CH203037A - 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
- CH203037A CH203037A CH203037DA CH203037A CH 203037 A CH203037 A CH 203037A CH 203037D A CH203037D A CH 203037DA CH 203037 A CH203037 A CH 203037A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- chromium
- preparation
- dye containing
- containing complexed
- 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 Azofar bstoffes. Es wurde gefunden, dass ein komplexge bundenes Chrom enthaltender Azofarbstoff hergestellt werden kann, wenn der Azofarb- stoff der Formel
EMI0001.0007
mit chromabgebenden Mitteln behandelt wird.
Die - neue Chromverbindung stellt ein grauschwarzes Pulver dar, das sich in Wasser, in 10 % iger Sodalösung, sowie in 10 % iger Natronlauge mit braunoranger und in konzentrierter Schwefelsäure mit gelb oranger Farbe löst. Sie erzeugt auf anima lischen Fasern braune Töne von sehr .guten Echtheitseigenschaften.
Der dem Verfahren als Ausgangsstoff dienende Azofarbstoff der obigen Formel kann -durch Kupplung in alkalischem Me dium von diazotierter 2-Amino-1-carboxy- benzol-5-sulfonsäure und 5-Aminoperinaphth- indandion erhalten werden.
Die Behandlung mit chromabgebenden Mitteln erfolgt nach .den bekannten Metho- @den, beispielsweise durch Erhitzen in wäs seriger Lösung mit Salzen des dreiwertigen Chroms.
Beispiel: 4,4 Teile des durch alkalische Kupplung hergestellten Azofarbstoffes aus diazotierter 2-Amino-il-carbogybenzol-5@sulfonsäure und 5-A.minoperinaphthindandion werden in 100 Teilen Wasser .gelöst und mit einer Chrom- formiatlösung, enthaltend 0g83 Teile Cr2O3, 24 Stunden zum (Sieden erhitzt.
Die neue Chromverbindung wird durch Beigabe von Kochsalz abgeschieden, abfiltriert und ge trocknet.
;, A process for the preparation of an azo dye containing complexed chromium. It has been found that an azo dye containing complex bonded chromium can be produced if the azo dye of the formula
EMI0001.0007
is treated with chromium-releasing agents.
The - new chromium compound is a gray-black powder that dissolves in water, in 10% soda solution, as well as in 10% sodium hydroxide solution with brown-orange color and in concentrated sulfuric acid with yellow-orange color. It produces brown tones with very good fastness properties on animal fibers.
The azo dye of the above formula serving as starting material for the process can be obtained by coupling in alkaline medium of diazotized 2-amino-1-carboxy-benzene-5-sulfonic acid and 5-aminoperinaphth-indanedione.
Treatment with chromium-releasing agents takes place according to the known methods, for example by heating in aqueous solution with salts of trivalent chromium.
Example: 4.4 parts of the azo dye produced by alkaline coupling from diazotized 2-amino-il-carbogybenzene-5 @ sulfonic acid and 5-a-minoperinaphthindanedione are dissolved in 100 parts of water and dissolved with a chromium formate solution containing 0.63 parts of Cr2O3, Heated to boiling for 24 hours.
The new chromium compound is deposited by adding sodium chloride, filtered off and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH203037T | 1937-05-22 | ||
CH199462T | 1938-08-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH203037A true CH203037A (en) | 1939-02-15 |
Family
ID=25723301
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH203037D CH203037A (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) | CH203037A (en) |
-
1937
- 1937-05-22 CH CH203037D patent/CH203037A/en unknown
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