GB583413A - Dyestuff preparations for dyeing or printing textile fibres - Google Patents

Dyestuff preparations for dyeing or printing textile fibres

Info

Publication number
GB583413A
GB583413A GB6019/42A GB601942A GB583413A GB 583413 A GB583413 A GB 583413A GB 6019/42 A GB6019/42 A GB 6019/42A GB 601942 A GB601942 A GB 601942A GB 583413 A GB583413 A GB 583413A
Authority
GB
United Kingdom
Prior art keywords
acid
leuco
compounds
chloride
water
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
GB6019/42A
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.)
Durand and Huguenin AG
Original Assignee
Durand and Huguenin 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 Durand and Huguenin AG filed Critical Durand and Huguenin AG
Publication of GB583413A publication Critical patent/GB583413A/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/22General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using vat dyestuffs including indigo
    • D06P1/28Esters of vat dyestuffs
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B67/00Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
    • C09B67/0071Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
    • C09B67/0077Preparations with possibly reduced vat, sulfur or indigo dyes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Coloring (AREA)

Abstract

A preparation for use in printing or dyeing textiles comprises a salt of an acid polybasic acid ester of an enolic reduction product of a cyclic poly-ketone yielding a water-insoluble dyestuff on acid oxidation, a water-soluble organic onium compound and a water-soluble organic acid amide. The enolic ester compound present in the dyestuff preparation may be a derivative of a dyestuff or a dyestuff intermediate which yields a water-insoluble dyestuff on acid oxidation, e.g., enolic ester compounds derived from vat dyestuffs. In the numerous specific Examples given the enolic ester compounds used are the acid sulphuric acid esters of (a) leuco-2 : 1-naphthioindigo, (b) leuco-dibromanthanthrone, (c) leuco-dichloranthanthrone, (d) leuco-6 : 61-dichloro-4 : 41-dimethyl-thionidigo, (e) leuco-2 : 1- : 5-anthraquinone-diphenylthiazole, (f) leuco-tribromisodibenzanthrone, (g) leuco-dichlorisodibenzanthrone, (h) leuco-dibromo-3 : 4-8 : 9-de-benzpyrenequinone, and (i) leuco-pyranthrone. Specified polybasic acids are malonic, phthalic, m-sulphobenzoic, phosphoric and sulphuric acids. Water-soluble organic onium compounds may be compounds with internal salt formation, e.g. betaines and onium groups may be those of a quaternary ammonium, phosphonium or ternary sulphonium compounds. The onium compounds may contain water-solubilizing groups such as hydroxyl, carboxylic and sulphonic acid groups and polyether radicals. Particularly useful are quaternary ammonium compounds obtainable by converting tertiary alkylolamines with the aid of methyl chloride, dimethyl sulphate and p-toluene sulphonic acid esters, or by reacting alkylene oxides with salts of tertiary amines or alkylol-amines. Organic onium compounds containing hydroxyl and polyether groups may be made by causing alkylene oxide to react with onium compounds. In the Examples, the following are specified:-the addition product of dimethyl or diethyl sulphate with tri-b -hydroxyethyl ether of triethanolamine; the addition products of dimethyl sulphate with tetrahydroxy-polyethyl ether, with asym: diethyl-diethanol-ethylene diamine, with piperidine - N - b - hydroxy - triethyl ether, with morpholine - N - b - hydroxyethyl ether, or with b -hydroxyethyl ether of N-b -hydroxyethylmorpholine; the addition product of methyl chloride with tri-b -hydroxyethyl ether of triethanolamine; the internal salts of dimethylphenylbenzyl - ammonium - monophonic acid or trimethylphenyl-ammonium-sulphonic acid, the mono sodium salt or the mono-diethylamine salt of the internal salt of dimethylphenyl-benzyl-ammonium disulphonic acid, N-b -hydroxyethyl-pyridinium chloride, b -hydroxyethyl ether of N-b -hydroxyethyl pyridnium chloride, N - methyl - pyridinium-methylsulphonate, acetamidopyridinium chloride, tetraethanolammonium chloride or triethanol-sulphonium chloride, p and the addition product of dimethyl sulphate with the tetrahydroxy polyethylether obtainable by the action of ethylene oxide on tetraethanol ethylene diamine. Specified organic acid amides (which may be partially replaced by compounds containing hydroxy groups such as phenol, furfuryl alcohol, thiodiglycol or turkey red oil) are carboxylic acid amides, e.g., formamide, acetamide, chloracetamide, hydroxyacetamide, diethanoloxamide, tartaric acid amide or benzamide, urea and its derivatives, e.g., urethane, dicyandiamide, biuret, hydantoin, asym: diethyl urea or 5 : 5-dimethylhydantoin; also sulphonic acid amides, e.g., toluene-sulphonamide. Specification 15722/10, [Class 2 (iii)], is referred to.
GB6019/42A 1941-05-05 1942-05-05 Dyestuff preparations for dyeing or printing textile fibres Expired GB583413A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH583413X 1941-05-05

Publications (1)

Publication Number Publication Date
GB583413A true GB583413A (en) 1946-12-18

Family

ID=4521650

Family Applications (1)

Application Number Title Priority Date Filing Date
GB6019/42A Expired GB583413A (en) 1941-05-05 1942-05-05 Dyestuff preparations for dyeing or printing textile fibres

Country Status (1)

Country Link
GB (1) GB583413A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1245648A2 (en) * 2001-03-29 2002-10-02 Air Products And Chemicals, Inc. Low foam n,n'-dialkyltartaramide wetting agents

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1245648A2 (en) * 2001-03-29 2002-10-02 Air Products And Chemicals, Inc. Low foam n,n'-dialkyltartaramide wetting agents
EP1245648A3 (en) * 2001-03-29 2004-02-04 Air Products And Chemicals, Inc. Low foam n,n'-dialkyltartaramide wetting agents

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