CH246186A - Process for the production of a metallizable polyazo dye. - Google Patents
Process for the production of a metallizable polyazo dye.Info
- Publication number
- CH246186A CH246186A CH246186DA CH246186A CH 246186 A CH246186 A CH 246186A CH 246186D A CH246186D A CH 246186DA CH 246186 A CH246186 A CH 246186A
- Authority
- CH
- Switzerland
- Prior art keywords
- mole
- dye
- mol
- acid
- production
- 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
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
- C09B35/38—Trisazo dyes ot the type
- C09B35/40—Trisazo dyes ot the type the component K being a dihydroxy or polyhydroxy compound
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 242845. Verfahren zur Herstellung eines metallisierbaren Polyazofarbatoffes. Das vorliegende Patent betrifft ein Ver fahren zur Herstellung eines braunen Poly- azofarbstoffes und ist dadurch gekennzeich net, dass man 1 Mol Resorcin, 1 Mol der Ver bindung,
erhältlich durch Verseifen und Diazotieren des Farbstoffes aus 1 Mol diazo- tierter Sulfauilsäure und 1 Mol 1-Acetamino- 2-oxybenzol und 1 Mol der aus 1 Mol tetrazo- tiertem 4,4'-Diaminobenzanilid und 1 Mol Salicylsäure erhältlichen Zwischenverbindung aufeinander einwirken lässt.
<I>Beispiel:</I> 17,3 g Sulfanilsäure werden wie üblich diazotiert und mit einer Lösung von 15,1 g 1-Acetamino-2-oxybenzol, 13,3 .g 30%iger Natronlauge und Wasser in Gegenwart von Soda gekuppelt. Der Farbstoff wird durch Salzsäure abgeschieden. Er wird durch Er wärmen mit verdünnter Schwefelsäure ver seift. Das Verseifungsprodukt wird filtriert und mit Wasser gewaschen. Es besitzt mut masslich die Formel
EMI0001.0031
Zur Weiterdiazotierung wird der Monoazo- farbstoff in Wasser und Natronlauge gelöst.
Man gibt eine Lösung von 7 g Natriumnitrit zu und lässt die Lösung unter Kühlung und gutem Rühren in Salzsäure einfliessen. Nach beendeter Diazotierung kuppelt man mit einer Lösung von 11 g Resorcin und Wasser in Gegenwart von Soda. Der @isazofarbstoff wird mit Salzsäure abgeschieden und fil triert. Er wird in Wasser und Soda gelöst und mit der in üblicher Weise hergestellten Zwischenverbindung aus 22,7 g 4,4'-Diamino- benzanilid und 13,8 g Salicylsäure in Gegen wart von Soda gekuppelt.
Der Tetrakisazo- farbstoff wird in der Wärme unter Zusatz von Kochsalz abgeschieden, filtriert und ge trocknet.
Der neue Farbstoff stellt ein dunkles Pulver dar, das Baumwolle und regenerierte Cellulose in orangebraunen Tönen färbt. Mit Kupfersulfat nachbehandelt, werden die Fär bungen in der Wasch-, Licht-, Säure- und Alkaliechtheit erheblich verbessert.
Additional patent to main patent no. 242845. Process for the production of a metallizable polyazo-carbate. The present patent relates to a process for the production of a brown poly azo dye and is characterized in that 1 mole of resorcinol, 1 mole of the compound,
obtainable by saponifying and diazotizing the dye from 1 mole of diazotized sulfauilic acid and 1 mole of 1-acetamino-2-oxybenzene and 1 mole of the intermediate compound obtainable from 1 mole of tetrazotized 4,4'-diaminobenzanilide and 1 mole of salicylic acid.
<I> Example: </I> 17.3 g of sulfanilic acid are diazotized as usual and with a solution of 15.1 g of 1-acetamino-2-oxybenzene, 13.3 g of 30% sodium hydroxide solution and water in the presence of soda coupled. The dye is deposited by hydrochloric acid. It is soaped by warming it with dilute sulfuric acid. The saponification product is filtered and washed with water. It presumably has the formula
EMI0001.0031
For further diazotization, the monoazo dye is dissolved in water and sodium hydroxide solution.
A solution of 7 g of sodium nitrite is added and the solution is allowed to flow into hydrochloric acid while cooling and stirring well. When the diazotization is complete, coupling is carried out with a solution of 11 g of resorcinol and water in the presence of soda. The @isazo dye is deposited with hydrochloric acid and filtered. It is dissolved in water and soda and coupled with the intermediate compound prepared in the usual manner from 22.7 g of 4,4'-diamino benzanilide and 13.8 g of salicylic acid in the presence of soda.
The tetrakisazo dye is deposited in the warm with the addition of common salt, filtered and dried.
The new dye is a dark powder that dyes cotton and regenerated cellulose in orange-brown tones. Post-treated with copper sulphate, the colors are considerably improved in terms of washing, light, acid and alkali fastness.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH242845T | 1945-04-16 | ||
CH246186T | 1945-04-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH246186A true CH246186A (en) | 1946-12-15 |
Family
ID=25728762
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH246186D CH246186A (en) | 1945-04-16 | 1945-04-16 | Process for the production of a metallizable polyazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH246186A (en) |
-
1945
- 1945-04-16 CH CH246186D patent/CH246186A/en unknown
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