GB525642A - Manufacture of disazo dyestuffs - Google Patents
Manufacture of disazo dyestuffsInfo
- Publication number
- GB525642A GB525642A GB6187/39A GB618739A GB525642A GB 525642 A GB525642 A GB 525642A GB 6187/39 A GB6187/39 A GB 6187/39A GB 618739 A GB618739 A GB 618739A GB 525642 A GB525642 A GB 525642A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- phenol
- coupled
- diazotized
- dyestuff
- 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
- C09B35/02—Disazo dyes
- C09B35/039—Disazo dyes characterised by the tetrazo component
- C09B35/04—Disazo dyes characterised by the tetrazo component the tetrazo component being a benzene derivative
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
525,642. Dyes. GEIGY AKT.-GES., J. R. Feb. 24, 1939, No. 6187. Convention date, Feb. 26,1938. Addition to 507,967. [Class 2(iii)] Disazo dyes of the general formula (where A=aryl, R=a benzene residue coupled in p-position, and Y=OH, alkyl, aryl, aralkyl or an amino or substituted amino group) are made by coupling the diazo compound of a monoazo dye of the formula with a phenol coupling in p-position and treating the product with an arylsulphochloride, only coupling the diazo compound of a monoazo dye of the formula with 2:8:3:6-acid and treating the product with an arylsulphochloride. In examples, (1) the dyestuff 4-nitraniline-6-sulphonic acid# 2:8:3:6- acid is reduced, diazotized, coupled with phenol or m-cresol and the product treated with p-toluenesulphochloride (violet on wool) ; other aryl-sulphochlorides, e.g., benzene- or p-chlorbenzene-sulphochloride may be used, (2) the dyestuff 4-nitraniline-6-sulphoethylanilide# 2:8: 3:6-acid is reduced, diazotized, coupled with phenol, and treated with p-toluene sulphochloride ; other specified components are the corresponding sulphonic acid amides or diethyl- or dimethyl-amides or the methyl-sulphone, and (3) the dyestuff 4-nitro-2-methoxyaniline- 5-sulphonic acid# phenol is reduced, diazotized, coupled with 2:8:3:6-acid and treated with ptoluenesulphochloride.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH525642X | 1938-02-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB525642A true GB525642A (en) | 1940-09-02 |
Family
ID=4518179
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB6187/39A Expired GB525642A (en) | 1938-02-26 | 1939-02-24 | Manufacture of disazo dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB525642A (en) |
-
1939
- 1939-02-24 GB GB6187/39A patent/GB525642A/en not_active Expired
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