IL92954A - Prevention of marcaptan odor in biocides containing organophosphate - Google Patents
Prevention of marcaptan odor in biocides containing organophosphateInfo
- Publication number
- IL92954A IL92954A IL9295490A IL9295490A IL92954A IL 92954 A IL92954 A IL 92954A IL 9295490 A IL9295490 A IL 9295490A IL 9295490 A IL9295490 A IL 9295490A IL 92954 A IL92954 A IL 92954A
- Authority
- IL
- Israel
- Prior art keywords
- solution
- accordance
- solvent
- thiophos
- phate
- Prior art date
Links
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 title claims abstract description 24
- 239000003139 biocide Substances 0.000 title description 5
- 230000005764 inhibitory process Effects 0.000 title description 2
- 239000000203 mixture Substances 0.000 claims abstract description 31
- 238000009472 formulation Methods 0.000 claims abstract description 24
- 238000000034 method Methods 0.000 claims abstract description 24
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 claims abstract description 18
- 150000001875 compounds Chemical class 0.000 claims abstract description 17
- 239000003513 alkali Substances 0.000 claims abstract description 4
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 claims abstract description 4
- 229910001854 alkali hydroxide Inorganic materials 0.000 claims abstract description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 18
- 230000003115 biocidal effect Effects 0.000 claims description 11
- 239000002904 solvent Substances 0.000 claims description 11
- 239000008187 granular material Substances 0.000 claims description 9
- 235000011121 sodium hydroxide Nutrition 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 239000003701 inert diluent Substances 0.000 claims description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000011593 sulfur Substances 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 239000008096 xylene Substances 0.000 claims description 3
- 150000003738 xylenes Chemical class 0.000 claims 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 claims description 2
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical class [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 2
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 229910052760 oxygen Chemical group 0.000 claims description 2
- 239000001301 oxygen Chemical group 0.000 claims description 2
- 235000011118 potassium hydroxide Nutrition 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 5
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 3
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 claims 2
- KOITVPOIFJTHPW-UHFFFAOYSA-N 2-(sulfanylmethyl)isoindole-1,3-dione Chemical group C1=CC=C2C(=O)N(CS)C(=O)C2=C1 KOITVPOIFJTHPW-UHFFFAOYSA-N 0.000 claims 1
- DUFKCOQISQKSAV-UHFFFAOYSA-N Polypropylene glycol (m w 1,200-3,000) Chemical compound CC(O)COC(C)CO DUFKCOQISQKSAV-UHFFFAOYSA-N 0.000 claims 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 239000000356 contaminant Substances 0.000 claims 1
- NAGJZTKCGNOGPW-UHFFFAOYSA-K dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [O-]P([O-])([S-])=S NAGJZTKCGNOGPW-UHFFFAOYSA-K 0.000 claims 1
- 229940051250 hexylene glycol Drugs 0.000 claims 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims 1
- 235000019645 odor Nutrition 0.000 abstract description 9
- 239000003795 chemical substances by application Substances 0.000 abstract description 7
- -1 thiophosphate compound Chemical class 0.000 abstract description 6
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 abstract description 3
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical class Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 abstract description 2
- ICIWUVCWSCSTAQ-UHFFFAOYSA-N iodic acid Chemical class OI(=O)=O ICIWUVCWSCSTAQ-UHFFFAOYSA-N 0.000 abstract description 2
- 238000002360 preparation method Methods 0.000 abstract description 2
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 239000013020 final formulation Substances 0.000 abstract 1
- 230000000717 retained effect Effects 0.000 abstract 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical class OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 description 13
- 239000004480 active ingredient Substances 0.000 description 11
- 239000007788 liquid Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- 239000006227 byproduct Substances 0.000 description 5
- 239000012071 phase Substances 0.000 description 5
- VEDTXTNSFWUXGQ-UHFFFAOYSA-N Carbophenothion Chemical compound CCOP(=S)(OCC)SCSC1=CC=C(Cl)C=C1 VEDTXTNSFWUXGQ-UHFFFAOYSA-N 0.000 description 4
- MUMQYXACQUZOFP-UHFFFAOYSA-N Dialifor Chemical compound C1=CC=C2C(=O)N(C(CCl)SP(=S)(OCC)OCC)C(=O)C2=C1 MUMQYXACQUZOFP-UHFFFAOYSA-N 0.000 description 4
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 4
- VBKKVDGJXVOLNE-UHFFFAOYSA-N Dioxation Chemical compound CCOP(=S)(OCC)SC1OCCOC1SP(=S)(OCC)OCC VBKKVDGJXVOLNE-UHFFFAOYSA-N 0.000 description 4
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
- 239000004927 clay Substances 0.000 description 4
- RIZMRRKBZQXFOY-UHFFFAOYSA-N ethion Chemical compound CCOP(=S)(OCC)SCSP(=S)(OCC)OCC RIZMRRKBZQXFOY-UHFFFAOYSA-N 0.000 description 4
- KVGLBTYUCJYMND-UHFFFAOYSA-N fonofos Chemical compound CCOP(=S)(CC)SC1=CC=CC=C1 KVGLBTYUCJYMND-UHFFFAOYSA-N 0.000 description 4
- 238000004817 gas chromatography Methods 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- BULVZWIRKLYCBC-UHFFFAOYSA-N phorate Chemical compound CCOP(=S)(OCC)SCSCC BULVZWIRKLYCBC-UHFFFAOYSA-N 0.000 description 4
- 125000004437 phosphorous atom Chemical group 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 125000004434 sulfur atom Chemical group 0.000 description 4
- XLNZEKHULJKQBA-UHFFFAOYSA-N terbufos Chemical compound CCOP(=S)(OCC)SCSC(C)(C)C XLNZEKHULJKQBA-UHFFFAOYSA-N 0.000 description 4
- 229910000365 copper sulfate Inorganic materials 0.000 description 3
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 3
- 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 3
- 238000006467 substitution reaction Methods 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 2
- 239000005921 Phosmet Substances 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 229960000892 attapulgite Drugs 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- 230000004071 biological effect Effects 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000013270 controlled release Methods 0.000 description 2
- 125000004093 cyano group Chemical group *C#N 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- VJYFKVYYMZPMAB-UHFFFAOYSA-N ethoprophos Chemical compound CCCSP(=O)(OCC)SCCC VJYFKVYYMZPMAB-UHFFFAOYSA-N 0.000 description 2
- 239000003337 fertilizer Substances 0.000 description 2
- 239000003630 growth substance Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000003094 microcapsule Substances 0.000 description 2
- 229910052625 palygorskite Inorganic materials 0.000 description 2
- LMNZTLDVJIUSHT-UHFFFAOYSA-N phosmet Chemical compound C1=CC=C2C(=O)N(CSP(=S)(OC)OC)C(=O)C2=C1 LMNZTLDVJIUSHT-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000011550 stock solution Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
- 239000010455 vermiculite Substances 0.000 description 2
- 229910052902 vermiculite Inorganic materials 0.000 description 2
- 235000019354 vermiculite Nutrition 0.000 description 2
- 238000005903 acid hydrolysis reaction Methods 0.000 description 1
- 229910000272 alkali metal oxide Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 239000003986 organophosphate insecticide Substances 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000004557 technical material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/025—Purification; Separation; Stabilisation; Desodorisation of organo-phosphorus compounds
-
- 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
- A01N57/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having alternatively specified atoms bound to the phosphorus atom and not covered by a single one of groups A01N57/10, A01N57/18, A01N57/26, A01N57/34
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Molecular Biology (AREA)
- Agronomy & Crop Science (AREA)
- Biochemistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IL10821990A IL108219A (en) | 1989-01-04 | 1990-01-03 | Prevention of marcaptan odor in biocides containing organophosphate |
| IL10821993A IL108219A0 (en) | 1989-01-04 | 1993-12-29 | Inhibition of mercaptan odor in organothiophosphate biocides |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/293,244 US4948787A (en) | 1989-01-04 | 1989-01-04 | Inhibition of mercaptan odor in organothiophosphate biocides |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL92954A0 IL92954A0 (en) | 1990-09-17 |
| IL92954A true IL92954A (en) | 1994-06-24 |
Family
ID=23128302
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL9295490A IL92954A (en) | 1989-01-04 | 1990-01-03 | Prevention of marcaptan odor in biocides containing organophosphate |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US4948787A (da) |
| EP (1) | EP0378303B1 (da) |
| JP (1) | JP2826358B2 (da) |
| AT (1) | ATE120612T1 (da) |
| AU (1) | AU635512B2 (da) |
| BR (1) | BR9000026A (da) |
| CA (1) | CA2007189C (da) |
| DE (1) | DE69018274T2 (da) |
| DK (1) | DK0378303T3 (da) |
| ES (1) | ES2071002T3 (da) |
| HU (1) | HUT53657A (da) |
| IL (1) | IL92954A (da) |
| IN (1) | IN170289B (da) |
| PL (1) | PL163944B1 (da) |
| ZA (1) | ZA9029B (da) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0673667B1 (en) * | 1989-04-21 | 2000-09-20 | Asahi Kogaku Kogyo Kabushiki Kaisha | Filter sheet |
| IL102242A (en) * | 1991-06-18 | 1996-12-05 | Gouws & Scheepers Pty Ltd | Pesticide and method of eradication |
| US6265542B1 (en) * | 1997-10-24 | 2001-07-24 | Genentech, Inc. | Purification of molecules |
| US7494602B2 (en) * | 2005-04-11 | 2009-02-24 | Piezotech, Llc | Compositions for high power piezoelectric ceramics |
| EP2324838A1 (en) | 2005-09-12 | 2011-05-25 | Abela Pharmaceuticals, Inc. | Compositions Comprising Dimethyl Sulfoxide (DMSO) |
| US8435224B2 (en) | 2005-09-12 | 2013-05-07 | Abela Pharmaceuticals, Inc. | Materials for facilitating administration of dimethyl sulfoxide (DMSO) and related compounds |
| CA2622204C (en) | 2005-09-12 | 2016-10-11 | Abela Pharmaceuticals, Inc. | Systems for removing dimethyl sulfoxide (dmso) or related compounds, or odors associated with same |
| US8480797B2 (en) | 2005-09-12 | 2013-07-09 | Abela Pharmaceuticals, Inc. | Activated carbon systems for facilitating use of dimethyl sulfoxide (DMSO) by removal of same, related compounds, or associated odors |
| US10046078B2 (en) * | 2008-01-18 | 2018-08-14 | Kenneth R. Code | Liquid iodine mist treatment of separated odor-emitting dry waste within a waste management facility |
| BRPI0921494A2 (pt) | 2008-11-03 | 2018-10-30 | Prad Reasearch And Development Ltd | método de planejamento de uma operação de amostragem para uma formação subterrãnea, método de contolar uma operação de amostragem de formação subterrânea, método de controlar uma operação de perfuração para uma formação subterrãnea, e método de realizar uma amostragem durante a operação de perfuração. |
| WO2011053874A1 (en) | 2009-10-30 | 2011-05-05 | Tandem Abela Development Group Llc | Dimethyl sulfoxide (dmso) and methylsulfonylmethane (msm) formulations to treat osteoarthritis |
| WO2015142609A1 (en) | 2014-03-20 | 2015-09-24 | Fmc Corporation | Odor-reduced pyrethroid-organothiophosphate formulations |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB748299A (en) * | 1952-08-01 | 1956-04-25 | Bayer Ag | Neutral esters of dithiophosphoric acid |
| US2767194A (en) * | 1955-03-18 | 1956-10-16 | Stauffer Chemical Co | Compositions of matter |
| NL267577A (da) * | 1960-07-28 | |||
| US3642960A (en) * | 1969-01-27 | 1972-02-15 | Stauffer Chemical Co | Method of producing thiono- or dithio-phosphonic acid esters |
| US4000271A (en) * | 1972-08-25 | 1976-12-28 | Mobil Oil Corporation | Deodorized organothiophosphorus compounds with reduced toxicity |
| US4370301A (en) * | 1979-11-28 | 1983-01-25 | Mitsubishi Denki Kabushiki Kaisha | Dry deodorizing apparatus |
| NL8104616A (nl) * | 1981-10-09 | 1983-05-02 | Nalco Chemical Co | Werkwijze voor het door omzetting verwijderen van mercaptanen uit organische vloeistoffen. |
| JPS60140418A (ja) * | 1983-12-28 | 1985-07-25 | Nec Corp | 座標入力装置 |
| JPS60178894A (ja) * | 1984-02-23 | 1985-09-12 | Nippon Tokushu Noyaku Seizo Kk | 有機チオリン酸エステル原体の還元脱臭法 |
| US4752604A (en) * | 1985-07-29 | 1988-06-21 | Stauffer Chemical Company | S,S-di-(tertiary alkyl) thiophosphonate insecticides |
-
1989
- 1989-01-04 US US07/293,244 patent/US4948787A/en not_active Expired - Lifetime
- 1989-12-28 JP JP1345044A patent/JP2826358B2/ja not_active Expired - Lifetime
- 1989-12-29 IN IN952/MAS/89A patent/IN170289B/en unknown
-
1990
- 1990-01-03 HU HU9020A patent/HUT53657A/hu unknown
- 1990-01-03 ZA ZA9029A patent/ZA9029B/xx unknown
- 1990-01-03 IL IL9295490A patent/IL92954A/en not_active IP Right Cessation
- 1990-01-03 AU AU47656/90A patent/AU635512B2/en not_active Ceased
- 1990-01-04 DE DE69018274T patent/DE69018274T2/de not_active Expired - Fee Related
- 1990-01-04 EP EP90300080A patent/EP0378303B1/en not_active Expired - Lifetime
- 1990-01-04 PL PL90283184A patent/PL163944B1/pl unknown
- 1990-01-04 ES ES90300080T patent/ES2071002T3/es not_active Expired - Lifetime
- 1990-01-04 CA CA002007189A patent/CA2007189C/en not_active Expired - Fee Related
- 1990-01-04 AT AT90300080T patent/ATE120612T1/de not_active IP Right Cessation
- 1990-01-04 DK DK90300080.0T patent/DK0378303T3/da active
- 1990-01-04 BR BR909000026A patent/BR9000026A/pt not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| US4948787A (en) | 1990-08-14 |
| EP0378303A3 (en) | 1991-04-24 |
| JPH02288812A (ja) | 1990-11-28 |
| ES2071002T3 (es) | 1995-06-16 |
| HUT53657A (en) | 1990-11-28 |
| ATE120612T1 (de) | 1995-04-15 |
| DE69018274D1 (de) | 1995-05-11 |
| CA2007189A1 (en) | 1990-07-04 |
| BR9000026A (pt) | 1990-10-09 |
| DK0378303T3 (da) | 1995-07-31 |
| IN170289B (da) | 1992-03-07 |
| HU900020D0 (en) | 1990-03-28 |
| AU4765690A (en) | 1990-07-12 |
| JP2826358B2 (ja) | 1998-11-18 |
| PL163944B1 (pl) | 1994-05-31 |
| AU635512B2 (en) | 1993-03-25 |
| EP0378303B1 (en) | 1995-04-05 |
| IL92954A0 (en) | 1990-09-17 |
| DE69018274T2 (de) | 1995-08-03 |
| EP0378303A2 (en) | 1990-07-18 |
| ZA9029B (en) | 1991-01-30 |
| CA2007189C (en) | 2000-04-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0095907B1 (en) | Biocidal or biostatic compositions containing 3-isothiazolones, their method of preparation and their uses | |
| IL92954A (en) | Prevention of marcaptan odor in biocides containing organophosphate | |
| JP5437363B2 (ja) | 有機リンおよび／または有機硫黄汚染物質を破壊するための組成物およびプロセス | |
| US2938831A (en) | Control of nematodes using dialkyl pyrazinyl phosphorothioates | |
| US3078298A (en) | 3-alkyl (sulfonyl and sulfoxyl) acrylic acid esters and nitriles | |
| EP0304492A1 (en) | Stable solid pesticidal preparation | |
| CA1090249A (en) | Insecticidal compositions | |
| CS244129B2 (en) | Insecticide and method of its production | |
| IL108219A (en) | Prevention of marcaptan odor in biocides containing organophosphate | |
| SU1028235A3 (ru) | Гербицидное средство | |
| US4383991A (en) | O-Alkyl-S-alkyl-S-branched alkylphosphorodithioate soil insecticides | |
| EP0373775A2 (en) | Insecticides | |
| SU1222185A3 (ru) | Гербицидное средство | |
| SU710501A3 (ru) | Гербицидный состав | |
| US4639538A (en) | Deodorized compositions based on organothiophosphorus compounds | |
| EP0921725B1 (en) | Aqueous malathion emulsions with improved properties as to stability, toxicity and smell | |
| US3275718A (en) | O, o-dialkyl-o-(2, 5-dichloro-4-bromophenyl)-thiophosphates | |
| JPS63290803A (ja) | 安定な農薬固型製剤 | |
| US3764698A (en) | Insecticides compositions and methods employing 3,4, substituted phenylmethylsulfinates | |
| KR100379712B1 (ko) | 제올라이트 제형의 농약 제조방법 | |
| US3632758A (en) | Insecticidal oximes | |
| JP2647071B2 (ja) | 農薬固型製剤 | |
| CA1305717C (en) | Thiophosphoric acid ester as a soil pest controlling agent | |
| US3086059A (en) | 4-halo-2-butynyl sulfides and use for controlling nematodes | |
| US3939263A (en) | Methods of combatting insects and acarina using oxygenated derivatives of S-(tert-bulythio)methyl O,O-diethyl phosphorodithioate and phosphorothioate |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| KB | Patent renewed | ||
| FF | Patent granted | ||
| KB | Patent renewed | ||
| RH1 | Patent not in force |