CH235449A - Process for the preparation of a trisazo dye. - Google Patents
Process for the preparation of a trisazo dye.Info
- Publication number
- CH235449A CH235449A CH235449DA CH235449A CH 235449 A CH235449 A CH 235449A CH 235449D A CH235449D A CH 235449DA CH 235449 A CH235449 A CH 235449A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- amino
- combined
- acid
- blue
- 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
- C09B31/16—Trisazo dyes
- C09B31/22—Trisazo dyes from a coupling component "D" containing directive hydroxyl and amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 231710. Verfahren zur Herstellung eines Trisazofarbstoffes. Vorliegendes Patent bezieht sich auf ein Verfahren zur Herstellung eines Trisazo- farbstoffes, dadurch gekennzeichnet, dass man 1-Diazo-4-axyben.zol-3-carbonsäure in saurem Medium mit 1-Amino-naphthalin-7-sulfon- säure vereinigt,
den so erhaltenen Aminoazo- Farbstoff @diazo-fnert, die Diazöverbindung in saurem Medium mit 1-Amino-2.5-dimethoxy- benzol vereinigt,
wieder .diazotiert und die Diazoverbindung des so erhaltenen Amino- disazofarbs.toffes in alkalischem Medium mit 2 - Mefhydamino - 5 - oxynap@htdialin - 7 -@sulf on- säure vereinigt.
Der so erhaltene Trisazofarbstoff ist ein dunkles Pulver, das sich in Wasser mit grünstichig blauer, in konzentrierter Schwe felsäure mit blauschwarzer Farbe löst, und färbt Baumwolle in lebhaften, grünstichig- blauen, lichtechten Tönen.
Die Färbungen werden durch Nachbehandeln mit Chromi- oder Kupfersalzen ohne merkliche Tan- änclerung sehr waschecht. <I>Beispiel:
</I> Die aus 15,3 Teilen 1-Amino-4-oxybenzol- 3-carbo@nsäure hergestellte Diazoverbindung wird in Geigenwart von überschüssigem Na-, triumacetat mit einer Lösung des Natrium- salzes von 22,
3 Teilen 1-Amino-naphthalin-7- sulfonsäure vereinigt. Nach beendeter Kupp lung wird der Farbstoff weiterdiäzotiert und ,die Diazoverbindung in essigsaurer Lösung mit 15 Teilen 1- Amino-2.5-@dimethoxybenzol vereinigt. Der Farbstoff wird abgeschieden und weiterdiazotiert.
Die Diazosuspension vereinigt man bei 0-5 mit einer so,daalkalis;chen Lösung von 25,3 Teilen 2-MethyIamino-5-oxynaphthalin- 7-sulfo@nsäure, wobei sich ein Zusatz von Pyridin,als vorteilhaft erweist.
Additional patent to main patent No. 231710. Process for the production of a trisazo dye. The present patent relates to a process for the preparation of a trisazo dye, characterized in that 1-diazo-4-axyben.zene-3-carboxylic acid is combined with 1-amino-naphthalene-7-sulfonic acid in an acidic medium,
the aminoazo-dye @ diazo-fnert thus obtained, the diazo compound combined with 1-amino-2,5-dimethoxybenzene in an acidic medium,
again .diazotized and the diazo compound of the amino disazofarbs.toff thus obtained is combined in an alkaline medium with 2 - mefhydamino - 5 - oxynap @ htdialin - 7 - @ sulfonic acid.
The trisazo dye thus obtained is a dark powder which dissolves in water with a greenish blue color and in concentrated sulfuric acid with a blue-black color, and dyes cotton in lively, greenish blue, lightfast shades.
After treatment with chromium or copper salts, the dyeings become very washable without noticeable tan. <I> example:
</I> The diazo compound produced from 15.3 parts of 1-amino-4-oxybenzene-3-carbonic acid is in Geigenwart of excess sodium, trium acetate with a solution of the sodium salt of 22,
3 parts of 1-amino-naphthalene-7-sulfonic acid combined. After the coupling has ended, the dye is further diacetized and the diazo compound is combined in acetic acid solution with 15 parts of 1- amino-2.5-@dimethoxybenzene. The dye is deposited and further diazotized.
The diazo suspension is combined at 0-5 with an alkaline solution of 25.3 parts of 2-methylamino-5-oxynaphthalene-7-sulfonic acid, the addition of pyridine proving to be advantageous.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE235449X | 1942-06-02 | ||
CH231710T | 1943-05-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH235449A true CH235449A (en) | 1944-11-30 |
Family
ID=25727620
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH235449D CH235449A (en) | 1942-06-02 | 1943-05-14 | Process for the preparation of a trisazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH235449A (en) |
-
1943
- 1943-05-14 CH CH235449D patent/CH235449A/en unknown
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