GB330349A - Manufacture of new azo-dyestuffs insoluble in water - Google Patents
Manufacture of new azo-dyestuffs insoluble in waterInfo
- Publication number
- GB330349A GB330349A GB1137429A GB1137429A GB330349A GB 330349 A GB330349 A GB 330349A GB 1137429 A GB1137429 A GB 1137429A GB 1137429 A GB1137429 A GB 1137429A GB 330349 A GB330349 A GB 330349A
- Authority
- GB
- United Kingdom
- Prior art keywords
- naphthol
- carboxylic acid
- carboxylic
- amino
- diazo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/10—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
- C09B29/18—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides
- C09B29/20—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides of the naphthalene series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
330,349. Groves, W. W., (I. G. Farbenindustrie Akt.-Ges.). April 12, 1929. Azo dyes are made in substance or on a sub. tratum by combining any diazo, tetrazo or diazo. azo compound free from sulphonic or carboxylic . groups with a 6-amino-2-naphthol-3-carboxylic acid arylide of the general formula where Y = -NH2, -NH-aryl or .N< alkyl. Two series of dyestuffs are obtainable according to the coupling conditions used. The following components are specified : 6-phenylamino-2-naphthol- 3-carboxylic acid anilide or o-toluidide, 6-p-methyl (or chlor)-phenylamino-2 - naphthol - 3 - carboxylic acid-o-anisidide, 6-o-chlorphenylamino-2-naphthol- 3-carboxylic acid anilide, 6-p-chlorphenylamino-2- naphthol-3-carboxylic c acid-p-chloranilide, 6-N- methylphenylamino-2-naphthol-3-carboxylic acid. anilide and 6-amino-2-naphthol-3-carboxylic acidp-toluidide; diazo components specified are alphanaphthylamine, 4-chloro-o-anisidine, 5-chlor-otoluidine, p-nitraniline, m-nitro-p-toluidine, mnitro-o-anisidine, o-aminoazotoluene, alpha-aminoazotoluene, alpha-aminoanthraquinone, - dianiside, 2 : 5-dichloraniline, and 2 : 4 : 5-trichloraniline. 6-Amino-2-naphthol-3-carboxylic acid arylides are made from 6-amino-2-naphthol-3-carboxylic acids (c.f. Specification 326,971) or substitution products thereof according to Specification 23732/13.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1137429A GB330349A (en) | 1929-04-12 | 1929-04-12 | Manufacture of new azo-dyestuffs insoluble in water |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1137429A GB330349A (en) | 1929-04-12 | 1929-04-12 | Manufacture of new azo-dyestuffs insoluble in water |
Publications (1)
Publication Number | Publication Date |
---|---|
GB330349A true GB330349A (en) | 1930-06-12 |
Family
ID=9985056
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1137429A Expired GB330349A (en) | 1929-04-12 | 1929-04-12 | Manufacture of new azo-dyestuffs insoluble in water |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB330349A (en) |
-
1929
- 1929-04-12 GB GB1137429A patent/GB330349A/en not_active Expired
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