CH163546A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH163546A CH163546A CH163546DA CH163546A CH 163546 A CH163546 A CH 163546A CH 163546D A CH163546D A CH 163546DA CH 163546 A CH163546 A CH 163546A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- blue
- production
- new azo
- mol
- 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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/24—Disazo or polyazo compounds
- C09B45/28—Disazo or polyazo compounds containing copper
-
- 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
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
- C09B35/02—Disazo dyes
- C09B35/039—Disazo dyes characterised by the tetrazo component
- C09B35/205—Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of a diaryl- or triaryl- alkane or-alkene
- C09B35/215—Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of a diaryl- or triaryl- alkane or-alkene of diarylethane or diarylethene
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 Azofarbstoffes. Es wurde gefunden, dass man einen neuen Azofarbstoff erhält, wenn man 1 Mol tetrazo- tierte 4.4'-Diaminostilben-3.3'-dikarbon- säure mit 2' Mol 1-Amino-8-oxynaphthalin- 4-sulfonsäure kuppelt.
Der erhaltene Azofarbstoff stellt ein graues Pulver dar, das sich in konzentrier ter Schwefelsäure mit blauer und in Wasser mit violetter Farbe löst. Er färbt Baumwolle aus neutralem oder schwach alkalischem Bade in graublauen Tönen, die beim Nachbehan deln mit Kupfersalzen in ein echtes Grün blau umschlagen.
<I>Beispiel:</I> 29,8 Teile 4.4'-Diaminostilben-3.8'-di- karbonsäure werden in 304 Teilen Wasser suspendiert und durch Beigabe der zur Bil dung des Dinatriumsalzes notwendigen Menge Natronlauge in Lösung gebracht. Zu der neutralen oder schwach alkalischen Lösung gibt man 14 Teile Natriumnitrit als 20%ige Lösung hinzu und lässt das 'Ganze unter gu tem Rühren langsam in ein Gemisch von 70 Teilen konz. Salzsäure und Eis einlaufen. Nach einigem Rühren hat die Tetrazolösung eine hellbraune Farbe angenommen.
Dann lässt man diese Lösung in eine abgekühlte, sodaalkalisehe Lösung von 48 Teilen 1- Amino-8-oxynaphthalin-4-sulfonsäure ein laufen. Nach beendeter Kupplung wird der Farbstoff nach Zugabe von etwas Kochsalz abfiltriert, gegebenenfalls umgelöst und ge trocknet.
Process for the production of a new azo dye. It has been found that a new azo dye is obtained if 1 mole of tetrazoated 4,4'-diaminostilbene-3,3'-dicarboxylic acid is coupled with 2 'mole of 1-amino-8-oxynaphthalene-4-sulfonic acid.
The azo dye obtained is a gray powder which dissolves in concentrated sulfuric acid with a blue color and in water with a purple color. It dyes cotton from neutral or weakly alkaline baths in gray-blue tones that turn into a real green blue when treated with copper salts.
<I> Example: </I> 29.8 parts of 4.4'-diaminostilbene-3.8'-dicarboxylic acid are suspended in 304 parts of water and brought into solution by adding the amount of sodium hydroxide required to form the disodium salt. 14 parts of sodium nitrite as a 20% solution are added to the neutral or weakly alkaline solution and the whole is slowly converted into a mixture of 70 parts of conc. Run in hydrochloric acid and ice. After some stirring, the tetrazo solution has turned a light brown color.
This solution is then allowed to run into a cooled, soda-alkaline solution of 48 parts of 1-amino-8-oxynaphthalene-4-sulfonic acid. After coupling has ended, the dye is filtered off after adding a little sodium chloride, if necessary redissolved and dried.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH163546T | 1932-02-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH163546A true CH163546A (en) | 1933-08-31 |
Family
ID=4416609
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH163546D CH163546A (en) | 1932-02-18 | 1932-02-18 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH163546A (en) |
-
1932
- 1932-02-18 CH CH163546D patent/CH163546A/en unknown
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