CH101614A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH101614A CH101614A CH101614DA CH101614A CH 101614 A CH101614 A CH 101614A CH 101614D A CH101614D A CH 101614DA CH 101614 A CH101614 A CH 101614A
- Authority
- CH
- Switzerland
- Prior art keywords
- blue
- azo dye
- production
- 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)
Description
Verfahren zur Herstellung eines neuen Azofarbstoffes. Es -wurde gefunden, idass man einen neuen Azofarbstoff erhält, wenn man das 1-Oxy- naphta,lin-8-sulia,mi,d mit der Diazoverbin- dung der 1-Amino-2-oxynaphtalin-4-sulfo- säure kuppelt.
<I>Beispiel:</I> 22,3 Teile 1-Oxynaphtalin-8-sulfa-mid, kalt in einer überschüssigen, wässerigen Ätz- kalilösung gelöst, werden mit<B>27,2</B> Teilen Diazoverbindung der 1-Amino-2-oxynapht-,it- lin-4-suliosäure als Natronsalz versetzt.
Lt ,die sofort einsetzende Kupplung, welche zweckmässig unter<B>10'</B> gehalten wird,<B>be-</B> endet, so wirddie Masse mit verdünnter Salz- sä,ure neutral gestellt, worauf der ausgeschie dene neue Azofarbstoff abfiltriert wird. Er stellt ein dunkles Pulver dar, welches in reinem Wasser mit rotvioletter, in konzen trierter Schwefelsäure mit blauer, in ver dünnter Natronlauge mit blauroter Fa.Ae löst. Er färbt aus saurem Bade die Wolle rotviolett an, durch Nacheliromieren schlägt ,der Farbton nach blau um.
Process for the production of a new azo dye. It has been found that a new azo dye is obtained when 1-oxynaphta, lin-8-sulia, mi, d is coupled with the diazo compound of 1-amino-2-oxynaphthalene-4-sulfonic acid .
<I> Example: </I> 22.3 parts of 1-oxynaphthalene-8-sulfa-mid, dissolved cold in an excess, aqueous caustic potash solution, are mixed with <B> 27.2 </B> parts of diazo compound of 1 -Amino-2-oxynapht-, it-lin-4-sulioic acid added as sodium salt.
If the coupling, which starts immediately and which is expediently kept below <B> 10 ', <B> ends </B>, the mass is rendered neutral with dilute hydrochloric acid, whereupon the rejected new azo dye is filtered off. It is a dark powder which dissolves in pure water with red-violet, in concentrated sulfuric acid with blue, in dilute sodium hydroxide with blue-red Ae. He dyes the wool red-violet from an acidic bath; by re-eliomizing, the color changes to blue.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH101614T | 1922-11-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH101614A true CH101614A (en) | 1923-12-17 |
Family
ID=4360037
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH101614D CH101614A (en) | 1922-11-18 | 1922-11-18 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH101614A (en) |
-
1922
- 1922-11-18 CH CH101614D patent/CH101614A/en unknown
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