CH203034A - 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
- CH203034A CH203034A CH203034DA CH203034A CH 203034 A CH203034 A CH 203034A CH 203034D A CH203034D A CH 203034DA CH 203034 A CH203034 A CH 203034A
- Authority
- CH
- Switzerland
- Prior art keywords
- chromium
- azo dye
- 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 komplex gebundenes Chrom enthaltenden Azofarbstoffes. Es wurde gefunden, dass ein komplex ge bundenes Chrom enthaltender Azofaribstoff hergestellt werden kann, wenn der Azofarb- stoff aus 1 Mol diazotierter 2-Amino-l-oxy- benzol-4-sulfonsäure und 1 Mol 5-Oxyperi- naphthindandion mit chromabgebenden Mit teln behandelt wird.
Die neue Chromverbindung stellt ein schwarzes Pulver dar, das sich in Wasser und in 10%iger Sodalösung mit braunroter, in 10%iger Natronlauge mit braunoranger und in konzentrierter Schwefelsäure mit oliv gelber Farbe löst. Sie färbt Leder in violett braunen Tönen von sehr guten Echtheits eigenschaften.
Der dem Verfahren als Ausgangsstoff dienende Azofarbstoff kann durch Kupplung in alkalischem Medium von äquimolekularen Mengen diazotierter 2-Amino-l-oxybenzol-4- sulfonsäure und 5-Oxyperinaphthindandion erhalten werden.
Die Behandlung mit chromabgebenden Mitteln erfolgt nach den bekannten Metho den, beispielsweise durch Erhitzen in wäss- riger Lösung mit Salzen des - dreiwertigen Chroms. <I>Beispiel:</I> 4,1 Teile 'des Azofarbstoffes aus diazo- tierter 2 - Amino -1- oxybenzol - 4 - sulfonsäure und 5-Oxyperinaphthindandion werden in 80 Teilen Wasser gelöst und mit einer Chrom- formiatlösung,
enthaltend 0,9 Teile Cr2O3, 24 Stunden zum Sieden erhitzt. Hierauf fil triert man heiss von vorhandenen unlöslichen Bestandteilen ab, scheidet die 'Chromverbin- dung durch Beigabe von Kochsalz ab, fil triert 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 is made from 1 mol of diazotized 2-amino-1-oxybenzene-4-sulfonic acid and 1 mol of 5-oxyperinaphthindanedione with chromium-releasing agents is treated.
The new chromium compound is a black powder that dissolves in water and in 10% sodium carbonate solution with brown-red, in 10% sodium hydroxide solution with brown-orange and in concentrated sulfuric acid with an olive-yellow color. It dyes leather in violet-brown shades with very good fastness properties.
The azo dye used as starting material for the process can be obtained by coupling in an alkaline medium equimolecular amounts of diazotized 2-amino-1-oxybenzene-4-sulfonic acid and 5-oxyperinaphthindanedione.
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. <I> Example: </I> 4.1 parts of the azo dye from diazotized 2 - amino -1- oxybenzene - 4 - sulfonic acid and 5-oxyperinaphthindanedione are dissolved in 80 parts of water and treated with a chromium formate solution,
containing 0.9 parts Cr2O3, heated to boiling for 24 hours. The insoluble constituents are then filtered while hot, the chromium compound is separated off by adding table salt, filtered and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH203034T | 1937-05-22 | ||
CH199462T | 1938-08-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH203034A true CH203034A (en) | 1939-02-15 |
Family
ID=25723298
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH203034D CH203034A (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) | CH203034A (en) |
-
1937
- 1937-05-22 CH CH203034D patent/CH203034A/en unknown
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