GB190210243A - Manufacture of Azo-dyestuffs. - Google Patents

Manufacture of Azo-dyestuffs.

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Publication number
GB190210243A
GB190210243A GB190210243DA GB190210243A GB 190210243 A GB190210243 A GB 190210243A GB 190210243D A GB190210243D A GB 190210243DA GB 190210243 A GB190210243 A GB 190210243A
Authority
GB
United Kingdom
Prior art keywords
acid
dyes
sulphonic acid
sulphonic
naphthylenediamine
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
Inventor
Oliver Imray
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Application granted granted Critical
Publication of GB190210243A publication Critical patent/GB190210243A/en
Expired legal-status Critical Current

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

Abstract

10,243. Imray, O., [Farbwerke vorm. Meister, Lucius, & Br³ning]. May 3. Dyes, artificial.-(1) Monoazo dyes, which are stable and are apparently derived from a 1 : 8- amidonaphthol sulphonic acid, are produced by heating with mineral acids the monazo dyes obtained from 1:8-naphthylenediamine sulphonic acid. An example is given in which the dye-stuff obtained by combining diazotized naphthionic acid with a molecular proportion of 1 : 8 : 4- naphthylenediamine sulphonic acid in acetic acid or feebly alkaline solution is heated with dilute hydrochloric acid at about 90‹ C. for 18 hours. The product dyes wool violet. Dyes from 1 : 8 : 4- naphthylenediamine sulphonic acid and picramic acid, o-amidophenol-p-sulphonic acid, o amidop-cresol-o-sulphonic acid, o amido-o-nitrophenolp-sulphonic acid, p - nitro - o - amidophenol, and chloramidophenol sulphonic acids [OH : NA2 : SO3H :Cl and OH : NH2 : Cl : SO3H = 1 : 2 : 4 : 6] are also similarly treated. (2) Disazo dyes are produced by combining a diazotized amine, such as diazotized aniline, p-toluidine, alpha- or #-naphthylamine, or p-nitraniline in acid solution, with the foregoing products, especially those obtained from an amidosulphonic acid, for example with those obtained by the action of mineral acids upon the monazo dyes derived from 1:8:4-naphthylenediamine sulphonic acid and naphthionic acid or sulphanilic acid.
GB190210243D 1902-05-03 1902-05-03 Manufacture of Azo-dyestuffs. Expired GB190210243A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB190210243T 1902-05-03

Publications (1)

Publication Number Publication Date
GB190210243A true GB190210243A (en) 1903-03-05

Family

ID=32154277

Family Applications (1)

Application Number Title Priority Date Filing Date
GB190210243D Expired GB190210243A (en) 1902-05-03 1902-05-03 Manufacture of Azo-dyestuffs.

Country Status (1)

Country Link
GB (1) GB190210243A (en)

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