GB748421A - New metallisable mono-azo dyestuffs - Google Patents

New metallisable mono-azo dyestuffs

Info

Publication number
GB748421A
GB748421A GB2183653A GB2183653A GB748421A GB 748421 A GB748421 A GB 748421A GB 2183653 A GB2183653 A GB 2183653A GB 2183653 A GB2183653 A GB 2183653A GB 748421 A GB748421 A GB 748421A
Authority
GB
United Kingdom
Prior art keywords
radicle
dyestuffs
sulphon
aminophenol
sulphonamide
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
GB2183653A
Inventor
Charles Hugh Reece
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 GB2183653A priority Critical patent/GB748421A/en
Publication of GB748421A publication Critical patent/GB748421A/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
    • C09B45/00Complex metal compounds of azo dyes
    • C09B45/02Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
    • C09B45/14Monoazo compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Developing Agents For Electrophotography (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Coloring (AREA)

Abstract

The invention comprises dyestuffs of formula:-<FORM:0748421/IV(c)/1> where X is H, NO2 or Hlg, R is H, an aryl radicle of the benzene series free of sulphonamido groups, an alkyl radicle of 1-3 C atoms or a hydroxyalkyl radicle of 2 or 3 C atoms, and of Y and Z one is H and the other - NH.CO.R1 where R1 is alkyl (C1-C4), alkoxy (C1-C4) or O.C3H4.O AIK where AIK is Me or Et. The invention also comprises chromium and cobalt complexes of the above dyestuffs which contain 0.5-0.75, preferably 0.5, atomic proportions of metal per mol. proportion of dyestuff. The dyestuffs are made by coupling the required diazotized amino-benzesulphonamide and naphthol and they may be metallized in the usual way in a weakly acid or alkaline medium preferably in the presence of an organic solvent and optionally with the addition of dispersing agents. Specified diazo components are 2 - aminophenol - 4 - sulphonamide - sulphon - N - methyl, - isopropyl -, b - hydroxy - ethyl - and - y - hydroxy - n - propyl - amide - sulphoanilide and sulphon - N - d - toluidide and 6 - nitro - and - chloro - 2 - aminophenol - 4 - sulphonamide and sulphon - N - methylamide. Specified coupling components are 1 - acetyl -, - n - butyryl - n - valeryl - car - bomethoxy -, - carboethoxy -, - carbo - n - butoxy -, - carbo - (21 - methoxy) - ethoxy -, and - carbo - (21 - ethoxy) - ethoxy - amino - 6 - naphthol, 2 - acetyl -, - n - butyryl -, - carbomethoxy -, - carboethoxy - and - carboisopropoxyamino - 7 - naphthol. The metallized dyestuffs yield red to violet to grey shades on wool and are also used to dye other nitrogeneous fibres and lacquers, varnishes and other plastic materials. Examples are provided of the use of certain of the above specified components in the preparation of unmetallized and metallized dyestuffs. In the Provisional Specification the sulphonamide group is - SO2 N R1 R2 where R1 is H or a short chain alkyl or hydroxyalkyl radicle and R2 is an aryl radicle of the benzene series free of sulphonamide groups, H or a short chain alkyl or hydroxyalkyl radicle and "AIK" is alkyl of C1 to C4. Additional diazo components specified are 2 - aminophenol - 4 - sulphon - N - di - (b - hydroxyethyl) - and - n - butyl - amide and 2 - aminophenol - 4 - sulphone - N - b - hydroxyethylanilide.
GB2183653A 1953-08-07 1953-08-07 New metallisable mono-azo dyestuffs Expired GB748421A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2183653A GB748421A (en) 1953-08-07 1953-08-07 New metallisable mono-azo dyestuffs

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2183653A GB748421A (en) 1953-08-07 1953-08-07 New metallisable mono-azo dyestuffs

Publications (1)

Publication Number Publication Date
GB748421A true GB748421A (en) 1956-05-02

Family

ID=10169627

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2183653A Expired GB748421A (en) 1953-08-07 1953-08-07 New metallisable mono-azo dyestuffs

Country Status (1)

Country Link
GB (1) GB748421A (en)

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