CH106449A - Process for the production of a new indigoid dye. - Google Patents
Process for the production of a new indigoid dye.Info
- Publication number
- CH106449A CH106449A CH106449DA CH106449A CH 106449 A CH106449 A CH 106449A CH 106449D A CH106449D A CH 106449DA CH 106449 A CH106449 A CH 106449A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- new
- indigoid dye
- blue
- new indigoid
- 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
- C09B7/12—Other thionaphthene indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen indigoiden Farbstoffes. Es wurde gefunden, da,ss ein neuer, wert voller, indigoider Farbstoff entsteht, wenn man das 1-Chlor-2,3-naphththioindoxyl mit Acenaphthenchinon kondensiert.
Der neue Farbstoff stellt ein blaurotes Pulver dar, das sich in .S@chwefelsäjure mit grüner Farbe löst. Er bildot eine orange- braune Küpe und färbt Baumwolle in blau roten Tönen von sehr guter Echtheit.
Beispiel: 234,5 Teile 1-Chlor-2,3-naphththioina.oxyl und 182 Teile Acenaphthenchinon werden in 5000 Teilen Alkohol suspendiert und zum Sieden erhitzt. Dann gibt man 5 Teile kon zentrierte Salzsäure zu. Nach kurzem K0- chen ist die Kondensation beendigt. Es wird h,eiss@ filtriert, ,gewaschen und getrocknet..
Process for the production of a new indigoid dye. It has been found that a new, valuable, indigoid dye is formed when 1-chloro-2,3-naphththioindoxyl is condensed with acenaphthenquinone.
The new dye is a blue-red powder that dissolves in .S @ sulfuric acid with a green color. It forms an orange-brown vat and dyes cotton in blue-red shades of very good fastness.
Example: 234.5 parts of 1-chloro-2,3-naphththioina.oxyl and 182 parts of acenaphthenquinone are suspended in 5000 parts of alcohol and heated to the boil. Then 5 parts of concentrated hydrochloric acid are added. After a short cooking, the condensation is over. It is h, eiss @ filtered, washed and dried ..
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH100705T | 1922-11-18 | ||
CH106449T | 1923-03-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH106449A true CH106449A (en) | 1924-09-01 |
Family
ID=25705864
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH106449D CH106449A (en) | 1922-11-18 | 1923-03-29 | Process for the production of a new indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH106449A (en) |
-
1923
- 1923-03-29 CH CH106449D patent/CH106449A/en unknown
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