CH215833A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH215833A CH215833A CH215833DA CH215833A CH 215833 A CH215833 A CH 215833A CH 215833D A CH215833D A CH 215833DA CH 215833 A CH215833 A CH 215833A
- Authority
- CH
- Switzerland
- Prior art keywords
- sep
- azo dye
- preparation
- dye
- acid
- 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
- C09B1/32—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
- C09B1/34—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated
-
- 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
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/08—Amino benzenes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines Azofarbstoffes. Es wurde gefunden, dass man einen neuen, wertvollen Azofarbstoff erhält, wenn man di- azotiertes 4-Nitro-2. 6 - dichlor-l- aminobenzol mit ss-N-Äthyl-N-3-methylphenylaminopro- pionsäure -,P'- ogyäthylester entsprechend der Formel
EMI0001.0012
kuppelt.
Der neue Azofarbstoff eignet sich beson ders zum Färben von Celluloseestern und -äthern, wobei man klare rotbraune Töne von ausgezeichneter Lichtechtheit erhält. Der Farb stoff lässt sich mit Hilfe geeigneter Dispergier- mittel so fein in Wasser verteilen, dass man kolloidale Lösungen erhält, die sich nicht von echten Lösungen unterscheiden.
Solche Lösun gen besitzen ein vorzügliches Durchfärbever- mögen für dichtgeschlagenes Acetatseiden- gewebe und stark gezwirntes Acetatseidengarn. <I>Beispiel:
</I> Die Diazoverbindung aus 209 Teilen 1- Amino - 2 . 6 - dichlor - 4 - nitrobenzol wird bei 0--5 o C langsam in die mit Wasser auf etwa 5000 Teile verdünnte Lösung von 265 Teilen ss - N -Äthyl - N - 3 - methylphenylaminopropion- säure-P'-ogyäthylester in 110 Teilen 35 /oiger Salzsäure eingegossen. Die Kupplung ist sehr rasch beendet.
Man versetzt mit so viel Na triumacetat oder verdünnter Natronlauge, dass das pH der Lösung 5 beträgt, saugt ab, wäscht gut aus, trocknet bei 50 o C und vermahlt mit der gleichen Menge eines Dispergiermittels.
Der Farbstoff bildet ein dunkelbraunes Pulver und liefert aus Glaubersalz oder Chlor ammonium enthaltenden wässrigen Bädern kräftige rotbraune Färbungen auf Acetatseide, die gut durchgefärbt und lichtecht sind.
Process for the preparation of an azo dye. It has been found that a new, valuable azo dye is obtained when diazotized 4-nitro-2. 6 - dichloro-l-aminobenzene with ss-N-ethyl-N-3-methylphenylaminopropionic acid -, P'-ogyäthylester according to the formula
EMI0001.0012
clutch.
The new azo dye is particularly suitable for dyeing cellulose esters and ethers, giving clear red-brown shades of excellent lightfastness. With the help of a suitable dispersing agent, the dye can be distributed so finely in water that colloidal solutions are obtained that do not differ from real solutions.
Such solutions have excellent through-dyeing properties for tightly twisted acetate silk and heavily twisted acetate silk yarn. <I> example:
</I> The diazo compound from 209 parts 1- amino - 2. 6 - dichloro - 4 - nitrobenzene is slowly added to the solution of 265 parts of ss - N - ethyl - N - 3 - methylphenylaminopropionic acid P'-ogyäthylester in 110 parts diluted with water to about 5000 parts 35% hydrochloric acid poured in. The coupling is completed very quickly.
Sufficient sodium acetate or dilute sodium hydroxide solution is added so that the pH of the solution is 5, and the product is filtered off with suction, washed thoroughly, dried at 50 ° C. and ground with the same amount of a dispersant.
The dye forms a dark brown powder and, from aqueous baths containing Glauber's salt or chlorine ammonium, produces strong red-brown colorations on acetate silk that are well colored and lightfast.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE215833X | 1938-07-28 | ||
CH212647T | 1940-11-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH215833A true CH215833A (en) | 1941-07-15 |
Family
ID=25725298
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH215833D CH215833A (en) | 1938-07-28 | 1939-06-27 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH215833A (en) |
-
1939
- 1939-06-27 CH CH215833D patent/CH215833A/en unknown
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