CH267295A - Process for the preparation of an acidic disazo dye. - Google Patents
Process for the preparation of an acidic disazo dye.Info
- Publication number
- CH267295A CH267295A CH267295DA CH267295A CH 267295 A CH267295 A CH 267295A CH 267295D A CH267295D A CH 267295DA CH 267295 A CH267295 A CH 267295A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- acidic
- sulfonic acid
- blue
- preparation
- 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
- C09B31/00—Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
- C09B31/02—Disazo dyes
- C09B31/08—Disazo dyes from a coupling component "C" containing directive hydroxyl and amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 263651. Verfahren zur Herstellung eines sauren Disazofarhstoffes. Es wurde gefunden, dass man zu einem neuen, wertvollen sauren Disazofarbstoff 0.e- langt, wenn man diazotiertes p-Tertiä,r-Amyl- anilin alkalisch auf 1-Amino-3- (4'-methyl)- plienylsulfoylaminobenzol-6-sulfonsäure kup pelt,
den erhaltenen 111onoazofa.rbstoff in der Sulfoylatninogrttppe metliyliert, weiterdiazo- tiert. und die Diazoverbindung des Aminoazo- farbstoffes in saurem Medium mit 2 --lethyl- amitio-8-oxynaphthaiin-6-stilfonsäure ver einigt.
Beispiel; 16,3 Teile p-Tertiär-Amylanilin werden di- azotiert und die Diazolösung mit der soda- alkalischen Lösung von 34,2 Teilen 1-Amino- 3 - (4'-inetltyl) - phenylsulfoylaminobenzol-6-sul- fonsäure vereinigt.
Nach beendeter Kupplung wird der Aminoazofarbstoff abgetrennt, in Wasser mittels 80 Teilen 301/oiger Natron- lauge gelöst und bei gewöhnlicher Tempera tur mit 20 Teilen Dimeth5-lsulfat behandelt, bis der ausschliesslich in der substituierten Aminogruppe methylierte Farbstoff ausge schieden ist.
Er wird in Wasser angerührt und bei etwa 50 mit 7 Teilen Natriumnitrit und 35 Teilen konzentrierter Salzsäure diazo- tiert, die Diazoverbindung abfiltriert und mit 24 Teilen 2-Methy lamino-8-oxynaplithalin-6- sulfonsäure in essiusaurem iHedium vereinigt. Der ausgeschiedene Disazofarbstoff wird ab filtriert und getroeknet.
Er stellt ein blaues Pulver dar, das sich in Wasser mit blauer Farbe löst und Wolle und Seide in neutralem oder schwach saurem Bad in blauen Tönen von guter Schwefel-, Walk und Lichtechtheit färbt.
Er besitzt die Formel:
EMI0001.0054
<B> Additional patent </B> to main patent No. 263651. Process for the production of an acidic disazo raw material. It has been found that a new, valuable acidic disazo dye 0.e- is obtained if diazotized p-tertiary, r-amylaniline is alkaline to 1-amino-3- (4'-methyl) - plienylsulfoylaminobenzene-6- sulfonic acid coupling,
the obtained 111onoazofa dye in the sulfoylatninogrttppe metliyliert, further diazo- tiert. and the diazo compound of the aminoazo dye is combined in an acidic medium with 2 -lethyl-amitio-8-oxynaphthaiine-6-stilfonic acid.
Example; 16.3 parts of p-tertiary amylaniline are diazoated and the diazo solution is combined with the soda-alkaline solution of 34.2 parts of 1-amino-3- (4'-ethyl) -phenylsulfoylaminobenzene-6-sulfonic acid.
After coupling has ended, the aminoazo dye is separated off, dissolved in water using 80 parts of 301% sodium hydroxide solution and treated with 20 parts of dimeth5 sulfate at normal temperature until the dye methylated exclusively in the substituted amino group is eliminated.
It is stirred in water and diazo- ated at about 50 with 7 parts of sodium nitrite and 35 parts of concentrated hydrochloric acid, the diazo compound is filtered off and combined with 24 parts of 2-methylamino-8-oxynaplithalin-6-sulfonic acid in acidic iHedium. The precipitated disazo dye is filtered off and dried.
It is a blue powder that dissolves in water with a blue color and dyes wool and silk in a neutral or weakly acidic bath in blue shades of good fastness to sulfur, milled and light.
It has the formula:
EMI0001.0054
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH267295T | 1948-02-17 | ||
CH263651T | 1950-02-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH267295A true CH267295A (en) | 1950-03-15 |
Family
ID=25730660
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH267295D CH267295A (en) | 1948-02-17 | 1948-02-17 | Process for the preparation of an acidic disazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH267295A (en) |
-
1948
- 1948-02-17 CH CH267295D patent/CH267295A/en unknown
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