DD202229A5 - Waessrige pestizidkonzentrate - Google Patents

Waessrige pestizidkonzentrate Download PDF

Info

Publication number: DD202229A5
Authority: DD; German Democratic Republic
Prior art keywords: component; concentrate according; pesticide; item; concentrate
Prior art date: 1981-09-09

Application number

DD82239802A

Other languages

German (de)

English (en)

Inventor

Edward Nowak

Ross M Dyer

Ernst Neuenschwander

Original Assignee

Ciba Geigy

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.)

1981-09-09

Filing date

1982-05-12

Publication date

1983-09-07

1982-05-12 Application filed by Ciba Geigy filed Critical Ciba Geigy

1983-09-07 Publication of DD202229A5 publication Critical patent/DD202229A5/de

Links

239000012141 concentrate Substances 0.000 title claims abstract description 33
239000000575 pesticide Substances 0.000 title claims abstract description 23
239000007787 solid Substances 0.000 claims abstract description 22
239000007788 liquid Substances 0.000 claims abstract description 17
239000007864 aqueous solution Substances 0.000 claims abstract description 15
239000001257 hydrogen Substances 0.000 claims abstract description 6
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 6
150000003839 salts Chemical class 0.000 claims abstract description 6
125000003118 aryl group Chemical group 0.000 claims abstract description 5
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 4
229910052783 alkali metal Inorganic materials 0.000 claims abstract description 3
150000001340 alkali metals Chemical class 0.000 claims abstract description 3
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 3
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 claims abstract 4
125000001302 tertiary amino group Chemical group 0.000 claims abstract 2
239000000203 mixture Substances 0.000 claims description 27
238000009472 formulation Methods 0.000 claims description 21
239000000243 solution Substances 0.000 claims description 20
239000005822 Propiconazole Substances 0.000 claims description 11
STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 claims description 11
239000005807 Metalaxyl Substances 0.000 claims description 10
ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 claims description 10
238000000034 method Methods 0.000 claims description 9
150000001875 compounds Chemical class 0.000 claims description 8
239000004094 surface-active agent Substances 0.000 claims description 8
230000000361 pesticidal effect Effects 0.000 claims description 6
239000005752 Copper oxychloride Substances 0.000 claims description 5
239000002518 antifoaming agent Substances 0.000 claims description 5
HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical compound [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 claims description 5
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 claims description 4
239000003795 chemical substances by application Substances 0.000 claims description 4
239000002562 thickening agent Substances 0.000 claims description 4
PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 claims description 3
239000005795 Imazalil Substances 0.000 claims description 3
FSAVDKDHPDSCTO-WQLSENKSSA-N [(z)-2-chloro-1-(2,4-dichlorophenyl)ethenyl] diethyl phosphate Chemical group CCOP(=O)(OCC)O\C(=C/Cl)C1=CC=C(Cl)C=C1Cl FSAVDKDHPDSCTO-WQLSENKSSA-N 0.000 claims description 3
229960002125 enilconazole Drugs 0.000 claims description 3
LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 claims description 2
125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims description 2
239000005745 Captan Substances 0.000 claims description 2
239000005789 Folpet Substances 0.000 claims description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
239000005870 Ziram Substances 0.000 claims description 2
239000000853 adhesive Substances 0.000 claims description 2
230000001070 adhesive effect Effects 0.000 claims description 2
125000000217 alkyl group Chemical group 0.000 claims description 2
MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 claims description 2
229940117949 captan Drugs 0.000 claims description 2
HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 claims description 2
150000002431 hydrogen Chemical class 0.000 claims description 2
239000002245 particle Substances 0.000 claims description 2
229910052700 potassium Inorganic materials 0.000 claims description 2
239000011591 potassium Substances 0.000 claims description 2
238000002360 preparation method Methods 0.000 claims description 2
125000000467 secondary amino group Chemical class [H]N([*:1])[*:2] 0.000 claims description 2
KVCGISUBCHHTDD-UHFFFAOYSA-M sodium;4-methylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1 KVCGISUBCHHTDD-UHFFFAOYSA-M 0.000 claims description 2
239000004308 thiabendazole Substances 0.000 claims description 2
WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 claims description 2
229960004546 thiabendazole Drugs 0.000 claims description 2
235000010296 thiabendazole Nutrition 0.000 claims description 2
239000008096 xylene Substances 0.000 claims description 2
DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 claims description 2
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 claims 2
ZZXDRXVIRVJQBT-UHFFFAOYSA-N 2,3-dimethylbenzenesulfonic acid Chemical compound CC1=CC=CC(S(O)(=O)=O)=C1C ZZXDRXVIRVJQBT-UHFFFAOYSA-N 0.000 claims 1
125000002947 alkylene group Chemical group 0.000 claims 1
239000012752 auxiliary agent Substances 0.000 claims 1
238000004519 manufacturing process Methods 0.000 claims 1
239000003960 organic solvent Substances 0.000 claims 1
GIPRGFRQMWSHAK-UHFFFAOYSA-M sodium;2-propan-2-ylbenzenesulfonate Chemical compound [Na+].CC(C)C1=CC=CC=C1S([O-])(=O)=O GIPRGFRQMWSHAK-UHFFFAOYSA-M 0.000 claims 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 26
QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract description 5
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 abstract description 3
CXENHBSYCFFKJS-OXYODPPFSA-N (Z,E)-alpha-farnesene Chemical compound CC(C)=CCC\C(C)=C\C\C=C(\C)C=C CXENHBSYCFFKJS-OXYODPPFSA-N 0.000 abstract 1
150000003335 secondary amines Chemical class 0.000 abstract 1
239000013543 active substance Substances 0.000 description 13
235000008504 concentrate Nutrition 0.000 description 13
239000004495 emulsifiable concentrate Substances 0.000 description 13
239000003752 hydrotrope Substances 0.000 description 10
239000004480 active ingredient Substances 0.000 description 9
QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 description 7
-1 aromatic sulfonic acids Chemical class 0.000 description 6
239000002904 solvent Substances 0.000 description 6
TWFZGCMQGLPBSX-UHFFFAOYSA-N Carbendazim Natural products C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 5
239000006013 carbendazim Substances 0.000 description 5
JNPZQRQPIHJYNM-UHFFFAOYSA-N carbendazim Chemical compound C1=C[CH]C2=NC(NC(=O)OC)=NC2=C1 JNPZQRQPIHJYNM-UHFFFAOYSA-N 0.000 description 5
239000000843 powder Substances 0.000 description 5
239000000047 product Substances 0.000 description 5
239000000725 suspension Substances 0.000 description 5
229910002012 Aerosil® Inorganic materials 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
LUAVFCBYZUMYCE-UHFFFAOYSA-N azanium;2-propan-2-ylbenzenesulfonate Chemical compound [NH4+].CC(C)C1=CC=CC=C1S([O-])(=O)=O LUAVFCBYZUMYCE-UHFFFAOYSA-N 0.000 description 4
239000003995 emulsifying agent Substances 0.000 description 4
239000000839 emulsion Substances 0.000 description 4
238000002844 melting Methods 0.000 description 4
230000008018 melting Effects 0.000 description 4
239000003921 oil Substances 0.000 description 4
235000019198 oils Nutrition 0.000 description 4
239000004215 Carbon black (E152) Substances 0.000 description 3
239000006185 dispersion Substances 0.000 description 3
229930195733 hydrocarbon Natural products 0.000 description 3
150000002430 hydrocarbons Chemical class 0.000 description 3
229920001296 polysiloxane Polymers 0.000 description 3
239000007921 spray Substances 0.000 description 3
238000001238 wet grinding Methods 0.000 description 3
QFMDFTQOJHFVNR-UHFFFAOYSA-N 1-[2,2-dichloro-1-(4-ethylphenyl)ethyl]-4-ethylbenzene Chemical compound C1=CC(CC)=CC=C1C(C(Cl)Cl)C1=CC=C(CC)C=C1 QFMDFTQOJHFVNR-UHFFFAOYSA-N 0.000 description 2
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 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
FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 description 2
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
239000007900 aqueous suspension Substances 0.000 description 2
230000000052 comparative effect Effects 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
238000004090 dissolution Methods 0.000 description 2
239000003814 drug Substances 0.000 description 2
229940079593 drug Drugs 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
229920000151 polyglycol Polymers 0.000 description 2
239000010695 polyglycol Substances 0.000 description 2
229920002451 polyvinyl alcohol Polymers 0.000 description 2
239000012266 salt solution Substances 0.000 description 2
229940079842 sodium cumenesulfonate Drugs 0.000 description 2
QEKATQBVVAZOAY-UHFFFAOYSA-M sodium;4-propan-2-ylbenzenesulfonate Chemical compound [Na+].CC(C)C1=CC=C(S([O-])(=O)=O)C=C1 QEKATQBVVAZOAY-UHFFFAOYSA-M 0.000 description 2
239000004546 suspension concentrate Substances 0.000 description 2
239000004563 wettable powder Substances 0.000 description 2
JIRHAGAOHOYLNO-UHFFFAOYSA-N (3-cyclopentyloxy-4-methoxyphenyl)methanol Chemical compound COC1=CC=C(CO)C=C1OC1CCCC1 JIRHAGAOHOYLNO-UHFFFAOYSA-N 0.000 description 1
WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 description 1
YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 description 1
241000196324 Embryophyta Species 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
ZZXDRXVIRVJQBT-UHFFFAOYSA-M Xylenesulfonate Chemical compound CC1=CC=CC(S([O-])(=O)=O)=C1C ZZXDRXVIRVJQBT-UHFFFAOYSA-M 0.000 description 1
229960001413 acetanilide Drugs 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
235000004279 alanine Nutrition 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
230000002528 anti-freeze Effects 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
NRKHRDIKEPQOCU-UHFFFAOYSA-N azane;sulfurochloridic acid Chemical compound N.OS(Cl)(=O)=O NRKHRDIKEPQOCU-UHFFFAOYSA-N 0.000 description 1
229920001400 block copolymer Polymers 0.000 description 1
125000004112 carboxyamino group Chemical group [H]OC(=O)N([H])[*] 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
235000019864 coconut oil Nutrition 0.000 description 1
239000003240 coconut oil Substances 0.000 description 1
239000013066 combination product Substances 0.000 description 1
229940127555 combination product Drugs 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
NSFKBZXCXCJZDQ-UHFFFAOYSA-N cumene;sodium Chemical compound [Na].CC(C)C1=CC=CC=C1 NSFKBZXCXCJZDQ-UHFFFAOYSA-N 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
239000000428 dust Substances 0.000 description 1
238000010410 dusting Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
239000012467 final product Substances 0.000 description 1
238000005187 foaming Methods 0.000 description 1
231100001261 hazardous Toxicity 0.000 description 1
239000012456 homogeneous solution Substances 0.000 description 1
125000005191 hydroxyalkylamino group Chemical group 0.000 description 1
231100001231 less toxic Toxicity 0.000 description 1
239000002609 medium Substances 0.000 description 1
238000003801 milling Methods 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical class CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 1
230000035515 penetration Effects 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
229920002401 polyacrylamide Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920000136 polysorbate Polymers 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
239000012439 solid excipient Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
235000020354 squash Nutrition 0.000 description 1
239000000126 substance Substances 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
229940071104 xylenesulfonate 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
- 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

Landscapes

Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Toxicology (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Dispersion Chemistry (AREA)
Chemical & Material Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

DD82239802A 1981-09-09 1982-05-12 Waessrige pestizidkonzentrate DD202229A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB8127203		1981-09-09

Publications (1)

Publication Number	Publication Date
DD202229A5 true DD202229A5 (de)	1983-09-07

Family

ID=10524393

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD82239802A DD202229A5 (de)	1981-09-09	1982-05-12	Waessrige pestizidkonzentrate

Country Status (24)

Country	Link
EP (1)	EP0074329B1 (fr)
JP (1)	JPS5846001A (fr)
AT (1)	ATE37468T1 (fr)
AU (1)	AU555932B2 (fr)
BG (1)	BG38781A3 (fr)
BR (1)	BR8203105A (fr)
CA (1)	CA1186217A (fr)
CS (1)	CS248701B2 (fr)
DD (1)	DD202229A5 (fr)
DE (1)	DE3279068D1 (fr)
DK (1)	DK163554C (fr)
EG (1)	EG16710A (fr)
FI (1)	FI69235C (fr)
GR (1)	GR75428B (fr)
HU (1)	HU196878B (fr)
IE (1)	IE54464B1 (fr)
IL (1)	IL65674A (fr)
NZ (1)	NZ200452A (fr)
OA (1)	OA07094A (fr)
PH (1)	PH18670A (fr)
PL (1)	PL135500B1 (fr)
RO (2)	RO93895B (fr)
TR (1)	TR21438A (fr)
ZA (1)	ZA822972B (fr)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0095242A3 (fr) *	1982-05-17	1985-12-27	Imperial Chemical Industries Plc	Compositions fongicides et procédés pour traiter les semences et pour lutter contre les champignons nuisibles
GB8613913D0 (en) *	1986-06-07	1986-07-09	Ciba Geigy Ag	Microbicidal agrochemical compositions
ES2080063T3 (es) *	1988-04-08	1996-02-01	Janssen Pharmaceutica Nv	Composiciones sinergicas que contienen imazalil.
UA66388C2 (en) *	1998-08-05	2004-05-17	Syngenta Participations Ag	Surfactant salt of aromatic sulfonic acid neutralized by alkoxylated amine, a method for the preparation thereof and pesticide composition
US6521785B2 (en)	1999-08-03	2003-02-18	Syngenta Participations Ag	Pesticide formulations containing alkoxylated amine neutralized aromaticsulfonic acid surfactants
GB0318448D0 (en) *	2003-08-06	2003-09-10	Syngenta Ltd	Formulation
AU2011236046B2 (en) *	2003-08-06	2012-11-15	Syngenta Limited	Agrochemical concentrate comprising an adjuvant and a hydrotrope
PL2629605T3 (pl)	2010-10-21	2017-07-31	Syngenta Limited	Koncentraty agrochemiczne zawierające alkoksylowane adiuwanty
CN104365587B (zh) *	2013-08-15	2016-08-10	沈阳中化农药化工研发有限公司	一种制成水乳化型羧酸类农药的方法
RU2711811C2 (ru) *	2014-02-19	2020-01-22	Басф Се	Водная совместная композиция металаксила

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3307931A (en) *	1964-12-31	1967-03-07	Rohm & Haas	Herbicidal composition and method
CH501364A (de) *	1967-04-11	1971-01-15	Du Pont	Verfahren zur Bekämpfung von Pilzerkrankungen bei Pflanzen
DE1792688A1 (de) *	1967-05-03	1971-11-25	Du Pont	Fungicid
US4195083A (en) *	1968-09-11	1980-03-25	Emby Gordon N	Veterinary compositions and method for controlling anthropod ectoparasites
DE2328192A1 (de) *	1972-06-06	1974-01-03	Procter & Gamble	Herbizide zusammensetzungen
IT1006584B (it) *	1972-06-06	1976-10-20	Procter & Gamble	Composizioni insetticide
US4107302A (en) *	1976-11-16	1978-08-15	Osaka Kasei Company Limited	Novel aqueous insecticidal concentrate composition
DE3111934A1 (de) *	1981-03-26	1982-10-07	Bayer Ag, 5090 Leverkusen	Oel-in-wasser-emulsionen, verfahren zu deren herstellung und deren verwendung

1982
- 1982-04-26 IE IE974/82A patent/IE54464B1/en not_active IP Right Cessation
- 1982-04-27 DK DK187882A patent/DK163554C/da not_active IP Right Cessation
- 1982-04-28 FI FI821482A patent/FI69235C/fi not_active IP Right Cessation
- 1982-04-28 NZ NZ200452A patent/NZ200452A/en unknown
- 1982-04-29 AT AT82810178T patent/ATE37468T1/de not_active IP Right Cessation
- 1982-04-29 EP EP82810178A patent/EP0074329B1/fr not_active Expired
- 1982-04-29 AU AU83123/82A patent/AU555932B2/en not_active Ceased
- 1982-04-29 DE DE8282810178T patent/DE3279068D1/de not_active Expired
- 1982-04-30 GR GR68037A patent/GR75428B/el unknown
- 1982-04-30 CA CA000402067A patent/CA1186217A/fr not_active Expired
- 1982-04-30 ZA ZA822972A patent/ZA822972B/xx unknown
- 1982-05-03 IL IL65674A patent/IL65674A/xx not_active IP Right Cessation
- 1982-05-05 TR TR21438A patent/TR21438A/xx unknown
- 1982-05-05 PL PL1982236301A patent/PL135500B1/pl unknown
- 1982-05-06 RO RO122538A patent/RO93895B/ro unknown
- 1982-05-06 BG BG056538A patent/BG38781A3/xx unknown
- 1982-05-06 RO RO82107454A patent/RO89556A/fr unknown
- 1982-05-07 OA OA57681A patent/OA07094A/fr unknown
- 1982-05-10 HU HU821460A patent/HU196878B/hu not_active IP Right Cessation
- 1982-05-11 JP JP57079089A patent/JPS5846001A/ja active Granted
- 1982-05-12 DD DD82239802A patent/DD202229A5/de not_active IP Right Cessation
- 1982-05-12 CS CS823460A patent/CS248701B2/cs unknown
- 1982-05-22 EG EG28982A patent/EG16710A/xx active
- 1982-05-27 BR BR8203105A patent/BR8203105A/pt not_active IP Right Cessation
- 1982-07-13 PH PH27561A patent/PH18670A/en unknown

Also Published As

Publication number	Publication date
JPH0349882B2 (fr)	1991-07-31
EP0074329A2 (fr)	1983-03-16
IE54464B1 (en)	1989-10-25
DK163554C (da)	1992-08-03
DK163554B (da)	1992-03-16
IL65674A0 (en)	1982-08-31
PL236301A1 (en)	1983-03-14
DE3279068D1 (en)	1988-11-03
PL135500B1 (en)	1985-10-31
ZA822972B (en)	1983-04-27
EP0074329B1 (fr)	1988-09-28
CS248701B2 (en)	1987-02-12
IL65674A (en)	1985-12-31
IE820974L (en)	1983-03-09
FI821482A0 (fi)	1982-04-28
NZ200452A (en)	1985-07-12
HU196878B (en)	1989-02-28
PH18670A (en)	1985-08-29
BG38781A3 (en)	1986-02-28
RO93895B (ro)	1988-03-31
EG16710A (en)	1995-07-27
ATE37468T1 (de)	1988-10-15
JPS5846001A (ja)	1983-03-17
FI821482L (fi)	1983-03-10
BR8203105A (pt)	1983-05-10
FI69235C (fi)	1986-01-10
EP0074329A3 (en)	1984-03-28
DK187882A (da)	1983-03-10
TR21438A (tr)	1984-06-04
CA1186217A (fr)	1985-04-30
GR75428B (fr)	1984-07-17
RO89556A (fr)	1986-12-10
RO93895A (fr)	1988-03-30
FI69235B (fi)	1985-09-30
AU555932B2 (en)	1986-10-16
OA07094A (fr)	1987-01-31
AU8312382A (en)	1983-03-17

Legal Events

Date	Code	Title	Description
1996-06-20	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
DE69904058T2 (de)	2003-04-17	Glyphosat-formulierung
US4853026A (en)	1989-08-01	Herbicidal emulsions
DE69330588T2 (de)	2002-04-25	Lagerstabile, pestizide, wässrige Emulsionen
EP0117999B1 (fr)	1986-10-15	Agents protecteurs de plantes en forme de dispersions mélangées
DE3225703C1 (de)	1984-01-19	Phospholipidkonzentrat und seine Verwendung als Hilfsstoff zum Herstellen und Austragen von Pflanzenschutzmittel enthaltenden Spritzbruehen
DE3881753T2 (de)	1993-10-07	Peptizide Formulierungen.
EP0088049B1 (fr)	1985-10-23	Mélanges herbicides
DE69923868T2 (de)	2005-07-28	Pestizidformulierungen, welche mit alkoxylierten Aminen neutralisierte alkoxylierte Tristyrylphenolhemi-Sulfatestertenside enthalten
DE69605598T2 (de)	2000-07-27	Stabile Mikroemulsionen von bestimmten 3-Isothiazolonverbindungen
DE3786845T2 (de)	1994-03-03	Wässrige Suspensionskonzentrate von Pendimethalin.
DE4013930A1 (de)	1990-11-08	Fluessige konzentrierte zusammensetzungen auf der basis von n-phosphonomethylglycin
DE3240862A1 (de)	1984-05-10	Fluessige pestizide mittel in form von suspensionskonzentraten
DE69907211T2 (de)	2004-02-19	Pyrimethanil enthaltendes suspensionskonzentrat
EP0257286A2 (fr)	1988-03-02	Microémulsions aqueuses concentrées
EP0702896A1 (fr)	1996-03-27	Suspension aqueuse thixotropique de produits phytosanitaires
DE3752093T2 (de)	1997-12-04	Wässerige Suspensionskonzentrate
DD202229A5 (de)	1983-09-07	Waessrige pestizidkonzentrate
EP0976329B1 (fr)	2003-03-19	Suspension aqueuse concentrée contenant thidiazuron et ethephon
EP0499798B1 (fr)	1996-04-03	Préparations liquides de mélanges d'herbicides à base de glufosinate
DE69323498T2 (de)	1999-06-17	Schaumarme, alkylpolyglucosid enthaltende zusammensetzungen
DE60019004T2 (de)	2005-08-18	Nicht-wässriges Suspensionskonzentrat
EP0185185B1 (fr)	1990-01-24	Procédé pour inhibiter l'évaporation et moyen pour sa mise en oeuvre
DE69600890T2 (de)	1999-06-24	Mikroemulsionen von 3-Isothiazolonverbindungen
DE3874594T2 (de)	1993-01-28	Gaenzlich waesserige formulierungen von organophosphorpestiziden.
EP0592880B1 (fr)	1997-04-09	Dispersion concentrée aqueuse, contenant le linuron comme agent actif