CH160672A - Process for the preparation of a water-insoluble azo dye. - Google Patents

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

Info

Publication number
CH160672A
CH160672A CH160672DA CH160672A CH 160672 A CH160672 A CH 160672A CH 160672D A CH160672D A CH 160672DA CH 160672 A CH160672 A CH 160672A
Authority
CH
Switzerland
Prior art keywords
water
preparation
azo dye
insoluble azo
dye
Prior art date
Application number
Other languages
German (de)
Inventor
Aktiengesellsc Farbenindustrie
Original Assignee
Ig Farbenindustrie 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
Application filed by Ig Farbenindustrie Ag filed Critical Ig Farbenindustrie Ag
Publication of CH160672A publication Critical patent/CH160672A/en

Links

Landscapes

  • Coloring (AREA)

Description

  

  Verfahren zur Darstellung eines     wasseruDiöslichen        Azofarbstoffes.       Gegenstand dieses Zusatzpatentes ist ein  Verfahren zur     Darstelluno-    eines     wa,sser-          unlöslichen        Azofarbstoffes,    das dadurch ge  kennzeichnet ist,     dass    man die     Diazoverbin-          dung    von     m-Chloranilin    mit     Terephtaloyl-          bis   <B>-</B>     essigsäure   <B>- 1 -</B>     amino   <B>- 3,

   -</B>     ühlor   <B>-</B> 4<B>.</B>     6-          diin,-thoxybenzol    kuppelt. Die, Einwirkung  der beiden Komponenten aufeinander kann  auch in Gegenwart eines Substrates erfolgen.  



  Der in Substanz hergestellte Farbstoff  bildet ein gelbes Pulver; die Färbungen be  sitzen einen lebhaften gelben Farbton und  sind sehr     cut    lichtecht.  



  <I>Beispiel:</I>  <B>58,9</B>     gr        Terephtaloyl   <B>-</B> bis<B>-</B>     essigsäure   <B>-</B>     1-          amino   <B>- 3 -</B>     ehlor   <B>-</B> 4<B>. 6 -</B>     dimathcxybenzol     werden in<B>100</B> cm' doppelt normaler -Natron  lauge und Wasser heiss gelöst.

   Diese Lösung       lä,uft    zu einer wie folgt bereiteten     D#iazo-          lösung:   <B>25,6</B>     gr        m-Chlo#ranilin    werden mit  <B>52</B> cm' Salzsäure von 22' B6 und 14,4     gr          Natriumnitrit    unter Eiszusatz wie     üblieh          diazotiert    und mit     Natriumacetat    auf     Konoo-          neutralität    abgestumpft.

      Die     Farbstoffbildung    ist nach     mehrst-au-          di-em        Nachrühren    beendet. Man saugt ab,  wäscht gut mit Wasser und trocknet.  



  Man erhält ein gelbes Pulver. Die     Dar-          stellun,g    des Farbstoffes kann auch in Gegen  wart eines Substrates erfolgen. Wird der  Farbstoff auf der Faser erzeugt, so erhält  man einen sehr lichtechten, lebhaften gelben  Farbton.



  Process for the preparation of a water-soluble azo dye. The subject of this additional patent is a process for the preparation of a water-insoluble azo dye, which is characterized in that the diazo compound of m-chloroaniline with terephtaloyl- to <B> - </B> acetic acid <B> - 1 - </B> amino <B> - 3,

   - </B> ühlor <B> - </B> 4 <B>. </B> 6- diine, -thoxybenzene couples. The action of the two components on one another can also take place in the presence of a substrate.



  The dye produced in substance forms a yellow powder; the colors have a lively yellow shade and are very lightfast.



  <I> Example: </I> <B> 58.9 </B> gr terephtaloyl <B> - </B> to <B> - </B> acetic acid <B> - </B> 1- amino <B> - 3 - </B> ehlor <B> - </B> 4 <B>. 6 - </B> dimethylbenzene are dissolved in <B> 100 </B> cm 'double normal caustic soda and hot water.

   This solution leads to a diazo solution prepared as follows: <B> 25.6 </B> gr m-chloraniline are mixed with <B> 52 </B> cm 'hydrochloric acid of 22' B6 and 14.4 g sodium nitrite with the addition of ice, diazotized as usual and blunted with sodium acetate to neutrality.

      The formation of the dyestuff has ended after several additional stirring times. It is suctioned off, washed well with water and dried.



  A yellow powder is obtained. The presentation of the dye can also take place in the presence of a substrate. If the dye is produced on the fiber, a very lightfast, vivid yellow color is obtained.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Darstellung eines wasser unlöslichen Azofarbstoffes, dadurch gekenn zeichnet, dass man die Diazoverbindung von m-Chleranilin mit Terephtaloyl <B>-</B> bis<B>-</B> essig- sä,ure <B>- 1 -</B> amino <B>- 3 -</B> chlor <B>-</B> 4.<B>6 -</B> dimeth- oxybenzol kuppelt. Der in Substanz hergestellte Farbstoff bildet ein gelbes Pulver; die Färbungen be sitzen einen lebhaften, gelben Farbton und sind sehr out lichtecht. <B>C</B> PATENT CLAIM: Process for the preparation of a water-insoluble azo dye, characterized in that the diazo compound of m-chloraniline with terephtaloyl <B> - </B> to <B> - </B> acetic acid, ure <B> - 1 - </B> amino <B> - 3 - </B> chlorine <B> - </B> 4. <B> 6 - </B> dimethoxybenzene couples. The dye produced in substance forms a yellow powder; the colors have a lively, yellow hue and are very lightfast. <B> C </B>
CH160672D 1930-09-09 1931-05-07 Process for the preparation of a water-insoluble azo dye. CH160672A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE160672X 1930-09-09
CH153828T 1931-05-07

Publications (1)

Publication Number Publication Date
CH160672A true CH160672A (en) 1933-03-15

Family

ID=25716321

Family Applications (1)

Application Number Title Priority Date Filing Date
CH160672D CH160672A (en) 1930-09-09 1931-05-07 Process for the preparation of a water-insoluble azo dye.

Country Status (1)

Country Link
CH (1) CH160672A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2492907A (en) * 1946-03-27 1949-12-27 Gen Aniline & Film Corp Azo dyes

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2492907A (en) * 1946-03-27 1949-12-27 Gen Aniline & Film Corp Azo dyes

Similar Documents

Publication Publication Date Title
CH160672A (en) Process for the preparation of a water-insoluble azo dye.
CH157528A (en) Process for the preparation of a water-insoluble azo dye.
CH157544A (en) Process for the preparation of a water-insoluble azo dye.
CH157555A (en) Process for the preparation of a water-insoluble azo dye.
CH160673A (en) Process for the preparation of a water-insoluble azo dye.
CH157530A (en) Process for the preparation of a water-insoluble azo dye.
CH157553A (en) Process for the preparation of a water-insoluble azo dye.
CH157533A (en) Process for the preparation of a water-insoluble azo dye.
CH160671A (en) Process for the preparation of a water-insoluble azo dye.
CH157552A (en) Process for the preparation of a water-insoluble azo dye.
CH157531A (en) Process for the preparation of a water-insoluble azo dye.
CH160670A (en) Process for the preparation of a water-insoluble azo dye.
CH157557A (en) Process for the preparation of a water-insoluble azo dye.
CH157547A (en) Process for the preparation of a water-insoluble azo dye.
CH154709A (en) Process for the preparation of a water-insoluble azo dye.
CH154715A (en) Process for the preparation of a water-insoluble azo dye.
CH154711A (en) Process for the preparation of a water-insoluble azo dye.
CH154710A (en) Process for the preparation of a water-insoluble azo dye.
CH157532A (en) Process for the preparation of a water-insoluble azo dye.
CH157556A (en) Process for the preparation of a water-insoluble azo dye.
CH157551A (en) Process for the preparation of a water-insoluble azo dye.
CH157543A (en) Process for the preparation of a water-insoluble azo dye.
CH157554A (en) Process for the preparation of a water-insoluble azo dye.
CH157538A (en) Process for the preparation of a water-insoluble azo dye.
CH154713A (en) Process for the preparation of a water-insoluble azo dye.