CH110877A - Process for the production of a new dye. - Google Patents
Process for the production of a new dye.Info
- Publication number
- CH110877A CH110877A CH110877DA CH110877A CH 110877 A CH110877 A CH 110877A CH 110877D A CH110877D A CH 110877DA CH 110877 A CH110877 A CH 110877A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- new dye
- production
- dissolves
- parts
- 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)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. <B>110287.</B> Verfahren zur Herstellung eines neuen Farbstoffes. Es wurde gefunden, dass man einen neuen Farbstoff erhält, wenn man die 3-Oxytiaph- thalin-1,8-dikarbonsäure mit diazotierter 4-Me- thyl-2-amitio-l-phenol-6-sulfosätii,e kuppelt und den so erhaltenen Farbstoff mit Chromformiat behandelt.
Der neue Farbstoff bildet ein schwärzliches Pulver, löst sich in Wasser unter Zusatz von Natronlauge mit rotvioletter Farbe und erzeugt im Chromdruck auf Baum wolle sehr echte violette Töne. <I>Beispiel:</I> <B>25</B> Teile 4-Methyl-2-amino-l-phenol-6-sulfo- säure werden wie üblich diazotiert und in eine Lösung von<B>21,6</B> Teilen 3-Oxynaphtbaliii- 1,8-dikarbonsäureanhydrid, <B>8</B> Teilen Natron- lange und 40 Teilen Soda in<B>500</B> Teilen Wasser eingetragen. Man rührt, bis die Diazo- verbindung verschwunden ist.
Hierauf salzt man mit Kochsalz aus und filtriert den aus geschiedenen Farbstoff. <B>25,6</B> Teile dieses Farbstoffes werden in <B>500</B> Teilen Wasser heiss gelöst Lind mit einer Chromformiatmenge, entsprechend 12,5 Teilen C'r20s, versetzt. Man kocht einige Zeit und filtriert den durch Kochsalzzusatz abgeschie denen Farbstoff.
Additional patent to main patent no. <B> 110287. </B> Process for the production of a new dye. It has been found that a new dye is obtained if the 3-oxytiaphthalene-1,8-dicarboxylic acid is coupled with diazotized 4-methyl-2-amitio-1-phenol-6-sulfosätii, e and the like obtained dye treated with chromium formate.
The new dye forms a blackish powder, dissolves in water with the addition of caustic soda with a red-violet color and creates very real violet tones when printed with chrome on cotton. <I> Example: </I> <B> 25 </B> parts of 4-methyl-2-amino-1-phenol-6-sulfonic acid are diazotized as usual and converted into a solution of <B> 21.6 Parts 3-Oxynaphtbaliii- 1,8-dikarbonsäureanhydrid, <B> 8 </B> parts of long soda and 40 parts of soda in <B> 500 </B> parts of water. Stir until the diazo compound has disappeared.
It is then salted out with common salt and the dye which has separated out is filtered off. <B> 25.6 </B> parts of this dye are dissolved in <B> 500 </B> parts of hot water and an amount of chromium formate corresponding to 12.5 parts of C'r20s is added. It is boiled for some time and the dye separated by the addition of common salt is filtered off.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH110287T | 1923-12-28 | ||
CH110877T | 1923-12-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH110877A true CH110877A (en) | 1925-07-01 |
Family
ID=25707668
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH110877D CH110877A (en) | 1923-12-28 | 1923-12-28 | Process for the production of a new dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH110877A (en) |
-
1923
- 1923-12-28 CH CH110877D patent/CH110877A/en unknown
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