CH303911A - Process for the preparation of a disazo dye. - Google Patents
Process for the preparation of a disazo dye.Info
- Publication number
- CH303911A CH303911A CH303911DA CH303911A CH 303911 A CH303911 A CH 303911A CH 303911D A CH303911D A CH 303911DA CH 303911 A CH303911 A CH 303911A
- Authority
- CH
- Switzerland
- Prior art keywords
- disazo dye
- preparation
- oxy
- parts
- good
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 301446. Verfahren zur Herstellung eines Disazofarbstoffes. Gegenstand des vorliegenden Patentes ist ein Verfahren zur Herstellung eines Disazo- farbstoffes, welches darin besteht, dass man 2 -Hol der Diazov erbindung aus 2-Amino-l- oxy-4-nitrobenzol mit 1 Mol Fumarsäure-di- [5-oxy-7-sulfonaphthyl-(2)]-amid kuppelt.
Im naehfolgenden Beispiel bedeuten die Teile Gewichtsteile, und die Prozente sind in Gewichtsprozenten angegeben.
<I>Beispiel.:</I> 34 Teile 2-Amino-l-oxy-4-nitrobenzol (da- @on 3,2 Teile L?berschuss) werden diazotiert. Man giesst die Diazosuspension innerhalb von 2 Stunden zu einer Lösung von 55,8 Teilen Fumarsäure-di- [5 - oxy -7-sulfonaphthyl- (2) ] - amid in 2000 Teilen Wasser,
40 Teilen Na triumhydroxydlösung 30 /o ig und 120 Teilen Pyridin. Nach einiger Zeit scheidet das Kupp lungsprodukt in kristalliner Form aus. Er wird abfiltriert und getrocknet. Der neue Disazofarbstoff ist ein dunkles Pulver, das sich in konzentrierter Schwefel säure mit blauroter Farbe löst und Baumwolle und Fasern aus regenerierter Cellulose im Nachkupferungsverfahren in bordeauxroten Tönen von sehr guter Lichtechtheit und guter Waschechtheit färbt.
<B> Additional patent </B> to main patent no. 301446. Process for the production of a disazo dye. The subject of the present patent is a process for the preparation of a disazo dye, which consists in that 2 -hol of the Diazov compound from 2-amino-l-oxy-4-nitrobenzene with 1 mole of fumaric acid-di- [5-oxy- 7-sulfonaphthyl- (2)] - amide couples.
In the example below, the parts are parts by weight and the percentages are percentages by weight.
<I> Example: </I> 34 parts of 2-amino-1-oxy-4-nitrobenzene (3.2 parts of excess L) are diazotized. The diazo suspension is poured over the course of 2 hours into a solution of 55.8 parts of di- [5-oxy-7-sulfonaphthyl- (2)] amide in 2000 parts of water,
40 parts of sodium hydroxide solution 30% and 120 parts of pyridine. After a while, the coupling product separates out in crystalline form. It is filtered off and dried. The new disazo dye is a dark powder that dissolves in concentrated sulfuric acid with a blue-red color and dyes cotton and fibers made of regenerated cellulose in the post-coppering process in burgundy shades of very good lightfastness and good washfastness.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH303911T | 1952-01-17 | ||
CH301446T | 1952-01-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH303911A true CH303911A (en) | 1954-12-15 |
Family
ID=25734396
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH303911D CH303911A (en) | 1952-01-17 | 1952-01-17 | Process for the preparation of a disazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH303911A (en) |
-
1952
- 1952-01-17 CH CH303911D patent/CH303911A/en unknown
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