CH190326A - Process for the preparation of an azo dye. - Google Patents

Process for the preparation of an azo dye.

Info

Publication number
CH190326A
CH190326A CH190326DA CH190326A CH 190326 A CH190326 A CH 190326A CH 190326D A CH190326D A CH 190326DA CH 190326 A CH190326 A CH 190326A
Authority
CH
Switzerland
Prior art keywords
azo dye
brown
red
preparation
varnishes
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 CH190326A publication Critical patent/CH190326A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/06Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
    • C09B29/08Amino benzenes
    • C09B29/0805Amino benzenes free of acid groups
    • C09B29/0807Amino benzenes free of acid groups characterised by the amino group
    • C09B29/0809Amino benzenes free of acid groups characterised by the amino group substituted amino group
    • C09B29/0811Amino benzenes free of acid groups characterised by the amino group substituted amino group further substituted alkylamino, alkenylamino, alkynylamino, cycloalkylamino aralkylamino or arylamino
    • C09B29/0823Amino benzenes free of acid groups characterised by the amino group substituted amino group further substituted alkylamino, alkenylamino, alkynylamino, cycloalkylamino aralkylamino or arylamino substituted by CN
    • C09B29/0826Amino benzenes free of acid groups characterised by the amino group substituted amino group further substituted alkylamino, alkenylamino, alkynylamino, cycloalkylamino aralkylamino or arylamino substituted by CN having N(-alkenylene/-alkynylene-O)(-alkenylene/-alkynylene-CN)
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/06Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
    • C09B29/08Amino benzenes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Description

  

      Zusatzpatent    zum Hauptpatent Nr. 188027.    Verfahren zur Herstellung eines     Azofarbstoffes.       Gegenstand des Hauptpatentes ist ein  Verfahren zur Herstellung eines neuen     Azo-          farbstoffes    durch Kuppeln der     Diazoverbin-          dung    von     1-Amino-4-nitrobenzol    mit     (N-Ox-          äthyl-N-[3-inethyl-phenyl]        )-ss-aminopropion-          säurenitril.     



  Es wurde nun gefunden, dass man einen  ähnlichen, wertvollen     Azofarbstoff    erhält,  wenn man die     Diazoverbindung    von     1-Amino-          2,6-dichlor-4-nitrobenzol    mit     (N-Oxäthyl-N-          [3    -     methyl    -     phenyl])        -ss    -     aminopropionsäure        -          nitril    kuppelt.  



  Der neue     Azofarbstoff    eignet sich vor  züglich zum Färben von     Zelluloseestern    und       -äthern,    die er in kräftig rotbraunen Tönen  färbt, ferner zur Herstellung gefärbter Fir  nisse. Spiritus- oder     Nitrozelluloselacke,    die  damit rotbraune Überzüge geben; Stearin.  Paraffin, Fette und Öle werden rotbraun ge  färbt.  



  <I>Beispiel:</I>  207 Teile     1-Amino-2,6-dichlor-4-nitroben-          zol    werden     diazotiert    und mit 214 Teilen         (N-Oxäthyl-N-[3-methyl-phenyl])        -ss-amino-          propionsäurenitril,    gelöst in 250 Teilen kon  zentrierter Salzsäure und 1000 Teilen Was  ser, gekuppelt. Die Kupplung ist nach kur  zer Zeit beendet. Der Farbstoff wird abge  saugt, säurefrei gewaschen und getrocknet.



      Additional patent to main patent No. 188027. Process for the production of an azo dye. The subject of the main patent is a process for the preparation of a new azo dye by coupling the diazo compound of 1-amino-4-nitrobenzene with (N-oxethyl-N- [3-ynethyl-phenyl]) -ss-aminopropion- acid nitrile.



  It has now been found that a similar, valuable azo dye is obtained if the diazo compound of 1-amino-2,6-dichloro-4-nitrobenzene is used with (N-oxethyl-N- [3-methyl-phenyl]) -ss - aminopropionic acid - nitrile couples.



  The new azo dye is particularly suitable for dyeing cellulose esters and ethers, which it dyes in strong red-brown tones, and also for producing colored varnishes. Spirit or nitrocellulose lacquers that give them red-brown coatings; Stearin. Paraffin, fats and oils are colored red-brown.



  <I> Example: </I> 207 parts of 1-amino-2,6-dichloro-4-nitrobenzene are diazotized and mixed with 214 parts of (N-oxethyl-N- [3-methyl-phenyl]) -ss- aminopropiononitrile, dissolved in 250 parts of concentrated hydrochloric acid and 1000 parts of water, coupled. The coupling ends after a short time. The dye is filtered off with suction, washed acid-free and dried.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines Azofarb- stoffes, dadurch gekennzeichnet, dass man die Diazoverbindung von 1-Amino-2,6-dichlor-4- nitrobenzol mit (N-Oxäthyl-N- [3-methyl- phenyl])-ss-aminopropionsäurenitril kuppelt. PATENT CLAIM: Process for the production of an azo dye, characterized in that the diazo compound of 1-amino-2,6-dichloro-4-nitrobenzene with (N-oxethyl-N- [3-methyl-phenyl]) - ss- aminopropionitrile couples. Der neue Azofarbstoff eignet sich vorzüg lich zum Färben von Zelluloseestern und -äthern, die er in kräftig rotbraunen Tönen färbt, ferner zur Herstellung gefärbter Fir nisse, Spiritus- oder Nitrozelluloselacke, die damit rotbraune Überzüge geben; Stearin, Paraffin, Fette und Öle werden rotbraun gefärbt. The new azo dye is especially suitable for dyeing cellulose esters and ethers, which it dyes in strong red-brown tones, and also for producing colored varnishes, spirit or nitrocellulose varnishes, which give them red-brown coatings; Stearin, paraffin, fats and oils are colored red-brown.
CH190326D 1935-12-05 1935-12-05 Process for the preparation of an azo dye. CH190326A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH188027T 1935-12-05
CH190326T 1935-12-05

Publications (1)

Publication Number Publication Date
CH190326A true CH190326A (en) 1937-04-15

Family

ID=25721605

Family Applications (1)

Application Number Title Priority Date Filing Date
CH190326D CH190326A (en) 1935-12-05 1935-12-05 Process for the preparation of an azo dye.

Country Status (1)

Country Link
CH (1) CH190326A (en)

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