CH199462A - Process for the preparation of an azo dye containing complexed chromium. - Google Patents
Process for the preparation of an azo dye containing complexed chromium.Info
- Publication number
- CH199462A CH199462A CH199462DA CH199462A CH 199462 A CH199462 A CH 199462A CH 199462D A CH199462D A CH 199462DA CH 199462 A CH199462 A CH 199462A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- chromium
- dye containing
- preparation
- red
- 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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/14—Monoazo compounds
- C09B45/16—Monoazo compounds containing chromium
-
- 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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/14—Monoazo compounds
- C09B45/18—Monoazo compounds containing copper
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines komplex gebundenes Chrom enthaltenden Azofarbstoffes. Es wurde gefunden, dass ein komplex ge bundenes Chrom enthaltender Azofarbstoff hergestellt werden kann, wenn der Azofarb- stoff der Formel
EMI0001.0006
mit chromabgebenden Mitteln behandelt wird.
Die neue Chromverbindung stellt ein graues Pulver dar, das sich in Wasser mit roter, in 10 0%iger Sodalösung, sowie in 10 %iger Natronlauge mit braunroter und in konzentrierter Schwefelsäure mit oranger Farbe löst. Sie erzeugt auf Leder bordeaux rote Töne von sehr guten Echtheitseigen schaften.
Der dem Verfahren als Ausgangsstoff dienende Azofarbstoff der obigen Formel kann durch Kupplung in alkalischem Medium von dianotierter 2-Amino-6-nitro-l-oxybenzol-4- sulfonsäure und 5-Nitroperinaphthindandion erhalten werden.
Die Behandlung mit chromabgebenden Mitteln erfolgt nach den bekannten Methoden, beispielsweise durch Erhitzen in wässeriger Lösung mit Salzen des dreiwertigen Chroms. Beispiel: 48,6 Teile des Azofarbstoffes aus diano tierter 6-Nitro-2-amino-l-oxybenzol-4-sulfon- säure und 5-Nitroperinaphthindandion werden in 1000 Teilen Wasser gelöst und mit einer Chromfluoridlösung, enthaltend 9,1 Teile Cr20s, 24 Stunden zum Sieden erhitzt.
Hier auf filtriert man heiss von beigemengten un löslichen Bestandteilen ab, scheidet die Chromverbindung durch Beigabe von Koch salz aus, filtriert und trocknet.
Process for the preparation of an azo dye containing complexed chromium. It has been found that an azo dye containing complexly bound chromium can be produced if the azo dye of the formula
EMI0001.0006
is treated with chromium-releasing agents.
The new chromium compound is a gray powder that dissolves in water with red, in 10 0% soda solution, as well as in 10% sodium hydroxide solution with brownish red and in concentrated sulfuric acid with orange color. It produces burgundy red tones with very good fastness properties on leather.
The azo dye of the above formula which is used as starting material for the process can be obtained by coupling in an alkaline medium dianotated 2-amino-6-nitro-1-oxybenzene-4-sulfonic acid and 5-nitroperinaphthindanedione.
The treatment with chromium-releasing agents takes place according to the known methods, for example by heating in an aqueous solution with salts of trivalent chromium. Example: 48.6 parts of the azo dye from diano-tated 6-nitro-2-amino-1-oxybenzene-4-sulfonic acid and 5-nitroperinaphthindanedione are dissolved in 1000 parts of water and treated with a chromium fluoride solution containing 9.1 parts of Cr20s Heated to the boil for 24 hours.
Here, added insoluble constituents are filtered off while hot, the chromium compound is separated out by adding sodium chloride, filtered and dried.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH199462T | 1938-08-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH199462A true CH199462A (en) | 1938-08-31 |
Family
ID=4441846
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH199462D CH199462A (en) | 1938-08-31 | 1937-05-22 | Process for the preparation of an azo dye containing complexed chromium. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH199462A (en) |
-
1937
- 1937-05-22 CH CH199462D patent/CH199462A/en unknown
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