CH131257A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH131257A CH131257A CH131257DA CH131257A CH 131257 A CH131257 A CH 131257A CH 131257D A CH131257D A CH 131257DA CH 131257 A CH131257 A CH 131257A
- Authority
- CH
- Switzerland
- Prior art keywords
- blue
- production
- dye
- amino
- azo dye
- 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
- C09B33/00—Disazo and polyazo dyes of the types A->K<-B, A->B->K<-C, or the like, prepared by diazotising and coupling
- C09B33/02—Disazo dyes
- C09B33/08—Disazo dyes in which the coupling component is a hydroxy-amino compound
- C09B33/10—Disazo dyes in which the coupling component is a hydroxy-amino compound in which the coupling component is an amino naphthol
-
- 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
- C09B45/26—Disazo or polyazo compounds containing chromium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. <B>128006.</B> Verfahren zur Herstellung eines neuen Azolarbstoffes. Es wurde gefunden, dass man einen neuen wertvollen Farbstoff erhält, wenn man den o-Oxyazofarbstoff, welcher durch Vereinigen von 2 Mol. diazotiertem 5-Nitro- -#-amino-l-phenol mit<B>1</B> Mol. des Harnstoffes der2-Amino-5-oxynaphtalin-7-sulfoeureent-- steht, mit Chrom abgebenden Mitteln be handelt.
Der neue Farbstoff stellt ein blau graues Pulver dar, löst sieh in Wasser und I in verdünnten Alkalien mit blauer, in kon zentrierter Schwefelsäure mit blauvioletter Farbe auf und färbt Baumwolle aus neu tralem Glaubersalzbade in blauen Tönen mit U ten Eehtheitseigenschaften.
<I>Beispiel:</I> Die 2 Mol. entsprechende Menge von diazc.- tiertem 5-Nitro-2-amino-l-phenol wird mit <B>1</B> Mol. des Harnstoffes der 2-Amino-5-cxy- naphtalin-7-sulfosä,ure wie üblich vereinigt. Der gebildete Farbstoff wird in<B>8000</B> Teilen Wasser gelöst, mit Chromfluoridlösung, die <B>30</B> Teile Cr203 enthält, versetzt, liierauf36 Stunden unter Ersatz des verdampfenden Wassers gekocht, ausgesalzen und getrock net.
Additional patent to main patent no. <B> 128006. </B> Process for the production of a new azo substance. It has been found that a new valuable dye is obtained if the o-oxyazo dye, which is obtained by combining 2 moles of diazotized 5-nitro- - # - amino-1-phenol with 1 mole. of urea der2-amino-5-oxynaphthalene-7-sulfoeureent-- is treated with chromium-releasing agents.
The new dye is a blue-gray powder, dissolves in water and I in dilute alkalis with blue, in concentrated sulfuric acid with blue-violet color and dyes cotton from neutral Glauber's salt bath in blue tones with U ten integrity properties.
<I> Example: </I> The 2 mol. Corresponding amount of diacetated 5-nitro-2-amino-1-phenol is mixed with <B> 1 </B> mol. Of the urea of the 2-amino- 5-cxynaphthalene-7-sulphonic acid combined as usual. The dye formed is dissolved in 8000 parts of water, mixed with chromium fluoride solution containing 30 parts of Cr203, boiled for 36 hours, replacing the evaporating water, salted out and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH131257T | 1927-04-23 | ||
CH128006T | 1927-08-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH131257A true CH131257A (en) | 1929-01-31 |
Family
ID=25711018
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH131257D CH131257A (en) | 1927-04-23 | 1927-04-23 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH131257A (en) |
-
1927
- 1927-04-23 CH CH131257D patent/CH131257A/en unknown
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