GB306843A - Process for the manufacture of azo dyestuffs containing chromium - Google Patents

Process for the manufacture of azo dyestuffs containing chromium

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Publication number
GB306843A
GB306843A GB6156/29A GB615629A GB306843A GB 306843 A GB306843 A GB 306843A GB 6156/29 A GB6156/29 A GB 6156/29A GB 615629 A GB615629 A GB 615629A GB 306843 A GB306843 A GB 306843A
Authority
GB
United Kingdom
Prior art keywords
carboxylic acids
sulphonic
compounds
aminodiphenylsulphone
methylpyrazolone
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
GB6156/29A
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 GB306843A publication Critical patent/GB306843A/en
Expired legal-status Critical Current

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Abstract

306,843. I. G. Farbenindustrie Akt.- Ges. Feb. 25, 1928, [Convention date]. Azo dyes, soluble chromium compounds of: lakes.-Azo dyes obtained by coupling diazo compounds with the methyl pyrazolones or pyrazolone carboxylic acids derived from salicylic sulphones as described in Specification 245,765 are converted into soluble chromium compounds by boiling with chromium salts. The products dye wool m even clear greenish yellow snades fast tolight, fulling, perspiration, steaming, and car. bonizing, and are suitable for the preparation of lakes on account of their fastness to light, water and lime. In examples the soluble chromium compounds of the following dyestuffs are prepared by boiling the dyestuffs under reflux with chromium formate solution :-(1) 2-chloro-4- toluidine # the methylpyrazolone from 4<1>-oxy- 3<1> - carboxy-2-aminodiphenylsulphone-4-sulphonic acid; (2) aniline-3-sulphonic acid # the same methylpyrazolone. Aniline, toluidines, xylidines, naphthylamines, and sulphonic acids, sulphonamides, sulphonanilides halogen derivatives, and carboxylic acids thereof may be used as diazo components, and other methyl pyrazolones or pyrazolone carboxylic acids from 4<1>-oxy-3<1>-carboxy-2-aminodiphenylsulphone or sulphonic or other derivatives thereof may be used as coupling components.
GB6156/29A 1928-02-25 1929-02-25 Process for the manufacture of azo dyestuffs containing chromium Expired GB306843A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE306843X 1928-02-25

Publications (1)

Publication Number Publication Date
GB306843A true GB306843A (en) 1930-05-26

Family

ID=6121237

Family Applications (1)

Application Number Title Priority Date Filing Date
GB6156/29A Expired GB306843A (en) 1928-02-25 1929-02-25 Process for the manufacture of azo dyestuffs containing chromium

Country Status (1)

Country Link
GB (1) GB306843A (en)

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