GB719631A - Manufacture of azo-dyestuffs - Google Patents
Manufacture of azo-dyestuffsInfo
- Publication number
- GB719631A GB719631A GB24384/51A GB2438451A GB719631A GB 719631 A GB719631 A GB 719631A GB 24384/51 A GB24384/51 A GB 24384/51A GB 2438451 A GB2438451 A GB 2438451A GB 719631 A GB719631 A GB 719631A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- dyestuffs
- trisazo
- components
- aminosalicylic
- 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
- C09B39/00—Other azo dyes prepared by diazotising and coupling
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Abstract
The invention comprises (1) the production of azo dyestuffs by coupling a diazo component in alkaline solutions with a p-aminosalicylic acid of the formula:- <FORM:0719631/IV(c)/1> and (2) monoazo, disazo and trisazo dyestuffs of the following formulae:- <FORM:0719631/IV(c)/2> and <FORM:0719631/IV(c)/3> where there is at least one solubilising group in one of the residues R; in all the formulae X and Y are hydrogen, chlorine, methyl or sulphonic acid. The disazo and trisazo dyestuffs are made by diazotizing the monoazo compounds and coupling with suitable components, and repeating the process if necessary. The products may be metallized (especially chromed) in substance or on the fibre, e.g. by the metachrome process. Examples show the production of the following dyestuffs:- 4-chloro-2-aminophenol --> 4-aminosalicylic acid, 6-nitro-2-aminophenol-4-sulphonic acid --> 4-aminosalicylic acid, sulphanilic acid --> 4-aminosalicylic acid --> 1-phenyl-3-methyl-5-pyrazolone, and sulphanilic acid --> 4-aminosalicylic acid --> 1-naphthylamine --> 2-naphthol. Other suitable starting materials are listed:- diazo components of the benzene and naphthalene series, end components for disazo (and middle components for trisazo) of the benzene, naphthalene and pyrazolone series, and as end components for trisazo resorcinol, naphthols and phenylmethylpyrazolone. Substituted 4-aminosalicylic acids are also mentioned.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE719631X | 1950-10-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB719631A true GB719631A (en) | 1954-12-08 |
Family
ID=6627257
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB24384/51A Expired GB719631A (en) | 1950-10-18 | 1951-10-18 | Manufacture of azo-dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB719631A (en) |
-
1951
- 1951-10-18 GB GB24384/51A patent/GB719631A/en not_active Expired
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