GB464330A - Improvements relating to disinfection - Google Patents

Improvements relating to disinfection

Info

Publication number
GB464330A
GB464330A GB2812335A GB2812335A GB464330A GB 464330 A GB464330 A GB 464330A GB 2812335 A GB2812335 A GB 2812335A GB 2812335 A GB2812335 A GB 2812335A GB 464330 A GB464330 A GB 464330A
Authority
GB
United Kingdom
Prior art keywords
sulphonium
dodecyl
compounds
obtainable
para
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
GB2812335A
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.)
Chemische Fabrik Von Heyden AG
Original Assignee
Chemische Fabrik Von Heyden AG
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
Application filed by Chemische Fabrik Von Heyden AG filed Critical Chemische Fabrik Von Heyden AG
Priority to GB2812335A priority Critical patent/GB464330A/en
Publication of GB464330A publication Critical patent/GB464330A/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N31/00Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Agronomy & Crop Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

Disinfectant and fungicidal preparations comprise a mixture of two or more sulphonium compounds. The preparations may be made by mixing two or more sulphonium compounds or by starting from mixed parent materials such as naturally occurring mixtures of fatty acids or fatty alcohols made therefrom by hydrogenation. Liquid agents may be made by dissolving or dispersing two or more sulphonium compounds in water, or in an inert organic liquid, e.g. an alcohol, hydrocarbon or chlorine substitution product of a hydrocarbon. The sulphonium compounds may also be mixed with indifferent solids, e.g. a soluble salt such as sodium sulphate or with bolus, talc, kieselguhr to produce dry powders. The disinfectant agents may be used for the preservation of preparations containing proteins or starch or for the preservation of cosmetics. Compounds containing radicals derived from fatty acids or alcohols of from 10 to 20 carbon atoms are particularly suitable, e.g. dodecyl-benzylmethyl-sulphonium methosulphate obtainable from dodecyl-benzyl-thioether and dimethyl sulphate and the corresponding tetradecyl, cetyl or octadecyl derivatives; dodecyl-paratolyl-methyl-sulphonium methosulphate obtainable from dodecyl-para-tolyl-thioether and dimethyl sulphate; dodecyl-dimethyl-sulphonium para-toluene sulphonate and higher derivatives obtainable from dodecyl-mercaptan and corresponding higher mercaptans and 2 mols of para-toluene-sulphonic acid methyl ester; di-decyl-methyl-sulphonium-methosulphate obtainable from didecyl-thioether and dimethyl sulphate. The groups contained in the sulphonium chains may be of varied nature and may be substituted or interrupted. Examples describe the disinfection of a solution of proteins, the preparation of an ointment having a petroleum jelly base and the preparation of aqueous disinfectant solutions, the active ingredients in each case being mixtures of sulphonium compounds having long chain alkyl radicals and in addition radicals such as methyl, phenyl, benzyl, tolyl.ALSO:Disinfectant and fungicidal preparations comprise a mixture of two or more sulphonium compounds. The preparations may be made by mixing two or more sulphonium compounds or by starting from mixed parent materials such as naturally occurring mixtures of fatty acids or fatty alcohols made therefrom by hydrogenation. Liquid agents may be made by dissolving or dispersing two or more sulphonium compounds in water, or in an inert organic liquid, e.g. an alcohol; hydrocarbon or chlorine substitution product of a hydrocarbon. The sulphonium compounds may also be mixed with indifferent solids, e.g. a soluble salt such as sodium sulphite for the preparation of liquid agents or with bolus, talc, kieselguhr to produce dry powders. The disinfectant agents may be used for the preservation of preparations containing proteins or starch or for the preservation of cosmetics. Compounds containing radicals derived from fatty acids or alcohols of from 10 to 20 carbon atoms are particularly suitable, e.g. dodecyl-benzyl-methyl-sulphonium methosulphate obtainable from dodecyl-benzyl-thioether and dimethyl sulphate and the corresponding tetradecyl, cetyl or octadecyl derivatives; dodecyl-para-tolyl-methyl-sulphonium methosulphate obtainable from dodecyl-para-tolylthioether and dimethyl sulphate; dodecyldimethyl-sulphonium para-toluene sulphonate and higher p derivatives obtainable from dodecylmercaptan and corresponding higher mercaptans and 2 mols. of para-toluene-sulphonic acid methyl ester; di - decyl - methyl - sulphonium-methosulphate obtainable from didecylthioether and dimethyl sulphate. The groups contained in the sulphonium chains may be of varied nature and may be substituted or interrupted. Examples describe the disinfection of a solution of proteins, the preparation of an ointment having a petroleum jelly base and the preparation of aqueous disinfectant solutions, the active ingredients in each case being mixtures of sulphonium compounds having long chain alkyl radicals and in addition radicals such as methyl, phenyl, benzyl, tolyl.
GB2812335A 1935-10-11 1935-10-11 Improvements relating to disinfection Expired GB464330A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2812335A GB464330A (en) 1935-10-11 1935-10-11 Improvements relating to disinfection

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2812335A GB464330A (en) 1935-10-11 1935-10-11 Improvements relating to disinfection

Publications (1)

Publication Number Publication Date
GB464330A true GB464330A (en) 1937-04-12

Family

ID=10270619

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2812335A Expired GB464330A (en) 1935-10-11 1935-10-11 Improvements relating to disinfection

Country Status (1)

Country Link
GB (1) GB464330A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2467547A1 (en) * 1979-10-22 1981-04-30 Elf Aquitaine Pesticidal tetra:decyl di:alkyl sulphonium salts - useful as bactericides, fungicides, algicides and corrosion inhibitors
EP0064441A1 (en) * 1981-04-27 1982-11-10 Societe Nationale Elf Aquitaine Biocidal composition based on sulfonium salts and organo tin compounds
US4376787A (en) 1979-12-03 1983-03-15 Economics Laboratory, Inc. Control of mastitis
US6379685B1 (en) * 1997-09-26 2002-04-30 Ecolab Inc. Acidic aqueous chlorite teat dip with improved emollient providing shelf life, sanitizing capacity and tissue protection
US6749869B1 (en) 1997-09-26 2004-06-15 Ecolab Acidic aqueous chlorite teat dip providing shelf life, sanitizing capacity and tissue protection
US10900128B2 (en) 2018-08-29 2021-01-26 Championx Usa Inc. Use of sulfonium salts as corrosion inhibitors
GB2615788A (en) * 2022-02-18 2023-08-23 Univ Exeter Fungicides and uses thereof

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2467547A1 (en) * 1979-10-22 1981-04-30 Elf Aquitaine Pesticidal tetra:decyl di:alkyl sulphonium salts - useful as bactericides, fungicides, algicides and corrosion inhibitors
US4376787A (en) 1979-12-03 1983-03-15 Economics Laboratory, Inc. Control of mastitis
EP0064441A1 (en) * 1981-04-27 1982-11-10 Societe Nationale Elf Aquitaine Biocidal composition based on sulfonium salts and organo tin compounds
US6379685B1 (en) * 1997-09-26 2002-04-30 Ecolab Inc. Acidic aqueous chlorite teat dip with improved emollient providing shelf life, sanitizing capacity and tissue protection
US6436444B1 (en) 1997-09-26 2002-08-20 Ecolab Inc. Acidic aqueous chlorite teat dip providing shelf life sanitizing capacity and tissue protection
US6699510B2 (en) 1997-09-26 2004-03-02 Ecolab Inc. Acidic aqueous chlorite teat dip with improved visual indicator stability, extended shelf life, sanitizing capacity and tissue protection
US6749869B1 (en) 1997-09-26 2004-06-15 Ecolab Acidic aqueous chlorite teat dip providing shelf life, sanitizing capacity and tissue protection
USRE41279E1 (en) 1997-09-26 2010-04-27 Ecolab Inc. Acidic aqueous chlorite teat dip with improved visual indicator stability, extended shelf life, sanitizing capacity and tissue protection
US10900128B2 (en) 2018-08-29 2021-01-26 Championx Usa Inc. Use of sulfonium salts as corrosion inhibitors
GB2615788A (en) * 2022-02-18 2023-08-23 Univ Exeter Fungicides and uses thereof

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