CH223710A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH223710A CH223710A CH223710DA CH223710A CH 223710 A CH223710 A CH 223710A CH 223710D A CH223710D A CH 223710DA CH 223710 A CH223710 A CH 223710A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- production
- new azo
- new
- dye
- 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
- C09B33/00—Disazo and polyazo dyes of the types A->K<-B, A->B->K<-C, or the like, prepared by diazotising and coupling
- C09B33/02—Disazo dyes
- C09B33/12—Disazo dyes in which the coupling component is a heterocyclic compound
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 220751. Verfahren zur Herstellung eines neuen Azofarbstoffes. Es wurde gefunden, dass man einen neuen Azofarbstoff erhält, wenn man 1 Mol der Diphenyl-4',4"-di-(3-methyl-5-pyrazo- lon)-2',2"-disulfonsäure mit 2 Mol der Diazo- verbindung der 1-Aminobenzol-2-carbonsäure vereinigt.
Der neue Farbstoff stellt ein gelbes Pulver dar; seine nachchromierten Färbungen auf Wolle weisen gelbe Töne von sehr guten Echtheitseigenschaften auf.
Beispiel: Man löst 13,7 Teile 1-Aminobenzol-2- carbonsäure in 90 Teilen 10%iger Salzsäure, kühlt mit Eis auf 0, und dianotiert mit einer Lösung von 7 Teilen Natriumnitrit in 30 Teilen Wasser.
Diese Diazolösung gibt man langsam zu einer eiskalten Lösung von 25,3 Teilen Diphenyl-4',4"-di-(3-methyl-5- pyrazolon)-2',2"-disulfonsäure in 150 Teilen Wasser und 18 Teilen Natriumcarbonat. Nach beendigter Kupplung wird der Farbstoff aus gesalzen, filtriert und getrocknet.
<B> Additional patent </B> to main patent no. 220751. Process for the production of a new azo dye. It has been found that a new azo dye is obtained if 1 mole of diphenyl-4 ', 4 "-di- (3-methyl-5-pyrazolone) -2', 2" -disulfonic acid is mixed with 2 moles of diazo - Combined compound of 1-aminobenzene-2-carboxylic acid.
The new dye is a yellow powder; his re-chrome-plated dyeings on wool show yellow tones with very good fastness properties.
Example: 13.7 parts of 1-aminobenzene-2-carboxylic acid are dissolved in 90 parts of 10% strength hydrochloric acid, cooled to 0 with ice and dianotized with a solution of 7 parts of sodium nitrite in 30 parts of water.
This diazo solution is slowly added to an ice-cold solution of 25.3 parts of diphenyl-4 ', 4 "-di- (3-methyl-5-pyrazolone) -2', 2" -disulfonic acid in 150 parts of water and 18 parts of sodium carbonate. After coupling is complete, the dye is salted out, filtered and dried.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH220751T | 1941-03-29 | ||
| CH223710T | 1941-03-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH223710A true CH223710A (en) | 1942-09-30 |
Family
ID=25726497
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH223710D CH223710A (en) | 1941-03-29 | 1941-03-29 | Process for the production of a new azo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH223710A (en) |
-
1941
- 1941-03-29 CH CH223710D patent/CH223710A/en unknown
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