CH109646A - Process for the production of a new vat dye. - Google Patents
Process for the production of a new vat dye.Info
- Publication number
- CH109646A CH109646A CH109646DA CH109646A CH 109646 A CH109646 A CH 109646A CH 109646D A CH109646D A CH 109646DA CH 109646 A CH109646 A CH 109646A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- new
- vat dye
- new vat
- 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
- C09B49/00—Sulfur dyes
- C09B49/12—Sulfur dyes from other compounds, e.g. other heterocyclic compounds
- C09B49/128—Sulfur dyes from other compounds, e.g. other heterocyclic compounds from hydroxy compounds of the benzene or naphthalene series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 108932. Verfahren zur Herstellung eines neuen Küpenfarhstoffes. Es wurde gefunden, dass man einen neuen Nüpenfarbstoff erhält, wenn nnan Thionyl- c:lilorid auf ?,S-Di-ss-nap@t@y@a,midobenzoc@i- non einwirken lässt.
Die Reaktion wird zweckm#issig in Gegenwart von Verdünnungs mitteln, wie Nitrobenzol, gegebenenfalls in Gegenwart von säurebindenden Dritteln, durchgeführt. Der neue Farbstoff bildet ein clunkelrötlichbraunes Pulver,
das sich in konzentrierter Schwefelsäure mit rötlich blauer Farbe löst und Wolle aus der Hy- drosulfitl@üpe in braunen Nuancen färbt.
Beispiel: 9,8 Teile 2,5-Di-ss-nitphthylamidobenzo- chinori werden in 150 Teilen Nitrobenzol kalt mit 9 Teilen Thionyl-chlorid versetzt und längere Zeit bei Zimmertemperatur ge rührt. Hierauf wird filtriert, mit Alkohol gewaschen und zetrocl:net.
Additional patent to the main patent No. 108932. Process for the production of a new vat raw material. It has been found that a new pimple dye is obtained if nnan thionyl- c: liloride is allowed to act on?, S-Di-ss-nap @ t @ y @ a, midobenzoc @ i-non.
The reaction is expediently carried out in the presence of diluents such as nitrobenzene, if appropriate in the presence of acid-binding thirds. The new dye forms a dark reddish brown powder,
which dissolves in concentrated sulfuric acid with a reddish blue color and dyes wool from the hydrosulphite oil in shades of brown.
Example: 9.8 parts of 2,5-di-ss-nitphthylamidobenzoquinori in 150 parts of cold nitrobenzene are mixed with 9 parts of thionyl chloride and the mixture is stirred for a long time at room temperature. It is then filtered, washed with alcohol and zetrocl: net.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH108932T | 1923-10-27 | ||
| CH109646T | 1923-11-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH109646A true CH109646A (en) | 1925-04-01 |
Family
ID=25707489
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH109646D CH109646A (en) | 1923-10-27 | 1923-11-24 | Process for the production of a new vat dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH109646A (en) |
-
1923
- 1923-11-24 CH CH109646D patent/CH109646A/en unknown
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