GB995875A - Reactive metallised azo dyestuffs - Google Patents

Reactive metallised azo dyestuffs

Info

Publication number
GB995875A
GB995875A GB1868662A GB1868662A GB995875A GB 995875 A GB995875 A GB 995875A GB 1868662 A GB1868662 A GB 1868662A GB 1868662 A GB1868662 A GB 1868662A GB 995875 A GB995875 A GB 995875A
Authority
GB
United Kingdom
Prior art keywords
dyes
group
radical
hydrazine
formula
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
GB1868662A
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 GB1868662A priority Critical patent/GB995875A/en
Publication of GB995875A publication Critical patent/GB995875A/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
    • C09B62/032Metal complex azo dyes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Electroplating And Plating Baths Therefor (AREA)

Abstract

The invention comprises the copper, chromium or cobalt complexes of sulphonated mono-, dis- or tris-azo dyes which contain in o,o1-position to a least one azo group two hydroxy groups or a hydroxy group and a carboxy group, and which contain attached to a benzene or naphthalene ring in the dyes, one or two groups of formula <FORM:0995875/C4-C5/1> wherein V is a phenylene or sulphophenylene radical; m and p are 1 or 2: R is a hydrogen atom or a C1- 4 alkyl group; R1 and R2 are methyl groups and R3 and R4 are hydrogen atoms or methyl groups, or when R3 and R4 are hydrogen atoms R1 and R2 are joined to form a tetra- or penta-methylene radical, or R1 and R3 and R2 and R4 are joined together to form in each case a trimethylene radical and X is a divalent mono- or di-chloropyrimidyl, 5-cyanomonochloropyrimidyl radical or divalent 1,3,5-triazinyl radical substituted in the 6-position by a hydrogen atom, C1- 4 alkyl, C1- 4 alkoxy, phenyl, phenoxy, amino or substituted amino group. The dyes are prepared by reacting an appropriate metallized dye containing a group of formula <FORM:0995875/C4-C5/2> with a hydrazine of formula <FORM:0995875/C4-C5/3> Specified hydrazines include N,N,N1-trimethyl-and N,N,N1,N1 - tetramethyl - hydrazine, N-aminopiperidine or - pyrrolidine, 1,5 - diazabicyclo - (0: 3: 3) - octane and, preferably, N,N - dimethyl - hydrazine. The dyes may be used to colour wool, silk, polyamide and, preferably, cellulose fibres by the usual processes for reactive dyes. Examples describe the preparation of the dyes. Specifications 846,949, 850,559, 859,198, 863,758, 870,985, 882,890, 887,867, 895,449, 896,675, 896,785, 902,726 and 923,886 are referred to.
GB1868662A 1962-05-15 1962-05-15 Reactive metallised azo dyestuffs Expired GB995875A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1868662A GB995875A (en) 1962-05-15 1962-05-15 Reactive metallised azo dyestuffs

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1868662A GB995875A (en) 1962-05-15 1962-05-15 Reactive metallised azo dyestuffs

Publications (1)

Publication Number Publication Date
GB995875A true GB995875A (en) 1965-06-23

Family

ID=10116674

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1868662A Expired GB995875A (en) 1962-05-15 1962-05-15 Reactive metallised azo dyestuffs

Country Status (1)

Country Link
GB (1) GB995875A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5123930A (en) * 1984-04-27 1992-06-23 Sandoz Ltd. 1:2 chromium and cobalt complexes of monoazo compounds for drying porous oxide layers on aluminum and aluminum alloy substrates
US5283325A (en) * 1984-04-27 1994-02-01 Sandoz Ltd. 1:2 chromium and cobalt complexes of monoazo compounds having further unsubstituted or substituted nitro-2-hydroxyphenyl diazo component radicals and 6- or 7-acyl-amino-1-hydroxy-3-sulfonaphthalene coupling component radicals

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5123930A (en) * 1984-04-27 1992-06-23 Sandoz Ltd. 1:2 chromium and cobalt complexes of monoazo compounds for drying porous oxide layers on aluminum and aluminum alloy substrates
US5283325A (en) * 1984-04-27 1994-02-01 Sandoz Ltd. 1:2 chromium and cobalt complexes of monoazo compounds having further unsubstituted or substituted nitro-2-hydroxyphenyl diazo component radicals and 6- or 7-acyl-amino-1-hydroxy-3-sulfonaphthalene coupling component radicals

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