NL8001849A - Vloeibaar pesticidepreparaat. - Google Patents

Vloeibaar pesticidepreparaat. Download PDF

Info

Publication number: NL8001849A
Authority: NL; Netherlands
Prior art keywords: water; polyoxyethylene; preparation; group; pesticide
Prior art date: 1979-03-28

Application number

NL8001849A

Other languages

English (en)

Dutch (nl)

Original Assignee

Kao Corp

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.)

1979-03-28

Filing date

1980-03-28

Publication date

1980-09-30

1980-03-28 Application filed by Kao Corp filed Critical Kao Corp

1980-09-30 Publication of NL8001849A publication Critical patent/NL8001849A/nl

Links

239000000575 pesticide Substances 0.000 title claims description 35
238000002360 preparation method Methods 0.000 title claims description 22
239000007788 liquid Substances 0.000 title claims description 11
-1 polyoxyethylene phenylphenol Polymers 0.000 claims description 33
239000000203 mixture Substances 0.000 claims description 29
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 24
239000002562 thickening agent Substances 0.000 claims description 19
125000003118 aryl group Chemical group 0.000 claims description 18
239000002736 nonionic surfactant Substances 0.000 claims description 18
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 14
125000003710 aryl alkyl group Chemical group 0.000 claims description 8
239000007864 aqueous solution Substances 0.000 claims description 7
125000002947 alkylene group Chemical group 0.000 claims description 5
239000006185 dispersion Substances 0.000 claims description 5
238000000034 method Methods 0.000 claims description 5
239000000243 solution Substances 0.000 claims description 5
125000004432 carbon atom Chemical group C* 0.000 claims description 4
150000001875 compounds Chemical class 0.000 claims description 3
LRMHFDNWKCSEQU-UHFFFAOYSA-N ethoxyethane;phenol Chemical compound CCOCC.OC1=CC=CC=C1 LRMHFDNWKCSEQU-UHFFFAOYSA-N 0.000 claims description 3
239000004094 surface-active agent Substances 0.000 claims description 3
125000000217 alkyl group Chemical group 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
239000000725 suspension Substances 0.000 description 24
239000002518 antifoaming agent Substances 0.000 description 7
239000002917 insecticide Substances 0.000 description 6
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 5
239000007900 aqueous suspension Substances 0.000 description 5
239000003795 chemical substances by application Substances 0.000 description 5
230000000052 comparative effect Effects 0.000 description 5
230000000361 pesticidal effect Effects 0.000 description 5
229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 5
229920001451 polypropylene glycol Polymers 0.000 description 5
NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 5
239000000600 sorbitol Substances 0.000 description 5
NMWKWBPNKPGATC-UHFFFAOYSA-N 4,5,6,7-tetrachloro-2-benzofuran-1(3H)-one Chemical compound ClC1=C(Cl)C(Cl)=C2COC(=O)C2=C1Cl NMWKWBPNKPGATC-UHFFFAOYSA-N 0.000 description 4
RNMDNPCBIKJCQP-UHFFFAOYSA-N 5-nonyl-7-oxabicyclo[4.1.0]hepta-1,3,5-trien-2-ol Chemical compound C(CCCCCCCC)C1=C2C(=C(C=C1)O)O2 RNMDNPCBIKJCQP-UHFFFAOYSA-N 0.000 description 4
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
229920001400 block copolymer Polymers 0.000 description 4
238000010790 dilution Methods 0.000 description 4
239000012895 dilution Substances 0.000 description 4
230000002070 germicidal effect Effects 0.000 description 4
229910052698 phosphorus Inorganic materials 0.000 description 4
239000011574 phosphorus Substances 0.000 description 4
239000007787 solid Substances 0.000 description 4
STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 3
LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 3
238000000354 decomposition reaction Methods 0.000 description 3
AWZOLILCOUMRDG-UHFFFAOYSA-N edifenphos Chemical compound C=1C=CC=CC=1SP(=O)(OCC)SC1=CC=CC=C1 AWZOLILCOUMRDG-UHFFFAOYSA-N 0.000 description 3
ZNOLGFHPUIJIMJ-UHFFFAOYSA-N fenitrothion Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C(C)=C1 ZNOLGFHPUIJIMJ-UHFFFAOYSA-N 0.000 description 3
239000008233 hard water Substances 0.000 description 3
239000004009 herbicide Substances 0.000 description 3
229920002545 silicone oil Polymers 0.000 description 3
XDESGXRLUIHEJT-UHFFFAOYSA-N 2,3,4-tribenzylphenol Chemical compound C=1C=CC=CC=1CC1=C(CC=2C=CC=CC=2)C(O)=CC=C1CC1=CC=CC=C1 XDESGXRLUIHEJT-UHFFFAOYSA-N 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
230000000895 acaricidal effect Effects 0.000 description 2
239000000642 acaricide Substances 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 description 2
XFMJUIKWKVJNDY-UHFFFAOYSA-N diethoxyphosphorylsulfanylmethylbenzene Chemical compound CCOP(=O)(OCC)SCC1=CC=CC=C1 XFMJUIKWKVJNDY-UHFFFAOYSA-N 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
150000004676 glycans Chemical class 0.000 description 2
VOEYXMAFNDNNED-UHFFFAOYSA-N metolcarb Chemical compound CNC(=O)OC1=CC=CC(C)=C1 VOEYXMAFNDNNED-UHFFFAOYSA-N 0.000 description 2
238000005191 phase separation Methods 0.000 description 2
150000008379 phenol ethers Chemical class 0.000 description 2
229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 2
229920001282 polysaccharide Polymers 0.000 description 2
239000005017 polysaccharide Substances 0.000 description 2
239000002002 slurry Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000000230 xanthan gum Substances 0.000 description 2
229920001285 xanthan gum Polymers 0.000 description 2
235000010493 xanthan gum Nutrition 0.000 description 2
229940082509 xanthan gum Drugs 0.000 description 2
WRIYPTGFYKBSFU-UHFFFAOYSA-N ()-Conen Chemical compound CCCCOP(=O)(SCC)SCC1=CC=CC=C1 WRIYPTGFYKBSFU-UHFFFAOYSA-N 0.000 description 1
WCVOGSZTONGSQY-UHFFFAOYSA-N 2,4,6-trichloroanisole Chemical compound COC1=C(Cl)C=C(Cl)C=C1Cl WCVOGSZTONGSQY-UHFFFAOYSA-N 0.000 description 1
CDMGNVWZXRKJNS-UHFFFAOYSA-N 2-benzylphenol Chemical compound OC1=CC=CC=C1CC1=CC=CC=C1 CDMGNVWZXRKJNS-UHFFFAOYSA-N 0.000 description 1
YKFRAOGHWKADFJ-UHFFFAOYSA-N Aramite Chemical compound ClCCOS(=O)OC(C)COC1=CC=C(C(C)(C)C)C=C1 YKFRAOGHWKADFJ-UHFFFAOYSA-N 0.000 description 1
229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
IVHVNMLJNASKHW-UHFFFAOYSA-M Chlorphonium chloride Chemical compound [Cl-].CCCC[P+](CCCC)(CCCC)CC1=CC=C(Cl)C=C1Cl IVHVNMLJNASKHW-UHFFFAOYSA-M 0.000 description 1
241000196324 Embryophyta Species 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
229920002907 Guar gum Polymers 0.000 description 1
229920000084 Gum arabic Polymers 0.000 description 1
241000238631 Hexapoda Species 0.000 description 1
240000007472 Leucaena leucocephala Species 0.000 description 1
239000005949 Malathion Substances 0.000 description 1
NPPQSCRMBWNHMW-UHFFFAOYSA-N Meprobamate Chemical compound NC(=O)OCC(C)(CCC)COC(N)=O NPPQSCRMBWNHMW-UHFFFAOYSA-N 0.000 description 1
FQYUMYWMJTYZTK-UHFFFAOYSA-N Phenyl glycidyl ether Chemical compound C1OC1COC1=CC=CC=C1 FQYUMYWMJTYZTK-UHFFFAOYSA-N 0.000 description 1
206010035148 Plague Diseases 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
241000607479 Yersinia pestis Species 0.000 description 1
VXSIXFKKSNGRRO-MXOVTSAMSA-N [(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate;[(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-3-[(e)-3-methoxy-2-methyl-3-oxoprop-1-enyl Chemical class CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1.CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VXSIXFKKSNGRRO-MXOVTSAMSA-N 0.000 description 1
BZMIHNKNQJJVRO-LVZFUZTISA-N [(e)-c-(3-chloro-2,6-dimethoxyphenyl)-n-ethoxycarbonimidoyl] benzoate Chemical compound COC=1C=CC(Cl)=C(OC)C=1C(=N/OCC)\OC(=O)C1=CC=CC=C1 BZMIHNKNQJJVRO-LVZFUZTISA-N 0.000 description 1
JAWMENYCRQKKJY-UHFFFAOYSA-N [3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-ylmethyl)-1-oxa-2,8-diazaspiro[4.5]dec-2-en-8-yl]-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]methanone Chemical compound N1N=NC=2CN(CCC=21)CC1=NOC2(C1)CCN(CC2)C(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F JAWMENYCRQKKJY-UHFFFAOYSA-N 0.000 description 1
239000000205 acacia gum Substances 0.000 description 1
235000010489 acacia gum Nutrition 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
150000005215 alkyl ethers Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
239000003146 anticoagulant agent Substances 0.000 description 1
229940127219 anticoagulant drug Drugs 0.000 description 1
125000006251 butylcarbonyl group Chemical group 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
125000004181 carboxyalkyl group Chemical group 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
230000001112 coagulating effect Effects 0.000 description 1
238000005345 coagulation Methods 0.000 description 1
230000015271 coagulation Effects 0.000 description 1
229930003836 cresol Natural products 0.000 description 1
UOAMTSKGCBMZTC-UHFFFAOYSA-N dicofol Chemical compound C=1C=C(Cl)C=CC=1C(C(Cl)(Cl)Cl)(O)C1=CC=C(Cl)C=C1 UOAMTSKGCBMZTC-UHFFFAOYSA-N 0.000 description 1
JXSJBGJIGXNWCI-UHFFFAOYSA-N diethyl 2-[(dimethoxyphosphorothioyl)thio]succinate Chemical compound CCOC(=O)CC(SP(=S)(OC)OC)C(=O)OCC JXSJBGJIGXNWCI-UHFFFAOYSA-N 0.000 description 1
125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
RDYMFSUJUZBWLH-UHFFFAOYSA-N endosulfan Chemical compound C12COS(=O)OCC2C2(Cl)C(Cl)=C(Cl)C1(Cl)C2(Cl)Cl RDYMFSUJUZBWLH-UHFFFAOYSA-N 0.000 description 1
RIZMRRKBZQXFOY-UHFFFAOYSA-N ethion Chemical compound CCOP(=S)(OCC)SCSP(=S)(OCC)OCC RIZMRRKBZQXFOY-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
DIRFUJHNVNOBMY-UHFFFAOYSA-N fenobucarb Chemical compound CCC(C)C1=CC=CC=C1OC(=O)NC DIRFUJHNVNOBMY-UHFFFAOYSA-N 0.000 description 1
238000005187 foaming Methods 0.000 description 1
239000000665 guar gum Substances 0.000 description 1
235000010417 guar gum Nutrition 0.000 description 1
229960002154 guar gum Drugs 0.000 description 1
125000002768 hydroxyalkyl group Chemical group 0.000 description 1
229920003063 hydroxymethyl cellulose Polymers 0.000 description 1
229940031574 hydroxymethyl cellulose Drugs 0.000 description 1
FCOAHACKGGIURQ-UHFFFAOYSA-N iprobenfos Chemical compound CC(C)OP(=O)(OC(C)C)SCC1=CC=CC=C1 FCOAHACKGGIURQ-UHFFFAOYSA-N 0.000 description 1
230000005923 long-lasting effect Effects 0.000 description 1
229960000453 malathion Drugs 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
244000005700 microbiome Species 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000012053 oil suspension Substances 0.000 description 1
239000002245 particle Substances 0.000 description 1
235000010987 pectin Nutrition 0.000 description 1
239000001814 pectin Substances 0.000 description 1
229920001277 pectin Polymers 0.000 description 1
CXPDTERMVIRXSR-UHFFFAOYSA-N phenol;prop-2-enylbenzene Chemical compound OC1=CC=CC=C1.C=CCC1=CC=CC=C1 CXPDTERMVIRXSR-UHFFFAOYSA-N 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000002243 precursor Substances 0.000 description 1
239000000047 product Substances 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 description 1
229940070846 pyrethrins Drugs 0.000 description 1
239000002728 pyrethroid Substances 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000006228 supernatant Substances 0.000 description 1
YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 description 1
230000001256 tonic effect Effects 0.000 description 1
229920003169 water-soluble polymer 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

Landscapes

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

NL8001849A 1979-03-28 1980-03-28 Vloeibaar pesticidepreparaat. NL8001849A (nl)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
JP3645679A JPS55129201A (en)	1979-03-28	1979-03-28	Fluid pesticidal composition
JP3645679		1979-03-28

Publications (1)

Publication Number	Publication Date
NL8001849A true NL8001849A (nl)	1980-09-30

Family

ID=12470312

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8001849A NL8001849A (nl)	1979-03-28	1980-03-28	Vloeibaar pesticidepreparaat.

Country Status (6)

Country	Link
JP (1)	JPS55129201A (pt)
BR (1)	BR8001833A (pt)
CA (1)	CA1145252A (pt)
DE (1)	DE3011611A1 (pt)
FR (1)	FR2452250A1 (pt)
NL (1)	NL8001849A (pt)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3111934A1 (de) *	1981-03-26	1982-10-07	Bayer Ag, 5090 Leverkusen	Oel-in-wasser-emulsionen, verfahren zu deren herstellung und deren verwendung
DE3236240A1 (de) *	1982-09-30	1984-04-05	Bayer Ag, 5090 Leverkusen	Homogene waessrige formulierungen
NO151026C (no) *	1982-11-26	1985-01-30	Saetersmoen A S	Insekticid og akaricid blanding inneholdende gelatin, og anvendelse av blandingen til aa bekjempe insekter og midd
JPS601101A (ja) *	1983-06-15	1985-01-07	Yuukou Yakuhin Kogyo Kk	水性懸濁農薬製剤
JPH0759481B2 (ja) *	1983-11-10	1995-06-28	日本農薬株式会社	安定なる水中懸濁状農薬製剤
ATE86067T1 (de) *	1984-04-09	1993-03-15	American Cyanamid Co	Insektizide waessrige mikroemulsionen.
DE3430611A1 (de) *	1984-08-20	1986-02-20	Werner & Mertz Gmbh, 6500 Mainz	Mittel zur abtoetung von hausstaubmilben und dessen verwendung
EP0217125B1 (en) *	1985-09-27	1990-08-16	American Cyanamid Company	Pesticidal aqueous flowable compositons
DE3628575A1 (de) *	1986-08-22	1988-02-25	Hoechst Ag	Waessrige fungizide dispersionen
JPH07121842B2 (ja) *	1986-09-09	1995-12-25	有恒薬品工業株式会社	水性懸濁状殺生剤組成物
IT1219699B (it) *	1988-05-27	1990-05-24	Geronazzo Spa	Agente tensio attivo a base di (fenil 1 etil) fenoli poliossialchilenati,suo procedimento di preparazione e suo impiego per ottenere soluzioni concentrate emulsionabili di sostanze attive
EP0499587A1 (de) *	1991-02-15	1992-08-19	Ciba-Geigy Ag	Insektizide Mikroemulsionen
JP2546200B2 (ja) *	1991-02-20	1996-10-23	東ソー株式会社	田植前湛水下水田除草用水性懸濁製剤および散布方法
DE4322211A1 (de) *	1993-07-03	1995-01-12	Basf Ag	Wäßrige, mehrphasige, stabile Fertigformulierung für Pflanzenschutz-Wirkstoffe und Verfahren zu ihrer Herstellung
DE4343856A1 (de) *	1993-12-22	1995-06-29	Hoechst Ag	Öl-in-Wasser-Emulsionen
US5912220A (en) *	1996-09-20	1999-06-15	S. C. Johnson & Son, Inc.	Surfactant complex with associative polymeric thickener
DE102008032537A1 (de) *	2008-07-10	2010-01-14	Gerstner, Alexander, Dipl.-Ing.	Direktanwendungs-Unkrautvernichtungszusammensetzung
CN103734135B (zh) *	2014-01-26	2016-03-16	上海艳紫化工科技有限公司	氯氟吡氧乙酸和炔草酯复配的农药悬浮剂
WO2025229996A1 (ja) *	2024-05-02	2025-11-06	花王株式会社	節足動物防除用噴霧剤組成物

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Publication number	Priority date	Publication date	Assignee	Title
DE851858C (de) *	1949-04-27	1952-10-09	Bayer Ag	Schaedlingsbekaempfungsmittel
US3364071A (en) *	1963-04-10	1968-01-16	Union Carbide Corp	Fuel cell with capillary supply means
US3575718A (en) *	1968-09-23	1971-04-20	Engelhard Min & Chem	Composite electrolyte member for fuel cell
US3948636A (en) *	1972-11-09	1976-04-06	Diamond Shamrock Corporation	Flowable aqueous composition of water-insoluble pesticide
IT989329B (it) *	1973-06-20	1975-05-20	Montedison Spa	Processo per la preparazione di acido 3 cheto glutarico per car bossilazione di acetone in glime
US4017664A (en) *	1975-09-02	1977-04-12	United Technologies Corporation	Silicon carbide electrolyte retaining matrix for fuel cells
US4000006A (en) *	1975-09-02	1976-12-28	United Technologies Corporation	Screen printing fuel cell electrolyte matrices
GB1510076A (en) *	1975-09-02	1978-05-10	United Technologies Corp	Screen printing of fuel cell electrolyte-retaining matrices
US4035551A (en) *	1976-09-01	1977-07-12	United Technologies Corporation	Electrolyte reservoir for a fuel cell
US4064322A (en) *	1976-09-01	1977-12-20	United Technologies Corporation	Electrolyte reservoir for a fuel cell
JPS5346889A (en) *	1976-10-09	1978-04-26	Nippon Totsukiyo Kanri Kk	Method of packing rice cake
US4115627A (en) *	1977-08-15	1978-09-19	United Technologies Corporation	Electrochemical cell comprising a ribbed electrode substrate
US4129685A (en) *	1977-08-15	1978-12-12	United Technologies Corp.	Fuel cell structure
FR2674586B1 (fr) *	1991-03-26	1995-06-02	Valeo	Garniture de frottement et disque de friction comportant une pluralite de garnitures de frottement, notamment pour embrayage de vehicule automobile.
JP2836351B2 (ja) *	1992-02-15	1998-12-14	三菱自動車工業株式会社	油圧式ハンドル角感応型後輪操舵装置

1979
- 1979-03-28 JP JP3645679A patent/JPS55129201A/ja active Granted
1980
- 1980-03-26 BR BR8001833A patent/BR8001833A/pt not_active IP Right Cessation
- 1980-03-26 DE DE19803011611 patent/DE3011611A1/de not_active Withdrawn
- 1980-03-27 FR FR8006815A patent/FR2452250A1/fr active Granted
- 1980-03-28 CA CA000348640A patent/CA1145252A/en not_active Expired
- 1980-03-28 NL NL8001849A patent/NL8001849A/nl not_active Application Discontinuation

Also Published As

Publication number	Publication date
BR8001833A (pt)	1980-11-18
FR2452250B1 (pt)	1983-04-01
DE3011611A1 (de)	1980-11-20
CA1145252A (en)	1983-04-26
JPS55129201A (en)	1980-10-06
JPS5761322B2 (pt)	1982-12-23
FR2452250A1 (fr)	1980-10-24

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Legal Events

Date	Code	Title
1985-01-01	A85	Still pending on 85-01-01
1987-03-02	BA	A request for search or an international-type search has been filed
1987-04-01	BB	A search report has been drawn up
1987-05-04	BC	A request for examination has been filed
1992-11-02	BV	The patent application has lapsed