CH200534A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH200534A CH200534A CH200534DA CH200534A CH 200534 A CH200534 A CH 200534A CH 200534D A CH200534D A CH 200534DA CH 200534 A CH200534 A CH 200534A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- azo dye
- new
- new azo
- 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
- C09B31/00—Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
- C09B31/02—Disazo dyes
- C09B31/06—Disazo dyes from a coupling component "C" containing a directive hydroxyl group
Description
Zusatzpatent zum Hauptpatent Nr. 198138. Verfahren zur Herstellung eines neuen Azofarbstoffes. Es wurde gefunden, dass man einen neuen Azofarbstoff erhält, wenn man auf 4-Methyl- 2-benzylphenol diazotiertes 4-Amino-3.2'- dimethyl-1 . 1'-azobenzol einwirken lässt.
Der neue Farbstoff stellt ein braunes Pul ver dar; auf Baumwolle hergestellt erzeugt der neue Farbstoff gelbbraune Töne. Beispiel: 22,6 Teile 4-Amino-3.2'-dimethyl-1.1'- azobenzol werden wie üblich diazotiert. Die filtrierte Diazoniumlösung lässt man ein fliessen in eine Lösung von 19,8 Teilen 4-Me- thyl-2-benzylphenol, 10 Teilen Natrium- hydrogyd, 5 Teilen Natriumcarbonat in 200 Teilen Wasser.
Der gebildete Farbstoff fällt sofort aus, wird filtriert, gewaschen und getrocknet. Er bildet ein braunes Pulver, das aus Chlorbenzol kristallisiert bei 165 bis 167 schmilzt.
Additional patent to main patent No. 198138. Process for the production of a new azo dye. It has been found that a new azo dye is obtained if 4-amino-3.2'-dimethyl-1 which has been diazotized onto 4-methyl-2-benzylphenol. 1'-azobenzene can act.
The new dye is a brown powder; Made on cotton, the new dye creates yellow-brown tones. Example: 22.6 parts of 4-amino-3.2'-dimethyl-1.1'-azobenzene are diazotized as usual. The filtered diazonium solution is allowed to flow into a solution of 19.8 parts of 4-methyl-2-benzylphenol, 10 parts of sodium hydrogen, 5 parts of sodium carbonate in 200 parts of water.
The dye formed precipitates immediately and is filtered, washed and dried. It forms a brown powder that crystallizes from chlorobenzene and melts at 165 to 167.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH200534T | 1936-11-16 | ||
CH198138T | 1936-11-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH200534A true CH200534A (en) | 1938-10-15 |
Family
ID=25723068
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH200534D CH200534A (en) | 1936-11-16 | 1936-11-16 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH200534A (en) |
-
1936
- 1936-11-16 CH CH200534D patent/CH200534A/en unknown
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