TW327595B - Stabilized microbicidally active 3-isothiazolone composition and method of stabilizing microbicidally active 3-isothiazolone in water solution - Google Patents
Stabilized microbicidally active 3-isothiazolone composition and method of stabilizing microbicidally active 3-isothiazolone in water solutionInfo
- Publication number
- TW327595B TW327595B TW085106402A TW85106402A TW327595B TW 327595 B TW327595 B TW 327595B TW 085106402 A TW085106402 A TW 085106402A TW 85106402 A TW85106402 A TW 85106402A TW 327595 B TW327595 B TW 327595B
- Authority
- TW
- Taiwan
- Prior art keywords
- acids
- isothiazolone
- microbicidally active
- stabilized
- microbicidally
- Prior art date
Links
- MGIYRDNGCNKGJU-UHFFFAOYSA-N isothiazolinone Chemical compound O=C1C=CSN1 MGIYRDNGCNKGJU-UHFFFAOYSA-N 0.000 title abstract 3
- 230000000087 stabilizing effect Effects 0.000 title abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title abstract 2
- 239000002253 acid Substances 0.000 abstract 4
- 150000007513 acids Chemical class 0.000 abstract 3
- -1 3-isothiazolone compound Chemical class 0.000 abstract 2
- TULKVGVRFUJFST-UHFFFAOYSA-N 2-(2-iodosylphenyl)acetic acid Chemical class OC(=O)CC1=CC=CC=C1I=O TULKVGVRFUJFST-UHFFFAOYSA-N 0.000 abstract 1
- CGSORKPMFGNTTJ-UHFFFAOYSA-N 2-(2-iodylphenyl)acetic acid Chemical class OC(=O)CC1=CC=CC=C1I(=O)=O CGSORKPMFGNTTJ-UHFFFAOYSA-N 0.000 abstract 1
- RKCPTJNBAMWIRW-UHFFFAOYSA-N 2-[2-(carboxymethyl)-3-iodosylphenyl]acetic acid Chemical class OC(=O)CC1=CC=CC(I=O)=C1CC(O)=O RKCPTJNBAMWIRW-UHFFFAOYSA-N 0.000 abstract 1
- SKCXSHSASMBUNN-UHFFFAOYSA-N 2-[2-(carboxymethyl)-3-iodylphenyl]acetic acid Chemical class OC(=O)CC1=CC=CC(I(=O)=O)=C1CC(O)=O SKCXSHSASMBUNN-UHFFFAOYSA-N 0.000 abstract 1
- ZNZFKDGMZIGWPD-UHFFFAOYSA-N 2-iodosylbenzamide Chemical class NC(=O)C1=CC=CC=C1I=O ZNZFKDGMZIGWPD-UHFFFAOYSA-N 0.000 abstract 1
- GKVXFNMJNIBRIL-UHFFFAOYSA-N 2-iodosylbenzenesulfonic acid Chemical class OS(=O)(=O)C1=CC=CC=C1I=O GKVXFNMJNIBRIL-UHFFFAOYSA-N 0.000 abstract 1
- YATDZQPWPZULMU-UHFFFAOYSA-N 2-iodosylnaphthalene-1-carboxylic acid Chemical class C1=CC=C2C(C(=O)O)=C(I=O)C=CC2=C1 YATDZQPWPZULMU-UHFFFAOYSA-N 0.000 abstract 1
- RRGZYVZQRWEAJL-UHFFFAOYSA-N 2-iodosylpyridin-1-ium-1-carboxylate Chemical class [O-]C(=O)[N+]1=CC=CC=C1I=O RRGZYVZQRWEAJL-UHFFFAOYSA-N 0.000 abstract 1
- LAUULDMKOCSHGZ-UHFFFAOYSA-N 2-iodylbenzamide Chemical class NC(=O)C1=CC=CC=C1I(=O)=O LAUULDMKOCSHGZ-UHFFFAOYSA-N 0.000 abstract 1
- HLFJXNCNYFCETF-UHFFFAOYSA-N 2-iodylnaphthalene-1-carboxylic acid Chemical class C1=CC=C2C(C(=O)O)=C(I(=O)=O)C=CC2=C1 HLFJXNCNYFCETF-UHFFFAOYSA-N 0.000 abstract 1
- ZAVSNPXZJYBRKG-UHFFFAOYSA-N 2-iodylpyridin-1-ium-1-carboxylate Chemical class [O-]C(=O)[N+]1=CC=CC=C1I(=O)=O ZAVSNPXZJYBRKG-UHFFFAOYSA-N 0.000 abstract 1
- TYGJHXDCSMYJAK-UHFFFAOYSA-N 3-iodosyl-2-sulfobenzoic acid Chemical class OC(=O)C1=CC=CC(I=O)=C1S(O)(=O)=O TYGJHXDCSMYJAK-UHFFFAOYSA-N 0.000 abstract 1
- DGXHFAKXEPXLDF-UHFFFAOYSA-N 3-iodosyl-2-sulfonaphthalene-1-carboxylic acid Chemical class C1=CC=C2C(C(=O)O)=C(S(O)(=O)=O)C(I=O)=CC2=C1 DGXHFAKXEPXLDF-UHFFFAOYSA-N 0.000 abstract 1
- PHTQXKFTVUUGGU-UHFFFAOYSA-N 3-iodosylnaphthalene-1,2-dicarboxylic acid Chemical class C1=CC=CC2=C(C(O)=O)C(C(=O)O)=C(I=O)C=C21 PHTQXKFTVUUGGU-UHFFFAOYSA-N 0.000 abstract 1
- BYCXIFMOPJEEOC-UHFFFAOYSA-N 3-iodosylphthalic acid Chemical class OC(=O)C1=CC=CC(I=O)=C1C(O)=O BYCXIFMOPJEEOC-UHFFFAOYSA-N 0.000 abstract 1
- YSKRZGKAUKSOPI-UHFFFAOYSA-N 3-iodyl-2-sulfobenzoic acid Chemical class OC(=O)C1=CC=CC(I(=O)=O)=C1S(O)(=O)=O YSKRZGKAUKSOPI-UHFFFAOYSA-N 0.000 abstract 1
- DUJOLUIYODMGGF-UHFFFAOYSA-N 3-iodyl-2-sulfonaphthalene-1-carboxylic acid Chemical class C1=CC=C2C(C(=O)O)=C(S(O)(=O)=O)C(I(=O)=O)=CC2=C1 DUJOLUIYODMGGF-UHFFFAOYSA-N 0.000 abstract 1
- ZENQFUGNZCYPMS-UHFFFAOYSA-N 3-iodylnaphthalene-1,2-dicarboxylic acid Chemical class C1=CC=CC2=C(C(O)=O)C(C(=O)O)=C(I(=O)=O)C=C21 ZENQFUGNZCYPMS-UHFFFAOYSA-N 0.000 abstract 1
- UQXKWWLGGQVMTA-UHFFFAOYSA-N 3-iodylphthalic acid Chemical class OC(=O)C1=CC=CC(I(=O)=O)=C1C(O)=O UQXKWWLGGQVMTA-UHFFFAOYSA-N 0.000 abstract 1
- BHCZBQIDEDDBHQ-UHFFFAOYSA-N 4-iodosyl-3-sulfophthalic acid Chemical class OC(=O)C1=CC=C(I=O)C(S(O)(=O)=O)=C1C(O)=O BHCZBQIDEDDBHQ-UHFFFAOYSA-N 0.000 abstract 1
- IBTZHFVXFXUBAE-UHFFFAOYSA-N 4-iodyl-3-sulfophthalic acid Chemical class OC(=O)C1=CC=C(I(=O)=O)C(S(O)(=O)=O)=C1C(O)=O IBTZHFVXFXUBAE-UHFFFAOYSA-N 0.000 abstract 1
- IFPHDUVGLXEIOQ-UHFFFAOYSA-N ortho-iodosylbenzoic acid Chemical class OC(=O)C1=CC=CC=C1I=O IFPHDUVGLXEIOQ-UHFFFAOYSA-N 0.000 abstract 1
- FIYYMXYOBLWYQO-UHFFFAOYSA-N ortho-iodylbenzoic acid Chemical class OC(=O)C1=CC=CC=C1I(=O)=O FIYYMXYOBLWYQO-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 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
- A01N43/74—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 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
-
- 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- General Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Cosmetics (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/450,190 US5594017A (en) | 1995-05-25 | 1995-05-25 | Stabilization of aqueous 3-isothiazolone solutions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW327595B true TW327595B (en) | 1998-03-01 |
Family
ID=23787138
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW085106402A TW327595B (en) | 1995-05-25 | 1996-05-30 | Stabilized microbicidally active 3-isothiazolone composition and method of stabilizing microbicidally active 3-isothiazolone in water solution |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US5594017A (zh) |
| EP (1) | EP0745326B1 (zh) |
| JP (1) | JPH08325251A (zh) |
| KR (1) | KR100443313B1 (zh) |
| CN (1) | CN1071540C (zh) |
| AT (1) | ATE184753T1 (zh) |
| AU (1) | AU705075B2 (zh) |
| BR (1) | BR9602461A (zh) |
| CA (1) | CA2176536A1 (zh) |
| DE (1) | DE69604332T2 (zh) |
| ES (1) | ES2138792T3 (zh) |
| HU (1) | HUP9601407A3 (zh) |
| NZ (1) | NZ286572A (zh) |
| SG (1) | SG44940A1 (zh) |
| TW (1) | TW327595B (zh) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5910503A (en) * | 1997-10-28 | 1999-06-08 | Rohm And Haas Company | Stable microbicide formulation |
| JP4903745B2 (ja) * | 2007-05-08 | 2012-03-28 | ローム アンド ハース カンパニー | 安定化された流体 |
| JP7326083B2 (ja) * | 2019-09-18 | 2023-08-15 | アクアス株式会社 | 藻類抑制剤組成物及び藻類抑制方法 |
| JP7326084B2 (ja) * | 2019-09-18 | 2023-08-15 | アクアス株式会社 | スライム抑制剤組成物及びスライム抑制方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| USRE34185E (en) * | 1985-03-08 | 1993-02-23 | Rohm And Haas Company | Stabilization of non-aqueous solutions of 3-isothiazolones |
| US4906274A (en) * | 1987-11-06 | 1990-03-06 | Rohm And Haas Company | Organic stabilizers |
| ATE105139T1 (de) * | 1989-06-06 | 1994-05-15 | Rohm & Haas | Organische stabilisatoren fuer isothiazolone. |
| DE58906847D1 (de) * | 1989-11-10 | 1994-03-10 | Thor Chemie Gmbh | Stabilisierte wässrige Lösungen von 3-Isothiazolinonen. |
-
1995
- 1995-05-25 US US08/450,190 patent/US5594017A/en not_active Expired - Fee Related
-
1996
- 1996-05-13 DE DE69604332T patent/DE69604332T2/de not_active Expired - Fee Related
- 1996-05-13 ES ES96303342T patent/ES2138792T3/es not_active Expired - Lifetime
- 1996-05-13 AT AT96303342T patent/ATE184753T1/de not_active IP Right Cessation
- 1996-05-13 EP EP96303342A patent/EP0745326B1/en not_active Expired - Lifetime
- 1996-05-13 AU AU52235/96A patent/AU705075B2/en not_active Ceased
- 1996-05-14 NZ NZ286572A patent/NZ286572A/en unknown
- 1996-05-14 CA CA002176536A patent/CA2176536A1/en not_active Abandoned
- 1996-05-15 SG SG1996009802A patent/SG44940A1/en unknown
- 1996-05-23 KR KR1019960017705A patent/KR100443313B1/ko not_active Expired - Fee Related
- 1996-05-23 CN CN96108124A patent/CN1071540C/zh not_active Expired - Fee Related
- 1996-05-24 BR BR9602461A patent/BR9602461A/pt not_active Application Discontinuation
- 1996-05-24 JP JP8151844A patent/JPH08325251A/ja not_active Withdrawn
- 1996-05-24 HU HU9601407A patent/HUP9601407A3/hu unknown
- 1996-05-30 TW TW085106402A patent/TW327595B/zh active
Also Published As
| Publication number | Publication date |
|---|---|
| AU705075B2 (en) | 1999-05-13 |
| NZ286572A (en) | 1998-07-28 |
| KR100443313B1 (ko) | 2004-10-20 |
| US5594017A (en) | 1997-01-14 |
| ES2138792T3 (es) | 2000-01-16 |
| CA2176536A1 (en) | 1996-11-26 |
| HUP9601407A2 (en) | 1997-02-28 |
| DE69604332D1 (de) | 1999-10-28 |
| JPH08325251A (ja) | 1996-12-10 |
| HUP9601407A3 (en) | 1997-09-29 |
| BR9602461A (pt) | 1998-04-22 |
| ATE184753T1 (de) | 1999-10-15 |
| CN1071540C (zh) | 2001-09-26 |
| EP0745326B1 (en) | 1999-09-22 |
| CN1140542A (zh) | 1997-01-22 |
| DE69604332T2 (de) | 2000-05-11 |
| EP0745326A1 (en) | 1996-12-04 |
| AU5223596A (en) | 1996-12-05 |
| HU9601407D0 (en) | 1996-07-29 |
| KR960040156A (ko) | 1996-12-17 |
| SG44940A1 (en) | 1997-12-19 |
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