GB265553A - Improvements in tetrakisazo dyes, and the process of manufacture - Google Patents
Improvements in tetrakisazo dyes, and the process of manufactureInfo
- Publication number
- GB265553A GB265553A GB32187/26A GB3218726A GB265553A GB 265553 A GB265553 A GB 265553A GB 32187/26 A GB32187/26 A GB 32187/26A GB 3218726 A GB3218726 A GB 3218726A GB 265553 A GB265553 A GB 265553A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- sodium
- pyrazolone
- toluidine
- coupling
- 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
- C09B31/30—Other polyazo dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
265,553. Newport Co., (Assignees of Oesch, J. B.). Feb. 6, 1926, [Convention date]. Tetrakisazo dyes are made by coupling a diazotized aminoazo body of the benzene series, containing one or two sulphonic groups and two to four methyl groups, with m-toluidine, rediazotizing and again coupling with m-toluidine, and rediazot.izing the trisazo dye thus formed and coupling with 1-phenyl-3-methyl-5-pyrazolone or a substitution product, particularly a sulphonic acid thereof. The products dye unmordanted cotton orange to brown shades of great fastness to light. In an example, sodium aminoazotoluene disulphonate used as the first component, and 1- p-sulphophenyl-3-methyl-5-pyrazolone (sodium salt) as end component. Strong reducing agents split up the dyestuff at the azo groups, yielding sodium 2-toluidine-5-sulphonate, sodium 2 : 5- diaminotoluene-3-sulphonate, methyl-p-phenylenediamine, and 1-p-sulphophenyl-3-methyl-4- amino-5-pyrazolone. Specifi cation 208,265 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US265553XA | 1926-02-06 | 1926-02-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB265553A true GB265553A (en) | 1928-03-20 |
Family
ID=21832480
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB32187/26A Expired GB265553A (en) | 1926-02-06 | 1926-12-20 | Improvements in tetrakisazo dyes, and the process of manufacture |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB265553A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2457823A (en) * | 1944-12-01 | 1949-01-04 | Ilford Ltd | Production of pyrazolone azo dyes |
US4081437A (en) * | 1974-04-25 | 1978-03-28 | Produits Chimiques Ugine Kuhlmann | Water soluble polyazo dyestuffs |
US4169831A (en) * | 1974-04-25 | 1979-10-02 | Produits Chimiques Ugine Kuhlmann | Water-soluble tetrakisazo dyestuffs derived from 4,4'-diaminoazobenzene |
-
1926
- 1926-12-20 GB GB32187/26A patent/GB265553A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2457823A (en) * | 1944-12-01 | 1949-01-04 | Ilford Ltd | Production of pyrazolone azo dyes |
US4081437A (en) * | 1974-04-25 | 1978-03-28 | Produits Chimiques Ugine Kuhlmann | Water soluble polyazo dyestuffs |
US4169831A (en) * | 1974-04-25 | 1979-10-02 | Produits Chimiques Ugine Kuhlmann | Water-soluble tetrakisazo dyestuffs derived from 4,4'-diaminoazobenzene |
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