CH293869A - 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
- CH293869A CH293869A CH293869DA CH293869A CH 293869 A CH293869 A CH 293869A CH 293869D A CH293869D A CH 293869DA CH 293869 A CH293869 A CH 293869A
- Authority
- CH
- Switzerland
- Prior art keywords
- copper
- brown
- parts
- acid
- 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—
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- 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 kupferbaren Polyazofarbstoffes. Das Verfahren ist da durch gekennzeichnet, dass man 1 Mol der Tetrazoverbindung von 1- (3'-Amino-4'-oxy - benzoylamino)
- 4- amino - benzol-3-earbonsäur e einerseits mit 1 Mol 4-Acetylamino-acetessig- säureanilid und anderseits mit 1 Mol 2-Oxy- naphthalin-6-sulfonsäure kuppelt.
Der erhaltene neue Disazofarbstoff stellt ein br aunsehwarzes Pulver dar, das sieh in Wasser mit brauner und in konz. Schwefel säure mit olivbrauner Farbe löst und Fasern aus natürlicher oder regenerierter Zellulose naehgekupfert in braunen Tönen von sehr guten Echtheiten anfärbt.
<I>Beispiel:</I> 28,7 Teile 1-(3'-Amino-4'-oxy-benzoyl- amino)-4-amino-ben7ol-3-earbonsäure werden in 400 Teilen Wasser mit 8 Teilen Natron lauge kalt gelöst, mit 13,8 Teilen Natrium nitrit vermischt und in der Kälte unter Rüh ren auf 40 Teile konz. Salzsäure und 80 Teile Wasser aufgetropft, die überschüssige Mine ralsäure mit Soda abgestumpft und dann mit 23,4 Teilen 4-Acety lamino-acetessigsäureani- lid, gelöst in 200 Teilen Wasser bei CTegen- wart von 20 Teilen Natriumbicarbonat, zum Zwischenprodukt vereinigt.
Nach beendigter Kupplung wird alsdann eine wässerige Lo sung von 22,4 Teilen 2-Oxy-naphthalin-6-sul- , fonsä.ure, 20 Teilen Soda und 150 Teilen Pyridin hinzufliessen gelassen. Die Kupplung ist nach mehrstündigem Rühren bei Raum temperatur beendigt, und der gebildete Disazo- farbstoff der Formel
EMI0001.0038
<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 in that 1 mol of the tetrazo compound of 1- (3'-amino-4'-oxy - benzoylamino)
- 4- amino-benzene-3-carboxylic acid coupled on the one hand with 1 mol of 4-acetylamino-acetic acid anilide and on the other hand with 1 mol of 2-oxynaphthalene-6-sulfonic acid.
The new disazo dye obtained is a brownish-black powder, which looks in water with brown and in conc. Sulfuric acid with an olive-brown color dissolves and stains fibers made of natural or regenerated cellulose, sewn in copper, in brown shades of very good fastness properties.
<I> Example: </I> 28.7 parts of 1- (3'-amino-4'-oxy-benzoyl-amino) -4-amino-ben7ol-3-carboxylic acid are dissolved 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, the excess mineral acid blunted with soda and then combined with 23.4 parts of 4-acetylamino-acetic acid anilide, dissolved in 200 parts of water with 20 parts of sodium bicarbonate present, to form the intermediate.
After the coupling has ended, an aqueous solution of 22.4 parts of 2-oxynaphthalene-6-sulphonic acid, 20 parts of soda and 150 parts of pyridine is allowed to flow in. The coupling is complete after several hours of stirring at room temperature, and the disazo dye formed of the formula
EMI0001.0038
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH293869T | 1948-08-06 | ||
CH261125T | 1948-08-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH293869A true CH293869A (en) | 1953-10-15 |
Family
ID=25730383
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH293869D CH293869A (en) | 1948-08-06 | 1948-08-06 | Process for the preparation of a copper-compatible polyazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH293869A (en) |
-
1948
- 1948-08-06 CH CH293869D patent/CH293869A/en unknown
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