GB443902A - New textile assistants - Google Patents

New textile assistants

Info

Publication number
GB443902A
GB443902A GB2544034A GB2544034A GB443902A GB 443902 A GB443902 A GB 443902A GB 2544034 A GB2544034 A GB 2544034A GB 2544034 A GB2544034 A GB 2544034A GB 443902 A GB443902 A GB 443902A
Authority
GB
United Kingdom
Prior art keywords
prepared
sulphonated
stearic
sulphonating
treating
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
GB2544034A
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
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB2544034A priority Critical patent/GB443902A/en
Publication of GB443902A publication Critical patent/GB443902A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/402Amides imides, sulfamic acids
    • D06M13/438Sulfonamides ; Sulfamic acids

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

Products stated to be wetting, foaming, cleansing and emulsifying agents, e.g. for use in the textile and leather industries are prepared by sulphonating acylaminoethers having the formula RCO.NR<1>(CH2)nOQ when R is a normal saturated aliphatic hydrocarbon radicle containing at least seven carbons, R<1> is hydrogen or alkyl, Q is aryl and n is 2, 3 or 4. The parent materials may be made by reacting a higher fatty acid with an aminoalkylarylether or by reacting a fatty acid amide or alkali metal derivative thereof with an inorganic ester of an aryloxyalkyl alcohol. In examples: (1) b -aminoethylphenylether and b -methylaminoethylphenylether (prepared from b -phenoxyethylchloride and methylamine) are acylated with stearic or lauric acid and sulphonated; (2) b -aminoethyltolylether, prepared from the pure cresol or from mixed cresols by first forming the toloxyethylchloride and then treating with ammonia is condensed with stearic and lauric acids and then sulphonated. A sample furnished under Sect. 2 (5) is prepared from g -chlorpropylphenylether by treating the latter with methylamine, acylating with laurylchloride and sulphonating.ALSO:Products stated to be emulsifying agents, e.g. for use in the textile and leather industries are prepared by sulphonating acylaminoethers having the formula RCO.NR<1>(CH2)n O Q when R is a normal saturated aliphatic hydrocarbon radicle containing at least seven carbons, R<1> is hydrogen or alkyl, Q is aryl, and n is 2, 3 or 4. In examples: (1) b -aminoethylphenylether and b -methylaminoethyl - phenylether are acylated with stearic or lauric acid and sulphonated; (2) b -aminoethyltolyl ether, prepared from the pure cresol or from mixed cresols by first forming the toloxyethylchloride and then treating with ammonia is condensed with stearic and lauric acids and then sulphonated.
GB2544034A 1934-09-04 1934-09-04 New textile assistants Expired GB443902A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2544034A GB443902A (en) 1934-09-04 1934-09-04 New textile assistants

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2544034A GB443902A (en) 1934-09-04 1934-09-04 New textile assistants

Publications (1)

Publication Number Publication Date
GB443902A true GB443902A (en) 1936-03-04

Family

ID=10227698

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2544034A Expired GB443902A (en) 1934-09-04 1934-09-04 New textile assistants

Country Status (1)

Country Link
GB (1) GB443902A (en)

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