CH104914A - Process for the preparation of a new azo dye. - Google Patents
Process for the preparation of a new azo dye.Info
- Publication number
- CH104914A CH104914A CH104914DA CH104914A CH 104914 A CH104914 A CH 104914A CH 104914D A CH104914D A CH 104914DA CH 104914 A CH104914 A CH 104914A
- Authority
- CH
- Switzerland
- Prior art keywords
- blue
- preparation
- azo dye
- red
- new 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen Azofarbstoffs. Es wurde gefunden, dass man einen neuen Azofarbstoff erhält, wenn man das 1-Oxynaph- thalin-8-sulfamid mit der bromierten Diazo- verbindung der 1-Amino-2-oxynaphthalin-4- sulfosäure kuppelt.
<I>Beispiel:</I> 22,3 Teile 1-Oxynaphthalin-8-sulfamid, kalt in einer überschüssigen, wässerigen Aetzkali- lösung gelöst, werden mit 35,1 Teilen bro- mierter Diazoverbindung der 1-Amino-2-oxy- naphtbalin-4-sulfosäure versetzt. Ist die sofort einsetzende Kupplung, welche zweckmässig unter 10' gehalten wird, beendet, so wird die Masse mit verdünnter Salzsäure neutral gestellt, worauf der ausgeschiedene neue Azofarbstoff abfiltriert wird.
Er stellt ein dunkles Pulver dar, welches sich in reinem Wasser mit rotvioletter, in konzentrierter Schwefelsäure mit blauer, in verdünnter Natronlauge mit 'blauroter Farbe löst. Er färbt aus saurem Bade die Wolle rotviolett an, durch Nachchromieren schlägt der Farb ton nach blau um.
Process for the preparation of a new azo dye. It has been found that a new azo dye is obtained when 1-oxynaphthalene-8-sulfamide is coupled with the brominated diazo compound of 1-amino-2-oxynaphthalene-4-sulfonic acid.
<I> Example: </I> 22.3 parts of 1-oxynaphthalene-8-sulfamide, dissolved cold in an excess, aqueous caustic potash solution, are mixed with 35.1 parts of brominated diazo compound of 1-amino-2-oxy - Naphtbalin-4-sulfonic acid added. When the coupling, which starts immediately and which is expediently kept below 10 ', has ended, the mass is neutralized with dilute hydrochloric acid, whereupon the new azo dye which has separated out is filtered off.
It is a dark powder which dissolves in pure water with red-violet color, in concentrated sulfuric acid with blue, in dilute sodium hydroxide solution with blue-red color. He dyes the wool red-violet from an acidic bath; after chrome plating, the color changes to blue.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH101614T | 1922-11-18 | ||
CH104914T | 1922-11-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH104914A true CH104914A (en) | 1924-05-16 |
Family
ID=25706013
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH104914D CH104914A (en) | 1922-11-18 | 1922-11-18 | Process for the preparation of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH104914A (en) |
-
1922
- 1922-11-18 CH CH104914D patent/CH104914A/en unknown
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