CH192979A - Process for the preparation of an azo dye which is capable of forming metal compounds. - Google Patents
Process for the preparation of an azo dye which is capable of forming metal compounds.Info
- Publication number
- CH192979A CH192979A CH192979DA CH192979A CH 192979 A CH192979 A CH 192979A CH 192979D A CH192979D A CH 192979DA CH 192979 A CH192979 A CH 192979A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- forming metal
- azo dye
- metal compounds
- 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
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. <B>188320.</B> Verfahren zur Herstellung eines Azofarbstoffes, der zur Bildung von 31etallverbindungen befähigt ist. Vorliegendes Patent bezieht sich auf ein Verfahren zur Herstellung eines Azofarb- stoffes, der zur Bildung von Metallverbin dungen befähigt ist, dadurch gekennzeich net," dass man 2-Naplithylamin-8-sulfosäure diazotiert, mit 4-Amino-aziminobenzol kup pelt,
den erhaltenen Aminoazofarbstoff wei ter Jiazotiert und mit 2-Phenylamino-ä- napht,hol-7-suliosäure kuppelt.
Der so erhaltene Farbstoff hat in Form seiner Kupferkomplexverbindung ein dunkles .Äusseres, löst sich in Wasser violett und in konzentrierter Schwefelsäure hellblau. Er zieht auf Baumwolle in graublauen Tönen kräftig auf, während,der ungekupferte Farb stoff ein Violett ist.
<I>Beispiel:</I> 24,5 Teile 2#-naphthylamin-8-sulfosaures Natrium werden bei<B>0<I>'</I> C</B> mit Salzsäure und <B>6,9</B> Teilen Natriumnitrit,diazotiert. Darauf- hin lässt man die Diazolösung einlaufen in eine salzsaure Lösung von 13,4 Teilen 4- Amin,o-aziminobenzol und rülirt bis zur Be endigung der Kupplung.
Dann salzt man den Aminoazofarbstoff aus, filtriert und löst ihn mit einer verdünnten Sodalösung. Dann kühlt man ab, versetzt die Lösung mit<B>6,9</B> Teilen Natriumnitrit und lässt die Verbin- #dung in Salzsäure einlaufen, welche mit ge nügend Eis vermengt ist. Nach kurzer Zeit ist die Weiterdiazotierung beendet.
Nun lässt man die Diazoverbindung in eine soda- alkalische Lösung von 34 Teilen 2-Phenyl- amino-,5-naplithol-7-sulfosäur,e einlaufen. Der Disazofarbstoff wird dann durch Anwärmen in Lösung gebracht, durch Zugabe von Salz gefällt, abfiltriert und Jurcli Auswaschen gereinigt.
Additional patent to main patent no. <B> 188320. </B> Process for the production of an azo dye which is capable of forming metal compounds. The present patent relates to a process for the production of an azo dye which is capable of forming metal compounds, characterized in that "2-naplithylamine-8-sulfonic acid is diazotized with 4-amino-aziminobenzene,
the aminoazo dye obtained is further jiazotized and coupled with 2-phenylamino-a- naphtha, hol-7-sulioic acid.
The dye thus obtained has a dark appearance in the form of its copper complex compound, dissolves violet in water and light blue in concentrated sulfuric acid. It pulls heavily on cotton in gray-blue tones, while the unplated dye is a violet.
<I> Example: </I> 24.5 parts of 2 # -naphthylamine-8-sulfonic acid sodium are added at <B> 0 <I> '</I> C </B> with hydrochloric acid and <B> 6.9 </B> Parts of sodium nitrite, diazotized. The diazo solution is then allowed to run into a hydrochloric acid solution of 13.4 parts of 4-amine, o-aziminobenzene and stirred until the coupling is complete.
Then the aminoazo dye is salted out, filtered and dissolved with a dilute soda solution. It is then cooled, the solution is mixed with 6.9 parts of sodium nitrite and the compound is allowed to run into hydrochloric acid, which is mixed with sufficient ice. The further diazotization is complete after a short time.
The diazo compound is now allowed to run into a soda-alkaline solution of 34 parts of 2-phenylamino, 5-naplithol-7-sulfonic acid. The disazo dye is then brought into solution by heating, precipitated by adding salt, filtered off and Jurcli rinsing is purified.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE192979X | 1935-01-04 | ||
CH188320T | 1935-12-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH192979A true CH192979A (en) | 1937-09-15 |
Family
ID=25721628
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH192979D CH192979A (en) | 1935-01-04 | 1935-12-18 | Process for the preparation of an azo dye which is capable of forming metal compounds. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH192979A (en) |
-
1935
- 1935-12-18 CH CH192979D patent/CH192979A/en unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CH192979A (en) | Process for the preparation of an azo dye which is capable of forming metal compounds. | |
DE850042C (en) | Process for the production of copper-containing trisazo dyes | |
CH194344A (en) | Process for the preparation of a polyazo dye. | |
CH215064A (en) | Process for the production of a copper-containing trisazo dye. | |
CH148005A (en) | Process for the preparation of a disazo dye. | |
CH251584A (en) | Process for the preparation of an azo dye. | |
CH144489A (en) | Process for the preparation of a disazo dye. | |
CH192049A (en) | Process for the production of a new azo dye. | |
CH86851A (en) | Process for the preparation of a new chromable orthoxyazo dye. | |
CH117270A (en) | Process for the production of a new dye. | |
CH132807A (en) | Process for the preparation of a new green tetrakisazo dye. | |
CH200370A (en) | Process for the preparation of a chromable o-oxydisazo dye. | |
CH238518A (en) | Process for the production of a new azo dye. | |
CH209107A (en) | Process for the preparation of an azo dye. | |
CH200999A (en) | Process for the preparation of an azo dye. | |
CH191739A (en) | Process for the preparation of an azo dye. | |
CH143890A (en) | Process for the preparation of an o-cyanarylrhodane compound. | |
CH193929A (en) | Process for the preparation of a secondary polyazo dye. | |
CH192047A (en) | Process for the production of a new azo dye. | |
CH209516A (en) | Process for the preparation of a disazo dye. | |
CH153829A (en) | Process for the production of a new metal-containing dye. | |
CH86986A (en) | Process for the production of an azo dye particularly suitable for cotton printing. | |
CH215044A (en) | Process for the preparation of a trisazo dye. | |
CH238336A (en) | Process for the preparation of a new disazo dye. | |
CH237130A (en) | Process for the production of a new azo dye. |