GB551434A - Dyes and dyeing - Google Patents

Dyes and dyeing

Info

Publication number
GB551434A
GB551434A GB929941A GB929941A GB551434A GB 551434 A GB551434 A GB 551434A GB 929941 A GB929941 A GB 929941A GB 929941 A GB929941 A GB 929941A GB 551434 A GB551434 A GB 551434A
Authority
GB
United Kingdom
Prior art keywords
amino
diethyl
acetanilide
benzthiazole
hydroxyethyl
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
GB929941A
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to GB929941A priority Critical patent/GB551434A/en
Publication of GB551434A publication Critical patent/GB551434A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/06Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
    • C09B29/08Amino benzenes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Abstract

551,434. Dyes and dyeing ; artificial silk : cellulose derivative compositions. ARGYLE, C. S. July 23, 1941, No. 9299. [Classes 2 (ii), (iii) and 15 (ii)] Azo dyes are obtained by coupling a diazotized 2-aminothiazole with . a mono-acidvl-mphenylenediamine. Specified diazo components are 4-methyl-2-aminothiazole, 2-amino-benzthiazole and its 6-methyl, 6-methoxy, 6- ethoxy, 6-chloro, 6-acetylamino and 6-benzoylamino derivatives and 2-amino-4:5-benzobenzthiazole, and specified coupling components are m-amino-acetamilide and its N- diethyl, N-di-(#-hydroxyethyl) and N-ethyl-N- #-hydroxyethyl derivatives, N-dimethyl-maminopropionanilide, 3-dietliylamino-4-methylacetanilide, 3-diethylamino-4-methoxy-acetanilide, N-diethyl-m-amino-stearanilide and N- diethyl-m-amino-benzanilide. The products give dischargable brilliant red shades on cellulose ester or ether materials and are applicable also for colouring synthetic linear superpolyamide materials. They may also be incorporated in cellulose ester or ether lacquers or spinning solutions. The dyestuffs containing diazotizable amino groups may be diazotized upon the materials and developed, e.g. with N-diethylaniline, N-di-(#-hydroxyethyl)-m-toluidine, N-diethyl-m-amino acetanilide or N-ethyl-1-naphthylamine. Examples relate to the production of the dyestuffs, (1) 2-amino-benzthiazole # N-diethyl-mamino-acetanilide or N-diethyl-m-amino-stearanilide, (2) 6-ethoxy-2-amino-benzthiazole - m-amino-acetanilide, which gives on cellulose acetate yarn, from an aqueous dispersion, bright bluish red dyeings capable of diazotization on the fibre and development with N-diethylaniline, N-di-(#-hydroxyethyl)-m-toluidine or N-diethyl-m-amino-acetanilide, (3) 6-acetylamino-2-amino-benzthiazole # N-di-(#- hydroxylethyl)-m-amino-acetanilide. An example is also given of the dyeing of a cellulose acetate knitted fabric with the azo dye of (1) above. Specification 440,113 is referred to. 6- Acetylamino-2-aminobenzthiazole and 6- benzoylamino-2-aminobenzthiazole are obtained by adding bromine to solutions of p-aminoacetanilide and p-aminobenzanilide respectively in glacial acetic acid containing ammonium thiocyanate. N-diethyl-m-amino-stearanilide and N-diethyl-m-amino-benzanilide are obtained by the action of stearic acid chloride and benzoyl chloride respectively on 3-diethylaminoaniline.
GB929941A 1941-07-23 1941-07-23 Dyes and dyeing Expired GB551434A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB929941A GB551434A (en) 1941-07-23 1941-07-23 Dyes and dyeing

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB929941A GB551434A (en) 1941-07-23 1941-07-23 Dyes and dyeing

Publications (1)

Publication Number Publication Date
GB551434A true GB551434A (en) 1943-02-22

Family

ID=9869283

Family Applications (1)

Application Number Title Priority Date Filing Date
GB929941A Expired GB551434A (en) 1941-07-23 1941-07-23 Dyes and dyeing

Country Status (1)

Country Link
GB (1) GB551434A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2683709A (en) * 1951-12-21 1954-07-13 Eastman Kodak Co 5-nitrothiazoleazo-nu, nu-substituted aniline-compounds
US2683708A (en) * 1951-12-21 1954-07-13 Eastman Kodak Co Azo compounds prepared from a 2-amino-5-nitrothiazole and an nu-monosubstituted aniline compound
US2746953A (en) * 1951-12-21 1956-05-22 Eastman Kodak Co 5-nitrothiazoleazoaniline compounds

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2683709A (en) * 1951-12-21 1954-07-13 Eastman Kodak Co 5-nitrothiazoleazo-nu, nu-substituted aniline-compounds
US2683708A (en) * 1951-12-21 1954-07-13 Eastman Kodak Co Azo compounds prepared from a 2-amino-5-nitrothiazole and an nu-monosubstituted aniline compound
US2746953A (en) * 1951-12-21 1956-05-22 Eastman Kodak Co 5-nitrothiazoleazoaniline compounds

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