KR910018365A - 3-이소티아졸론의 안정화방법 및 안정한 3-이소티아졸론 조성물 - Google Patents
3-이소티아졸론의 안정화방법 및 안정한 3-이소티아졸론 조성물 Download PDFInfo
- Publication number
- KR910018365A KR910018365A KR1019910005431A KR910005431A KR910018365A KR 910018365 A KR910018365 A KR 910018365A KR 1019910005431 A KR1019910005431 A KR 1019910005431A KR 910005431 A KR910005431 A KR 910005431A KR 910018365 A KR910018365 A KR 910018365A
- Authority
- KR
- South Korea
- Prior art keywords
- isothiazolone
- composition
- phenoxyalkanol
- dichloro
- octyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 9
- MGIYRDNGCNKGJU-UHFFFAOYSA-N isothiazolinone Chemical compound O=C1C=CSN1 MGIYRDNGCNKGJU-UHFFFAOYSA-N 0.000 title claims 8
- 230000000087 stabilizing effect Effects 0.000 title claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 4
- JLHMJWHSBYZWJJ-UHFFFAOYSA-N 1,2-thiazole 1-oxide Chemical compound O=S1C=CC=N1 JLHMJWHSBYZWJJ-UHFFFAOYSA-N 0.000 claims 2
- IBLKWZIFZMJLFL-UHFFFAOYSA-N 1-phenoxypropan-2-ol Chemical compound CC(O)COC1=CC=CC=C1 IBLKWZIFZMJLFL-UHFFFAOYSA-N 0.000 claims 2
- JRQLZCFSWYQHPI-UHFFFAOYSA-N 4,5-dichloro-2-cyclohexyl-1,2-thiazol-3-one Chemical compound O=C1C(Cl)=C(Cl)SN1C1CCCCC1 JRQLZCFSWYQHPI-UHFFFAOYSA-N 0.000 claims 2
- PORQOHRXAJJKGK-UHFFFAOYSA-N 4,5-dichloro-2-n-octyl-3(2H)-isothiazolone Chemical compound CCCCCCCCN1SC(Cl)=C(Cl)C1=O PORQOHRXAJJKGK-UHFFFAOYSA-N 0.000 claims 2
- 238000002144 chemical decomposition reaction Methods 0.000 claims 2
- DHNRXBZYEKSXIM-UHFFFAOYSA-N chloromethylisothiazolinone Chemical group CN1SC(Cl)=CC1=O DHNRXBZYEKSXIM-UHFFFAOYSA-N 0.000 claims 2
- BEGLCMHJXHIJLR-UHFFFAOYSA-N methylisothiazolinone Chemical compound CN1SC=CC1=O BEGLCMHJXHIJLR-UHFFFAOYSA-N 0.000 claims 2
- JPMIIZHYYWMHDT-UHFFFAOYSA-N octhilinone Chemical compound CCCCCCCCN1SC=CC1=O JPMIIZHYYWMHDT-UHFFFAOYSA-N 0.000 claims 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 2
- 229940106026 phenoxyisopropanol Drugs 0.000 claims 2
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 claims 1
- -1 3-isothiazolone compound Chemical class 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 230000005494 condensation Effects 0.000 claims 1
- 238000009833 condensation Methods 0.000 claims 1
- 239000002270 dispersing agent Substances 0.000 claims 1
- 239000003906 humectant Substances 0.000 claims 1
- 229960005323 phenoxyethanol Drugs 0.000 claims 1
- 229920000642 polymer Polymers 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 239000004034 viscosity adjusting agent Substances 0.000 claims 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
- C07D275/02—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings
- C07D275/03—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Pest Control & Pesticides (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Cosmetics (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (13)
- 화학적 분해에 대하여 이소티아졸론을 안정화시키기 위하여 충분한 량의 페녹시 알카놀에 3-이소티아졸론을 용해시킴을 포함하는 3-이소티아졸론의 안정화 방법.
- 1항에 있어서, 페녹시알카놀에 대한 3-이소티아졸론의 중량비가 약 0.1 : 99∼25 : 75 임을 특징으로 하는 방법.
- 1항에 있어서, 결과용액은 나아가 계면활성제, 무기염, 중합체 분산제, 보습제, 점도조절제 및 응결점 강하제로 구성된 그룹에서 선택된 보조제를 약 25중량%까지 포함함을 특징으로 하는 방법.
- 1항에 있어서, 상기 3-이소티아졸론은 5-클로로-2-메틸-3-이소티아졸론, 2-메틸-3-이소티아졸론, 2-옥틸-3-이소티아졸론, 4,5-디클로로-2-시클로헥실-3-이소티아졸론, 및 4,5-디클로로-2-옥틸-이소티아졸론으로 구성되는 그룹에서 선택됨을 특징으로 하는 방법.
- 1항에 있어서, 결과용액은 약 5중량%이하의 수분을 포함함을 특징으로 하는 방법.
- 5항에 있어서, 상기 용액은 물을 포함하지 않음을 특징으로 하는 방법.
- 1항에 있어서, 상기 페녹시알카놀을 페녹시 에탄올과 페녹시 이소프로판올로 구성되는 그룹에서 선택됨을 특징으로 하는 방법.
- 3-이소티아졸론 화합물, 및 상기 이소티아졸론을 화학적 분해에 대하여 안정시키기에 충분한 량의 페녹시 알카놀을 포함한 조성물.
- 8항에 있어서, 상기 페녹시알카놀을 페녹시알카놀에 대한 3-이소티아졸론의 중량비가 약 0.1 : 99.9∼25 : 75 로 존재함을 특징으로 하는 조성물.
- 8항에 있어서, 상기 3-이소티아졸론은 5-클로로-2-메틸-3-이소티아졸론, 2-메틸-3-이소티아졸론, 2-옥틸-3-이소티아졸론, 4,5-디클로로-2-시클로헥실-3-이소티아졸론, 및 4,5-디클로로-2-옥틸-이소티아졸론으로 구성된 그룹에서 선택됨을 특징으로 하는 조성물.
- 8항에 있어서, 상기 조성물은 약 5%이하의 물을 포함함을 특징으로 하는 조성물.
- 8항에 있어서, 상기 조성물은 물을 포함하지 않음을 특징으로 하는 조성물.
- 8항에 있어서, 상기 페녹시알카놀은 페녹시알카놀 및 페녹시이소프로판올로 구성되는 그룹에서 선택됨을 특징으로 하는 조성물.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US505,201 | 1990-04-05 | ||
US07/505,201 US5037989A (en) | 1990-04-05 | 1990-04-05 | Phenoxyalkanol as a stabilizer for isothiazolone concentrates |
Publications (2)
Publication Number | Publication Date |
---|---|
KR910018365A true KR910018365A (ko) | 1991-11-30 |
KR0171601B1 KR0171601B1 (ko) | 1999-02-01 |
Family
ID=24009415
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019910005431A KR0171601B1 (ko) | 1990-04-05 | 1991-04-04 | 3-이소티아졸론의 안정화방법 및 안정한 3-이소티아졸론 조성물 |
Country Status (13)
Country | Link |
---|---|
US (1) | US5037989A (ko) |
EP (1) | EP0450916B1 (ko) |
JP (1) | JP3119672B2 (ko) |
KR (1) | KR0171601B1 (ko) |
AT (1) | ATE133833T1 (ko) |
AU (1) | AU643766B2 (ko) |
CA (1) | CA2038982A1 (ko) |
DE (1) | DE69116916T2 (ko) |
ES (1) | ES2084101T3 (ko) |
HU (1) | HU213251B (ko) |
IE (1) | IE75699B1 (ko) |
IL (1) | IL97749A (ko) |
PT (1) | PT97259B (ko) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9003871D0 (en) * | 1990-02-21 | 1990-04-18 | Rohm & Haas | Stabilization of isothiazolones |
DE4301295C2 (de) * | 1993-01-15 | 1999-04-08 | Schuelke & Mayr Gmbh | Wäßriges Desinfektionsmittelkonzentrat und Desinfektionsmittel auf Aldehyd- und Alkoholbasis und deren Verwendung |
US5599827A (en) * | 1995-05-16 | 1997-02-04 | Rohm And Haas Company | Stable microemulsions of certain 3-isothiazolone compounds |
DE19534532C2 (de) * | 1995-09-08 | 1999-04-08 | Schuelke & Mayr Gmbh | Additivmischungen für Kühlschmiermittelprodukte und deren Verwendung |
US6121302A (en) * | 1999-05-11 | 2000-09-19 | Lonza, Inc. | Stabilization of isothiazolone |
FR2795328B1 (fr) * | 1999-06-23 | 2002-08-02 | H F F F Haut Fourneau Forges E | Procede et composition de protection contre la contamination pour articles sanitaires |
US6511673B1 (en) * | 2000-05-10 | 2003-01-28 | Rohm And Haas Company | Microbicidal composition |
WO2002067685A1 (en) * | 2001-02-26 | 2002-09-06 | Lonza Inc. | Stable preservative formulations comprising halopropynyl compounds and butoxydiglycol solvent |
EP1488699B1 (en) * | 2002-01-31 | 2013-01-16 | Rohm And Haas Company | Synergistic microbicidal combinations |
US9034905B2 (en) | 2003-02-05 | 2015-05-19 | Rohm And Haas Company | Synergistic microbicidal combinations |
DE102005012123A1 (de) | 2005-03-16 | 2006-09-28 | Schülke & Mayr GmbH | Isothiazolon-haltiges Konservierungsmittel mit verbesserter Wirksamkeit |
EP1772055A1 (en) * | 2005-10-04 | 2007-04-11 | Rohm and Haas France SAS | Synergistic microbicidal compositions comprising a N-alkyl-1,2-benzoisothiazolin-3-one |
CN107920527B (zh) * | 2015-09-09 | 2021-02-19 | 托尔有限公司 | 储存稳定的生物杀灭剂组合物 |
CN109566633A (zh) * | 2019-01-03 | 2019-04-05 | 三博生化科技(上海)有限公司 | 一种防腐剂及其制备方法 |
US20200390666A1 (en) * | 2019-05-01 | 2020-12-17 | Church & Dwight Co., Inc. | Rinse-free shampoo composition |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3508928A1 (de) * | 1985-03-13 | 1986-09-18 | Giulini Chemie Gmbh, 6700 Ludwigshafen | Kombination zur antimikrobiellen und antioxidativen stabilisierung von externa und koerperpflegemitteln |
DE68904828T2 (de) * | 1988-06-08 | 1993-06-03 | Ichikawa Gosei Kagaku Kk | Verfahren zur stabilisierung einer 3-isothiazolon-loesung. |
GB9003871D0 (en) * | 1990-02-21 | 1990-04-18 | Rohm & Haas | Stabilization of isothiazolones |
-
1990
- 1990-04-05 US US07/505,201 patent/US5037989A/en not_active Expired - Lifetime
-
1991
- 1991-03-25 CA CA002038982A patent/CA2038982A1/en not_active Abandoned
- 1991-04-02 AT AT91302884T patent/ATE133833T1/de not_active IP Right Cessation
- 1991-04-02 IL IL9774991A patent/IL97749A/en not_active IP Right Cessation
- 1991-04-02 DE DE69116916T patent/DE69116916T2/de not_active Expired - Lifetime
- 1991-04-02 ES ES91302884T patent/ES2084101T3/es not_active Expired - Lifetime
- 1991-04-02 EP EP91302884A patent/EP0450916B1/en not_active Expired - Lifetime
- 1991-04-04 IE IE112491A patent/IE75699B1/en not_active IP Right Cessation
- 1991-04-04 JP JP03071795A patent/JP3119672B2/ja not_active Expired - Lifetime
- 1991-04-04 KR KR1019910005431A patent/KR0171601B1/ko not_active IP Right Cessation
- 1991-04-04 PT PT97259A patent/PT97259B/pt not_active IP Right Cessation
- 1991-04-04 AU AU74088/91A patent/AU643766B2/en not_active Expired
- 1991-04-05 HU HU911119A patent/HU213251B/hu not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
HU213251B (en) | 1997-04-28 |
JP3119672B2 (ja) | 2000-12-25 |
DE69116916D1 (de) | 1996-03-21 |
EP0450916B1 (en) | 1996-02-07 |
US5037989A (en) | 1991-08-06 |
HUT60318A (en) | 1992-08-28 |
IE911124A1 (en) | 1991-10-09 |
ES2084101T3 (es) | 1996-05-01 |
PT97259A (pt) | 1992-01-31 |
ATE133833T1 (de) | 1996-02-15 |
AU7408891A (en) | 1991-10-10 |
DE69116916T2 (de) | 1996-09-05 |
PT97259B (pt) | 1998-07-31 |
AU643766B2 (en) | 1993-11-25 |
HU911119D0 (en) | 1991-10-28 |
EP0450916A1 (en) | 1991-10-09 |
IL97749A0 (en) | 1992-06-21 |
IL97749A (en) | 1995-06-29 |
CA2038982A1 (en) | 1991-10-06 |
JPH04221374A (ja) | 1992-08-11 |
IE75699B1 (en) | 1997-09-10 |
KR0171601B1 (ko) | 1999-02-01 |
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