CH162150A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH162150A CH162150A CH162150DA CH162150A CH 162150 A CH162150 A CH 162150A CH 162150D A CH162150D A CH 162150DA CH 162150 A CH162150 A CH 162150A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- azo dye
- new azo
- dye
- azo
- 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
- C09B33/04—Disazo dyes in which the coupling component is a dihydroxy or polyhydroxy compound
- C09B33/048—Disazo dyes in which the coupling component is a dihydroxy or polyhydroxy compound the coupling component being a bis-naphthol
Description
Verfahren zur Herstellung eines neuen Azofarbstoffes. Es wurde gefunden, dass man einen neuen Azofarbstoff der Formel -
EMI0001.0004
erhält, wenn man das 1-Diazo-2.5-diäthoxy- 4-ber)zoylaininobenzol mit dem Di-(2. 8-oxy- naphthoyl)-bei)zidiiiid kuppelt. Der so erhal tene Farbstoff bildet ein violettschwarzes Pulver. Auf geeigneten Substraten, wie zum Beispiel Baumwolle, Wolle, Kunstseide her gestellt, färbt er diese in reinen, echten, violetten Tönen.
<I>Beispiel:</I> <B>60</B> Teile 1-Amino-2 .5-diäthoxy-4-benzoyl- aminobenzol werden wie üblich diazotiert und in eine Lösung von 52,4 Teilen des Di-(2,8- oxynaphthoyl)-benzidinid, 100 Teilen 30 %iger Natriumhydroxydlösung, <B>30</B> Teilen Soda und 2000 Teilen Wasser eingetragen. Der ge bildete Farbstoff fällt sofort aus. Er wird filtriert, gewaschen und. getrocknet.
Process for the production of a new azo dye. It has been found that a new azo dye of the formula -
EMI0001.0004
obtained when the 1-diazo-2,5-diethoxy-4-ber) zoylaininobenzene is coupled with the di- (2,8-oxynaphthoyl) -bei) zidiiiid. The dye obtained in this way forms a purple-black powder. Placed on suitable substrates such as cotton, wool, rayon, he dyes them in pure, genuine, purple tones.
<I> Example: </I> <B> 60 </B> parts of 1-amino-2 .5-diethoxy-4-benzoyl-aminobenzene are diazotized as usual and dissolved in a solution of 52.4 parts of the di- ( 2,8-oxynaphthoyl) benzidinide, 100 parts of 30% strength sodium hydroxide solution, 30 parts of soda and 2000 parts of water are added. The dye formed precipitates out immediately. It is filtered, washed and. dried.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH162150T | 1932-08-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH162150A true CH162150A (en) | 1933-06-15 |
Family
ID=4415368
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH162150D CH162150A (en) | 1932-08-05 | 1932-08-05 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH162150A (en) |
-
1932
- 1932-08-05 CH CH162150D patent/CH162150A/en unknown
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