CH263528A - 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
- CH263528A CH263528A CH263528DA CH263528A CH 263528 A CH263528 A CH 263528A CH 263528D A CH263528D A CH 263528DA CH 263528 A CH263528 A CH 263528A
- Authority
- CH
- Switzerland
- Prior art keywords
- chromium
- dye
- azo dye
- containing azo
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (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- 6-nitro-l-phenol-4-sulfonsäure und 2-Methyl- amino - 6 - methoxy - naphthalin erhältlichen Farbstoff mit. chromabgebenden Mitteln be handelt.
Der neue chromhaltige Farbstoff ist ein grünschwarzes Pulver, das sich in Wasser und verdünnter Sodalösung mit grüner Farbe löst und Wolle aus schwefelsaurem Bade in gleichmässigen gelbstichig grünen Tönen färbt.
Der dein vorliegenden Verfahren als Aus gangsstoff dienende Farbstoff kann aus den angegebenen Komponenten in bekannter Weise, z. B. durch Kupplung in saurem Me dium, erhalten werden. Als chromabgebende Mittel wählt man zweckmässig solche, die das Chrom in dreiwertiger Form enthalten und daher keine schädliche Oxydationswirkung besitzen, insbesondere Chrom-(III)-Salze. Die Umsetzung kann in an sich bekannter Weise in saurem, neutralem oder alkalischem Me dium, mit oder ohne Zusätze z. B. von Neu tralsalzen, gegebenenfalls komplexbildender Art, organischen Lösungsmitteln, wie Alko hol oder Pyridin, offen oder unter Druck durchgeführt werden.
<I>Beispiel:</I> 23,4 Teile 6-Nitro-2-amino-l-phenol-4-sul- fonsäure werden in bekannter Weise diazo- tiert und mit 19,5 Teilen 2-1llethylamino-6- metho.Yynaphthalin bei Gegenwart von Essig säure oder Alkohol gekuppelt. Der abfiltrierte Farbstoff wird in 1800 Teilen Wasser bei Siedehitze gelöst und mit einer Chromfor- miatlösung versetzt, die eine 8,4 Teilen Chromoxyd entsprechende Menge Chrom ent hält. Man erhitzt unter Rückflusskühlttng län gere Zeit zum Sieden und filtriert die erhal tene, in Wasser schwer lösliche Chromverbin dung ab.
Sie wird durch Lösen in verdünn ter Natronlauge in eine leicht lösliche Form übergeführt und getrocknet.
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-6-nitro-1-phenol-4-sulfonic acid and 2-methylamino-6-methoxy-naphthalene is used. chromium-releasing agents.
The new chromium-containing dye is a greenish-black powder that dissolves in water and dilute soda solution with a green color and dyes wool from a sulfuric acid bath in uniform yellowish green tones.
The present process as starting material from serving dye can be prepared from the specified components in a known manner, for. B. medium by coupling in acidic Me obtained. As chromium-releasing agents, it is expedient to choose those which contain 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 acidic, neutral or alkaline Me, with or without additives such. B. of neutralsalts, optionally complex-forming type, organic solvents such as alcohol or pyridine, can be carried out openly or under pressure.
<I> Example: </I> 23.4 parts of 6-nitro-2-amino-l-phenol-4-sulphonic acid are diazotized in a known manner and 19.5 parts of 2-1llethylamino-6-metho .Yynaphthalene coupled in the presence of acetic acid or alcohol. The filtered dye is dissolved in 1800 parts of water at the boiling point and a chromium formate solution is added which contains an amount of chromium corresponding to 8.4 parts of chromium oxide. The mixture is refluxed for a longer time and the chromium compound obtained, which is sparingly soluble in water, is filtered off.
It is converted into an easily soluble form by dissolving it in dilute sodium hydroxide solution and drying.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH263528T | 1943-12-02 | ||
CH258297T | 1948-11-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH263528A true CH263528A (en) | 1949-08-31 |
Family
ID=25730165
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH263528D CH263528A (en) | 1943-12-02 | 1943-12-02 | Process for the preparation of a chromium-containing azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH263528A (en) |
-
1943
- 1943-12-02 CH CH263528D patent/CH263528A/en unknown
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