CH293863A - 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
- CH293863A CH293863A CH293863DA CH293863A CH 293863 A CH293863 A CH 293863A CH 293863D A CH293863D A CH 293863DA CH 293863 A CH293863 A CH 293863A
- Authority
- CH
- Switzerland
- Prior art keywords
- copper
- amino
- parts
- mol
- oxy
- 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 kupferbaren Polyazofarbstoffes. Das Verfahren ist da durch gekennzeichnet, dass man 1.
Mol der Tetrazoverbindung von 1-(3'-Amino-4'-oxy- benzoylamino) - 4- aminö - benzol-3-carbonsäure einerseits mit 1 Mol 1-(4'-Amino-phenyl)-3- methyl.-5-pyrazolon und anderseits mit 1 Mol 2-Acetyl.amino-6-oxy - naphthalin-8-s ulfonsäure kuppelt..
Der erhaltene neue Disazofarbstoff stellt ein dunkelbraunes Pulver dar, welches sich in Wasser und in konz. Schwefelsäure mit rot stichig brauner Farbe löst und färbt Fasern aus Baumwolle und Zellwolle nachgekupfert in braunen Tönen von sehr guter Nass- und Lichtechtheit..
<I>Beispiel:</I> 28,7 Teile 1-(3'-Amino-4'-oxy -benzoyl- amino)-4-amino-benzol-3-carbonsäure werden in 400 Teilen Nasser mit 8 Teilen Natronlauge kalt gelöst, mit 13,8 Teilen Natriumnitrit ver mischt und in der Kälte unter Rühren auf 40 Teile konz. Salzsäure und 80 Teile Wasser aufgetropft. Nach dem Abstumpfen der über schüssigen Mineralsäure mit Natriumbicar- bonat vereinigt man die Tetrazov erbindung mit 18,9 Teilen 1-(4'-Amino-phenyl)
-3-methyl- 5-pyrazolon, gelöst in 200 Teilen Wasser und 20 Teilen Natriumbiearbonat. Zum Zwischen produkt lä.sst man alsdann eine wässerige Lö sung von 28,1 Teilen 2-Acetylamino-6-oxy- naphthalin-8-sulfonsäure, 20 Teilen Soda und 150 Teilen Py ridin fliessen.
Nach mehrstün digem Rühren bei Raumtemperatur wird der gebildete Disazofarbstoff der Formel
EMI0001.0044
finit Salz gefällt, abfiltriert und getrocknet.
<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'-oxybenzoylamino) -4-amino-benzene-3-carboxylic acid on the one hand with 1 mol of 1- (4'-aminophenyl) -3-methyl.-5 -pyrazolon and on the other hand with 1 mol of 2-acetyl.amino-6-oxy-naphthalene-8-sulfonic acid.
The new disazo dye obtained is a dark brown powder which is dissolved in water and in conc. Sulfuric acid with a red, tinged brown color dissolves and dyes fibers made of cotton and staple viscose after copper in brown shades of very good wet and light fastness.
<I> Example: </I> 28.7 parts of 1- (3'-amino-4'-oxy-benzoyl-amino) -4-amino-benzene-3-carboxylic acid are cold in 400 parts of water with 8 parts of sodium hydroxide solution dissolved, mixed ver 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 Tetrazov compound is combined with 18.9 parts of 1- (4'-aminophenyl)
-3-methyl-5-pyrazolone, dissolved in 200 parts of water and 20 parts of sodium carbonate. An aqueous solution of 28.1 parts of 2-acetylamino-6-oxynaphthalene-8-sulfonic acid, 20 parts of soda and 150 parts of pyridine is then allowed to flow into the intermediate product.
After several hours of stirring at room temperature, the disazo dye formed is of the formula
EMI0001.0044
finite salt precipitated, filtered off and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH293863T | 1948-08-06 | ||
CH261125T | 1948-08-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH293863A true CH293863A (en) | 1953-10-15 |
Family
ID=25730377
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH293863D CH293863A (en) | 1948-08-06 | 1948-08-06 | Process for the preparation of a copper-compatible polyazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH293863A (en) |
-
1948
- 1948-08-06 CH CH293863D patent/CH293863A/en unknown
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