CH233846A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH233846A CH233846A CH233846DA CH233846A CH 233846 A CH233846 A CH 233846A CH 233846D A CH233846D A CH 233846DA CH 233846 A CH233846 A CH 233846A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- azo dye
- yellow
- new
- new azo
- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/10—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
- C09B29/12—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group of the benzene series
Description
Verfahren zur Herstellung eines neuen Azofarbstofes. Es wurde gefunden, dass man einen. neuen Azofarbstoff erhält, wenn man diazotierten 4 - Aminobrenzkatechinäthylenäther mit 1- Ogy-4-methylbenzol vereinigt.
Der neue Farbstoff bildet in trockenem Zustande ein gelbes Pulver, das sich in orga nischen Lösungsmitteln, wie Alkohol, Essig säureäthylester mit gelber Farbe löst. Ver- mahlt man ihn mit einem Verteilungsmittel, wie z. B. Sulfitcelluloseablauge, so erhält man eine feine Paste, die in Wasser eine feine Suspension gibt, aus der man Acetatkunst- seide in gelben, echten Tönen färbt.
<I>Beispiel:</I> 15,1 Teile 4-Aminobrenzkatechinäthylen- äther werden in etwa 100 Teilen Wasser sus pendiert und mit 25 Teilen 30%iger Salz säure und 7 Teilen, Natriumnitrit diazotiert. Die kalte Lösung der Diazoniumverbindung i wird in eine kalte Lösung, enthaltend 10,8 Teile 1-Ogy-4-methylbenzol, 10 Teile 30 /woig,er Natriumhydrogydlösung und 15 Teile Natriumcarbonat,
gegeben. Der Farbstoff fällt aus. und wird nach beendeter Kupplung ab filtriert und gewaschen.
Process for the preparation of a new azo dye. It was found that one. new azo dye is obtained when diazotized 4-aminocatechol ethylene ether is combined with 1-Ogy-4-methylbenzene.
The new dye forms a yellow powder when dry, which dissolves in organic solvents such as alcohol, ethyl acetate with a yellow color. If you grind it with a distributing agent such as B. Sulphite cellulose waste liquor, a fine paste is obtained which is a fine suspension in water, from which acetate artificial silk is dyed in yellow, real shades.
<I> Example: </I> 15.1 parts of 4-aminocatechol ethylene ether are suspended in about 100 parts of water and diazotized with 25 parts of 30% hydrochloric acid and 7 parts of sodium nitrite. The cold solution of the diazonium compound i is in a cold solution containing 10.8 parts of 1-Ogy-4-methylbenzene, 10 parts of 30 / week, he sodium hydrogen solution and 15 parts of sodium carbonate,
given. The dye precipitates. and is filtered off and washed after the coupling has ended.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH233846T | 1942-10-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH233846A true CH233846A (en) | 1944-08-31 |
Family
ID=4458249
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH233846D CH233846A (en) | 1942-10-12 | 1942-10-12 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH233846A (en) |
-
1942
- 1942-10-12 CH CH233846D patent/CH233846A/en unknown
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