CH163280A - Process for the production of a new vat dye. - Google Patents
Process for the production of a new vat dye.Info
- Publication number
- CH163280A CH163280A CH163280DA CH163280A CH 163280 A CH163280 A CH 163280A CH 163280D A CH163280D A CH 163280DA CH 163280 A CH163280 A CH 163280A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- new
- chloro
- vat dye
- dye
- 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
- C09B7/00—Indigoid dyes
- C09B7/10—Bis-thionapthene indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen Nüpenfarbst ffes. Es wurde gefunden, dass man einen neuen Küpenfarbstoff erhält, wenn man das 2-(p- Dimethylamino-)anil des 5-Chlor-4. 7-dimethyl- 3-oxythionaphtens mit 1-Chlor-2. 3-naphtthio- indoxyl kondensiert.
Der neue Farbstoff der Formel
EMI0001.0014
stellt ein rotviolettes Pulver dar, das sich in konzentrierter Schwefelsäure mit grüner Farbe löst und Baumwolle aus oraugebraun ge färbter Küpe in blauvioletten Tönen von sehr guten Echtheiten färbt.
<I>Beispiel:</I> 344 Teile 2-(p-Dimethylamirro-)anil des 5-Chlor-4.7-dirnethyl-3-oxythionaphtens wer den mit 234,5 Teilen 1-Chlor-2. 3-naphtthio- indoxyl in 8000 Teilen Benzol zum Sieden erhitzt. Nach beendeter Kondensation wird der Farbstoff abfiltriert, gewaschen und ge trocknet.
Process for the production of a new pomple color. It has been found that a new vat dye is obtained if the 2- (p-dimethylamino) anil des 5-chloro-4. 7-dimethyl-3-oxythionaphthene with 1-chloro-2. 3-naphthioindoxyl condensed.
The new dye in the formula
EMI0001.0014
represents a red-violet powder that dissolves in concentrated sulfuric acid with a green color and dyes cotton from orange-brown vat in blue-violet shades of very good fastness properties.
<I> Example: </I> 344 parts of 2- (p-dimethylamirro-) anil des 5-chloro-4,7-dirnethyl-3-oxythionaphthene with 234.5 parts of 1-chloro-2. 3-naphthioindoxyl in 8000 parts of benzene heated to boiling. When the condensation has ended, the dye is filtered off, washed and dried.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH163280T | 1932-07-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH163280A true CH163280A (en) | 1933-08-15 |
Family
ID=4416352
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH163280D CH163280A (en) | 1932-07-15 | 1932-07-15 | Process for the production of a new vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH163280A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2539737A (en) * | 1943-10-28 | 1951-01-30 | Ciba Ltd | Mixtures of thioindigoid dyestuffs |
-
1932
- 1932-07-15 CH CH163280D patent/CH163280A/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2539737A (en) * | 1943-10-28 | 1951-01-30 | Ciba Ltd | Mixtures of thioindigoid dyestuffs |
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