CH224128A - Process for the preparation of a primary disazo dye. - Google Patents
Process for the preparation of a primary disazo dye.Info
- Publication number
- CH224128A CH224128A CH224128DA CH224128A CH 224128 A CH224128 A CH 224128A CH 224128D A CH224128D A CH 224128DA CH 224128 A CH224128 A CH 224128A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- blue
- preparation
- amino
- diazo
- 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
Zusatzpatent zum Hauptpatent Nr. 221927. 'Verfahren zur Herstellung eines primären Bisazofarbstoffes. Vorliegendes Patent bezieht sich auf ein Verfahren zur Herstellung eines primären Disazofarbstoffes, dadurch gekennzeichnet, dass man .die Diazoverbindung von 1-Amino- 2 -chlor- 6 -nitrobenzol in saurem Medium mit 1-Ami,no-8-oxynaphthalin-3,6-disulfon- säure und den so .erhaltenen Mon:
oazofarb- stoff in alkalischem Medium mit .der Diazo- verbindung aus 1-Amino - 4 - N - eyolohexyl- eaprinyl-aminobenzol vereinigt.
Der so erhaltene Disazofarbstoff ist ein dunkles Pulver, das sich in Wasser mit blauer, in konzentrierter Schwefelsäure mit blaugrüner Farbe löst, und färbt Wolle, Seide und künstliche Fasern auf Caseinbasis in blauschwarzen Tönen. Die Färbungen be sitzen sehr ;gute Wasch-, Walk-, Schweiss-, Seewasser- und Lichtechtheit.
<I>Beispiel:</I> <B>1,8</B> Teile 1-Amino - 2 -chlor -16 -,nitrobenzol werden qdurch Eintragen in eine Mischung aus etwa 40 Teilen :Schwefelsäure 94%ig und '29 Teilen Nitrosyls.chwefelsäure 45%ig bei<B>5-10'</B> diazotiert. Die Lösung wird auf Eis ,gegossen.
Nach Entfernung der über schüssigen salpeterigen,Säure und Filtrieren lässt man. die so erhaltene Diazolüsung in eine mineralsaure Lösung von 81,9 Teilen 1- Amino-@8-oxynap,hthalin-3;6 :
disu,Ifons5,urelau- fen. Nachbeendeter Bildung .des Monoazo- farbstoffes wird dieser abgeschieden und mit überschüssigem Natriumcarbonot wieder in Lösung .gebracht. In diese Lösung lässt man eine aus 34,4 Teilen 1-Amilno-4-N-cyclo- hexyl-,caprinyl-aminobenzol hergestellte Di- azolösung fliessen.
Der Disazofarbstoff wird abgeschieden, gewaschen und getrocknet.
Additional patent to main patent No. 221927. Process for the preparation of a primary bisazo dye. The present patent relates to a process for the preparation of a primary disazo dye, characterized in that the diazo compound of 1-amino-2-chloro-6-nitrobenzene in an acidic medium with 1-ami, no-8-oxynaphthalene-3,6 -disulfonic acid and the mon:
oazo dye combined in an alkaline medium with the diazo compound of 1-amino-4-N-eyolohexyl-eaprinyl-aminobenzene.
The disazo dye thus obtained is a dark powder which dissolves in water with a blue color and in concentrated sulfuric acid with a blue-green color, and dyes wool, silk and artificial fibers based on casein in blue-black shades. The dyeings are very good; good fastness to washing, fulling, perspiration, sea water and light.
<I> Example: </I> <B> 1.8 </B> parts of 1-amino - 2-chloro -16 -, nitrobenzene are q by adding to a mixture of about 40 parts: sulfuric acid 94% and '29 Share nitrosylsulfuric acid 45% diazotized at <B> 5-10 '</B>. The solution is poured onto ice.
After removing the excess nitric acid, and filtering, it is left. the diazo solution thus obtained in a mineral acid solution of 81.9 parts of 1- Amino- @ 8-oxynap, hthalin-3; 6:
disu, ifons5, run across. When the formation of the monoazo dye has ended, it is deposited and brought back into solution with excess sodium carbonate. A diazole solution prepared from 34.4 parts of 1-amino-4-N-cyclohexyl-, caprinyl-aminobenzene is allowed to flow into this solution.
The disazo dye is deposited, washed and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE224128X | 1940-09-07 | ||
CH221927T | 1941-07-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH224128A true CH224128A (en) | 1942-10-31 |
Family
ID=25726570
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH224128D CH224128A (en) | 1940-09-07 | 1941-07-18 | Process for the preparation of a primary disazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH224128A (en) |
-
1941
- 1941-07-18 CH CH224128D patent/CH224128A/en unknown
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