GB995502A - Reactive mono- and dis-azo dyestuffs - Google Patents

Reactive mono- and dis-azo dyestuffs

Info

Publication number
GB995502A
GB995502A GB1868462A GB1868462A GB995502A GB 995502 A GB995502 A GB 995502A GB 1868462 A GB1868462 A GB 1868462A GB 1868462 A GB1868462 A GB 1868462A GB 995502 A GB995502 A GB 995502A
Authority
GB
United Kingdom
Prior art keywords
radical
dyes
substituted
formula
hydrogen atom
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
GB1868462A
Inventor
Ian Knowles Barben
Cecil Vivian Stead
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 GB1868462A priority Critical patent/GB995502A/en
Priority to CH607363A priority patent/CH435497A/en
Priority to FR934959A priority patent/FR1364736A/en
Publication of GB995502A publication Critical patent/GB995502A/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
    • C09B62/00Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
    • C09B62/02Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring
    • C09B62/022Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring the heterocyclic ring being alternatively specified
    • C09B62/026Azo dyes

Landscapes

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

Abstract

The invention comprises azo dyes which in the form of the free acids are of formula <FORM:0995502/C4-C5/1> wherein R is a hydrogen atom or C1- 4 alkyl group; R1 and R2 are methyl groups and R3 and R4 are each independently a hydrogen atom or a methyl group, or when R3 and R4 are hydrogen atoms R1 and R2 are joined together to form a tetra- or penta-methylene radical, or R1 and R3 and R2 and R4 are joined togethe to form in each case a trimethylene radical; D is the residue of a diazo component of the benzene, naphthalene or stilbene series or a benzene or naphthalene radical substituted by a phenylazo or naphthylazo group; n is an integer from 1 to 6; E is a 1,4-phenylene or -naphthylene radical which may be substituted by ureido, acetylamino, methyl, methoxy, carboxylic or sulphonic acid groups and X is a divalent mono- or di-chloropyrimidyl, or 5-cyanochloropyrimidyl radical or a divalent 1,3,5-triazinyl radical substituted in the 6-position by a hydrogen atom or a C1- 4 alkyl, phenyl, C1- 4 alkoxy, phenoxy, amino or substituted amino group. The dyes are prepared by reacting an azo dye of formula <FORM:0995502/C4-C5/2> with a hydrazine of formula <FORM:0995502/C4-C5/3> Specified hydrazines include N:N:N1-trimethyl and N:N:N1:N1 - tetramethyl - hydrazine, N - aminopiperidine, N - aminopyrrolidine, 1,5 - diazabicyclo - (0,3,3) - octane and, preferably, N,N - dimethylhydrazine. The dyes may be used to colour wool, silk, synthetic polyamide and preferably cellulose materials by the usual reactive dye processes. The preparation of the dyes is described in examples.
GB1868462A 1962-05-15 1962-05-15 Reactive mono- and dis-azo dyestuffs Expired GB995502A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
GB1868462A GB995502A (en) 1962-05-15 1962-05-15 Reactive mono- and dis-azo dyestuffs
CH607363A CH435497A (en) 1962-05-15 1963-05-15 Process for the production of azo dyes
FR934959A FR1364736A (en) 1962-05-15 1963-05-15 New azo dyes for dyeing textile materials, in particular cellulose

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1868462A GB995502A (en) 1962-05-15 1962-05-15 Reactive mono- and dis-azo dyestuffs

Publications (1)

Publication Number Publication Date
GB995502A true GB995502A (en) 1965-06-16

Family

ID=10116644

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1868462A Expired GB995502A (en) 1962-05-15 1962-05-15 Reactive mono- and dis-azo dyestuffs

Country Status (2)

Country Link
CH (1) CH435497A (en)
GB (1) GB995502A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0122458A1 (en) * 1983-03-16 1984-10-24 Ciba-Geigy Ag Azo compounds

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0122458A1 (en) * 1983-03-16 1984-10-24 Ciba-Geigy Ag Azo compounds

Also Published As

Publication number Publication date
CH435497A (en) 1967-05-15

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