CH265726A - Process for the preparation of a copper-compatible polyazo dye. - Google Patents
Process for the preparation of a copper-compatible polyazo dye.Info
- Publication number
- CH265726A CH265726A CH265726DA CH265726A CH 265726 A CH265726 A CH 265726A CH 265726D A CH265726D A CH 265726DA CH 265726 A CH265726 A CH 265726A
- Authority
- CH
- Switzerland
- Prior art keywords
- copper
- amino
- yellow
- parts
- preparation
- 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
- C09B35/02—Disazo dyes
- C09B35/039—Disazo dyes characterised by the tetrazo component
- C09B35/28—Disazo dyes characterised by the tetrazo component the tetrazo component containing two aryl nuclei linked by at least one of the groups —CON<, —SO2N<, —SO2—, or —SO2—O—
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 261125. Verfahren zur Herstellung eines kupferbaren Polyazofarbstoffes. Gegenstand vorliegenden Patentes ist ein Verfahren zur Herstellung eines kupferbarer Polyazofarbstoffes. Das Verfahren ist da durch gekennzeichnet, dass man.
1 Mol der Tetrazoverbindung von 1-(3'.-Amino-4'-oxy- benzoyiamino) -4-amino-benzol.-3-carbonsäure einerseits mit 1 Mol 1-(4'-Am.ino-phenyl)-3- phenyl-5-pyrazolon und anderseits mit 1 11o1 1- (4'-Am ino-3'-sulfo-plienyl) -3-methyl - 5.- pyr- azolon kuppelt.
Der erhaltene neue Disazofarbstoff stellt ein dunkelbraunes Pulver dar, das sich in Wasser mit gelbbrauner und in konz. Schwe felsäure mit, gelber Farbe löst und Fasern aus natürlicher oder regenerierter Cellulose nachgekupfert in gelbbraunen Tönen anfärbt, welche vorzügliche Echtheiten aufweisen.
<I>Beispiel:</I> 28,7 Teile 1 - (3'- Amino - 4'- oxy - benzoyl- amino)-4-amino-benzol-3-carbonsätire werden in 400 Teilen Wasser mit 8 Teilen Natron lauge kalt gelöst, mit 13,8 Teilen Natrium nitrit vermischt und in der Kälte unter Rühren auf 40 Teile konz. Salzsäure und 80 Teile Wasser aufgetropft. Nach dem Ab stumpfen der überschüssigen Mineralsäure mit Natriumbicarbonat vereinigt man die Tetrazoverbindung mit 25,1 Teilen 1-(4' A.mino-phenyl)-3-phenyl-5-pyrazolon,
gelöst in 200 Teilen Wasser und 20 Teilen Natrium biearbonat. Zum Zwischenprodukt lä.sst man alsdann eine wässrige Lösung von 26,9 Teilen 1- (4'-Amino-3'-sulf o-phenyl) -3-metliyl - 5 - pyr- azolon, 20 Teilen Soda und 150 Teilen Pyr- idin fliessen. Nach mehrstündigem Rühren bei Raumtemperatur wird der gebildete Disa.zo- farbstoff der Formel
EMI0001.0044
<B> Additional patent </B> to main patent no. 261125. Process for the production of a copperable polyazo dye. The present patent relates to a process for the preparation of a copperable polyazo dye. The process is characterized by that one.
1 mol of the tetrazo compound of 1- (3 '.- Amino-4'-oxy-benzoyiamino) -4-aminobenzene-3-carboxylic acid on the one hand with 1 mol of 1- (4'-aminophenyl) -3 - phenyl-5-pyrazolone and on the other hand with 11o1 1- (4'-Amino-3'-sulfo-plienyl) -3-methyl-5-pyrazolone couples.
The new disazo dye obtained is a dark brown powder, which in water with yellow-brown and in conc. Sulfur acid with a yellow color dissolves and stains fibers made from natural or regenerated cellulose after copper-plating in yellow-brown tones, which have excellent fastness properties.
<I> Example: </I> 28.7 parts of 1- (3'-amino-4'-oxy-benzoyl-amino) -4-amino-benzene-3-carbonsätire are in 400 parts of water with 8 parts of sodium hydroxide solution dissolved cold, mixed with 13.8 parts of sodium nitrite and concentrated in the cold with stirring to 40 parts. Hydrochloric acid and 80 parts of water were added dropwise. After the excess mineral acid has been blunted with sodium bicarbonate, the tetrazo compound is combined with 25.1 parts of 1- (4 'A.mino-phenyl) -3-phenyl-5-pyrazolone,
dissolved in 200 parts of water and 20 parts of sodium bicarbonate. An aqueous solution of 26.9 parts of 1- (4'-amino-3'-sulfo-phenyl) -3-methyl-5-pyrazolone, 20 parts of soda and 150 parts of pyr- idin flow. After several hours of stirring at room temperature, the disa.zo dye formed is of the formula
EMI0001.0044
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH265726T | 1947-09-15 | ||
CH261125T | 1948-08-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH265726A true CH265726A (en) | 1949-12-15 |
Family
ID=25730370
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH265726D CH265726A (en) | 1947-09-15 | 1947-09-15 | Process for the preparation of a copper-compatible polyazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH265726A (en) |
-
1947
- 1947-09-15 CH CH265726D patent/CH265726A/en unknown
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