CH203038A - 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
- CH203038A CH203038A CH203038DA CH203038A CH 203038 A CH203038 A CH 203038A CH 203038D A CH203038D A CH 203038DA CH 203038 A CH203038 A CH 203038A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- chromium
- brown
- dye containing
- 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
- 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<B>komplex</B> gebundenes Chrom enthaltenden Azofarbstoffes. Es wurde gefunden, dass ein komplex ge bundenes Chrom enthaltender Azofarbstoff hergestellt werden kann, wenn der Azofarb- stoff aus<B>1</B> M ol diazotierter 2-Amino-l-oxy- 6-earboxybenzol-4-sulfonsäure <B>und 1</B> Mol 5- Oxyperinaplithindandion mit eli-romabgeben- den Mitteln behandelt wird.
Die neue Chromverbindung stellt ein graues Pulver dar, das sieh in Wasser, in 10%iger Sodalösung und in 10%iger Na tronlauge mit braunoranger, in konzentrierter Schwefelsäure mit olivbrauner Farbe löst. Sie erzeugt auf Leder braunviolette Töne von guten Echtheitseigenschaften.
Der dem Veziahren als Ausgangsstoff dienende Azofarbstoff kann durch Kupplung in alkalischem Medium von äquiniolekularen Mengen diazotierter 2-Amino-l-oxy-6-earb- oxybenzol-4-sulfonsäure und 5-Oxyperinaph- thindandion erhalten werden.
Die Behandung mit ehromabgebenden Mitteln erfolgt nac'h den bekannten Me- thoden, beispielsweise durch Erhitzen in wäs seriger Lösung mit Salzen des dreiwertigen Chroms.
Beispiel: 45,6 Teile des Azofarbstoffes aus diazo- tierter 2-Amino-l-oxy-6-earboxybenzol-4-sul- fonsäure und 5-Oxyperinaphthindandion wer den in<B>1000</B> Teilen Wasser gelöst und mit einer Fluorellromlösung, enthaltend<B>9,1,</B> Teile r,O" 24 Stunden zum Sieden erhitzt. Man gewinnt die neue Chromverbindung durch Beigabe von Kochsalz, Filtrieren und Trock nen.
Process for the production of an azo dye containing <B> complex </B> bound chromium. It has been found that an azo dye containing complexly bound chromium can be produced if the azo dye is composed of 1 mol of diazotized 2-amino-1-oxy-6-earboxybenzene-4-sulfonic acid > and 1 </B> mol of 5-oxyperinaplithindandione is treated with eli-rom-releasing agents.
The new chromium compound is a gray powder that dissolves in water, in 10% sodium carbonate solution and in 10% sodium hydroxide solution with brown-orange, in concentrated sulfuric acid with an olive-brown color. It produces brown-violet tones with good fastness properties on leather.
The azo dye used as the starting material for the process can be obtained by coupling in an alkaline medium equine molecular amounts of diazotized 2-amino-1-oxy-6-oxybenzene-4-sulfonic acid and 5-oxyperinaphthindanedione.
The treatment with blood-releasing agents takes place according to the known methods, for example by heating in an aqueous solution with salts of trivalent chromium.
Example: 45.6 parts of the azo dye from diazotized 2-amino-1-oxy-6-earboxybenzene-4-sulfonic acid and 5-oxyperinaphthindanedione are dissolved in 1000 parts of water and mixed with a Fluorellromium solution containing <B> 9.1, </B> parts r, O "heated to boiling for 24 hours. The new chromium compound is obtained by adding sodium chloride, filtering and drying.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH203038T | 1937-05-22 | ||
CH199462T | 1938-08-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH203038A true CH203038A (en) | 1939-02-15 |
Family
ID=25723302
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH203038D CH203038A (en) | 1937-05-22 | 1937-05-22 | Process for the preparation of an azo dye containing complexed chromium. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH203038A (en) |
-
1937
- 1937-05-22 CH CH203038D patent/CH203038A/en unknown
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