CH267871A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH267871A CH267871A CH267871DA CH267871A CH 267871 A CH267871 A CH 267871A CH 267871D A CH267871D A CH 267871DA CH 267871 A CH267871 A CH 267871A
- Authority
- CH
- Switzerland
- Prior art keywords
- acid
- dye
- production
- azo dye
- new 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
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
- C09B35/38—Trisazo dyes ot the type
- C09B35/44—Trisazo dyes ot the type the component K being a hydroxy amine
- C09B35/46—Trisazo dyes ot the type the component K being a hydroxy amine the component K being an amino naphthol
- C09B35/463—D being derived from diaminodiphenyl
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 264602. verfahren zur Herstellung eines neuen Azofarbstoffes. Das vorliegende Patent betrifft ein Ver fahren zur Herstellung eines neuen Azofarb- stoffes und ist dadurch gekennzeichnet, dass man die Zwischenverbindung aus 4,4'-Tetrazo- diphenyl und 1 Mol Salicylsäure mit dem Ace- tylaminoazofarbstoff, den man durch saure Kupplung von dianotierter Anilin-2,5-disttl- fonsäure mit.
2,8-Atninonaphthol-6-sulfon- säure und nachfolgende Aeetylierung erhält, vereinigt. und das erhaltene Kopplungspro dukt zwecks Verseifung der Acetylamino- gruppe mit verseifenden Mitteln behandelt. <I>Beispiel:</I> 18,4 Teile Zenzidin werden in bekannter Weise tetrazotiert und mit 13,8 Teilen Sali- cylsäure in alkalischer Lösung- zur Zwischen verbindung vereinigt.
Zu der orangebraunen Suspension derselben lässt tnan in Gegenwart von 20 Teilen calc. Soda die wässerige Lösung von 52 Teilen des Monoazofarbstoffes, den man durch Vereinigung von diazotierter Anilin-2,5- disulfonsäure mit 2,8-Aminonaphthol-6-sulfoti- säure in saurem Medium und nachfolgende Acet,ylierung erhält, bei 5 bis 100 zufliessen. Der entstehende Farbstoff geht mit violett- brauner Farbe in Lösung. Nach beendeter Kupplung wird ausgesalzen, filtriert und ge trocknet.
Der so erhaltene Trisazofarbstoff, ein dunkles Pulver, färbt Baumwolle in licht echten violettbraunen Tönen.
Durch Verseifen in l0o/oiger Sodalösung bei 90 erhält man den entsprechenden Amino- azofarbstoff, der Baumwolle in gelbstichig braunen, schweiss- und säureechten Nuancen von -uter Lichtechtheit. färbt.
<B> Additional patent </B> to main patent no. 264602. Process for the production of a new azo dye. The present patent relates to a process for the production of a new azo dye and is characterized in that the intermediate compound of 4,4'-tetrazodiphenyl and 1 mole of salicylic acid with the acetylaminoazo dye, which is obtained by acidic coupling of dianotated aniline -2,5-distl- fonic acid with.
2,8-Atninonaphthol-6-sulfonic acid and subsequent acetylation obtained, combined. and the coupling product obtained is treated with saponifying agents for the purpose of saponifying the acetylamino group. <I> Example: </I> 18.4 parts of zenzidine are tetrazotized in a known manner and combined with 13.8 parts of salicylic acid in an alkaline solution to form the intermediate compound.
The orange-brown suspension of the same can be added in the presence of 20 parts of calc. Soda the aqueous solution of 52 parts of the monoazo dye, which is obtained by combining diazotized aniline-2,5-disulfonic acid with 2,8-aminonaphthol-6-sulphonic acid in an acidic medium and subsequent acetylation, at 5 to 100 flow in . The resulting dye goes into solution with a violet-brown color. After the coupling has ended, the mixture is salted out, filtered and dried.
The trisazo dye obtained in this way, a dark powder, dyes cotton in light, genuine violet-brown shades.
Saponification in 10% soda solution at 90 gives the corresponding amino azo dye, cotton in yellow-tinged brown, sweat- and acid-fast shades of good lightfastness. colors.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH264602T | 1947-01-17 | ||
CH267871T | 1947-01-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH267871A true CH267871A (en) | 1950-04-15 |
Family
ID=25730753
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH267871D CH267871A (en) | 1947-01-17 | 1947-01-17 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH267871A (en) |
-
1947
- 1947-01-17 CH CH267871D patent/CH267871A/en unknown
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