JP2001517219A - 殺生物組成物および使用 - Google Patents
殺生物組成物および使用Info
- Publication number
- JP2001517219A JP2001517219A JP54049098A JP54049098A JP2001517219A JP 2001517219 A JP2001517219 A JP 2001517219A JP 54049098 A JP54049098 A JP 54049098A JP 54049098 A JP54049098 A JP 54049098A JP 2001517219 A JP2001517219 A JP 2001517219A
- Authority
- JP
- Japan
- Prior art keywords
- chloride
- composition
- quaternary ammonium
- aqueous system
- ammonium compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 24
- 230000003115 biocidal effect Effects 0.000 title description 5
- DHVLDKHFGIVEIP-UHFFFAOYSA-N 2-bromo-2-(bromomethyl)pentanedinitrile Chemical compound BrCC(Br)(C#N)CCC#N DHVLDKHFGIVEIP-UHFFFAOYSA-N 0.000 claims abstract description 15
- 150000003856 quaternary ammonium compounds Chemical class 0.000 claims abstract description 9
- 230000000845 anti-microbial effect Effects 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims abstract 10
- 239000004599 antimicrobial Substances 0.000 claims abstract 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims description 6
- 229960001927 cetylpyridinium chloride Drugs 0.000 claims description 6
- YMKDRGPMQRFJGP-UHFFFAOYSA-M cetylpyridinium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 YMKDRGPMQRFJGP-UHFFFAOYSA-M 0.000 claims description 6
- DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 claims description 5
- 235000019270 ammonium chloride Nutrition 0.000 claims description 3
- 244000005700 microbiome Species 0.000 claims description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 2
- 229940027983 antiseptic and disinfectant quaternary ammonium compound Drugs 0.000 claims description 2
- 239000000498 cooling water Substances 0.000 claims description 2
- 230000002195 synergetic effect Effects 0.000 claims description 2
- RLGQACBPNDBWTB-UHFFFAOYSA-N cetyltrimethylammonium ion Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)C RLGQACBPNDBWTB-UHFFFAOYSA-N 0.000 claims 3
- 125000005997 bromomethyl group Chemical group 0.000 claims 2
- GHPYJLCQYMAXGG-WCCKRBBISA-N (2R)-2-amino-3-(2-boronoethylsulfanyl)propanoic acid hydrochloride Chemical compound Cl.N[C@@H](CSCCB(O)O)C(O)=O GHPYJLCQYMAXGG-WCCKRBBISA-N 0.000 claims 1
- ZTOMUSMDRMJOTH-UHFFFAOYSA-N glutaronitrile Chemical compound N#CCCCC#N ZTOMUSMDRMJOTH-UHFFFAOYSA-N 0.000 claims 1
- 125000003944 tolyl group Chemical group 0.000 claims 1
- 230000000813 microbial effect Effects 0.000 abstract 1
- PUAQLLVFLMYYJJ-UHFFFAOYSA-N 2-aminopropiophenone Chemical compound CC(N)C(=O)C1=CC=CC=C1 PUAQLLVFLMYYJJ-UHFFFAOYSA-N 0.000 description 4
- 241000894006 Bacteria Species 0.000 description 4
- 230000001580 bacterial effect Effects 0.000 description 4
- 241000233866 Fungi Species 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000001629 suppression Effects 0.000 description 3
- 229940126062 Compound A Drugs 0.000 description 2
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- 230000006399 behavior Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000003643 water by type Substances 0.000 description 2
- GKQHIYSTBXDYNQ-UHFFFAOYSA-M 1-dodecylpyridin-1-ium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+]1=CC=CC=C1 GKQHIYSTBXDYNQ-UHFFFAOYSA-M 0.000 description 1
- QAQSNXHKHKONNS-UHFFFAOYSA-N 1-ethyl-2-hydroxy-4-methyl-6-oxopyridine-3-carboxamide Chemical compound CCN1C(O)=C(C(N)=O)C(C)=CC1=O QAQSNXHKHKONNS-UHFFFAOYSA-N 0.000 description 1
- 241000193400 Bacillus simplex Species 0.000 description 1
- 241000589513 Burkholderia cepacia Species 0.000 description 1
- 241000866631 Caballeronia glathei Species 0.000 description 1
- 241000203811 Curtobacterium flaccumfaciens Species 0.000 description 1
- RUPBZQFQVRMKDG-UHFFFAOYSA-M Didecyldimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCC[N+](C)(C)CCCCCCCCCC RUPBZQFQVRMKDG-UHFFFAOYSA-M 0.000 description 1
- 229920002444 Exopolysaccharide Polymers 0.000 description 1
- 241000588747 Klebsiella pneumoniae Species 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 241000589517 Pseudomonas aeruginosa Species 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000008485 antagonism Effects 0.000 description 1
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 1
- FADYGXGJTNYCHZ-UHFFFAOYSA-M benzyl-dodecyl-diethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](CC)(CC)CC1=CC=CC=C1 FADYGXGJTNYCHZ-UHFFFAOYSA-M 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- WLCFKPHMRNPAFZ-UHFFFAOYSA-M didodecyl(dimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCC WLCFKPHMRNPAFZ-UHFFFAOYSA-M 0.000 description 1
- 231100000673 dose–response relationship Toxicity 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 229940045505 klebsiella pneumoniae Drugs 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- JWZXKXIUSSIAMR-UHFFFAOYSA-N methylene bis(thiocyanate) Chemical compound N#CSCSC#N JWZXKXIUSSIAMR-UHFFFAOYSA-N 0.000 description 1
- 230000003134 recirculating effect Effects 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- SFVFIFLLYFPGHH-UHFFFAOYSA-M stearalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SFVFIFLLYFPGHH-UHFFFAOYSA-M 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 231100000440 toxicity profile Toxicity 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- YBNLWIZAWPBUKQ-UHFFFAOYSA-N trichloro(trichloromethylsulfonyl)methane Chemical compound ClC(Cl)(Cl)S(=O)(=O)C(Cl)(Cl)Cl YBNLWIZAWPBUKQ-UHFFFAOYSA-N 0.000 description 1
- CEYYIKYYFSTQRU-UHFFFAOYSA-M trimethyl(tetradecyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCC[N+](C)(C)C CEYYIKYYFSTQRU-UHFFFAOYSA-M 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/34—Nitriles
-
- 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/12—Quaternary ammonium compounds
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Description
Claims (1)
- 【特許請求の範囲】 1.相乗的に有効な量の(a)2−ブロモ−2−(ブロモメチル)−グルタロニ トリルおよび(b)第四アンモニウム化合物を含んでなる抗微生物組成物。 2.第四アンモニウム化合物が、アルキルジメチルベンジルアンモニウムクロ リド、ラウリルトリメチルアンモニウムクロリド、セチルトリメチルアンモニウ ムクロリドおよびセチルピリジニウムクロリドからなる群より選ばれる、請求項 1に記載の組成物。 3.(a)対(b)の重量比が、約3:1〜1:16である、請求項1に記載 の組成物。 4.(a)2−ブロモ−2−(ブロモメチル)−グルタロニトリルおよび(b )第四アンモニウム化合物の相乗的混合物を含んでなる組成物のために有効な量 を水性系に添加することを含んでなる、水性系における微生物の成長を制御する 方法。 5.前記組成物が、前記水性系100万につき約0.5〜約60部の量で前記 系に添加される、請求項4に記載の方法。 6.(a)対(b)の重量比が約3:1〜1:16である、請求項4に記載の 方法。 7.第四アンモニウム化合物が、アルキルジメチルベンジルアンモニウムクロ リド、ラウリルトリメチルアンモニウムクロリド、セチルトリメチルアンモニウ ムクロリドおよびセチルピリジニウムクロリドからなる群より選ばれる、請求項 4に記載の方法。 8.前記水性系が冷却水系を含んでなる、請求項4に記載の方法。 9.前記水性系がパルピングおよび製紙系を含んでなる、請求項4に記載の方 法。 10.本質的に相乗的に有効な量の(a)2−ブロモ−2−(ブロモメチル) −グルタロニトリルおよび(b)第四アンモニウム化合物からなる抗微生物組成 物。 11.第四アンモニウム化合物が、アルキルジメチルベンジルアンモニウムク ロリド、ラウリルトリメチルアンモニウムクロリド、セチルトリメチルアンモニ ウムクロリドおよびセチルピリジニウムクロリドからなる群より選ばれる、請求 項10に記載の組成物。 12.(a)対(b)の重量比が、約3:1〜1:16である、請求項10に記 載の組成物。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/821,746 US5763482A (en) | 1997-03-20 | 1997-03-20 | Biocidal composition and use |
US08/821,746 | 1997-03-20 | ||
PCT/US1998/002127 WO1998041088A1 (en) | 1997-03-20 | 1998-02-05 | Biocidal composition and use |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2001517219A true JP2001517219A (ja) | 2001-10-02 |
JP2001517219A5 JP2001517219A5 (ja) | 2005-10-06 |
JP4187272B2 JP4187272B2 (ja) | 2008-11-26 |
Family
ID=25234201
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP54049098A Expired - Fee Related JP4187272B2 (ja) | 1997-03-20 | 1998-02-05 | 殺生物組成物および使用 |
Country Status (16)
Country | Link |
---|---|
US (1) | US5763482A (ja) |
EP (1) | EP0984685B1 (ja) |
JP (1) | JP4187272B2 (ja) |
KR (1) | KR20010005499A (ja) |
CN (1) | CN1149922C (ja) |
AT (1) | ATE298503T1 (ja) |
AU (1) | AU726937B2 (ja) |
BR (1) | BR9808028B1 (ja) |
CA (1) | CA2284543C (ja) |
DE (1) | DE69830724T2 (ja) |
ES (1) | ES2241128T3 (ja) |
MY (1) | MY133559A (ja) |
NO (1) | NO994555L (ja) |
NZ (1) | NZ337937A (ja) |
WO (1) | WO1998041088A1 (ja) |
ZA (1) | ZA98364B (ja) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20020074903A (ko) * | 2001-03-22 | 2002-10-04 | 김용국 | 농약 조성물 및 그 용도 |
KR20020074899A (ko) * | 2001-03-22 | 2002-10-04 | 김용국 | 살균·살충·소독제 조성물 |
JP4534051B2 (ja) * | 2001-08-16 | 2010-09-01 | 株式会社片山化学工業研究所 | ウエットパルプの防腐防かび方法およびその防腐防かび組成物 |
US7008545B2 (en) * | 2002-08-22 | 2006-03-07 | Hercules Incorporated | Synergistic biocidal mixtures |
US20060231505A1 (en) * | 2002-08-22 | 2006-10-19 | Mayer Michael J | Synergistic biocidal mixtures |
MXPA05009294A (es) * | 2003-03-04 | 2005-10-05 | Valspar Sourcing Inc | Sistema de manejo de electrorrevestimiento. |
WO2004078222A1 (en) * | 2003-03-04 | 2004-09-16 | Valspar Sourcing Inc. | Treating an electrocoat system with a biosurfactant |
WO2004078997A2 (en) * | 2003-03-04 | 2004-09-16 | Valspar Sourcing Inc. | Method for detecting micro-organisms in an electrocoating process |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3054678A (en) * | 1958-04-16 | 1962-09-18 | Michener Harold David | Preservation process with quaternary ammonium compounds |
US3829586A (en) * | 1970-01-02 | 1974-08-13 | Betz Laboratories | Slime control compositions and their use |
US3833731A (en) * | 1970-12-28 | 1974-09-03 | Merck & Co Inc | Dihalomethylglutaronitriles used as antibacterial and antifungal agents |
US4655815A (en) * | 1985-03-27 | 1987-04-07 | Calgon Corporation | Admixtures of 2-bromo-2-bromomethylglutaronitrile and a formaldehyde donor |
US5034405A (en) * | 1985-03-27 | 1991-07-23 | Calgon Corporation | Admixtures of 2-bromo-2-bromomethyl-glutaronitrile, 2-methyl-4-isothiazolin-3-one and 5-chloro-2-methyl-4-isothiazolin-3-one |
GB9009529D0 (en) * | 1990-04-27 | 1990-06-20 | Ici Plc | Biocide composition and use |
NZ240129A (en) * | 1990-10-15 | 1993-07-27 | Calgon Corp | Synergistic microbiocide |
US5444088A (en) * | 1993-10-05 | 1995-08-22 | Nalco Chemical Company | Synergistic anti-microbial compositions comprising 2-bromo-2-(bromomethyl)-glutaronitrile and 2-bromo-2-nitro-propane-1,3-diol |
-
1997
- 1997-03-20 US US08/821,746 patent/US5763482A/en not_active Expired - Fee Related
-
1998
- 1998-01-14 MY MYPI98000155A patent/MY133559A/en unknown
- 1998-01-16 ZA ZA98364A patent/ZA98364B/xx unknown
- 1998-02-05 ES ES98909987T patent/ES2241128T3/es not_active Expired - Lifetime
- 1998-02-05 AT AT98909987T patent/ATE298503T1/de active
- 1998-02-05 AU AU64339/98A patent/AU726937B2/en not_active Ceased
- 1998-02-05 EP EP98909987A patent/EP0984685B1/en not_active Expired - Lifetime
- 1998-02-05 WO PCT/US1998/002127 patent/WO1998041088A1/en active IP Right Grant
- 1998-02-05 BR BRPI9808028-8A patent/BR9808028B1/pt not_active IP Right Cessation
- 1998-02-05 CA CA002284543A patent/CA2284543C/en not_active Expired - Fee Related
- 1998-02-05 CN CNB98805311XA patent/CN1149922C/zh not_active Expired - Fee Related
- 1998-02-05 KR KR1019997008556A patent/KR20010005499A/ko not_active Application Discontinuation
- 1998-02-05 JP JP54049098A patent/JP4187272B2/ja not_active Expired - Fee Related
- 1998-02-05 DE DE69830724T patent/DE69830724T2/de not_active Expired - Lifetime
- 1998-02-05 NZ NZ337937A patent/NZ337937A/xx not_active IP Right Cessation
-
1999
- 1999-09-20 NO NO994555A patent/NO994555L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
AU726937B2 (en) | 2000-11-23 |
KR20010005499A (ko) | 2001-01-15 |
NO994555D0 (no) | 1999-09-20 |
CN1149922C (zh) | 2004-05-19 |
WO1998041088A1 (en) | 1998-09-24 |
CA2284543C (en) | 2003-09-30 |
EP0984685A1 (en) | 2000-03-15 |
NZ337937A (en) | 2000-07-28 |
BR9808028B1 (pt) | 2009-05-05 |
ATE298503T1 (de) | 2005-07-15 |
EP0984685A4 (en) | 2004-08-18 |
EP0984685B1 (en) | 2005-06-29 |
DE69830724T2 (de) | 2006-05-04 |
DE69830724D1 (de) | 2005-08-04 |
JP4187272B2 (ja) | 2008-11-26 |
ZA98364B (en) | 1998-07-30 |
CA2284543A1 (en) | 1998-09-24 |
BR9808028A (pt) | 2000-03-28 |
CN1257405A (zh) | 2000-06-21 |
US5763482A (en) | 1998-06-09 |
ES2241128T3 (es) | 2005-10-16 |
MY133559A (en) | 2007-11-30 |
AU6433998A (en) | 1998-10-12 |
NO994555L (no) | 1999-11-02 |
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