GB511103A - Manufacture of substantive polyazo dyestuffs - Google Patents
Manufacture of substantive polyazo dyestuffsInfo
- Publication number
- GB511103A GB511103A GB25909/38A GB2590938A GB511103A GB 511103 A GB511103 A GB 511103A GB 25909/38 A GB25909/38 A GB 25909/38A GB 2590938 A GB2590938 A GB 2590938A GB 511103 A GB511103 A GB 511103A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- sulphonic acid
- naphthylamine
- sulphonic
- dyes
- 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
- C09B31/00—Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
- C09B31/16—Trisazo dyes
- C09B31/22—Trisazo dyes from a coupling component "D" containing directive hydroxyl and amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
511,103. Dyes. GEIGY AKT.-GES., J. R Sept. 5, 1938, No. 25909. Convention date Sept. 7, 1937. [Classes 2(iii) and 15(ii)] Substantive polyazo dyes are made by diazotizing disazo dyes of the formula A-N=N-M1-N=N-M2-NH2 and coupling with 2-aroylamino-6-naphthol-8- sulphonic acids, in which the aroyl residue may be substituted (A = the residue of a benzene or naphthalene sulphonic or carboxylic acid, M1 and M2=benzene and naphthalene residues containing the azo groups in p-position to one another or to the amido group). They produce fast blue to grey shades on cotton and viscose which may be developed on the fibre to fast green shades. In examples the following dyes are described (1) aniline-m-sulphonic acid# 1 - naphthylamine - 7 - sulphonic acid# amino - hydroquinone dimethylether# 2 - (4<1>- or 3<1> - amino) benzoylamino - 6 - naphthol - 8 - sulphonic acid# (on the fibre)- 1 - phenyl - 3 - methyl - 5 - pyrazolone : other middle components 'specified are aminohydroquinone diethyl or dibenzyl ether, cresidine, aminonaphthol ethers or alpha-naphthylamine, (2) 1-amino-4- acetylaminonaphthalene-7-sulphonic acid# 1- naphthylamine - 6 - sulphonic acid # 1 - naphthylamine - 7 - sulphonic acid # N - benzoyl - 2:6:8: - acid. Other initial components specified are aniline o - sulphonic acid, aniline-2:5-disulphonic acid, 4-chloraniline-3- sulphonic acid, 2-naphthylamine-4:8-disulphonic acid. Specifications 445,999 and 481,832 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH511103X | 1937-09-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB511103A true GB511103A (en) | 1939-08-14 |
Family
ID=4517437
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB25909/38A Expired GB511103A (en) | 1937-09-07 | 1938-09-05 | Manufacture of substantive polyazo dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB511103A (en) |
-
1938
- 1938-09-05 GB GB25909/38A patent/GB511103A/en not_active Expired
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