GB218568A - Manufacture of azo-dyestuffs - Google Patents

Manufacture of azo-dyestuffs

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Publication number
GB218568A
GB218568A GB3135923A GB3135923A GB218568A GB 218568 A GB218568 A GB 218568A GB 3135923 A GB3135923 A GB 3135923A GB 3135923 A GB3135923 A GB 3135923A GB 218568 A GB218568 A GB 218568A
Authority
GB
United Kingdom
Prior art keywords
nitro
chlor
toluidine
oxynaphthoyl
bis
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
GB3135923A
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.)
GRIESHEIM ELEKTRON CHEM FAB
Chemische Fabrik Griesheim Elektron
Original Assignee
GRIESHEIM ELEKTRON CHEM FAB
Chemische Fabrik Griesheim Elektron
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 GRIESHEIM ELEKTRON CHEM FAB, Chemische Fabrik Griesheim Elektron filed Critical GRIESHEIM ELEKTRON CHEM FAB
Priority to GB3135923A priority Critical patent/GB218568A/en
Publication of GB218568A publication Critical patent/GB218568A/en
Expired legal-status Critical Current

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Abstract

Azo dyes are produced by coupling diazo compounds with bis-(2 : 3-oxynaphthoyl)-4 : 41 diamino-3 : 31-dialkyloxydiaryls; the dyestuffs may be produced upon a substratum or upon the fibre, various shades of brown being thereby obtained. As diazo compounds may be used those of aniline and its substitution products, such as toluidines, anisidines, chlor- and nitro-anilines, chlor- and nitro-toluidine, chlor- and nitro-anisidines, naphthylamines, aminoanthraquinones, aminoazo-compounds, and diamines; nitrosamines may also be used. Prints may be produced by printing with diazo solutions upon goods padded with the 2 : 3-oxynaphthoic acid derivative. In an example an orange-brown shade is produced on cotton yarn impregnated with bis-(2 : 3-oxynaphthoyl)-dianisidine by developing, without drying, in a solution of diazotized 2 : 5-dichloraniline. A table is given showing the shades obtainable from bis-(2 : 3-oxynaphthoyl)-dianisidine or bis-(2 : 3-oxynaphthoyl)-diphenetidine on the one hand and the diazo or tetrazo compounds of the following bases:-o-toluidine, m-chloraniline, 2 : 5- or 3 : 5-dichloranaline, 4- or 5-chlor-2-toluidine, 4-chlor-3-toluidine, 4-chlor-2-anisidine, 4- or 5-nitro-2-toluidine, 3-nitro-4-toluidine, 4- or 5-nitro-2-anisidine, 5-nitro-3-anisidine, 4- or 5-chlor-2-nitraniline, 2- or 3-chlor-4-nitraniline, 3 : 5-dinitraniline, 4-nitro-anthranilic acid methyl ester, 5-nitro-3-aminobenzoic acid ethyl ester, a -aminoanthraquinone, m-aminoazotoluene, benzidine, dianisidine. Bis-(2 : 3-oxynaphthoyl)-4 : 41-diamino-3 : 31-dialkyloxy-diaryls are obtained by the action of 2 : 3-oxynaphthoic acid on 4 : 41 diamino-3 : 31-dialkyloxydiaryls; the properties of the compounds from dianisidine and diphenetidine are given.ALSO:Fast brown shades are produced upon the fibre by impregnating with a bis-(2 : 3-oxynaphthoyl)-4 : 41-diamino-diaryl and developing with a diazo compound; the latter may be applied by printing. As diazo compounds may be used those of aniline and its substitution products, such as toludines, anisidines, chlor- and nitro-anilines, chlor- and nitro-toluidines, chlor- and nitroanisidines, naphthylamines, aminoanthraquinones, aminoazo compounds, and diamines; nitrosamines may also be used. In an example an orange-brown shade is produced on cotton yarn by impregnating with bis-(2 : 3-oxynaphthoyl)-dianisidine and developing, without drying, in a solution of diazotized 2 : 5-dichloraniline. A table is given showing the shades obtainable from bis-(2 : 3-oxynaphthoyl)-dianisidine or diphenetidine on the one hand and the diazo or tetrazo compounds of the following bases:-o-toluidine, m-chloraniline, 2 : 5-or 3 : 5-dichloraniline, 4- or 5-chlor-2-toluidine, 4-chlor-3-toluidine, 4-chlor-2-anisidine, 4- or 5-nitro-2-toluidine, 3-nitro-4-toluidine, 4- or 5-nitro-2-anisidine, 5-nitro-3-anisidine, 4- or 5-chlor-2-nitraniline, 2- or 3-chlor-4-nitraniline, 3 : 5-dinitraniline, 4-nitro-anthranilic acid methyl ester, 5-nitro-3-aminobenzoic acid ethyl ester, a -aminoanthraquinone, m-aminoazotoluene, benzidine, dianisidine.
GB3135923A 1923-12-13 1923-12-13 Manufacture of azo-dyestuffs Expired GB218568A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3135923A GB218568A (en) 1923-12-13 1923-12-13 Manufacture of azo-dyestuffs

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3135923A GB218568A (en) 1923-12-13 1923-12-13 Manufacture of azo-dyestuffs

Publications (1)

Publication Number Publication Date
GB218568A true GB218568A (en) 1924-07-10

Family

ID=10321927

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3135923A Expired GB218568A (en) 1923-12-13 1923-12-13 Manufacture of azo-dyestuffs

Country Status (1)

Country Link
GB (1) GB218568A (en)

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