CH116510A - Process for the production of a new dye. - Google Patents
Process for the production of a new dye.Info
- Publication number
- CH116510A CH116510A CH116510DA CH116510A CH 116510 A CH116510 A CH 116510A CH 116510D A CH116510D A CH 116510DA CH 116510 A CH116510 A CH 116510A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- new dye
- dye
- new
- chloro
- 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 diazoüer- ter 4-Chlor-2-amino-l-phenol-6-sulfosäure mit Acetessiganilid erhalten wird, mit Chrom- fluorid behandelt. Der neue Farbstoff bildet ein oranges Pulver, löst sich in Wasser mit gelber Farbe und färbt Wolle aus saurem Bade in sehr gleichmässigen, echten gelben Tönen an.
<I>Beispiel:</I> 43,1 Teile des Natronsalzes des Farb stoffes, erhalten durch Kuppeln von 4-Chlor- 2-diazo-l-phenol-6-sulfosäure mit Acetessig- anilid, werden in 1000 Teilen Wasser gelöst, mit einer Chromfluoridlösung entsprechend 22,5 Teilen Crz03 versetzt und einige Zeit bei Gegenwart von 10 Teilen Glaspulver zum Sieden erhitzt. Die Lösung wird hier auf durch Verdampfen konzentriert und der Farbstoff mit Kochsalz ausgefällt.
Process for the production of a new dye. It has been found that a new dye is obtained if the azo dye, which is obtained by coupling diazoic 4-chloro-2-amino-1-phenol-6-sulfonic acid with acetoacetanilide, is treated with chromium fluoride . The new dye forms an orange powder, dissolves in water with a yellow color and dyes wool from an acid bath in very even, genuine yellow tones.
<I> Example: </I> 43.1 parts of the sodium salt of the dye, obtained by coupling 4-chloro-2-diazo-1-phenol-6-sulfonic acid with acetoacetic anilide, are dissolved in 1000 parts of water, with a chromium fluoride solution corresponding to 22.5 parts of Crz03 and heated to boiling for some time in the presence of 10 parts of glass powder. The solution is concentrated here by evaporation and the dye is precipitated with common salt.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH111564T | 1924-06-17 | ||
CH116510T | 1924-06-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH116510A true CH116510A (en) | 1926-09-01 |
Family
ID=25707876
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH116510D CH116510A (en) | 1924-06-17 | 1924-06-17 | Process for the production of a new dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH116510A (en) |
-
1924
- 1924-06-17 CH CH116510D patent/CH116510A/en unknown
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