GB443222A - The manufacture of azodyestuffs and dyeing and printing preparations - Google Patents

The manufacture of azodyestuffs and dyeing and printing preparations

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Publication number
GB443222A
GB443222A GB24243/34A GB2424334A GB443222A GB 443222 A GB443222 A GB 443222A GB 24243/34 A GB24243/34 A GB 24243/34A GB 2424334 A GB2424334 A GB 2424334A GB 443222 A GB443222 A GB 443222A
Authority
GB
United Kingdom
Prior art keywords
nitro
cyanamide
diazotized
amino
acid
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
GB24243/34A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Publication of GB443222A publication Critical patent/GB443222A/en
Expired legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Azo dyes; lakes; dye preparations; azo dyes, forming upon the material; printing.--Azo dyes are manufactured in substance or on a substratum, particularly vegetable fibres, by splitting up by the action of an acid medium a triazene compound obtained by condensing cyanamide, cyanamide-carboxylic acid or a salt thereof with a diazo compound of a base suitable for preparing water-insoluble azo dyes, in the presence of a coupling component free from solubilizing groups. Preparations for dyeing and printing purposes comprise a mixture of the said triazene compounds and coupling components, if desired with the addition of wetting or dispersing agents. The dyeing may be developed by treatment in an acid medium, or in some cases by merely hanging in the air. In examples: (1) cotton tissue is printed with an aqueous mixture of the condensation product from diazotized 5-nitro-2-amino-1-methoxybenzene and sodium cyanamide, 2 : 3-hydroxynaphthoic acid a -naphthylamide, highly sulphonated castor oil, caustic soda and starch tragacanth thickener, and a full Bordeaux is developed by exposure to superheated steam containing formic and acetic acid vapours or by treatment in an aqueous formic or acetic acid solution; (2) a similar printing colour containing the condensation product from diazotized 5-nitro-2-amino-1 methylbenzene and sodium cyanamide, and 2 : 3-hydroxynaphthoic acid o-toluidide yields a full reddish-Bordeaux; (3) a similar printing colour containing the condensation product from diazotized 4-chloro-2-anisidine and sodium cyanamide, and 2 : 3-hydroxynaphthoic acid o-anisidide yields a full clear red; (4) a similar printing colour containing the condensation product from diazotized 2-nitro-4-chloraniline and sodium cyanamide, and 2 : 3-hydroxynaphthoic acid anilide yields a full yellowish-red; there may similarly be employed the condensation products from sodium cyanamide and diazotized 4-nitro-2-toluidine, 2-nitro-4-toluidine, 4-chloro-2-toluidine, 2 : 5-dichloraniline, 5 - benzoylamino - 2 - amino - 1 : 4-diethoxybenzene, 4-amino-4<1>-nitro-3-methoxy-6-methylazobenzene, 2-aminocarbazole or 1-aminoanthraquinone; (5) a similar printing colour containing the condensation product from diazotized 5-nitro-2-amino-1-methoxy-benzene and the sodium salt of cyanamide-carboxylic acid, and 2 : 3-hydroxynaphthoic acid a -naphthylamide yields a full Bordeaux. The Specification as open to inspection under Sect. 91 comprises also the manufacture of the triazene compounds employed above. Additional examples describe the manufacture of the triazene compounds employed in (1), (2) and (5) above, and also of the condensation products of sodium cyanamide with diazotized 2 : 5 - dichloraniline or 4 - amino - 4<1> - nitro - 3-methoxy - 6 - methylazobenzene, and of the sodium salt of cyanamide-carboxylic acid with diazotized 5 - nitro - 2 - amino - 1 - methylbenzene. This subject-matter does not appear in the Specification as accepted.
GB24243/34A 1933-08-26 1934-08-22 The manufacture of azodyestuffs and dyeing and printing preparations Expired GB443222A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE443222X 1933-08-26

Publications (1)

Publication Number Publication Date
GB443222A true GB443222A (en) 1936-02-24

Family

ID=6527863

Family Applications (1)

Application Number Title Priority Date Filing Date
GB24243/34A Expired GB443222A (en) 1933-08-26 1934-08-22 The manufacture of azodyestuffs and dyeing and printing preparations

Country Status (1)

Country Link
GB (1) GB443222A (en)

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