CH205822A - Process for the preparation of a monoazo dye. - Google Patents
Process for the preparation of a monoazo dye.Info
- Publication number
- CH205822A CH205822A CH205822DA CH205822A CH 205822 A CH205822 A CH 205822A CH 205822D A CH205822D A CH 205822DA CH 205822 A CH205822 A CH 205822A
- Authority
- CH
- Switzerland
- Prior art keywords
- monoazo dye
- preparation
- dye
- diazotized
- aminophenol
- 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)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines Honoazofarbstoffes. Vorliegendes Patent bezieht sich auf ein Verfahren zur Hex^stellung eines Monoazo- farbstoffes,dadurch gekennzeichnet, dass man diazotiertes 4-Chlor=6-nitro-2-aminophenol in sodaalkasischer Lösung mit 1-Phenogyacetyl- amino- 6 -ogynaphthalin- 3 -sulfonsäure kup pelt.
Der so erhaltene Farbstoff ist ein dunkles Pulver und färbt Wolle beim Chromieren in blaugrauen Tönen von sehr guten Echtheits- eigenschaften.
<I>Beispiel:</I> 18,9 Teile 4-Chlor-6-nitro-2--aminophenol werden diazotiert. Die erhaltene Diazolösung lässt man m eine überschüssiges Natrium- carbonat enthaltende Lösung von 38 Teilen 1, - Phenogyacetylamino- 6; - oxynaphthalin-3- sulfonsäure laufen. Nach beendeter Kuppe- Jung wird,der gebildete Farbstoff abgeschie den und -getrocknet.
Process for the preparation of a honoazo dye. The present patent relates to a process for hex ^ position of a monoazo dye, characterized in that diazotized 4-chloro = 6-nitro-2-aminophenol in soda-alkaline solution with 1-phenogyacetylamino-6-gynaphthalene-3-sulfonic acid coupling.
The dye obtained in this way is a dark powder and, on chroming, dyes wool in blue-gray shades with very good fastness properties.
<I> Example: </I> 18.9 parts of 4-chloro-6-nitro-2-aminophenol are diazotized. The diazo solution obtained is left m a solution of 38 parts of 1-phenogyacetylamino-6; - run oxynaphthalene-3-sulfonic acid. After the Kuppe-Jung is finished, the dye formed is deposited and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE205822X | 1937-01-25 | ||
CH203140T | 1938-01-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH205822A true CH205822A (en) | 1939-06-30 |
Family
ID=25723893
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH205822D CH205822A (en) | 1937-01-25 | 1938-01-19 | Process for the preparation of a monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH205822A (en) |
-
1938
- 1938-01-19 CH CH205822D patent/CH205822A/en unknown
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