CH119368A - Process for the production of a new dye. - Google Patents
Process for the production of a new dye.Info
- Publication number
- CH119368A CH119368A CH119368DA CH119368A CH 119368 A CH119368 A CH 119368A CH 119368D A CH119368D A CH 119368DA CH 119368 A CH119368 A CH 119368A
- Authority
- CH
- Switzerland
- Prior art keywords
- new dye
- production
- parts
- acid
- new
- 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
Verfahren zur Herstellung eines neuen Farbstoffes. Es wurde gefunden, dass man einen neuen Farbstoff erhält, wenn man Barbitursäure mit diazotierter 4-Sulfo-2-amino-l-phenol-6- karbonsäure kuppelt und das so erhaltene Produkt mit Chromformiat behandelt. Der neue Farbstoff bildet ein braunes- Pulver, löst sich in verdünnter Sodalösung mit gel ber Farbe und erzeugt auf .Wolle, aus saurem Bade gefärbt, echte gelbe Töne.
Beispiel: 232 Teile 4-Sulfo-2-amino-l-phenol-6-kar- bonsäure werden wie üblich diazotiert und in ein Gemisch aus 134 Teilen Barbitur- säure, 133 Teilen 30 %iger Natronlauge, 170 Teilen Soda und 1500 Teilen Wasser einge tragen. Die Kupplung setzt sofort ein, zu ihrer Vervollständigung rührt man noch einige Zeit. Der gebildete Farbstoff wird dann filtriert und getrocknet.
37,7 Teile dieses Firbstoffes werden in <B>650</B> Teilen kochendem Wasser gelöst und mit einer Chromformiatlösung entsprechend 15,2 Teilen Cr203 versetzt. Man kocht mehrere Stunden am Rückflusskühler, dampft teil weise ein und gewinnt die neue Chromver bindung durch Filtrieren, gegebenenfalls un ter vorherigem Aussalzen.
Process for the production of a new dye. It has been found that a new dye is obtained if barbituric acid is coupled with diazotized 4-sulfo-2-amino-1-phenol-6-carboxylic acid and the product thus obtained is treated with chromium formate. The new dye forms a brown powder, dissolves in a dilute soda solution with a yellow color and dissolves. Wool, dyed from an acid bath, produces real yellow tones.
Example: 232 parts of 4-sulfo-2-amino-1-phenol-6-carboxylic acid are diazotized as usual and mixed with 134 parts of barbituric acid, 133 parts of 30% strength sodium hydroxide solution, 170 parts of soda and 1500 parts of water entered. The clutch works immediately, and stir for some time to complete. The dye formed is then filtered and dried.
37.7 parts of this dye are dissolved in 650 parts of boiling water and a chromium formate solution corresponding to 15.2 parts of Cr 2 O 3 is added. It is boiled for several hours on the reflux condenser, partially evaporated and the new chromium compound is obtained by filtering, if necessary with prior salting out.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH114283T | 1924-12-24 | ||
CH119368T | 1924-12-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH119368A true CH119368A (en) | 1927-03-01 |
Family
ID=25708295
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH119368D CH119368A (en) | 1924-12-24 | 1924-12-24 | Process for the production of a new dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH119368A (en) |
-
1924
- 1924-12-24 CH CH119368D patent/CH119368A/en unknown
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