GB778233A - New tetrakisazo-dyestuffs and process for making them - Google Patents
New tetrakisazo-dyestuffs and process for making themInfo
- Publication number
- GB778233A GB778233A GB28697/54A GB2869754A GB778233A GB 778233 A GB778233 A GB 778233A GB 28697/54 A GB28697/54 A GB 28697/54A GB 2869754 A GB2869754 A GB 2869754A GB 778233 A GB778233 A GB 778233A
- Authority
- GB
- United Kingdom
- Prior art keywords
- naphthol
- dyestuffs
- group
- sulphonic
- effected
- 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
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
- C09B35/50—Tetrazo dyes
- C09B35/56—Tetrazo dyes of the type
Abstract
The invention comprises dyestuffs of formula <FORM:0778233/IV(b)/1> where R1 is a diphenyl residue bound in the 4 and 41 positions to the azo linkage and containing in the 3, 31 positions an - O - O - CH2-COOH group or a COOH group and R2 and R3 are residues of naphthol sulphonic acids bound to - N=N - R1 in a position vicinal to the OH group and each containing a single sulphonic acid group bound to the naphthalene nucleus. The dyestuffs may be made by coupling a tetrazo compound of an appropriate diaminodiazo - dyestuff with 8 - oxyquinoline advantageously tetrazotization is effected by the indirect method and coupling in an alkaline medium optionally with the addition of a compound such as pyridine or alcohol. Preferably the 8 - oxyquinoline is coupled in a finely divided state e.g. as precipitated by alkali from a hydrochloric acid solution, before or after mixing with the tetrazocompound. The diazo dyestuffs are made by coupling the necessary tetrazotized diphenyl derivative with an appropriate naphthol sulphonic acid generally in an alkaline medium and advantageously a solution of the tetrazo compound is run into an alkaline solution of the sulphonic acid. The carboxymethoxy group is specified as a 3, 31 - substituent in the diphenyl compounds. Specified naphthol sulphonic acids are 2 - (41 - aminophenylamino) - 5 - naphthol - 7, 31 - disulphonic acid, <FORM:0778233/IV(b)/2> and 2 - amino - 5 - naphthol - 7 - and - 8 - naphthol - 6 - sulphonic acids the last two acids being preferred. Mixtures of sulphonic acids may be used. The dyestuffs dye wool, silk or leather and especially cellulose-containing materials such as cotton, linen and regenerated cellulose. They may be converted into metal compounds on the fibre, in substance or in the dyebath. Metallization, e.g. coppering may be effected as in Specification 455,274 [Group IV] and after-treatment with an aqueous solution containing a basic formaldehyde condensation product as in Specification 619,969 may be effected. Cellulose fibres yield coppered dyeings in navy blue, grey or black shades. Examples are provided of the preparation of the dyestuffs by the use of certain of the above specified components the products being used to give coppered dyeings on cellulosic materials.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH778233X | 1953-10-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB778233A true GB778233A (en) | 1957-07-03 |
Family
ID=4535987
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB28697/54A Expired GB778233A (en) | 1953-10-14 | 1954-10-05 | New tetrakisazo-dyestuffs and process for making them |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB778233A (en) |
-
1954
- 1954-10-05 GB GB28697/54A patent/GB778233A/en not_active Expired
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