CH263503A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH263503A CH263503A CH263503DA CH263503A CH 263503 A CH263503 A CH 263503A CH 263503D A CH263503D A CH 263503DA CH 263503 A CH263503 A CH 263503A
- Authority
- CH
- Switzerland
- Prior art keywords
- blue
- dye
- azo dye
- violet
- preparation
- Prior art date
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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/14—Monoazo compounds
- C09B45/16—Monoazo compounds containing chromium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Azofarbstoffes. Es wurde gefunden, dass ein wertvoller Azofarbstoff hergestellt werden kann, wenn man diazotierte 6-Nitro-2-amino-l-phenol-4- sulfonsäure mit Glycerin-mono-(6-oxy-2- naphthyl)-äther kuppelt.
Der neue Farbstoff stellt. ein schwärz liches Pulver dar, das sich in Wasser und verdünnter Sodalösung mit blauvioletter, in konzentrierter Schwefelsäure mit violettroter Farbe löst. Der Farbstoff färbt. Wolle aus saurem Bade in blauen Tönen, die durch Nachchromieren in ein echtes blaustichiges Olivgrau übergeführt. werden.
Die Kupplung erfolgt zweckmässig in al kalischem, z. B. Alkalihydroxy d und gegebe nenfalls Alkalicarbonat enthaltendem Medium. <I>Beispiel:</I> 23,4 Teile 6-Nitro-2-amino-l-phenol-4-sul- fonsäure werden in bekannter Weise diazotiert und in alkalischer Lösung mit 24 Teilen Glv- cerin-mono-(6-oxy-2-naphthyl)-äther gekup pelt. Nach beendeter Kupplung wird der Farbstoff durch Kochsalzzugabe abgeschie den, abfiltriert und getrocknet.
Process for the preparation of an azo dye. It has been found that a valuable azo dye can be produced if diazotized 6-nitro-2-amino-1-phenol-4-sulfonic acid is coupled with glycerol mono- (6-oxy-2-naphthyl) ether.
The new dye represents. a blackish powder that dissolves in water and dilute soda solution with a blue-violet color, in concentrated sulfuric acid with a violet-red color. The dye stains. Wool from an acid bath in blue tones, which are converted into a real blue-tinged olive-gray by re-chrome plating. will.
The coupling is expedient in al kalischem, z. B. Alkali hydroxide and optionally alkali carbonate-containing medium. <I> Example: </I> 23.4 parts of 6-nitro-2-amino-1-phenol-4-sulphonic acid are diazotized in a known manner and mixed with 24 parts of glycerin-mono- (6 -oxy-2-naphthyl) ether coupled. After coupling is complete, the dye is deposited by adding sodium chloride, filtered off and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH263503T | 1942-12-22 | ||
CH257111T | 1943-11-04 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH263503A true CH263503A (en) | 1949-08-31 |
Family
ID=25730042
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH263503D CH263503A (en) | 1942-12-22 | 1942-12-22 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH263503A (en) |
-
1942
- 1942-12-22 CH CH263503D patent/CH263503A/en unknown
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