CH101937A - Process for the production of an indigoid dye. - Google Patents
Process for the production of an indigoid dye.Info
- Publication number
- CH101937A CH101937A CH101937DA CH101937A CH 101937 A CH101937 A CH 101937A CH 101937D A CH101937D A CH 101937DA CH 101937 A CH101937 A CH 101937A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- indigoid dye
- dye
- indigoid
- thionaphthisatin
- 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)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines indigoiden Farbstoffes. Es wurde gefunden, dass man einen wert vollen indigoiden Farbstoff herstellen kann,. wenn man das 2,1-Thionaphthisatin in Form seines a-p-Dimethylaminoanils mit Oxy thio- naphthen kondensiert. Der Farbstoff bildet ein rotes Pulver, löst sich in konzentrier ter Schwefelsäure mit grünlicher Farbe und gibt mit Hydrosulfit und Natronlauge eine gelbe Küpe, aus welcher Baumwolle in sehr licht-, wasch- und chlorechten Bordeaux Tö nen gefärbt wird.
<I>Beispiel:</I> 332 Teile a-p-Dimethylaminoanil des 2,1-Thionaphthisatins und<B>150</B> Teile Oxythio- naphthen werden in 4000 Teilen Alkohol sus pendiert und nach Beigabe von 7 Teilen Soda zum Sieden erhitzt. Nach kurzem Kochen ist die Kondensation beendigt. Der in sehr guter Ausbeute abgeschiedene Farbstoff wird filtriert, gewaschen und getrocknet.
Process for the production of an indigoid dye. It has been found that a valuable indigoid dye can be produced. if the 2,1-thionaphthisatin in the form of its a-p-dimethylaminoanil is condensed with oxy thionaphthen. The dye forms a red powder, dissolves in concentrated sulfuric acid with a greenish color and, with hydrosulphite and sodium hydroxide solution, gives a yellow vat from which cotton is dyed in very light, wash and chlorine-fast Bordeaux tones.
<I> Example: </I> 332 parts of ap-dimethylaminoanil des 2,1-thionaphthisatin and <B> 150 </B> parts of oxythionaphthene are suspended in 4000 parts of alcohol and, after adding 7 parts of soda, heated to the boil . After a short boil, the condensation is over. The dyestuff deposited in very good yield is filtered, washed and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH100705T | 1922-11-18 | ||
CH101937T | 1923-02-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH101937A true CH101937A (en) | 1924-03-01 |
Family
ID=25705820
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH101937D CH101937A (en) | 1922-11-18 | 1923-02-09 | Process for the production of an indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH101937A (en) |
-
1923
- 1923-02-09 CH CH101937D patent/CH101937A/en unknown
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