredient Substances 0.000 claims description 27
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 21
MZZBPDKVEFVLFF-UHFFFAOYSA-N cyanazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C#N)=N1 MZZBPDKVEFVLFF-UHFFFAOYSA-N 0.000 claims description 20
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 claims description 20
239000005591 Pendimethalin Substances 0.000 claims description 19
239000013543 active substance Substances 0.000 claims description 17
MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 claims description 12
PUIYMUZLKQOUOZ-UHFFFAOYSA-N isoproturon Chemical compound CC(C)C1=CC=C(NC(=O)N(C)C)C=C1 PUIYMUZLKQOUOZ-UHFFFAOYSA-N 0.000 claims description 12
125000000217 alkyl group Chemical group 0.000 claims description 9
ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 claims description 9
ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 claims description 7
239000002253 acid Substances 0.000 claims description 7
XKJMBINCVNINCA-UHFFFAOYSA-N Alfalone Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XKJMBINCVNINCA-UHFFFAOYSA-N 0.000 claims description 6
239000005573 Linuron Substances 0.000 claims description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 6
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 6
239000004546 suspension concentrate Substances 0.000 claims description 6
239000007859 condensation product Substances 0.000 claims description 5
239000002562 thickening agent Substances 0.000 claims description 5
239000002270 dispersing agent Substances 0.000 claims description 4
239000003995 emulsifying agent Substances 0.000 claims description 4
239000000080 wetting agent Substances 0.000 claims description 4
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 3
150000001447 alkali salts Chemical class 0.000 claims description 3
JHRWWRDRBPCWTF-OLQVQODUSA-N captafol Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)C(Cl)Cl)C(=O)[C@H]21 JHRWWRDRBPCWTF-OLQVQODUSA-N 0.000 claims description 3
150000005690 diesters Chemical class 0.000 claims description 3
150000002148 esters Chemical class 0.000 claims description 3
239000000047 product Substances 0.000 claims description 3
RDJTWDKSYLLHRW-UHFFFAOYSA-N Dinoseb acetate Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(C)=O RDJTWDKSYLLHRW-UHFFFAOYSA-N 0.000 claims description 2
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 2
239000003513 alkali Substances 0.000 claims description 2
239000003795 chemical substances by application Substances 0.000 claims description 2
229910052731 fluorine Inorganic materials 0.000 claims description 2
JOOMJVFZQRQWKR-UHFFFAOYSA-N pyrazophos Chemical compound N1=C(C)C(C(=O)OCC)=CN2N=C(OP(=S)(OCC)OCC)C=C21 JOOMJVFZQRQWKR-UHFFFAOYSA-N 0.000 claims description 2
230000000361 pesticidal effect Effects 0.000 claims 4
229920000151 polyglycol Polymers 0.000 claims 2
239000010695 polyglycol Substances 0.000 claims 2
229910052910 alkali metal silicate Inorganic materials 0.000 claims 1
125000005907 alkyl ester group Chemical group 0.000 claims 1
150000001896 cresols Chemical class 0.000 claims 1
RDYMFSUJUZBWLH-SVWSLYAFSA-N endosulfan Chemical compound C([C@@H]12)OS(=O)OC[C@@H]1[C@]1(Cl)C(Cl)=C(Cl)[C@@]2(Cl)C1(Cl)Cl RDYMFSUJUZBWLH-SVWSLYAFSA-N 0.000 claims 1
150000002170 ethers Chemical class 0.000 claims 1
125000004494 ethyl ester group Chemical group 0.000 claims 1
239000011737 fluorine Substances 0.000 claims 1
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims 1
229920005610 lignin Polymers 0.000 claims 1
239000002736 nonionic surfactant Substances 0.000 claims 1
239000003090 pesticide formulation Substances 0.000 claims 1
150000002989 phenols Chemical class 0.000 claims 1
DFCVAXDGRDRJCT-UHFFFAOYSA-N phosphoric acid;2,3,4-tris(2-phenylethenyl)phenol Chemical compound OP(O)(O)=O.C=1C=CC=CC=1C=CC1=C(C=CC=2C=CC=CC=2)C(O)=CC=C1C=CC1=CC=CC=C1 DFCVAXDGRDRJCT-UHFFFAOYSA-N 0.000 claims 1
OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 claims 1
229910052939 potassium sulfate Inorganic materials 0.000 claims 1
239000001120 potassium sulphate Substances 0.000 claims 1
235000011151 potassium sulphates Nutrition 0.000 claims 1
239000002689 soil Substances 0.000 claims 1
150000001875 compounds Chemical class 0.000 abstract description 4
239000000575 pesticide Substances 0.000 abstract description 4
239000007900 aqueous suspension Substances 0.000 abstract description 3
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 18
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 12
XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 description 10
239000005510 Diuron Substances 0.000 description 9
239000000126 substance Substances 0.000 description 9
239000000725 suspension Substances 0.000 description 9
238000009472 formulation Methods 0.000 description 8
159000000000 sodium salts Chemical class 0.000 description 7
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
150000004676 glycans Chemical class 0.000 description 6
229920001282 polysaccharide Polymers 0.000 description 6
239000005017 polysaccharide Substances 0.000 description 6
TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 5
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
238000002156 mixing Methods 0.000 description 4
QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 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
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
229930003836 cresol Natural products 0.000 description 3
FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 3
239000000843 powder Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000011734 sodium Substances 0.000 description 3
SXERGJJQSKIUIC-UHFFFAOYSA-N 2-Phenoxypropionic acid Chemical class OC(=O)C(C)OC1=CC=CC=C1 SXERGJJQSKIUIC-UHFFFAOYSA-N 0.000 description 2
QIMMUPPBPVKWKM-UHFFFAOYSA-N 2-methylnaphthalene Chemical compound C1=CC=CC2=CC(C)=CC=C21 QIMMUPPBPVKWKM-UHFFFAOYSA-N 0.000 description 2
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 2
239000007798 antifreeze agent Substances 0.000 description 2
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 2
238000009835 boiling Methods 0.000 description 2
239000006013 carbendazim Substances 0.000 description 2
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 2
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
239000004088 foaming agent Substances 0.000 description 2
230000000855 fungicidal effect Effects 0.000 description 2
235000011187 glycerol Nutrition 0.000 description 2
238000000034 method Methods 0.000 description 2
BACHBFVBHLGWSL-UHFFFAOYSA-N methyl 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoate Chemical group C1=CC(OC(C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-UHFFFAOYSA-N 0.000 description 2
229910052901 montmorillonite Inorganic materials 0.000 description 2
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 2
150000003021 phthalic acid derivatives Chemical class 0.000 description 2
BACHBFVBHLGWSL-JTQLQIEISA-N rac-diclofop methyl Natural products C1=CC(O[C@@H](C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-JTQLQIEISA-N 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
125000004400 (C1-C12) alkyl group Chemical group 0.000 description 1
LJHSWQBHPNDHRQ-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-yl)-2-phenoxypropanoic acid Chemical compound N=1C2=CC=CC=C2SC=1C(C)(C(O)=O)OC1=CC=CC=C1 LJHSWQBHPNDHRQ-UHFFFAOYSA-N 0.000 description 1
FKZMQCJUCFNPCP-UHFFFAOYSA-N 2-(1,3-benzoxazol-2-yl)-2-phenoxypropanoic acid Chemical compound N=1C2=CC=CC=C2OC=1C(C)(C(O)=O)OC1=CC=CC=C1 FKZMQCJUCFNPCP-UHFFFAOYSA-N 0.000 description 1
ZRYCRPNCXLQHPN-UHFFFAOYSA-N 3-hydroxy-2-methylbenzaldehyde Chemical compound CC1=C(O)C=CC=C1C=O ZRYCRPNCXLQHPN-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
229920001732 Lignosulfonate Polymers 0.000 description 1
LKJPSUCKSLORMF-UHFFFAOYSA-N Monolinuron Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C=C1 LKJPSUCKSLORMF-UHFFFAOYSA-N 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
231100000674 Phytotoxicity Toxicity 0.000 description 1
CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
241000220317 Rosa Species 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
229910052915 alkaline earth metal silicate Inorganic materials 0.000 description 1
QPUYECUOLPXSFR-UHFFFAOYSA-N alpha-methyl-naphthalene Natural products C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
230000002528 anti-freeze Effects 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
239000003849 aromatic solvent Substances 0.000 description 1
JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
239000002585 base Substances 0.000 description 1
239000013065 commercial product Substances 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000004744 fabric Substances 0.000 description 1
238000005189 flocculation Methods 0.000 description 1
230000016615 flocculation Effects 0.000 description 1
231100001261 hazardous Toxicity 0.000 description 1
230000000749 insecticidal effect Effects 0.000 description 1
150000004702 methyl esters Chemical class 0.000 description 1
OLZQTUCTGLHFTQ-UHFFFAOYSA-N octan-2-yl 2-(4-amino-3,5-dichloro-6-fluoropyridin-2-yl)oxyacetate Chemical compound CCCCCCC(C)OC(=O)COC1=NC(F)=C(Cl)C(N)=C1Cl OLZQTUCTGLHFTQ-UHFFFAOYSA-N 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
KSSNXJHPEFVKHY-UHFFFAOYSA-N phenol;hydrate Chemical compound O.OC1=CC=CC=C1 KSSNXJHPEFVKHY-UHFFFAOYSA-N 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
238000005086 pumping Methods 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000002002 slurry Substances 0.000 description 1
229920005552 sodium lignosulfonate Polymers 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
229940093635 tributyl phosphate Drugs 0.000 description 1
GLEXFKSLNFMHOA-UHFFFAOYSA-N triphenylazanium hydroxide Chemical compound [OH-].C1(=CC=CC=C1)[NH+](C1=CC=CC=C1)C1=CC=CC=C1 GLEXFKSLNFMHOA-UHFFFAOYSA-N 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
238000002255 vaccination Methods 0.000 description 1
238000001238 wet grinding Methods 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
- 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
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing heterocyclic radicals

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)
Chemical & Material Sciences (AREA)
Dispersion Chemistry (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

SK4169-91A 1983-01-27 1991-12-30 Liquid herbicide composition based on water mixed dispersion SK416991A3 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19833302648 DE3302648A1 (de)	1983-01-27	1983-01-27	Pflanzenschutzmittel in form von mischdispersionen

Publications (1)

Publication Number	Publication Date
SK416991A3 true SK416991A3 (en)	1994-04-06

Family

ID=6189324

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK4169-91A SK416991A3 (en)	1983-01-27	1991-12-30	Liquid herbicide composition based on water mixed dispersion

Country Status (16)

Country	Link
US (1)	US4594096A (cs)
EP (1)	EP0117999B1 (cs)
AT (1)	ATE22774T1 (cs)
AU (1)	AU562412B2 (cs)
BR (1)	BR8400333A (cs)
CA (1)	CA1227352A (cs)
CZ (1)	CZ416991A3 (cs)
DE (2)	DE3302648A1 (cs)
DK (1)	DK163476C (cs)
HU (1)	HU199057B (cs)
IE (1)	IE56609B1 (cs)
IL (1)	IL70781A (cs)
PL (1)	PL142037B1 (cs)
SK (1)	SK416991A3 (cs)
TR (1)	TR21863A (cs)
ZA (1)	ZA84594B (cs)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3614788A1 (de) *	1986-05-02	1987-11-05	Hoechst Ag	Herbizide emulsionen
US4871392A (en) *	1986-05-23	1989-10-03	American Cyanamid Company	Aqueous suspension concentrate compositions of pendimethalin
US5679619A (en) *	1986-05-23	1997-10-21	American Cyanamid Company	Aqueous suspension concentrate compositions of pendimethalin
US4874425A (en) *	1986-05-23	1989-10-17	American Cyanamid Company	Stable aqueous suspension concentrate compositions
US5624884A (en) *	1986-05-23	1997-04-29	American Cyanamid Company	Aqueous suspension concentrate compositions of pendimethalin
CA1289065C (en) *	1986-05-23	1991-09-17	Leonard John Morgan	Aqueous suspension concentrate compositions
US4875929A (en) *	1986-05-23	1989-10-24	American Cyanamid Company	Aqueous suspension concentrate compositions
JP2579755B2 (ja) *	1986-07-17	1997-02-12	塩野義製薬株式会社	新規懸濁性農薬製剤
FR2601259B1 (fr)	1986-07-11	1990-06-22	Rhone Poulenc Chimie	Nouvelles compositions tensio-actives a base d'esters phosphoriques leur procede de preparation et leur application a la formulation de matieres actives.
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1983
- 1983-01-27 DE DE19833302648 patent/DE3302648A1/de not_active Withdrawn
1984
- 1984-01-23 HU HU84266A patent/HU199057B/hu unknown
- 1984-01-24 US US06/573,402 patent/US4594096A/en not_active Expired - Lifetime
- 1984-01-25 EP EP84100732A patent/EP0117999B1/de not_active Expired
- 1984-01-25 DE DE8484100732T patent/DE3460924D1/de not_active Expired
- 1984-01-25 TR TR21863A patent/TR21863A/xx unknown
- 1984-01-25 IL IL70781A patent/IL70781A/xx unknown
- 1984-01-25 AT AT84100732T patent/ATE22774T1/de not_active IP Right Cessation
- 1984-01-26 BR BR8400333A patent/BR8400333A/pt unknown
- 1984-01-26 DK DK036084A patent/DK163476C/da not_active IP Right Cessation
- 1984-01-26 CA CA000446107A patent/CA1227352A/en not_active Expired
- 1984-01-26 PL PL1984245911A patent/PL142037B1/pl unknown
- 1984-01-26 IE IE174/84A patent/IE56609B1/en not_active IP Right Cessation
- 1984-01-26 ZA ZA84594A patent/ZA84594B/xx unknown
- 1984-01-26 AU AU23837/84A patent/AU562412B2/en not_active Expired - Fee Related
1991
- 1991-12-30 CZ CS914169A patent/CZ416991A3/cs unknown
- 1991-12-30 SK SK4169-91A patent/SK416991A3/sk unknown

Also Published As

Publication number	Publication date
DK36084A (da)	1984-07-28
CA1227352A (en)	1987-09-29
DK163476B (da)	1992-03-09
US4594096A (en)	1986-06-10
DK163476C (da)	1992-08-03
IL70781A (en)	1987-02-27
AU2383784A (en)	1984-08-02
PL142037B1 (en)	1987-09-30
TR21863A (tr)	1987-12-25
IE56609B1 (en)	1991-10-09
ZA84594B (en)	1984-09-26
HU199057B (en)	1990-01-29
PL245911A1 (en)	1985-02-13
ATE22774T1 (de)	1986-11-15
BR8400333A (pt)	1984-08-28
DE3460924D1 (en)	1986-11-20
EP0117999A1 (de)	1984-09-12
DK36084D0 (da)	1984-01-26
EP0117999B1 (de)	1986-10-15
IL70781A0 (en)	1984-04-30
IE840174L (en)	1984-07-27
CZ416991A3 (en)	1993-01-13
AU562412B2 (en)	1987-06-11
DE3302648A1 (de)	1984-08-02

Publication	Publication Date	Title
SK416991A3 (en)	1994-04-06	Liquid herbicide composition based on water mixed dispersion
JP3152991B2 (ja)	2001-04-03	液状除草剤組成物
CA2379468C (en)	2009-05-19	Pesticide formulations containing phosphate ester surfactant and alkoxylated lignosulfonate
JP2593886B2 (ja)	1997-03-26	植物保護有効物質の新規なサスポエマルジヨン
JP2685504B2 (ja)	1997-12-03	液体農薬組成物
CZ332797A3 (cs)	1998-02-18	Formulace glyfosátu obsahující etheraminové povrchově aktivní látky
CZ2001859A3 (en)	2001-06-13	Glyphosate preparation
CZ291704B6 (cs)	2003-05-14	Pesticidní prostředek
HUT54273A (en)	1991-02-28	Concentrated liquid herbicidal compositions comprising n-phosphonomethylglycine
US7238645B1 (en)	2007-07-03	Pesticide formulations containing phosphate ester surfactant and alkoxylated lignosulfonate
PL188690B1 (pl)	2005-03-31	Olejowy koncentrat zawiesinowy, sposób wytwarzania olejowego koncentratu zawiesinowego, zastosowanie olejowego koncentratu zawiesinowego oraz sposób zwalczania albo kontroli niepożądanej wegetacji roślin
SK280910B6 (sk)	2000-09-12	Spôsob výroby stáleho vodného suspenzného koncentrátu pendimetalínu
IL143389A (en)	2006-08-01	Preparations of pesticides containing surfactants which are estersyl sulfate Esters of alkoxylated undergone neutralization by amine alkoxylated
JPH0324004A (ja)	1991-02-01	除草用混合物の液状配合物
US6521785B2 (en)	2003-02-18	Pesticide formulations containing alkoxylated amine neutralized aromaticsulfonic acid surfactants
CZ2001383A3 (cs)	2001-07-11	Pesticidní prostředky obsahující povrchově aktivní látky na bázi alkoxylovaných aminů neutralizovaných aromatickými sulfonovými kyselinami
KR102874630B1 (ko)	2025-10-23	농약 제제
US20120108427A1 (en)	2012-05-03	Aqueous herbicide concentrate
SK394787A3 (en)	2001-02-12	Aqueous suspension concentrated pesticidal composition and method for producing the same