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AT39956B - Process for the preparation of a water-insoluble monoazo dye. - Google Patents

Process for the preparation of a water-insoluble monoazo dye.

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Publication number
AT39956B
AT39956B AT39956DA AT39956B AT 39956 B AT39956 B AT 39956B AT 39956D A AT39956D A AT 39956DA AT 39956 B AT39956 B AT 39956B
Authority
AT
Austria
Prior art keywords
water
preparation
monoazo dye
insoluble monoazo
dye
Prior art date
Application number
Other languages
German (de)
Original Assignee
Basf Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from DE1906200263D external-priority patent/DE200263C/de
Application filed by Basf Ag filed Critical Basf Ag
Application granted granted Critical
Publication of AT39956B publication Critical patent/AT39956B/en

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Description

  

   <Desc/Clms Page number 1> 
 



  Verfahren zur Darstellung eines   wasserunlöslichen     Monoazofarbstoffs.   



   Es hat sich gezeigt, dass die Diazoverbindung des praktisch bisher noch nicht angewandten 2-Nitro-4-cbloranilins beim Kombinieren mit 8-Naphtol einen leuchtend orangefarbenen Farbstoff liefert, welcher infolge seiner Wasserunlöslichkeit, seiner ganz hervor- 
 EMI1.1 
   Kalkechtbeit   der mannigfachsten vorteilhaftesten Anwendungen fähig ist. Man kann den Farbstoff erzeugen, indem man die Diazoverbindung des 2-itro-4-chloranilins mit einer Lösung   von -Naphtolnatrium   kombiniert, die zweckmässig mit   Türkischrotöl,   Ölsäure, Seife und ähnlich wirkenden Mitteln versetzt worden ist. 



   Zur Herstellung von   Pigmentfarben   mittels dieses Farbstoffs kann entweder schon die Kupplung bei Gegenwart eines der bekannten Substrate der Lackfal) rikation (Tonerde- 
 EMI1.2 
 träglich mit Substraten vermischt (angeteigt oder trocken vermahlen) werden. Zur Erzeugung der Farbstoffe auf der Faser verfährt man in der üblichen Weise. 



   Beispiel :
34,5 Teile   2-Nitro-4-rhloranilin   werden in üblicher Weise diazotiert und die (eventuell filtrierte) Diazolösung unter gutem Rühren einlaufen gelassen in eine Lösung von 29 Teilen 
 EMI1.3 
 Wasser, der   260   Teile einer 25prozentigen Lösung von kristallisiertem Natriumacetat beigegeben sind. 



   Die Kombination verläuft sehr rasch. Der ausgeschiedene Azofarbstoff wird abfiltriert und leicht abgepresst. 



   In ganz analoger Weise verfährt man bei Erzeugung des Farbstoffs in Gegenwart von Substrat, wobei man das letztere mit dem   -Naphtol und eventucU   mit Türkischrotöl usw. vor dem Zusetzen der Diazolösung mischen kann. 

**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.



   <Desc / Clms Page number 1>
 



  Process for the preparation of a water-insoluble monoazo dye.



   It has been shown that the diazo compound of 2-nitro-4-cbloraniline, which has not yet been used in practice, when combined with 8-naphthol, produces a bright orange dye which, due to its insolubility in water, its very prominent
 EMI1.1
   Lime real work is capable of the most varied of advantageous applications. The dye can be produced by combining the diazo compound of 2-itro-4-chloroaniline with a solution of sodium naphthol to which Turkish red oil, oleic acid, soap and similar agents have been added.



   For the production of pigment colors by means of this dye, either the coupling in the presence of one of the known substrates of the lacquer application (alumina
 EMI1.2
 mixed with substrates (made into a paste or dry-ground). The usual procedure is used to produce the dyes on the fiber.



   Example:
34.5 parts of 2-nitro-4-chloroaniline are diazotized in the usual manner and the (possibly filtered) diazo solution is allowed to run into a solution of 29 parts with thorough stirring
 EMI1.3
 Water to which 260 parts of a 25 percent solution of crystallized sodium acetate are added.



   The combination is very quick. The precipitated azo dye is filtered off and gently squeezed out.



   The procedure for producing the dye in the presence of substrate is quite analogous, the latter being able to be mixed with the -naphtol and possibly with Turkish red oil etc. before the addition of the diazo solution.

** WARNING ** End of DESC field may overlap beginning of CLMS **.

 

Claims (1)

PATENT-ANSPRUCH : Verfahren zur Darstellung eines wasserunlöslichen Monoazofarbstoffs, dadurch gekennzeichnet, dass man die Diazoverbindung des 2-Nitro-4-chloranilins mit ss-Naphtol bei Gegenwart eines Substrats oder ohne ein solches, in beiden Fällen mit oder ohne Zugabe von Türkischrotöl, Ölsäure, Seife und ähnlich wirkenden Mitteln kombiniert. **WARNUNG** Ende CLMS Feld Kannt Anfang DESC uberlappen**. PATENT CLAIM: Process for the preparation of a water-insoluble monoazo dye, characterized in that the diazo compound of 2-nitro-4-chloroaniline with s-naphtol in the presence of a substrate or without such, in both cases with or without the addition of Turkish red oil, oleic acid, soap and the like acting means combined. ** WARNING ** End of CLMS field may overlap beginning of DESC **.
AT39956D 1906-05-21 1908-06-01 Process for the preparation of a water-insoluble monoazo dye. AT39956B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE1906200263D DE200263C (en) 1906-05-21

Publications (1)

Publication Number Publication Date
AT39956B true AT39956B (en) 1909-12-10

Family

ID=5760165

Family Applications (1)

Application Number Title Priority Date Filing Date
AT39956D AT39956B (en) 1906-05-21 1908-06-01 Process for the preparation of a water-insoluble monoazo dye.

Country Status (1)

Country Link
AT (1) AT39956B (en)

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