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GB423587A - The manufacture of diazoimino compounds and their application in dyeing and printing - Google Patents

The manufacture of diazoimino compounds and their application in dyeing and printing

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Publication number
GB423587A
GB423587A GB1828633A GB1828633A GB423587A GB 423587 A GB423587 A GB 423587A GB 1828633 A GB1828633 A GB 1828633A GB 1828633 A GB1828633 A GB 1828633A GB 423587 A GB423587 A GB 423587A
Authority
GB
United Kingdom
Prior art keywords
acid
diazoimino
piperazinoacetic
dyeing
compounds
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
GB1828633A
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 GB1828633A priority Critical patent/GB423587A/en
Publication of GB423587A publication Critical patent/GB423587A/en
Expired legal-status Critical Current

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Abstract

Diazoimino compounds soluble in water are made by coupling an aromatic diazo-, diazoazo-, or tetrazo-compound with a piperazinoacetic acid. They may be mixed with suitable azo coupling components and, if desired, with textile assistants and/or solid diluents, to form dry azo preparations for use in dyeing and printing. In examples: (1)--(3) diazoimino compounds from the following diazotized bases and piperazinoacetic acid are described: 4- or 5-chlor-o-toluidine, dianisidine, 4-methoxy-3-benzoylaminoaniline, aniline, m- and p-chloraniline and 4-benzoylamino-2 : 5-dimethoxyaniline; 4-carbothoxypiperazinoacetic acid may also be used. Azo dyes are formed on the material by applying the above diazoimino compounds and a coupling component, preferably in the form of a mixture, the colour being developed by means of an acid treatment. Examples are given in which the diazoimino compound is used with the anilide or o-toluidide of 2 : 3-oxynaphthoic acid or diacetoacetyl-o-tolidine, the colour being developed in an ager containing steam mixed with the vapours of formic and acetic acids. Piperazinoacetic acid is made by condensing piperazine with chloracetic acid or by hydrolysing ethyl 4-carbothoxy-1-piperazinoacetate with caustic soda.
GB1828633A 1933-06-27 1933-06-27 The manufacture of diazoimino compounds and their application in dyeing and printing Expired GB423587A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1828633A GB423587A (en) 1933-06-27 1933-06-27 The manufacture of diazoimino compounds and their application in dyeing and printing

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1828633A GB423587A (en) 1933-06-27 1933-06-27 The manufacture of diazoimino compounds and their application in dyeing and printing

Publications (1)

Publication Number Publication Date
GB423587A true GB423587A (en) 1935-01-28

Family

ID=10109849

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1828633A Expired GB423587A (en) 1933-06-27 1933-06-27 The manufacture of diazoimino compounds and their application in dyeing and printing

Country Status (1)

Country Link
GB (1) GB423587A (en)

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