CH203039A - Process for the preparation of an azo dye containing complex bonded copper. - Google Patents
Process for the preparation of an azo dye containing complex bonded copper.Info
- Publication number
- CH203039A CH203039A CH203039DA CH203039A CH 203039 A CH203039 A CH 203039A CH 203039D A CH203039D A CH 203039DA CH 203039 A CH203039 A CH 203039A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- copper
- preparation
- containing complex
- bonded copper
- 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 Kupfer enthaltenden Azofarbstoffes. Es wurde gefunden, dass ein komplex .ge bundenes Kupfer enthaltender Azofarbstoff hergestellt werden kann, wenn der Azofarb- stoff der Formel
EMI0001.0007
mit kupferabgebenden Mitteln behandelt wird.
Die neue Kupferverbindung stellt ein braunes Pulver dar, das sich in .Wasser mit gelboranger, in 1-0%iger Sololösung, sowie in 10 % iger Natronlauge mit orangeroter und in konzentrierter Schwefelsäure mit gelber Farbe löst. iSie erzeugt auf Leder lhellbraune Töne von sehr ,guten Echtheitseigenschaften.
Der dem- Verfahren als Ausgangsstoff dienende- AzoTarbstoff der obigen Formel kann durch Kupplung in alkalischem Me dium von diazotierter 2-Amino-6-carboxy-l- oxybenzol - 4 - sulfonsäure und Perinaphth- in.dandion-,5-sulfonsäure erhalten werden.
Die Behandlung mit kupferabgebenden Mitteln erfolgt nach den bekannten Metho den, beispielsweise durch Erhitzen in wässe riger Lösung mit Kupfersalzen. <I>Beispiel:</I> 52 Teile des Azofarbstoffes aus diazo- tierter 2-Amino-l-oxy-6-carboxybenzol-4-sul- fonsäure und Perinaphthindandion-5-sulfon- säure werden in 1000 Teilen Wasser gelöst und mit einer Kupfersulfatlösun.g, enthaltend 3,
0 Teile Kupfersulfat, so lange zum Sieden erhitzt, bis der Azofarb- stoff vollständig 'in die Kupferverbindung übergegangen ist. Hierauf scheidet man den Farbstoff durch Beigabe von Kochsalz aus, filtriert und trocknet.
Process for the preparation of an azo dye containing complex bonded copper. It has been found that an azo dye containing complex .ge bound copper can be produced if the azo dye of the formula
EMI0001.0007
is treated with copper-releasing agents.
The new copper compound is a brown powder that dissolves in water with yellow-orange color, in 1-0% strength solution, as well as in 10% sodium hydroxide solution with orange-red color and in concentrated sulfuric acid with yellow color. iSie produces light brown tones with very, good fastness properties on leather.
The azo dye of the above formula which serves as the starting material for the process can be obtained by coupling in alkaline medium of diazotized 2-amino-6-carboxy-l-oxybenzene-4-sulfonic acid and perinaphth-in.dandione-, 5-sulfonic acid.
The treatment with copper-releasing agents is carried out according to the known methods, for example by heating in an aqueous solution with copper salts. <I> Example: </I> 52 parts of the azo dye from diazotized 2-amino-1-oxy-6-carboxybenzene-4-sulphonic acid and perinaphthindanedione-5-sulphonic acid are dissolved in 1000 parts of water and mixed with a copper sulfate solution containing 3,
0 parts of copper sulphate, heated to the boil until the azo dye has completely converted into the copper compound. The dye is then separated out by adding common salt, filtered and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH203039T | 1937-05-22 | ||
CH199462T | 1938-08-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH203039A true CH203039A (en) | 1939-02-15 |
Family
ID=25723303
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH203039D CH203039A (en) | 1937-05-22 | 1937-05-22 | Process for the preparation of an azo dye containing complex bonded copper. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH203039A (en) |
-
1937
- 1937-05-22 CH CH203039D patent/CH203039A/en unknown
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