NZ227222A - Insecticidal aerosol containing a pyrethroidal compound - Google Patents
Insecticidal aerosol containing a pyrethroidal compoundInfo
- Publication number
- NZ227222A NZ227222A NZ227222A NZ22722288A NZ227222A NZ 227222 A NZ227222 A NZ 227222A NZ 227222 A NZ227222 A NZ 227222A NZ 22722288 A NZ22722288 A NZ 22722288A NZ 227222 A NZ227222 A NZ 227222A
- Authority
- NZ
- New Zealand
- Prior art keywords
- aerosol
- methyl ether
- glycol methyl
- container
- chrysanthemate
- Prior art date
Links
- 239000000443 aerosol Substances 0.000 title claims description 100
- 230000000749 insecticidal effect Effects 0.000 title claims description 22
- 150000001875 compounds Chemical class 0.000 title claims description 8
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims description 24
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 21
- 239000007853 buffer solution Substances 0.000 claims description 20
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 12
- 239000007788 liquid Substances 0.000 claims description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 10
- -1 3-phenoxybenzyl Chemical group 0.000 claims description 9
- 239000007791 liquid phase Substances 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 8
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 8
- 239000004480 active ingredient Substances 0.000 claims description 7
- SVKTYVVWVAOWIT-UHFFFAOYSA-N azanium;azane;benzoate Chemical compound N.[NH4+].[O-]C(=O)C1=CC=CC=C1 SVKTYVVWVAOWIT-UHFFFAOYSA-N 0.000 claims description 7
- RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 claims description 7
- 229960000490 permethrin Drugs 0.000 claims description 7
- 238000002360 preparation method Methods 0.000 claims description 7
- SBNFWQZLDJGRLK-RTWAWAEBSA-N (1R)-trans-phenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 SBNFWQZLDJGRLK-RTWAWAEBSA-N 0.000 claims description 6
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 claims description 6
- 238000004817 gas chromatography Methods 0.000 claims description 6
- 239000003960 organic solvent Substances 0.000 claims description 6
- 229960003536 phenothrin Drugs 0.000 claims description 6
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 6
- 239000003380 propellant Substances 0.000 claims description 6
- 239000005927 Pyriproxyfen Substances 0.000 claims description 5
- 235000019441 ethanol Nutrition 0.000 claims description 5
- NHDHVHZZCFYRSB-UHFFFAOYSA-N pyriproxyfen Chemical compound C=1C=CC=NC=1OC(C)COC(C=C1)=CC=C1OC1=CC=CC=C1 NHDHVHZZCFYRSB-UHFFFAOYSA-N 0.000 claims description 5
- 229940108410 resmethrin Drugs 0.000 claims description 5
- VEMKTZHHVJILDY-FIWHBWSRSA-N resmethrin Chemical compound CC1(C)[C@H](C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-FIWHBWSRSA-N 0.000 claims description 5
- WAEVWDZKMBQDEJ-UHFFFAOYSA-N 2-[2-(2-methoxypropoxy)propoxy]propan-1-ol Chemical compound COC(C)COC(C)COC(C)CO WAEVWDZKMBQDEJ-UHFFFAOYSA-N 0.000 claims description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 4
- 239000002356 single layer Substances 0.000 claims description 4
- CUDYYMUUJHLCGZ-UHFFFAOYSA-N 2-(2-methoxypropoxy)propan-1-ol Chemical compound COC(C)COC(C)CO CUDYYMUUJHLCGZ-UHFFFAOYSA-N 0.000 claims description 3
- SBNFWQZLDJGRLK-UHFFFAOYSA-N phenothrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 SBNFWQZLDJGRLK-UHFFFAOYSA-N 0.000 claims description 3
- RLLPVAHGXHCWKJ-IEBWSBKVSA-N (3-phenoxyphenyl)methyl (1s,3s)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-IEBWSBKVSA-N 0.000 claims description 2
- 230000000052 comparative effect Effects 0.000 claims description 2
- 230000001143 conditioned effect Effects 0.000 claims description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 11
- 239000000243 solution Substances 0.000 description 11
- 239000000203 mixture Substances 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 7
- 239000005028 tinplate Substances 0.000 description 7
- KWIPUXXIFQQMKN-UHFFFAOYSA-N 2-azaniumyl-3-(4-cyanophenyl)propanoate Chemical compound OC(=O)C(N)CC1=CC=C(C#N)C=C1 KWIPUXXIFQQMKN-UHFFFAOYSA-N 0.000 description 6
- 229940090948 ammonium benzoate Drugs 0.000 description 6
- 230000003750 conditioning effect Effects 0.000 description 6
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 5
- 239000010410 layer Substances 0.000 description 4
- YUGWDVYLFSETPE-JLHYYAGUSA-N Empenthrin Chemical compound CC\C=C(/C)C(C#C)OC(=O)C1C(C=C(C)C)C1(C)C YUGWDVYLFSETPE-JLHYYAGUSA-N 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000011259 mixed solution Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- CXBMCYHAMVGWJQ-CABCVRRESA-N (1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)methyl (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-CABCVRRESA-N 0.000 description 1
- XLOPRKKSAJMMEW-SFYZADRCSA-M (R,R)-chrysanthemate Chemical compound CC(C)=C[C@@H]1[C@@H](C([O-])=O)C1(C)C XLOPRKKSAJMMEW-SFYZADRCSA-M 0.000 description 1
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 1
- 101150027068 DEGS1 gene Proteins 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- NRAWNNRCLNRNLQ-UHFFFAOYSA-N azanium;benzoic acid;benzoate Chemical compound [NH4+].OC(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 NRAWNNRCLNRNLQ-UHFFFAOYSA-N 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- QABCGOSYZHCPGN-UHFFFAOYSA-N chloro(dimethyl)silicon Chemical compound C[Si](C)Cl QABCGOSYZHCPGN-UHFFFAOYSA-N 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 1
- 229960001826 dimethylphthalate Drugs 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- WLLGXSLBOPFWQV-OTHKPKEBSA-N molport-035-783-878 Chemical compound C([C@H]1C=C2)[C@H]2C2C1C(=O)N(CC(CC)CCCC)C2=O WLLGXSLBOPFWQV-OTHKPKEBSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 229960005235 piperonyl butoxide Drugs 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- UVVPZMPJAYXZDN-UHFFFAOYSA-M sodium;benzoic acid;benzoate Chemical compound [Na+].OC(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 UVVPZMPJAYXZDN-UHFFFAOYSA-M 0.000 description 1
- WGRULTCAYDOGQK-UHFFFAOYSA-M sodium;sodium;hydroxide Chemical compound [OH-].[Na].[Na+] WGRULTCAYDOGQK-UHFFFAOYSA-M 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229960005199 tetramethrin Drugs 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 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
- A01N25/06—Aerosols
-
- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Dispersion Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP31818487 | 1987-12-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NZ227222A true NZ227222A (en) | 1990-04-26 |
Family
ID=18096393
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NZ227222A NZ227222A (en) | 1987-12-15 | 1988-12-06 | Insecticidal aerosol containing a pyrethroidal compound |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US5064639A (enExample) |
| EP (1) | EP0320908B1 (enExample) |
| KR (1) | KR960011193B1 (enExample) |
| AU (1) | AU605652B2 (enExample) |
| BE (1) | BE1001443A3 (enExample) |
| BR (1) | BR8806604A (enExample) |
| CA (1) | CA1309337C (enExample) |
| CH (1) | CH676536A5 (enExample) |
| DE (1) | DE3863766D1 (enExample) |
| ES (1) | ES2009453A6 (enExample) |
| FR (1) | FR2624345B1 (enExample) |
| GB (1) | GB2213725B (enExample) |
| IT (1) | IT1227146B (enExample) |
| MX (1) | MX14191A (enExample) |
| MY (1) | MY103645A (enExample) |
| NZ (1) | NZ227222A (enExample) |
| ZA (1) | ZA889125B (enExample) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU610906B2 (en) * | 1987-07-31 | 1991-05-30 | Sumitomo Chemical Company, Limited | Method for preventing harm from bloodsucking insects |
| AU605939B2 (en) * | 1987-12-15 | 1991-01-24 | Sumitomo Chemical Company, Limited | Mono-layer water-based insecticidal aerosol |
| US5074252A (en) * | 1988-03-25 | 1991-12-24 | Morgan Jr Charles | Rechargeable insecticide dispenser providing controlled release of an insecticide composition |
| WO1994003056A1 (en) * | 1992-07-31 | 1994-02-17 | Ian Alexander Edwin Maccormick | Aerosol insecticide composition |
| FR2713235B1 (fr) * | 1993-11-29 | 1996-01-19 | Rhone Poulenc Agrochimie | Composition pour aérosol et système générateur d'aérosol la contenant. |
| CO4750805A1 (es) * | 1995-12-13 | 1999-03-31 | Sumitomo Chemical Co | Compuesto para champu |
| IE80657B1 (en) * | 1996-03-29 | 1998-11-04 | Merial Sas | Insecticidal combination to control mammal fleas in particular fleas on cats and dogs |
| RU2127517C1 (ru) * | 1997-03-11 | 1999-03-20 | Открытое акционерное общество "Арнест" | Инсектицидная композиция |
| JP4776757B2 (ja) * | 1999-10-01 | 2011-09-21 | 株式会社ダイゾー | エアゾール組成物 |
| RU2176448C2 (ru) * | 1999-11-19 | 2001-12-10 | Открытое акционерное общество "Арнест" | Инсектицидный препарат |
| US6482863B2 (en) * | 2000-12-15 | 2002-11-19 | S. C. Johnson & Son, Inc. | Insect repellant formulation deliverable by piezoelectric device |
| US6814956B2 (en) * | 2002-05-23 | 2004-11-09 | Mclaughlin Gormley King Company | Non-flammable aerosol insecticidal compositions |
| US8747875B2 (en) * | 2008-09-29 | 2014-06-10 | The Hartz Mountain Corporation | Photo-stable pest control |
| JP5876246B2 (ja) * | 2010-08-06 | 2016-03-02 | 住友化学株式会社 | 活性成分を空気中に送達するための組成物およびその利用 |
| AU2011265562A1 (en) | 2011-01-12 | 2012-07-26 | Sumitomo Chemical Company, Limited | Method of controlling harmful arthropod, composition, and electrostatic spray device |
| US10405552B2 (en) | 2017-05-22 | 2019-09-10 | S. C. Johnson & Son, Inc. | Composite insecticidal composition |
| CN109258680A (zh) * | 2018-11-06 | 2019-01-25 | 成都彩虹电器（集团）中南有限公司 | 一种均相透明水基气雾剂及其制备方法 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6056683B2 (ja) * | 1977-02-22 | 1985-12-11 | 第一製薬株式会社 | 安定化されたカルプロニウムクロライド配合剤 |
| LU79847A1 (fr) * | 1978-06-20 | 1980-01-22 | Airwick Ag | Systeme de pulverisation sous forme d'aerosol |
| EP0032779B1 (en) * | 1980-01-21 | 1983-06-29 | Pfw (Nederland) B.V. | Novel method for preparation of homogeneous dimethylether-propelled water-based aerosols |
| US4450253A (en) * | 1981-03-03 | 1984-05-22 | Ccl Industries Inc. | Propellant-active carrier system for water-based paints |
| US4518734A (en) * | 1981-06-22 | 1985-05-21 | Rust-Oleum Corporation | Water based aerosol coatings |
| DE3127061A1 (de) * | 1981-07-09 | 1983-01-27 | Bayer Ag, 5090 Leverkusen | Aerosol-formulierungen auf wasserbasis |
| JPS60104004A (ja) * | 1983-11-09 | 1985-06-08 | Fumakiraa Kk | 低薬害性エアゾ−ル農薬組成物 |
| JPS60104003A (ja) * | 1983-11-09 | 1985-06-08 | Fumakiraa Kk | 低薬害性エアゾ−ル農薬組成物 |
| JPH0618284B2 (ja) * | 1984-08-09 | 1994-03-09 | 富士通株式会社 | マイクロ波集積回路 |
| US4604226A (en) * | 1985-03-22 | 1986-08-05 | E. I. Du Pont De Nemours And Company | Aerosol corrosion inhibitors |
-
1988
- 1988-11-29 AU AU26346/88A patent/AU605652B2/en not_active Ceased
- 1988-12-02 MY MYPI88001402A patent/MY103645A/en unknown
- 1988-12-06 NZ NZ227222A patent/NZ227222A/en unknown
- 1988-12-06 FR FR888815942A patent/FR2624345B1/fr not_active Expired - Lifetime
- 1988-12-06 ZA ZA889125A patent/ZA889125B/xx unknown
- 1988-12-08 US US07/281,519 patent/US5064639A/en not_active Expired - Fee Related
- 1988-12-09 GB GB8828815A patent/GB2213725B/en not_active Expired - Lifetime
- 1988-12-12 CH CH4581/88A patent/CH676536A5/fr not_active IP Right Cessation
- 1988-12-13 CA CA000585772A patent/CA1309337C/en not_active Expired - Lifetime
- 1988-12-13 IT IT8848647A patent/IT1227146B/it active
- 1988-12-13 ES ES8803782A patent/ES2009453A6/es not_active Expired
- 1988-12-14 EP EP88120904A patent/EP0320908B1/en not_active Expired - Lifetime
- 1988-12-14 BE BE8801403A patent/BE1001443A3/fr not_active IP Right Cessation
- 1988-12-14 BR BR888806604A patent/BR8806604A/pt not_active Application Discontinuation
- 1988-12-14 DE DE8888120904T patent/DE3863766D1/de not_active Expired - Lifetime
- 1988-12-15 KR KR1019880016736A patent/KR960011193B1/ko not_active Expired - Lifetime
- 1988-12-15 MX MX1419188A patent/MX14191A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US5064639A (en) | 1991-11-12 |
| CA1309337C (en) | 1992-10-27 |
| BR8806604A (pt) | 1989-08-22 |
| IT1227146B (it) | 1991-03-19 |
| ZA889125B (en) | 1989-08-30 |
| GB8828815D0 (en) | 1989-01-18 |
| IT8848647A0 (it) | 1988-12-13 |
| GB2213725B (en) | 1991-07-31 |
| EP0320908A1 (en) | 1989-06-21 |
| KR960011193B1 (ko) | 1996-08-21 |
| CH676536A5 (enExample) | 1991-02-15 |
| FR2624345A1 (fr) | 1989-06-16 |
| GB2213725A (en) | 1989-08-23 |
| AU2634688A (en) | 1989-06-15 |
| KR890009265A (ko) | 1989-08-01 |
| ES2009453A6 (es) | 1989-09-16 |
| MY103645A (en) | 1993-08-28 |
| FR2624345B1 (fr) | 1990-06-01 |
| EP0320908B1 (en) | 1991-07-17 |
| AU605652B2 (en) | 1991-01-17 |
| DE3863766D1 (de) | 1991-08-22 |
| MX14191A (es) | 1993-10-01 |
| BE1001443A3 (fr) | 1989-10-31 |
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