CH238149A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH238149A CH238149A CH238149DA CH238149A CH 238149 A CH238149 A CH 238149A CH 238149D A CH238149D A CH 238149DA CH 238149 A CH238149 A CH 238149A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- production
- new azo
- dye
- blue
- 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)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Description
Verfahren zur Herstellung eines neuen Azofarbstoffes. Es wurde gefunden, dass man einen neuen Azofarbstoff erhält, wenn man die Diazover- bindung der 2-Amino-l-oxy-6-nitrobenzol-4- sulfonsäure in alkalischem Medium mit 1,4- Dioxynaphthalinmonoäthyläther vereinigt.
Der Farbstoff stellt ein dunkles Pulver dar, das sich in Wasser mit blauvioletter Farbe löst und Wolle aus saurem Bade in violettblauen Tönen färbt, die beim Nach- chromieren in Grün übergehen.
Beispiel: 23,4 Teile 2-Amino-l-oxy-6-nitrobenzol-4- sulfonsäure werden mit 6,9 Teilen Natrium- nitrit und 22 Teilen Salzsäure (30 %) diazotiert. Die Diazoverbindung lässt man bei 0-5 in eine Lösung von 18,8 Teilen 1,4-Dioxy- naphthalinmonoäthyläther,
15 Teilen Natron- lauge (30 %) und 25 Teilen Natriumcarbonat in 100 Teilen Wasser fliessen. Die Kupplung ist nach, vierstündigem Rühren bei 10-15o beendet. Der Farbstoff wird abfiltriert und getrocknet.
Process for the production of a new azo dye. It has been found that a new azo dye is obtained if the diazo compound of 2-amino-1-oxy-6-nitrobenzene-4-sulfonic acid is combined with 1,4-dioxynaphthalene monoethyl ether in an alkaline medium.
The dye is a dark powder that dissolves in water with a blue-violet color and dyes wool from an acid bath in violet-blue tones, which turn green when chromed.
Example: 23.4 parts of 2-amino-1-oxy-6-nitrobenzene-4-sulfonic acid are diazotized with 6.9 parts of sodium nitrite and 22 parts of hydrochloric acid (30%). The diazo compound is left at 0-5 in a solution of 18.8 parts of 1,4-dioxynaphthalene monoethyl ether,
15 parts of sodium hydroxide solution (30%) and 25 parts of sodium carbonate flow in 100 parts of water. The coupling is complete after stirring for four hours at 10-15 °. The dye is filtered off and dried.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH238149T | 1944-01-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH238149A true CH238149A (en) | 1945-06-30 |
Family
ID=4460436
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH238149D CH238149A (en) | 1944-01-12 | 1944-01-12 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH238149A (en) |
-
1944
- 1944-01-12 CH CH238149D patent/CH238149A/en unknown
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