CH116507A - Process for the production of a new dye. - Google Patents
Process for the production of a new dye.Info
- Publication number
- CH116507A CH116507A CH116507DA CH116507A CH 116507 A CH116507 A CH 116507A CH 116507D A CH116507D A CH 116507DA CH 116507 A CH116507 A CH 116507A
- Authority
- CH
- Switzerland
- Prior art keywords
- new dye
- production
- dye
- new
- toluidide
- 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 neuen Farbstoffes. Es wurde gefunden, dass man einen neuen Farbstoff erhält, wenn man den Azofarb- stoff, welcher durch Kuppeln von dia.zotier- ter 2-Amino-l-phenol-4-sulfo-6-karbonsäure mit Acetessig-o-toluidid erhalten wird, mit Natriumchromat behandelt. Der neue Farb stoff bildet ein braunes Pulver, löst sich in Wasser mit gelber Farbe und färbt Wolle aus saurem Bade in sehr gleichmässigen, echten gelben Tönen an.
<I>Beispiel:</I> 13,7 Teile des Farbstoffes aus 2-Diazo- 1-phenol-4-sulfo-6-karbonsäure und Acet- essig-o-toluidid werden in 150 Teilen Was ser gelöst; hierauf fügt man 6,7 Teile Na- triumchromat hinzu, und, sobald letzteres ge löst ist, 12,5 Teile Ammonsulfat und erhitzt am Rüekflusskühler längere Zeit zum Sieden. Wenn die Chromverbindung sich gebildet hat, wird die Lösung etwas eingedampft und der Farbstoff mit Kochsalz ausgesalzen.
Process for the production of a new dye. It has been found that a new dye is obtained when the azo dye, which is obtained by coupling dia.zotier- ter 2-amino-1-phenol-4-sulfo-6-carboxylic acid with acetoacetic-o-toluidide , treated with sodium chromate. The new dye forms a brown powder, dissolves in water with a yellow color and dyes wool from an acid bath in very even, genuine yellow tones.
<I> Example: </I> 13.7 parts of the dye from 2-diazo-1-phenol-4-sulfo-6-carboxylic acid and aceto-acetic-o-toluidide are dissolved in 150 parts of water; 6.7 parts of sodium chromate are then added and, as soon as the latter has dissolved, 12.5 parts of ammonium sulphate are added and the mixture is heated to the boil for a long time in a reflux condenser. When the chromium compound has formed, the solution is slightly evaporated and the dye is salted out with common salt.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH111564T | 1924-06-17 | ||
CH116507T | 1924-06-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH116507A true CH116507A (en) | 1926-09-01 |
Family
ID=25707873
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH116507D CH116507A (en) | 1924-06-17 | 1924-06-17 | Process for the production of a new dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH116507A (en) |
-
1924
- 1924-06-17 CH CH116507D patent/CH116507A/en unknown
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