GB685078A - New trisazo dyestuffs - Google Patents
New trisazo dyestuffsInfo
- Publication number
- GB685078A GB685078A GB1675650A GB1675650A GB685078A GB 685078 A GB685078 A GB 685078A GB 1675650 A GB1675650 A GB 1675650A GB 1675650 A GB1675650 A GB 1675650A GB 685078 A GB685078 A GB 685078A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- coupling
- diazotizing
- nitroaniline
- formula
- 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
- C09B35/38—Trisazo dyes ot the type
- C09B35/44—Trisazo dyes ot the type the component K being a hydroxy amine
- C09B35/46—Trisazo dyes ot the type the component K being a hydroxy amine the component K being an amino naphthol
- C09B35/461—D being derived from diaminobenzene
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
The invention comprises trisazo dyestuffs of the formula <FORM:0685078/IV (c)/1> where X is hydrogen or chlorine. These are made by diazotizing an amine of the formula <FORM:0685078/IV (c)/2> (Y=nitro or acylamino), coupling in acid medium with one mol. of the appropriate aminonaphtholsulphonic acid, coupling the product in alkaline solution with a diazotized aniline-sulphonic acid, converting Y to NH2, diazotizing the amino group and coupling in alkaline medium with m-aminophenol. The products dye leather in grey or black shades. In the examples the initial diazo component is p-nitroaniline, o-chloro-p-nitroaniline or p-amino-acetanilide, the naphthalene derivative is H acid or K acid and the second diazo component is sulphanilic acid or metanilic acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1675650A GB685078A (en) | 1950-07-05 | 1950-07-05 | New trisazo dyestuffs |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1675650A GB685078A (en) | 1950-07-05 | 1950-07-05 | New trisazo dyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB685078A true GB685078A (en) | 1952-12-31 |
Family
ID=10083071
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1675650A Expired GB685078A (en) | 1950-07-05 | 1950-07-05 | New trisazo dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB685078A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2216325A1 (en) * | 1973-02-06 | 1974-08-30 | Hoechst Ag | |
US4734489A (en) * | 1985-03-29 | 1988-03-29 | Taoka Chemical Company, Limited | Trisazo compounds useful in producing water-resistant ink compositions |
-
1950
- 1950-07-05 GB GB1675650A patent/GB685078A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2216325A1 (en) * | 1973-02-06 | 1974-08-30 | Hoechst Ag | |
US4734489A (en) * | 1985-03-29 | 1988-03-29 | Taoka Chemical Company, Limited | Trisazo compounds useful in producing water-resistant ink compositions |
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