GB482342A - Manufacture of disazo-dyestuffs soluble in water - Google Patents
Manufacture of disazo-dyestuffs soluble in waterInfo
- Publication number
- GB482342A GB482342A GB2595636A GB2595636A GB482342A GB 482342 A GB482342 A GB 482342A GB 2595636 A GB2595636 A GB 2595636A GB 2595636 A GB2595636 A GB 2595636A GB 482342 A GB482342 A GB 482342A
- Authority
- GB
- United Kingdom
- Prior art keywords
- resorcinol
- acid
- sulphonic acid
- sulphonic
- methyltaurine
- 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
- C09B33/00—Disazo and polyazo dyes of the types A->K<-B, A->B->K<-C, or the like, prepared by diazotising and coupling
- C09B33/02—Disazo dyes
- C09B33/04—Disazo dyes in which the coupling component is a dihydroxy or polyhydroxy compound
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
Disazo dyes soluble in water are made by coupling in any order of succession resorcinol with a diazo compound of the benzene series (1 mol) and a diazo compound from an amine of the benzene series containing besides the amino group to be diazotized a free amino group and/or at least one alkyl sulphonic group and containing no nitro group (1 mol), the components being selected so that the finished dyestuff contains at least two sulphonic acid groups, or 2 mols of the diazo compound substituted by amino and/or alkyl sulphonic groups are coupled with 1 mol of resorcinol. They dye leather in brown shades. In examples the following dyes are described: (1) 4-amino-1-benzylsulphonic acid \sQ resorcinol; (2) 4 - aminobenzene - 1 - methyltaurine - 2-sulphonic acid --> resorcinol \sM 4-nitro-aniline-2-sulphonic acid; (3) and (6) 1 : 4-diaminobenzene-sulphomethyltauride --> resorcinol \sM 2-nitroaniline-4-sulphonic acid or sulphanilic acid; (4) 1 : 4-diaminobenzene sulphonic acid --> resorcinol \sM sulphanilic acid or 1 : 4-diaminobenzene sulphonic acid; (5) 1 - aminobenzene - 3 - sulphotauride --> resorcinol \sM sulphanilic acid. 4 - Aminobenzene - 1 - methyltaurine - 2-sulphonic acid is made by condensing 4-nitro 1-chlorbenzene-2-sulphonic acid with methyltaurine and reducing. 1 : 4 - Diaminobenzene sulphomethyltauride is made by condensing 1-chlor-4-nitrobenzene-2-sulphochloride with methyltaurine, exchanging the chlorine for amino and reducing. 1 - Aminobenzene - 3 - sulphotauride is made by condensing 1-nitrobenzene-3-sulphochloride with taurine and reducing.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2595636A GB482342A (en) | 1936-09-24 | 1936-09-24 | Manufacture of disazo-dyestuffs soluble in water |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2595636A GB482342A (en) | 1936-09-24 | 1936-09-24 | Manufacture of disazo-dyestuffs soluble in water |
Publications (1)
Publication Number | Publication Date |
---|---|
GB482342A true GB482342A (en) | 1938-03-24 |
Family
ID=10236038
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2595636A Expired GB482342A (en) | 1936-09-24 | 1936-09-24 | Manufacture of disazo-dyestuffs soluble in water |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB482342A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3852263A (en) * | 1971-01-15 | 1974-12-03 | Bayer Ag | Substituted 4-(n-sulphoalkylene-aminosulphonyl)-phenyl-azo-phenyl compounds |
-
1936
- 1936-09-24 GB GB2595636A patent/GB482342A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3852263A (en) * | 1971-01-15 | 1974-12-03 | Bayer Ag | Substituted 4-(n-sulphoalkylene-aminosulphonyl)-phenyl-azo-phenyl compounds |
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