NO323350B1 - Synergistisk biocidsammensetning og anvendelse av denne for a bekjempe skadelige mikroorganismer. - Google Patents
Synergistisk biocidsammensetning og anvendelse av denne for a bekjempe skadelige mikroorganismer. Download PDFInfo
- Publication number
- NO323350B1 NO323350B1 NO20000749A NO20000749A NO323350B1 NO 323350 B1 NO323350 B1 NO 323350B1 NO 20000749 A NO20000749 A NO 20000749A NO 20000749 A NO20000749 A NO 20000749A NO 323350 B1 NO323350 B1 NO 323350B1
- Authority
- NO
- Norway
- Prior art keywords
- biocide
- composition according
- mit
- bit
- methylisothiazolin
- Prior art date
Links
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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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP97114397A EP0900525A1 (de) | 1997-08-20 | 1997-08-20 | Synergistische Biozidzusammensetzung |
| PCT/EP1998/005310 WO1999008530A1 (de) | 1997-08-20 | 1998-08-20 | Synergistische biozidzusammensetzung |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO20000749D0 NO20000749D0 (no) | 2000-02-15 |
| NO20000749L NO20000749L (no) | 2000-04-18 |
| NO323350B1 true NO323350B1 (no) | 2007-04-02 |
Family
ID=8227248
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20000749A NO323350B1 (no) | 1997-08-20 | 2000-02-15 | Synergistisk biocidsammensetning og anvendelse av denne for a bekjempe skadelige mikroorganismer. |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US6361788B1 (ko) |
| EP (2) | EP0900525A1 (ko) |
| JP (1) | JP3992433B2 (ko) |
| KR (1) | KR100397259B1 (ko) |
| CN (1) | CN1286370C (ko) |
| AT (1) | ATE227082T1 (ko) |
| AU (1) | AU731655B2 (ko) |
| BR (1) | BR9811955B1 (ko) |
| CA (1) | CA2299227C (ko) |
| CZ (1) | CZ294066B6 (ko) |
| DE (1) | DE59806209D1 (ko) |
| DK (1) | DK1005271T3 (ko) |
| ES (1) | ES2188013T3 (ko) |
| HU (1) | HU230127B1 (ko) |
| MX (1) | MX212024B (ko) |
| NO (1) | NO323350B1 (ko) |
| PL (1) | PL203139B1 (ko) |
| PT (1) | PT1005271E (ko) |
| TR (1) | TR200000437T2 (ko) |
| WO (1) | WO1999008530A1 (ko) |
Families Citing this family (67)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0900525A1 (de) * | 1997-08-20 | 1999-03-10 | Thor Chemie Gmbh | Synergistische Biozidzusammensetzung |
| FR2801767B1 (fr) * | 1999-12-01 | 2002-09-13 | Eastman Kodak Co | Materiau biocide ayant une activite amelioree |
| DE10042894A1 (de) * | 2000-08-31 | 2002-03-14 | Thor Chemie Gmbh | Synergistische Biozidzusammensetzung mit 2-Methylisothiazolin-3-on |
| KR20040073475A (ko) * | 2001-12-12 | 2004-08-19 | 아이에스피이 인베스트먼츠 인코포레이팃드 | 폴리에틸렌 글리콜, 폴리프로필렌 글리콜 또는폴리프로필렌 글리콜 글리세릴 에스테르 중의아이피비씨(ｉｐｂｃ) 액체 조성물 |
| EP1527684B1 (en) * | 2002-01-31 | 2013-02-27 | Rohm And Haas Company | Synergistic microbicidal combination |
| KR20040038041A (ko) * | 2002-10-31 | 2004-05-08 | 에스케이케미칼주식회사 | 살균제 조성물 및 이를 이용한 살균방법 |
| AU2002359562A1 (en) * | 2002-12-02 | 2004-06-23 | Lonza Inc. | Starch compositions containing biodegradation inhibitors |
| US9034905B2 (en) * | 2003-02-05 | 2015-05-19 | Rohm And Haas Company | Synergistic microbicidal combinations |
| AU2004201059B2 (en) | 2003-03-26 | 2009-06-04 | Rohm And Haas Company | Microbicidal composition |
| JP5194205B2 (ja) * | 2004-02-19 | 2013-05-08 | 住化エンビロサイエンス株式会社 | 工業用抗菌組成物 |
| US7105555B2 (en) * | 2004-04-06 | 2006-09-12 | Isp Investments Inc. | Stable, neutral pH VOC-free biocidal compositions of 1,2-benzisothiazolin-3-one |
| US7718715B2 (en) * | 2004-06-10 | 2010-05-18 | S.C. Johnson & Son, Inc. | pH-modified latex comprising a synergistic combination of biocides |
| DE102004052878A1 (de) * | 2004-11-02 | 2006-05-04 | Schülke & Mayr GmbH | Isothiazolonhaltige Konservierungsmittel mit verbesserter Stabilität |
| US7468384B2 (en) | 2004-11-16 | 2008-12-23 | Rohm And Haas Company | Microbicidal composition |
| DE102004059041A1 (de) * | 2004-12-07 | 2006-06-08 | Schülke & Mayr GmbH | Verwendung von Formaldehyd und Formaldehyd freisetzenden Verbindungen in einer Zusammensetzung zur Bekämpfung von Mykobakterien |
| DE102005001566A1 (de) * | 2005-01-13 | 2006-07-27 | Lanxess Deutschland Gmbh | Antimikrobiell ausgerüstete Feststoff-Zubereitungen |
| JP2006265390A (ja) * | 2005-03-24 | 2006-10-05 | Shachihata Inc | 水性インキ |
| WO2007104750A2 (de) * | 2006-03-13 | 2007-09-20 | Basf Se | Verfahren zur herstellung von polymeren nanopartikeln |
| JP4707138B2 (ja) * | 2005-05-27 | 2011-06-22 | 住化エンビロサイエンス株式会社 | 工業用抗菌組成物 |
| CN101257795B (zh) * | 2005-07-08 | 2012-06-06 | Isp投资有限公司 | 杀微生物组合物 |
| DE102005036314A1 (de) | 2005-07-29 | 2007-02-01 | Isp Biochema Schwaben Gmbh | Mikrobizide Zusammensetzung |
| RU2008112684A (ru) * | 2005-09-02 | 2009-10-10 | Тор Гмбх (De) | Синергическая серебросодержащая биоцидная композиция |
| 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 |
| JP4813896B2 (ja) * | 2005-12-22 | 2011-11-09 | 株式会社片山化学工業研究所 | 工業用抗菌剤およびそれを用いた工業的抗菌方法 |
| JP4840934B2 (ja) * | 2006-04-07 | 2011-12-21 | ローム アンド ハース カンパニー | 水処理方法 |
| US8309231B2 (en) | 2006-05-31 | 2012-11-13 | Usg Interiors, Llc | Acoustical tile |
| EP1873300A1 (de) | 2006-06-30 | 2008-01-02 | THOR GmbH | Antimikrobiell ausgerüstetes Textil |
| JP2008019215A (ja) * | 2006-07-13 | 2008-01-31 | Nippon Soda Co Ltd | 殺菌剤組成物 |
| JP5108264B2 (ja) * | 2006-08-08 | 2012-12-26 | アーチ・ケミカルズ・ジャパン株式会社 | 工業用防腐剤組成物 |
| DE102006061890A1 (de) * | 2006-12-28 | 2008-07-03 | Thor Gmbh | Kleb- und Dichtungsmassen mit antimikrobieller Ausrüstung |
| CA2632160C (en) * | 2007-06-21 | 2011-10-11 | Rohm And Haas Company | Microbicidal composition comprising n-methyl-1,2-benzisothiazolin-3-one and 2,2-dibromo-3-nitrilopropionamide |
| US20090035340A1 (en) * | 2007-07-30 | 2009-02-05 | Kimberly-Clark Worldwide, Inc. | Preservative compositions for moist wipes |
| JP5344862B2 (ja) * | 2008-07-23 | 2013-11-20 | 日本エンバイロケミカルズ株式会社 | 工業用防腐防かび剤 |
| EP2213166B1 (de) * | 2009-01-29 | 2012-03-21 | THOR GmbH | Biozidzusammensetzungen enthaltend 2-Methylisothiazolin-3-on und ein Haloalkylsulfon |
| PL2272348T3 (pl) | 2009-07-07 | 2015-08-31 | Lanxess Deutschland Gmbh | Kompozycje biobójcze |
| JP5210360B2 (ja) * | 2009-07-30 | 2013-06-12 | ローム アンド ハース カンパニー | 相乗的殺微生物組成物 |
| DE102009048188A1 (de) | 2009-10-02 | 2011-04-07 | Schülke & Mayr GmbH | Antimikrobiell wirksame Gebrauchslösungen enthaltend Kombinationen von Isothiazolonen und Aminen |
| DE102009048189A1 (de) * | 2009-10-02 | 2011-04-07 | Schülke & Mayr GmbH | Lagerstabile mikrobizide Konzentrate und deren Verwendung als Konservierungsmittel |
| WO2011115912A1 (en) * | 2010-03-15 | 2011-09-22 | Isp Investments Inc. | Synergistic preservative compositions |
| CN201712857U (zh) | 2010-05-10 | 2011-01-19 | S.C.约翰逊父子公司 | 用于挥发性材料的散发装置及其壳体和散发片 |
| EP2575476A1 (de) | 2010-05-26 | 2013-04-10 | THOR GmbH | Synergistische biozidzusammensetzung enthaltend wenigstens drei biozide komponenten |
| JP5550611B2 (ja) * | 2010-08-09 | 2014-07-16 | ダウ グローバル テクノロジーズ エルエルシー | １，２−ベンゾイソチアゾリン−３−オンを含む組成物 |
| US20130109728A1 (en) | 2011-10-27 | 2013-05-02 | Titan Chemicals Limited | Biocide composition |
| CN102559421B (zh) * | 2011-12-23 | 2014-06-25 | 广州立白企业集团有限公司 | 一种具有协同防腐作用的含酶织物洗涤剂 |
| US8957129B2 (en) | 2012-05-07 | 2015-02-17 | Rhodia Operations | Aqueous coatings and paints incorporating one or more antimicrobial biosurfactants and methods for using same |
| US9278151B2 (en) | 2012-11-27 | 2016-03-08 | S.C. Johnson & Son, Inc. | Volatile material dispenser |
| US9205163B2 (en) | 2012-11-27 | 2015-12-08 | S.C. Johnson & Son, Inc. | Volatile material dispenser |
| CN102986669A (zh) * | 2012-12-31 | 2013-03-27 | 大连百傲化学股份有限公司 | 稳定的杀菌剂组合物 |
| EP3003040A1 (en) | 2013-05-28 | 2016-04-13 | THOR GmbH | Microbicidal composition comprising 2-methyl-4-isothiazolin-3-one and an amineoxide |
| EP3003035A2 (en) | 2013-05-28 | 2016-04-13 | Thor Specialities (UK) Limited | Microbicidal composition comprising an isothiazolone and an amineoxide |
| EP2842425A1 (de) * | 2013-08-28 | 2015-03-04 | LANXESS Deutschland GmbH | Mikrobizide Mittel |
| EP3077462B2 (de) * | 2013-12-06 | 2023-11-08 | THOR GmbH | Verfahren zur herstellung eines beschichtungsmittels |
| JP5955899B2 (ja) * | 2014-07-16 | 2016-07-20 | 株式会社パイロットコーポレーション | 筆記具用水性インキ組成物およびそれを収容してなる製品 |
| US20170233585A1 (en) | 2014-09-02 | 2017-08-17 | Thor Gmbh | Products preserved with 5-chloro-2-methyl-4-isothiazolin-3-one |
| JP6377494B2 (ja) * | 2014-11-05 | 2018-08-22 | 株式会社パイロットコーポレーション | 筆記具用水性インキ組成物および水性インキ製品 |
| EP3346838B1 (de) | 2015-09-09 | 2020-06-24 | THOR GmbH | Lagerstabile biozidzusammensetzung |
| WO2017148572A1 (de) | 2016-03-01 | 2017-09-08 | Thor Gmbh | Verfahren zur verminderung des mikrobiellen befalls von technischen produkten |
| CN109068639A (zh) | 2016-04-05 | 2018-12-21 | 托尔有限公司 | 含有5-氯-2-甲基异噻唑啉-3-酮的协同杀生物剂组合物 |
| EP3439476A1 (de) | 2016-04-05 | 2019-02-13 | THOR GmbH | Synergistische biozidzusammensetzungen enthaltend 5-chlor-2-methylisothiazolin-3-on |
| CN110325039A (zh) | 2017-02-28 | 2019-10-11 | 托尔有限公司 | 含有5-氯-2-甲基异噻唑啉-3-酮的协同杀生物组合物 |
| US20210204548A1 (en) | 2017-04-04 | 2021-07-08 | Thor Gmbh | Stabilized Biocide Composition |
| HUE053827T2 (hu) | 2017-05-03 | 2021-07-28 | Vink Chemicals Gmbh & Co Kg | Tárolás során stabil mikrobicid koncentrátumok és alkalmazásuk tartósítószerként |
| CN111087653A (zh) * | 2019-11-13 | 2020-05-01 | 嘉兴学院 | 一种水性聚氨酯乳液用防腐剂及其制备方法 |
| WO2023061620A1 (de) | 2021-10-15 | 2023-04-20 | Thor Gmbh | Verfahren zur behandlung von technischen produkten |
| WO2024175245A1 (de) | 2023-02-23 | 2024-08-29 | Thor Gmbh | Synergistische zusammensetzungen enthaltend guanidin |
| WO2024175246A1 (de) | 2023-02-23 | 2024-08-29 | Thor Gmbh | Gegen mikrobiellen befall stabilisiertes wässriges technisches produkt |
| WO2024175248A1 (de) | 2023-02-23 | 2024-08-29 | Thor Gmbh | Zusammensetzungen enthaltend guanidin und 1,2-benzisothiazolin-3-on |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0737362B2 (ja) * | 1988-03-01 | 1995-04-26 | 治 梅川 | 工業用殺菌組成物 |
| US5028620A (en) * | 1988-09-15 | 1991-07-02 | Rohm And Haas Company | Biocide composition |
| EP0542721A3 (en) * | 1990-04-27 | 1993-08-25 | Imperial Chemical Industries Plc | Biocide composition and its use |
| GB9015786D0 (en) * | 1990-07-18 | 1990-09-05 | Ici Plc | Biocide composition |
| US5464850A (en) * | 1991-10-04 | 1995-11-07 | Ciba Corning Diagnostics Corp. | Synergistic preservative systems for chemistry reagents |
| JP3139167B2 (ja) * | 1992-09-11 | 2001-02-26 | 北興化学工業株式会社 | 安定な液状防菌防カビ製剤 |
| ATE185045T1 (de) * | 1994-04-07 | 1999-10-15 | Rohm & Haas | Halogenfreies biozid |
| EP0900525A1 (de) * | 1997-08-20 | 1999-03-10 | Thor Chemie Gmbh | Synergistische Biozidzusammensetzung |
-
1997
- 1997-08-20 EP EP97114397A patent/EP0900525A1/de not_active Withdrawn
-
1998
- 1998-08-20 WO PCT/EP1998/005310 patent/WO1999008530A1/de active IP Right Grant
- 1998-08-20 TR TR2000/00437T patent/TR200000437T2/xx unknown
- 1998-08-20 EP EP98946397A patent/EP1005271B1/de not_active Revoked
- 1998-08-20 CA CA002299227A patent/CA2299227C/en not_active Expired - Lifetime
- 1998-08-20 PT PT98946397T patent/PT1005271E/pt unknown
- 1998-08-20 AT AT98946397T patent/ATE227082T1/de not_active IP Right Cessation
- 1998-08-20 PL PL338711A patent/PL203139B1/pl unknown
- 1998-08-20 HU HU0003297A patent/HU230127B1/hu unknown
- 1998-08-20 CN CNB988083000A patent/CN1286370C/zh not_active Expired - Lifetime
- 1998-08-20 US US09/485,975 patent/US6361788B1/en not_active Expired - Lifetime
- 1998-08-20 BR BRPI9811955-9A patent/BR9811955B1/pt not_active IP Right Cessation
- 1998-08-20 KR KR20007001666A patent/KR100397259B1/ko not_active IP Right Cessation
- 1998-08-20 CZ CZ2000539A patent/CZ294066B6/cs not_active IP Right Cessation
- 1998-08-20 DK DK98946397T patent/DK1005271T3/da active
- 1998-08-20 AU AU93453/98A patent/AU731655B2/en not_active Expired
- 1998-08-20 ES ES98946397T patent/ES2188013T3/es not_active Expired - Lifetime
- 1998-08-20 DE DE59806209T patent/DE59806209D1/de not_active Revoked
- 1998-08-20 JP JP2000509290A patent/JP3992433B2/ja not_active Expired - Fee Related
-
2000
- 2000-02-10 MX MXPA00001460 patent/MX212024B/es unknown
- 2000-02-15 NO NO20000749A patent/NO323350B1/no not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| BR9811955B1 (pt) | 2011-02-08 |
| HUP0003297A3 (en) | 2002-02-28 |
| NO20000749L (no) | 2000-04-18 |
| KR100397259B1 (ko) | 2003-09-13 |
| PL203139B1 (pl) | 2009-08-31 |
| PL338711A1 (en) | 2000-11-20 |
| JP2001515016A (ja) | 2001-09-18 |
| CN1286370C (zh) | 2006-11-29 |
| TR200000437T2 (tr) | 2000-08-21 |
| HU230127B1 (hu) | 2015-08-28 |
| PT1005271E (pt) | 2003-03-31 |
| AU9345398A (en) | 1999-03-08 |
| ATE227082T1 (de) | 2002-11-15 |
| CA2299227A1 (en) | 1999-02-25 |
| EP1005271A1 (de) | 2000-06-07 |
| NO20000749D0 (no) | 2000-02-15 |
| AU731655B2 (en) | 2001-04-05 |
| BR9811955A (pt) | 2000-08-15 |
| WO1999008530A1 (de) | 1999-02-25 |
| DE59806209D1 (de) | 2002-12-12 |
| DK1005271T3 (da) | 2003-03-10 |
| MXPA00001460A (es) | 2001-06-01 |
| MX212024B (es) | 2002-12-11 |
| CN1267192A (zh) | 2000-09-20 |
| HUP0003297A2 (hu) | 2001-01-29 |
| JP3992433B2 (ja) | 2007-10-17 |
| EP1005271B1 (de) | 2002-11-06 |
| KR20010023049A (ko) | 2001-03-26 |
| CA2299227C (en) | 2003-04-29 |
| EP0900525A1 (de) | 1999-03-10 |
| ES2188013T3 (es) | 2003-06-16 |
| CZ294066B6 (cs) | 2004-09-15 |
| US6361788B1 (en) | 2002-03-26 |
| CZ2000539A3 (cs) | 2000-06-14 |
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Legal Events
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| MK1K | Patent expired |