CH120174A - Process for the production of a new dye. - Google Patents
Process for the production of a new dye.Info
- Publication number
- CH120174A CH120174A CH120174DA CH120174A CH 120174 A CH120174 A CH 120174A CH 120174D A CH120174D A CH 120174DA CH 120174 A CH120174 A CH 120174A
- Authority
- CH
- Switzerland
- Prior art keywords
- new dye
- production
- brown
- mol
- naphthylaminobenzoquinone
- 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
- C09B57/00—Other synthetic dyes of known constitution
- C09B57/002—Aminoketone dyes, e.g. arylaminoketone dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines neuen Farbstoffes. Es wurde gefunden, dass man einen neuen Farbstoff erhält, wenn man 2,5-Di-,B-naph- thylaminobenzochinon mit einer Lösung von Chlor in Schwefeldichlorid, entsprechend der Zusammensetzung SC14, und zwar im Ver hältnis von 1 Mol. 2,5-Di-,B-naphthylamino- benzochinon zu 2 Mol. SC14, behandelt.
Der neue Farbstoff bildet ein gelbbraunes Pul ver, das sich in konzentrierter Schwefelsäure mit rotbrauner Farbe und Wolle aus der Küpe gelbbraun färbt. <I>Beispiel:</I> 3,9 Teile 2,5-Di-B-naphthyla,minobenzo- ehinon werden in einem Gemisch von 33 Tei len Nitrobenzol und 66 Teilen o-Nitrotoluol suspendiert und unter starker Kühlung mit einer Lösung von Chlor in Schwefeldichlorid, entsprechend der Zusammensetzung SC14, versetzt. Nach einiger Zeit wird der neue Farbstoff filtriert, mit Alkohol nachgewa schen und getrocknet.
Process for the production of a new dye. It has been found that a new dye is obtained when 2,5-di-, B-naphthylaminobenzoquinone is mixed with a solution of chlorine in sulfur dichloride, corresponding to the composition SC14, in a ratio of 1 mol. 2.5 -Di-, B-naphthylamino-benzoquinone to 2 mol. SC14 treated.
The new dye forms a yellow-brown powder that turns yellow-brown in concentrated sulfuric acid with red-brown color and wool from the vat. <I> Example: </I> 3.9 parts of 2,5-di-B-naphthyla, minobenzo- ehinon are suspended in a mixture of 33 parts of nitrobenzene and 66 parts of o-nitrotoluene and with strong cooling with a solution of Chlorine is added to sulfur dichloride according to the composition SC14. After a while, the new dye is filtered, rewashed with alcohol and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH108932T | 1923-10-27 | ||
CH120174T | 1925-09-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH120174A true CH120174A (en) | 1927-05-02 |
Family
ID=25707513
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH120174D CH120174A (en) | 1923-10-27 | 1925-09-16 | Process for the production of a new dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH120174A (en) |
-
1925
- 1925-09-16 CH CH120174D patent/CH120174A/en unknown
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