CH106439A - Process for the production of a new indigoid dye. - Google Patents
Process for the production of a new indigoid dye.Info
- Publication number
- CH106439A CH106439A CH106439DA CH106439A CH 106439 A CH106439 A CH 106439A CH 106439D A CH106439D A CH 106439DA CH 106439 A CH106439 A CH 106439A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- production
- indigoid dye
- dissolves
- gray
- 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)
- Paper (AREA)
Description
Verfahren zur Herstellung eines indigoiden Farbstoffes. Es wurde gefunden, dass man einen indigoiden Farbstoff erhält, wenn man das 2,3-Thionaphthisatin, in welchem das a- Ketonsasuerstoffatom durch ein übspaltbares Radikal, wie zum Beispiel Halogen oder eine Anilgruppe, ersetzt ist, mit OxytIiiomaphthen- karbonsäure kondensiert.
Der Farbstoff stellt ein graublaues Pulver dar, das sich in Schwe felsäure mit grüner Farbe löst. Mit Hydro- sulfit und Natronlauge geht der Farbstoff mit orangebrauner Farbe in Lösung und färbt daraus Baumwolle in grauen Nuancen von guter Echtheit.
Beispiel: 332 Teile 2-(4'-Dimethylamino)-an11 des 2,3 - Thionaphthisatins und 194 Teile Oxy- thion.aphthenl#:.arbonsäure werden in 5000 Teilen Alkohol kurze Zeit am Rückflussküh- ler gelw-cht. Der gebildete Farbstoff wird fil triert, gewaschen und getrocknet.
Process for the production of an indigoid dye. It has been found that an indigoid dye is obtained if the 2,3-thionaphthisatin, in which the α-ketone oxygen atom has been replaced by a cleavable radical, such as halogen or an anil group, is condensed with oxytomaphthenecarboxylic acid.
The dye is a gray-blue powder that dissolves in sulfuric acid with a green color. The orange-brown dye dissolves with hydrosulfite and sodium hydroxide solution and dyes cotton in gray shades of good fastness.
Example: 332 parts of 2- (4'-dimethylamino) -an11 des 2,3-thionaphthisatin and 194 parts of oxythione.aphthenic acid are waxed in 5000 parts of alcohol for a short time on the reflux condenser. The dye formed is filtered off, washed and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH100705T | 1922-11-18 | ||
CH106439T | 1923-07-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH106439A true CH106439A (en) | 1924-09-01 |
Family
ID=25705854
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH106439D CH106439A (en) | 1922-11-18 | 1923-07-18 | Process for the production of a new indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH106439A (en) |
-
1923
- 1923-07-18 CH CH106439D patent/CH106439A/en unknown
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