CH267867A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH267867A CH267867A CH267867DA CH267867A CH 267867 A CH267867 A CH 267867A CH 267867D A CH267867D A CH 267867DA CH 267867 A CH267867 A CH 267867A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- azo dye
- production
- new azo
- new
- 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, da.ss inan die Zwischenverbindung aus 4,4'-Tetrazo- diphenyl und 1 --Hol Salicylsäure mit dem Di- acetyidiaminoazofarbstoff,
den man durch saure Kupplung von diazotiert.er 5-Acetyl- amino-2-aminobenzol-l-suifonsäure mit 2,8- Aminonaphthol-6-stulfoilsätire und nachfol gende Acetylierung erhält, vereinigt und das erhaltene Kupplungsprodukt zwecks Versei fung der im Naphthalinkern sitzenden Acetyl- aminogruppe mit verseifenden Mitteln behan delt.
<I>Beispiel:</I> 18,4 Teile Benzidin werden in bekannter Weise tetrazotiert und mit 13,8 Teilen Salicyl- säure in alkalischer Lösung zur Zwischenver bindung vereinigt. Zu der orangebraunen Sus pension derselben lässt man in Gegenwart von 20 Teilen calc. Soda die wässerige Lösung von 52 Teilen des Monoazofarbstoffes,
den man durch Vereinigung von diazotierter 5-Acetyl- amino - 2 - aminobenzol -1- sulfonsäure mit 2,8 Aminonaphthol-6-sulfonsäure in saurem Me dium und nachfolgende Acetylierung erhält, bei 5 bis 100 zufliessen. Der entstellende Farb stoff geht mit violettbrauner Farbe in Lösung. Nach beendeter Kupplung wird ausgesalzen, filtriert und getrocknet.
Der so erhaltene Tris- azofarbstoff, ein dunkles Pulver, färbt Baum wolle in lichtechten violettbraunen Tönen.
Durch Verseifen in 10 o/oiger Sodalösung bei<B>900</B> erhält man den entsprechenden Amino- azofarbstoff, der Baumwolle in gelbstichig braunen, sehweiss- und säureechten Nuancen von guter Liehtechtheit 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 -hol salicylic acid with the diacetyidiaminoazo dye,
which is obtained by acid coupling of diazotiert.er 5-acetyl-amino-2-aminobenzene-l-suifonic acid with 2,8-aminonaphthol-6-stulfoilsätire and subsequent acetylation, and the coupling product obtained is combined for the purpose of hydrolysis of those in the naphthalene core Acetyl amino group treated with saponifying agents.
<I> Example: </I> 18.4 parts of benzidine are tetrazotized in a known manner and combined with 13.8 parts of salicylic acid in an alkaline solution to form the intermediate compound. To the orange-brown Sus pension the same can be calc in the presence of 20 parts. Soda the aqueous solution of 52 parts of the monoazo dye,
which is obtained by combining diazotized 5-acetylamino-2-aminobenzene-1-sulfonic acid with 2.8 aminonaphthol-6-sulfonic acid in acidic Me and subsequent acetylation, at 5 to 100 flow. The disfiguring dye goes into solution with a purple-brown color. After the coupling has ended, it is salted out, filtered and dried.
The tris azo dye thus obtained, a dark powder, dyes cotton in lightfast violet-brown shades.
By saponifying in 10% soda solution at <B> 900 </B> the corresponding amino azo dye is obtained, which dyes cotton in yellowish brown, whitish-white and acid-fast shades of good lightfastness.
Claims (1)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH267869T | 1947-01-17 | ||
CH267867T | 1947-01-17 | ||
CH264602T | 1947-01-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH267867A true CH267867A (en) | 1950-04-15 |
Family
ID=27178089
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH267867D CH267867A (en) | 1947-01-17 | 1947-01-17 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH267867A (en) |
-
1947
- 1947-01-17 CH CH267867D patent/CH267867A/en unknown
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