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GB884541A - Process for the control of micro-organisms - Google Patents

Process for the control of micro-organisms

Info

Publication number
GB884541A
GB884541A GB2166059A GB2166059A GB884541A GB 884541 A GB884541 A GB 884541A GB 2166059 A GB2166059 A GB 2166059A GB 2166059 A GB2166059 A GB 2166059A GB 884541 A GB884541 A GB 884541A
Authority
GB
United Kingdom
Prior art keywords
water
benzisothiazolone
aqueous media
salt
micro
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.)
Expired
Application number
GB2166059A
Inventor
Anthony John Hinton
John Norman Turner
John Selwyn Morley
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority to NL268752D priority Critical patent/NL268752A/xx
Priority to BE607703D priority patent/BE607703A/xx
Priority to NL122753D priority patent/NL122753C/xx
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB2166059A priority patent/GB884541A/en
Priority to US33917A priority patent/US3065123A/en
Priority to FR831019A priority patent/FR1261520A/en
Priority to GB29994/60A priority patent/GB918869A/en
Priority to DE19611419483 priority patent/DE1419483A1/en
Priority to CH1004061A priority patent/CH409856A/en
Priority to CH1363361A priority patent/CH372026A/en
Priority to FR872072A priority patent/FR80284E/en
Publication of GB884541A publication Critical patent/GB884541A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
    • C07D275/04—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems
    • 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
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M7/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made of other substances with subsequent freeing of the treated goods from the treating medium, e.g. swelling, e.g. polyolefins
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/40—Reduced friction resistance, lubricant properties; Sizing compositions

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Textile Engineering (AREA)
  • Pest Control & Pesticides (AREA)
  • Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Agronomy & Crop Science (AREA)
  • Biochemistry (AREA)
  • Plant Pathology (AREA)
  • Microbiology (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Thiazole And Isothizaole Compounds (AREA)

Abstract

Aqueous media containing water paints have added thereto a 1 : 2 benziso thiazolone of formula:- <FORM:0884541/III/1> where R is a hydrogen or halogen, e.g. chlorine or bromine atom or a salt thereof, e.g. sodium, potassium, ammonium or amine such as triethanolamine salts to protect them against infection by micro-organisms. The 1 : 2 benzisothiazolone may be added par se or as a solution in water or diethylene glycol or as a water dispersible powder containing a wetting agent, e.g. an alkylated naphthalene sulphonic acid.ALSO:Aqueous natural or synthetic rubber dispersions are protected against infection by micro-organisms by adding a 1:2-benzisothiazolone of formula <FORM:0884541/IV (a)/1> where R is hydrogen or halogen or a salt thereof, e.g. sodium, potassium, ammonium or amine such as triethanolamine, salt. The benzisothiazolone may be added per se, as a solution in water or diethylene glycol or as a water-dispersible powder containing a wetting agent, e.g. an alkylated naphthalene sulphonic acid.ALSO:A process for protecting aqueous media containing proteins or protein degradation products, e.g. peptone, against infection by micro-organisms comprises adding a 1 : 2-benzisothiazolone of formula <FORM:0884541/IV (b)/1> where R is a hydrogen or halogen, e.g. chlorine or bromine atom or a salt thereof, e.g. sodium potassium, ammonium or amine, such as triethanolamine salts to said aqueous media. The 1 : 2 benzisothiazolone may be added per se or as a solution in water or diethylene glycol or as a water dispersible powder containing a wetting agent.ALSO:A process for the protection of aqueous media against infection by micro-organisms comprises the addition to the aqueous media of a 1 : 2-benzisothiazolone of formula <FORM:0884541/I/1> where R is a hydrogen or halogenatom e.g. chlorine or bromine, or a salt thereof, e.g. a sodium, potassium, ammonium or amine (such as triethanolamine) salt.ALSO:A water-dispersible powder for use in the protection of aqueous media, e.g. wood pulps, water paints, rubber latexes, cutting liquids and tannery soak liquors against infection by micro-organisms comprises a 1:2-benzisothiazolone of formula <FORM:0884541/VI/1> where R is an hydrogen or halogen atom, e.g. chlorine or bromine in admixture with a wetting or dispersing agent. A process for disinfecting aqueous media comprises adding a 1:2-benzisothiazolone of the above formula or a salt thereof, e.g. sodium, potassium, ammonium or amine such as triethanolamine salts to said aqueous media per se or as a solution in water or diethylene glycol or as the above powder. Alkylated napthalene sulphonic acids are specified as wetting agents.
GB2166059A 1959-06-24 1959-06-24 Process for the control of micro-organisms Expired GB884541A (en)

Priority Applications (11)

Application Number Priority Date Filing Date Title
NL268752D NL268752A (en) 1959-06-24
BE607703D BE607703A (en) 1959-06-24
NL122753D NL122753C (en) 1959-06-24
GB2166059A GB884541A (en) 1959-06-24 1959-06-24 Process for the control of micro-organisms
US33917A US3065123A (en) 1959-06-24 1960-06-06 Process for control of micro-organisms
FR831019A FR1261520A (en) 1959-06-24 1960-06-24 Process for combating microorganisms, in particular in industrial aqueous media
GB29994/60A GB918869A (en) 1959-06-24 1960-08-31 Process for the control of micro-organisms
DE19611419483 DE1419483A1 (en) 1959-06-24 1961-08-29 Process for the protection of textile treatment fluids against microorganisms
CH1004061A CH409856A (en) 1959-06-24 1961-08-29 Process for the protection of aqueous media containing textile auxiliaries against infection by microorganisms
CH1363361A CH372026A (en) 1959-06-24 1961-08-29 Process for protecting aqueous media containing textile treatment agents against infection by microorganisms
FR872072A FR80284E (en) 1959-06-24 1961-08-31 Process for combating microorganisms, in particular in industrial aqueous media

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2166059A GB884541A (en) 1959-06-24 1959-06-24 Process for the control of micro-organisms

Publications (1)

Publication Number Publication Date
GB884541A true GB884541A (en) 1961-12-13

Family

ID=32922842

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2166059A Expired GB884541A (en) 1959-06-24 1959-06-24 Process for the control of micro-organisms

Country Status (1)

Country Link
GB (1) GB884541A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3970755A (en) 1973-05-10 1976-07-20 Imperial Chemical Industries Limited Biocidal compositions
US4539071A (en) * 1982-04-19 1985-09-03 Dearborn Chemicals Limited Biocide
US4751311A (en) * 1985-07-10 1988-06-14 Imperial Chemical Industries Isothiazolone aqueous solutions
FR2620306A1 (en) * 1987-09-14 1989-03-17 Solvay COMPOSITIONS CONTAINING BIOSYNTHETIC PESTICIDE PRODUCTS, METHODS FOR THEIR PRODUCTION AND THEIR USE
US5328926A (en) * 1991-11-07 1994-07-12 Buckman Laboratories International, Inc. Synergistic combinations of iodopropargyl compounds with 1,2-benzisothiazolin-3-one in controlling fungal and bacterial growth in aqueous fluids
EP1184507A1 (en) * 2000-09-04 2002-03-06 Sanitized Ag Antimicrobial composition comprising 1,2-Benzisothiazolin-3-one and use thereof in textile finishing

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3970755A (en) 1973-05-10 1976-07-20 Imperial Chemical Industries Limited Biocidal compositions
US4539071A (en) * 1982-04-19 1985-09-03 Dearborn Chemicals Limited Biocide
US4751311A (en) * 1985-07-10 1988-06-14 Imperial Chemical Industries Isothiazolone aqueous solutions
FR2620306A1 (en) * 1987-09-14 1989-03-17 Solvay COMPOSITIONS CONTAINING BIOSYNTHETIC PESTICIDE PRODUCTS, METHODS FOR THEIR PRODUCTION AND THEIR USE
EP0307992A1 (en) * 1987-09-14 1989-03-22 Novo Nordisk A/S Compositions containing biosynthetic pesticidal products, process for their preparation and their use
US4915943A (en) * 1987-09-14 1990-04-10 Solvay & Cie (Societe Anonyme) Compositions containing biosynthetic pesticide products, processes for their production and their use
US5328926A (en) * 1991-11-07 1994-07-12 Buckman Laboratories International, Inc. Synergistic combinations of iodopropargyl compounds with 1,2-benzisothiazolin-3-one in controlling fungal and bacterial growth in aqueous fluids
EP1184507A1 (en) * 2000-09-04 2002-03-06 Sanitized Ag Antimicrobial composition comprising 1,2-Benzisothiazolin-3-one and use thereof in textile finishing

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