CH263526A - Process for the preparation of a chromium-containing azo dye. - Google Patents
Process for the preparation of a chromium-containing azo dye.Info
- Publication number
- CH263526A CH263526A CH263526DA CH263526A CH 263526 A CH263526 A CH 263526A CH 263526D A CH263526D A CH 263526DA CH 263526 A CH263526 A CH 263526A
- Authority
- CH
- Switzerland
- Prior art keywords
- chromium
- dye
- green
- amino
- containing azo
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
Description
Verfahren zur Herstellung eines chromhaltigen Azofarbstoffes. Es wurde gefunden, dass ein wertvoller chromhaltiger Azofarbstoff hergestellt werden kann, wenn man den aus diazotierter 2-Amino- 1-phenol-4,6-disulfonsäure und 2-Amino-6-me- thoxynaphthalin erhältlichen Farbstoff mit chromabgebenden Mitteln behandelt.
Der neue chromhaltige Farbstoff ist ein grünschwarzes Pulver, das sich in Wasser mit grüner, in verdünnter Sodalösung oder verdünnter Natronlauge mit blaugrüner und in konz. Schwefelsäure mit bordeauxroter Farbe löst und Wolle aus schwefelsaurem Färbebade in gleichmässigen und gelbstichig grünen Tönen färbt, die gut licht- und walk- echt sind.
Der dem vorliegenden Verfahren als Aus gangsstoff dienende Farbstoff kann aus den angegebenen Komponenten in bekannter Weise, z. B. durch Kupplung in saurem Me dium, vorteilhaft in Gegenwart von essigsau rem Pyridin, erhalten werden. Als chrom abgebende Mittel wählt man zweckmässig sol che, die das Chrom in dreiwertiger Form ent halten und daher keine schädliche Oxyda tionswirkung besitzen, insbesondere Chrom- (III)-Salze. Die Umsetzung kann in an sich bekannter Weise in saurem, neutralem oder alkalischem Medium,, mit oder ohne Zusätze z.
B. von Neutralsalzen, gegebenenfalls kom plexbildender Art, organischen Lösungsmit teln, wie Alkohol oder Pyridin, offen oder unter Druck durchgeführt werden. <I>Beispiel:</I> 26,9 Teile 2-Amino-l-phenol-4,6-disulfon- säure werden in bekannter Weise diazotiert und mit 18 Teilen 2-Amino-6-methoxy-naph- thalin bei Gegenwart von essigsaurem Pyridin gekuppelt.
Der abfiltrierte Farbstoff wird in 500 Teilen Wasser bei Siedehitze gelöst und mit einer Chromformiatlösung versetzt, die eine 8 Teilen Chromoxyd entsprechende Menge Chrom enthält. Man erhitzt unter Rückflusskühlung längere Zeit zum Sieden und dampft die erhaltene Farbstofflösung zur Trockne ein.
Process for the preparation of a chromium-containing azo dye. It has been found that a valuable chromium-containing azo dye can be produced if the dye obtainable from diazotized 2-amino-1-phenol-4,6-disulfonic acid and 2-amino-6-methoxynaphthalene is treated with chromium-donating agents.
The new chromium-containing dye is a greenish-black powder that dissolves in water with green, in dilute soda solution or dilute sodium hydroxide solution with blue-green and in conc. Sulfuric acid with a burgundy red color dissolves and dyes wool from a sulfuric acid dyebath in even, yellowish green tones that are very lightfast and whackfast.
The present process as starting material from serving dye can be prepared from the specified components in a known manner, for. B. by coupling in acidic Me medium, advantageously in the presence of acetic acid rem pyridine obtained. As a chromium-releasing agent, it is advisable to choose those which contain the chromium in trivalent form and therefore have no harmful oxidizing effect, in particular chromium (III) salts. The reaction can be carried out in a manner known per se in an acidic, neutral or alkaline medium, with or without additives such.
B. neutral salts, possibly complex-forming complex, organic solvents, such as alcohol or pyridine, can be carried out openly or under pressure. <I> Example: </I> 26.9 parts of 2-amino-1-phenol-4,6-disulfonic acid are diazotized in a known manner and with 18 parts of 2-amino-6-methoxynaphthalene in the presence coupled by pyridine acetic acid.
The filtered dye is dissolved in 500 parts of water at the boiling point and a chromium formate solution is added which contains an amount of chromium corresponding to 8 parts of chromium oxide. The mixture is refluxed for a long time and the resulting dye solution is evaporated to dryness.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH263526T | 1943-12-02 | ||
CH258297T | 1948-11-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH263526A true CH263526A (en) | 1949-08-31 |
Family
ID=25730163
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH263526D CH263526A (en) | 1943-12-02 | 1943-12-02 | Process for the preparation of a chromium-containing azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH263526A (en) |
-
1943
- 1943-12-02 CH CH263526D patent/CH263526A/en unknown
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