ZA200506601B - Microbicidal compositions including an ionene polymer and 2,4,4'-trichloro-2'-hydroxydiphenyl ether and methods of using the same - Google Patents
Microbicidal compositions including an ionene polymer and 2,4,4'-trichloro-2'-hydroxydiphenyl ether and methods of using the same Download PDFInfo
- Publication number
- ZA200506601B ZA200506601B ZA200506601A ZA200506601A ZA200506601B ZA 200506601 B ZA200506601 B ZA 200506601B ZA 200506601 A ZA200506601 A ZA 200506601A ZA 200506601 A ZA200506601 A ZA 200506601A ZA 200506601 B ZA200506601 B ZA 200506601B
- Authority
- ZA
- South Africa
- Prior art keywords
- composition
- alkyl
- medium
- product
- microorganism
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 67
- 238000000034 method Methods 0.000 title claims description 43
- LTMQZVLXCLQPCT-UHFFFAOYSA-N 1,1,6-trimethyltetralin Chemical compound C1CCC(C)(C)C=2C1=CC(C)=CC=2 LTMQZVLXCLQPCT-UHFFFAOYSA-N 0.000 title claims description 28
- 229920000642 polymer Polymers 0.000 title claims description 20
- XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 title claims description 14
- 230000003641 microbiacidal effect Effects 0.000 title description 7
- 244000005700 microbiome Species 0.000 claims description 32
- 239000000463 material Substances 0.000 claims description 31
- 241000894006 Bacteria Species 0.000 claims description 11
- 241000233866 Fungi Species 0.000 claims description 11
- 229960003500 triclosan Drugs 0.000 claims description 11
- 241000195493 Cryptophyta Species 0.000 claims description 10
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims description 8
- 238000009472 formulation Methods 0.000 claims description 8
- -1 leathers Substances 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 239000003973 paint Substances 0.000 claims description 4
- 239000000123 paper Substances 0.000 claims description 4
- 239000002023 wood Substances 0.000 claims description 4
- 239000003905 agrochemical Substances 0.000 claims description 3
- 238000000576 coating method Methods 0.000 claims description 3
- 239000000498 cooling water Substances 0.000 claims description 3
- 239000002537 cosmetic Substances 0.000 claims description 3
- 238000005553 drilling Methods 0.000 claims description 3
- 239000000839 emulsion Substances 0.000 claims description 3
- 239000012530 fluid Substances 0.000 claims description 3
- 239000000314 lubricant Substances 0.000 claims description 3
- 238000005555 metalworking Methods 0.000 claims description 3
- 239000003348 petrochemical agent Substances 0.000 claims description 3
- 239000008194 pharmaceutical composition Substances 0.000 claims description 3
- 239000004753 textile Substances 0.000 claims description 3
- 239000002351 wastewater Substances 0.000 claims description 3
- 229920001131 Pulp (paper) Polymers 0.000 claims description 2
- 239000000853 adhesive Substances 0.000 claims description 2
- 230000001070 adhesive effect Effects 0.000 claims description 2
- 239000000975 dye Substances 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims 19
- 150000002500 ions Chemical class 0.000 claims 12
- 125000000304 alkynyl group Chemical group 0.000 claims 7
- 125000003342 alkenyl group Chemical group 0.000 claims 5
- 229910052739 hydrogen Inorganic materials 0.000 claims 5
- 239000001257 hydrogen Substances 0.000 claims 5
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 4
- 125000002091 cationic group Chemical group 0.000 claims 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 3
- 125000006267 biphenyl group Chemical group 0.000 claims 2
- 239000003093 cationic surfactant Substances 0.000 claims 2
- 239000006185 dispersion Substances 0.000 claims 1
- 229910052500 inorganic mineral Inorganic materials 0.000 claims 1
- 239000011707 mineral Substances 0.000 claims 1
- 239000002002 slurry Substances 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 229940124561 microbicide Drugs 0.000 description 4
- 230000008901 benefit Effects 0.000 description 3
- 239000003619 algicide Substances 0.000 description 2
- 230000000844 anti-bacterial effect Effects 0.000 description 2
- 239000003899 bactericide agent Substances 0.000 description 2
- 239000003139 biocide Substances 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 239000012770 industrial material Substances 0.000 description 2
- 239000002855 microbicide agent Substances 0.000 description 2
- 241000589774 Pseudomonas sp. Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229920006317 cationic polymer Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/74—Synthetic polymeric materials
- A61K31/765—Polymers containing oxygen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/02—Local antiseptics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/383,121 US20040175352A1 (en) | 2003-03-06 | 2003-03-06 | Microbicidal compositions including an ionene polymer and 2,4,4-trichloro-2-hydroxydiphenyl ether, and methods of using the same |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200506601B true ZA200506601B (en) | 2006-06-28 |
Family
ID=32927026
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200506601A ZA200506601B (en) | 2003-03-06 | 2005-08-18 | Microbicidal compositions including an ionene polymer and 2,4,4'-trichloro-2'-hydroxydiphenyl ether and methods of using the same |
Country Status (10)
Country | Link |
---|---|
US (1) | US20040175352A1 (pt) |
EP (1) | EP1603390A2 (pt) |
JP (1) | JP2006522121A (pt) |
CN (1) | CN1756484A (pt) |
AU (1) | AU2004220618A1 (pt) |
BR (1) | BRPI0408673A (pt) |
CA (1) | CA2517610A1 (pt) |
MX (1) | MXPA05009475A (pt) |
WO (1) | WO2004080176A2 (pt) |
ZA (1) | ZA200506601B (pt) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006074255A1 (en) * | 2005-01-05 | 2006-07-13 | Dow Global Technologies Inc. | Enhanced efficacy of fungicides in paper and paperboard |
DE102005043428A1 (de) * | 2005-09-13 | 2007-03-15 | Lanxess Deutschland Gmbh | Verwendung von Triclosan für den Holzschutz |
EP2754350A3 (en) * | 2005-10-25 | 2014-11-12 | Dow Global Technologies LLC | Antimicrobial composition and method |
EP2385759A2 (en) * | 2009-01-08 | 2011-11-16 | Buckman Laboratories International, Inc. | Microbicidal compositions including activated nitrogenous compound and 1,4-bis (bromoacetoxy)-2-butene, and methods of using the same |
JP6427261B2 (ja) * | 2015-02-19 | 2018-11-21 | イェディテペ・ウニヴェルシテシYeditepe Universitesi | 種子および表面滅菌のためのコーティング製剤 |
WO2019071500A1 (en) * | 2017-10-12 | 2019-04-18 | The Procter & Gamble Company | ANTIMICROBIAL DETERGENT COMPOSITION FOR LAUNDRY |
Family Cites Families (46)
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US3231509A (en) * | 1964-06-11 | 1966-01-25 | Betz Laboratories | Slimicidal composition and method |
US3629477A (en) * | 1966-08-08 | 1971-12-21 | Geigy Chem Corp | Halogenated diphenyether-containing compositions and control of pests therewith |
DE1288747B (de) * | 1967-04-19 | 1969-02-06 | Henkel & Cie Gmbh | Verwendung von 2-Hydroxyd-diphenylaethern als Potenzierungsmittel in antimikrobiellen Mitteln |
US3898336A (en) * | 1970-05-11 | 1975-08-05 | California Inst Of Techn | Insoluble polymeric quaternary trihalogen salt coated substrates |
US3778476A (en) * | 1970-05-11 | 1973-12-11 | California Inst Of Techn | Polymeric organic halogen salts |
USRE28808E (en) * | 1972-02-04 | 1976-05-11 | American Cyanamid Company | Polyquaternary flocculants |
US3738945A (en) * | 1972-02-04 | 1973-06-12 | H Panzer | Polyquaternary flocculants |
US3894946A (en) * | 1973-04-02 | 1975-07-15 | American Cyanamid Co | Process for treating industrial wastes |
US3894947A (en) * | 1973-04-02 | 1975-07-15 | American Cyanamid Co | Process for treating industrial wastes |
US3930877A (en) * | 1973-08-13 | 1976-01-06 | Nalco Chemical Company | Cationic starch and condensates for making the same |
US4025627A (en) * | 1973-12-18 | 1977-05-24 | Millmaster Onyx Corporation | Microbiocidal polymeric quaternary ammonium compounds |
US3874870A (en) * | 1973-12-18 | 1975-04-01 | Mill Master Onyx Corp | Microbiocidal polymeric quarternary ammonium compounds |
US4027020A (en) * | 1974-10-29 | 1977-05-31 | Millmaster Onyx Corporation | Randomly terminated capped polymers |
US3931319A (en) * | 1974-10-29 | 1976-01-06 | Millmaster Onyx Corporation | Capped polymers |
US4010252A (en) * | 1974-12-19 | 1977-03-01 | Colgate-Palmolive Company | Antimicrobial compositions |
US4054542A (en) * | 1975-04-14 | 1977-10-18 | Buckman Laboratories, Inc. | Amine-epichlorohydrin polymeric compositions |
US4098877A (en) * | 1975-09-15 | 1978-07-04 | American Cyanamid Company | Antimicrobial composition (enhanced activity from combination of phenol and a quaternary compound) |
US4089977A (en) * | 1976-11-24 | 1978-05-16 | Kewanee Industries | Polymeric anti-microbial agent |
US4164521A (en) * | 1977-02-07 | 1979-08-14 | American Cyanamid Company | Mixtures of polycationic and polyanionic polymers for scale control |
US4147627A (en) * | 1977-02-07 | 1979-04-03 | American Cyanamid Company | Process for scale control using mixtures of polycationic and polyanionic polymers |
JPS6050163B2 (ja) * | 1977-06-10 | 1985-11-07 | ライオン株式会社 | シヤンプ−組成物 |
US4098788A (en) * | 1977-06-20 | 1978-07-04 | Bristol-Myers Company | Process for preparing quinazolines |
US4111679A (en) * | 1977-08-17 | 1978-09-05 | Chemed Corporation | Polyquaternary compounds for the control of microbiological growth |
US4166041A (en) * | 1977-12-15 | 1979-08-28 | American Cyanamid Company | Process for magnesium scale control using mixtures of polycationic and polyanionic polymers |
US4104161A (en) * | 1978-04-18 | 1978-08-01 | Nalco Chemical Company | Method for treating aqueous wastes containing at least 1% proteinaceous matter |
US4506081A (en) * | 1982-09-02 | 1985-03-19 | Buckman Laboratories, Inc. | Polymeric quaternary ammonium compounds and their uses |
US4581058A (en) * | 1982-09-02 | 1986-04-08 | Buckman Laboratories, Inc. | Polymeric quaternary ammonium compounds and their uses |
JPS59163427A (ja) * | 1983-03-07 | 1984-09-14 | Kanebo Ltd | 抗菌性アクリル系合成繊維の製造法 |
US4606773A (en) * | 1984-12-10 | 1986-08-19 | Nalco Chemical Company | Emulsification of alkenyl succinic anhydride sizing agents |
US4675178A (en) * | 1985-05-02 | 1987-06-23 | Calgon Corporation | Use of cationic polymers (polydimethyldialkyl ammonium chloride-acrylamide copolymers and dimethyldialkyl ammonium chloride) to increase deposition and/or retention of active agent (S) of deodorant formulations on surfaces |
US4769155A (en) * | 1987-08-19 | 1988-09-06 | Nalco Chemical Company | Turbidity reduction |
US4960590A (en) * | 1989-02-10 | 1990-10-02 | Buckman Laboratories International, Inc. | Novel polymeric quaternary ammonium trihalides |
ZA905554B (en) * | 1989-09-27 | 1991-04-24 | Buckman Labor Inc | Synergistic combinations of ionenes with hexahydro-1,3,5-tris(2-hydroxyethyl)-s-triazine in controlling fungal and bacterial growth in synthetic metalworking fluid |
US5051124A (en) * | 1989-10-24 | 1991-09-24 | Buckman Laboratories International, Inc. | Microbicidal compositions of dimethylamine-epichlorohydrin amines |
US5158596A (en) * | 1991-02-15 | 1992-10-27 | Rohm And Haas Company | Synergistic antialgal compositions comprising diphenylethers and certain commercial biocides, methods of controlling algae, and coating compositions comprising the antialgal compositions |
EP0580814A1 (en) * | 1991-04-15 | 1994-02-02 | The Procter & Gamble Company | Antibacterial mild liquid skin cleanser |
US5681862A (en) * | 1993-03-05 | 1997-10-28 | Buckman Laboratories International, Inc. | Ionene polymers as microbicides |
US5350679A (en) * | 1993-06-14 | 1994-09-27 | Dow Corning Corporation | Repeat insult microbial test method |
US6503952B2 (en) * | 1995-11-13 | 2003-01-07 | The Trustees Of Columbia University In The City Of New York | Triple antimicrobial composition |
BR9707318A (pt) * | 1996-02-07 | 1999-04-13 | Buckman Labor Inc | Composição microbicida e método para controlar o crescimento de pelos menos um microorganismo |
US5866016A (en) * | 1997-07-01 | 1999-02-02 | Buckman Laboratories International, Inc. | Methods and compositions for controlling biofouling using combinations of an ionene polymer and a salt of dodecylamine |
US5776960A (en) * | 1996-10-16 | 1998-07-07 | Buckman Laboratories International, Inc. | Synergistic antimicrobial compositions containing an ionene polymer and a pyrithione salt and methods of using the same |
US6133483A (en) * | 1998-07-30 | 2000-10-17 | Cleary; Thomas F. | Process for the production of 2,4,4'-trichloro-2'-methoxydiphenyl ether |
US6147120A (en) * | 1999-02-16 | 2000-11-14 | Ecolab Inc. | Synergistic antimicrobial skin washing compositions |
US6294589B1 (en) * | 2000-05-12 | 2001-09-25 | Shaw Industries, Inc. | Polyurethane composition containing antimicrobial agents and methods for use therefor |
US20030026833A1 (en) * | 2001-07-10 | 2003-02-06 | Payne Stephen A. | Synergistic antimicrobial textile finish |
-
2003
- 2003-03-06 US US10/383,121 patent/US20040175352A1/en not_active Abandoned
-
2004
- 2004-03-05 BR BRPI0408673-2A patent/BRPI0408673A/pt not_active IP Right Cessation
- 2004-03-05 JP JP2006509197A patent/JP2006522121A/ja not_active Withdrawn
- 2004-03-05 AU AU2004220618A patent/AU2004220618A1/en not_active Abandoned
- 2004-03-05 CA CA002517610A patent/CA2517610A1/en not_active Abandoned
- 2004-03-05 MX MXPA05009475A patent/MXPA05009475A/es unknown
- 2004-03-05 EP EP04718106A patent/EP1603390A2/en not_active Withdrawn
- 2004-03-05 CN CNA2004800060774A patent/CN1756484A/zh active Pending
- 2004-03-05 WO PCT/US2004/006861 patent/WO2004080176A2/en active Application Filing
-
2005
- 2005-08-18 ZA ZA200506601A patent/ZA200506601B/en unknown
Also Published As
Publication number | Publication date |
---|---|
EP1603390A2 (en) | 2005-12-14 |
MXPA05009475A (es) | 2005-11-23 |
JP2006522121A (ja) | 2006-09-28 |
WO2004080176A2 (en) | 2004-09-23 |
AU2004220618A1 (en) | 2004-09-23 |
WO2004080176A3 (en) | 2004-12-09 |
BRPI0408673A (pt) | 2006-03-28 |
US20040175352A1 (en) | 2004-09-09 |
CN1756484A (zh) | 2006-04-05 |
CA2517610A1 (en) | 2004-09-23 |
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