CH252289A - Process for the preparation of a polyazo dye. - Google Patents
Process for the preparation of a polyazo dye.Info
- Publication number
- CH252289A CH252289A CH252289DA CH252289A CH 252289 A CH252289 A CH 252289A CH 252289D A CH252289D A CH 252289DA CH 252289 A CH252289 A CH 252289A
- Authority
- CH
- Switzerland
- Prior art keywords
- benzene
- mol
- dye
- oxy
- diamino
- 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
- C09B35/40—Trisazo dyes ot the type the component K being a dihydroxy or polyhydroxy compound
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 246985. Verfahren zur Herstellung eines Polyazofarbstoffes. Gegenstand vorliegenden Patentes ist ein Verfahren zur Herstellung eines Polyazo- farbstoffes. Das Verfahren ist dadurch ge kennzeichnet, dass man 'die diazotierte Amino- azoverbindung 4-Amino-naphthyl-1,1'-azo-4'- oxy-benzol-3'-carbonsäure in alkalischem Me dium mit dem Disazofarbstoff vereinigt,
der erhältlich ist durch Kuppeln von 1 Mol tetrazotierter 1-Oxy-2,6-diamino-benzol-4-sul- fonsäure einerseits mit 1 Mol 1,3-Diamino- benzol und anderseits mit 1 Mol Resorcin.
Der erhaltene neue Polyazofarbstoff ,stellt ein dunkles Pulver dar, das sich in Wasser mit brauner und in konzentrierter Schwefel säure mit schmutzig graublauer Farbe löst. Baumwolle und Fasern aus regenerierter Cellulose werden in dunkelbraunen Tönen an gefärbt. Durch Nachbehandlung mit Kupfer sulfat werden Nass- und Lichtechtheit erheb lich verbessert.
<I>Beispiel:</I> 20,4 Teile 1-Oxy-2,6=diamino-benzol-4-sul- fonsäure werden in salzsaurer Lösung mit 132,8 Teilen Natriumnitrit tetrazotiert, die überschüssige Mineralsäure mit Natriumace- tat abgestumpft und bei Gegenwart von über schüssigem Natriumacetat mit einer neutra len Lösung von -10,8 Teilen 1,3-D.iamino-ben- zol vereinigt.
Das Zwischenprodukt ist sehr rasch gebildet. Nach zweistündigem Rühren wird weitergekuppelt, indem man die Zwi schenverbindung in eine Lösung von 11 Tei- len Resorcin, 40 Teilen Soda und 6,00 Teilen Wasser langsam einfliessen lässt, wobei sich der Disazofarbstoff augenblicklich bildet.
Der mit Sole resorcinfrei gewaschene Dis- azofarbstoff wird in sodaalkalischer Lösung mit 30,7 Teilen des diazotierten Aminoazo- fa.rbstoffes, erhalten durch saure Kupplung von diazotierter 5-Amino-2-oxy-benzol-car- bonsäure mit 1-Amino-naphthalin, vereinigt. Am andern Morgen wird der gebildete Poly- azofarbstoff ausgesalzt,
filtriert und ge trocknet.
<B> Additional patent </B> to main patent no. 246985. Process for the production of a polyazo dye. The present patent relates to a process for the production of a polyazo dye. The process is characterized in that 'the diazotized amino azo compound 4-amino-naphthyl-1,1'-azo-4'-oxy-benzene-3'-carboxylic acid is combined with the disazo dye in an alkaline medium,
which is obtainable by coupling 1 mol of tetrazotized 1-oxy-2,6-diamino-benzene-4-sulphonic acid on the one hand with 1 mol of 1,3-diamino-benzene and on the other hand with 1 mol of resorcinol.
The new polyazo dye obtained is a dark powder that dissolves in water with brown and in concentrated sulfuric acid with a dirty gray-blue color. Cotton and fibers made from regenerated cellulose are colored in dark brown tones. Subsequent treatment with copper sulfate improves wet and light fastness considerably.
<I> Example: </I> 20.4 parts of 1-oxy-2,6 = diamino-benzene-4-sulphonic acid are tetrazotized in hydrochloric acid solution with 132.8 parts of sodium nitrite, and the excess mineral acid is truncated with sodium acetate and in the presence of excess sodium acetate combined with a neutral solution of -10.8 parts of 1,3-D.iamino-benzene.
The intermediate product is formed very quickly. After two hours of stirring, the coupling is continued by slowly flowing the intermediate compound into a solution of 11 parts of resorcinol, 40 parts of soda and 6.00 parts of water, the disazo dye being formed immediately.
The disazo dye washed with brine free of resorcinol is obtained in a soda-alkaline solution with 30.7 parts of the diazotized aminoazo dye obtained by acidic coupling of diazotized 5-amino-2-oxy-benzene-carboxylic acid with 1-amino-naphthalene , united. The next morning the polyazo dye formed is salted out,
filtered and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH246985T | 1945-11-09 | ||
CH252289T | 1945-11-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH252289A true CH252289A (en) | 1947-12-15 |
Family
ID=25729163
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH252289D CH252289A (en) | 1945-11-09 | 1945-11-09 | Process for the preparation of a polyazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH252289A (en) |
-
1945
- 1945-11-09 CH CH252289D patent/CH252289A/en unknown
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