CH123736A - Process for the preparation of an azo dye. - Google Patents

Process for the preparation of an azo dye.

Info

Publication number
CH123736A
CH123736A CH123736DA CH123736A CH 123736 A CH123736 A CH 123736A CH 123736D A CH123736D A CH 123736DA CH 123736 A CH123736 A CH 123736A
Authority
CH
Switzerland
Prior art keywords
azo dye
preparation
dye
cresidine
nitroaniline
Prior art date
Application number
Other languages
German (de)
Inventor
Gesellschaft Fuer Chemis Basel
Original Assignee
Chem Ind Basel
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 Chem Ind Basel filed Critical Chem Ind Basel
Publication of CH123736A publication Critical patent/CH123736A/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
    • 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
    • C09B29/081Amino benzenes free of acid groups characterised by the amino group substituted amino group unsubstituted alkylamino, alkenylamino, alkynylamino, cycloalkylamino, aralkylamino or arylamino

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

Description

  

  Verfahren zur Herstellung eines     Azofarbstoffes.       Es wurde gefunden, dass man einen neuen       Azofarbstoff    erhält, wenn man     diazotiertes          o-Nitranilin    mit     Kresidin        (CHa    :     OCHa    :     NH2     1 :4: 3) kuppelt. Der Farbstoff bildet ein  gelbes Pulver; er färbt Gebilde aus     Zellu-          loseestern    und     -äthern,    wie zum Beispiel die       Acetatseide,    in echten, gelben Tönen, welche  den überraschenden Vorzug haben, nicht       phototrop    zu sein.

      <I>Beispiel</I>    In die durch     Diazotieren    von 138 Teilen       o-Nitranilin    erhaltene     Diazolösung    wird unter  Rühren eine wässerige Lösung des     Chlor-          hydrates    aus 137 Teilen     Kresidin        (C13s          OCHs    :     NHs    :1: 4 : 3) eingetragen. Dieses Ge  misch wird unter Kühlung tropfenweise mit  einer wässerigen Lösung von 365 Teilen Na-         triumacetat    versetzt. Der gebildete     Farbstoff     fällt sofort aus.

   Wenn keine     Diazoverbindung     mehr nachweisbar ist, wird mit     Sodalösung     neutral gestellt und filtriert.



  Process for the preparation of an azo dye. It has been found that a new azo dye is obtained when diazotized o-nitroaniline is coupled with cresidine (CHa: OCHa: NH2 1: 4: 3). The dye forms a yellow powder; he colors structures made from cellulose esters and ethers, such as acetate silk, in genuine yellow tones, which have the surprising advantage of not being phototropic.

      <I> Example </I> An aqueous solution of the chlorohydrate of 137 parts of cresidine (C13s OCHs: NHs: 1: 4: 3) is introduced into the diazo solution obtained by diazotizing 138 parts of o-nitroaniline. An aqueous solution of 365 parts of sodium acetate is added dropwise to this mixture while cooling. The dye formed precipitates immediately.

   If no more diazo compound can be detected, it is made neutral with soda solution and filtered.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines Azofarb- stoffes, dadurch gekennzeichnet, dass man diazotiertes o-Nitranilin mit Kresidin (CHs OCHS : NH.2 : 1 : 4 : 3) kuppelt. Der Farbstoff bildet ein gelbes Pulver; er färbt Gebilde aus Celluloseestern und -äthern, wie zum Beispiel die Acetatseide, in echten, gelben Tönen, w=elche den überraschenden Vorzug haben, nicht phototrop zu sein. PATENT CLAIM: Process for the production of an azo dye, characterized in that diazotized o-nitroaniline is coupled with cresidine (CHs OCHS: NH.2: 1: 4: 3). The dye forms a yellow powder; he colors structures made from cellulose esters and ethers, such as acetate silk, in genuine yellow tones, which have the surprising advantage of not being phototropic.
CH123736D 1926-10-02 1926-10-02 Process for the preparation of an azo dye. CH123736A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH123736T 1926-10-02

Publications (1)

Publication Number Publication Date
CH123736A true CH123736A (en) 1927-12-16

Family

ID=4382390

Family Applications (1)

Application Number Title Priority Date Filing Date
CH123736D CH123736A (en) 1926-10-02 1926-10-02 Process for the preparation of an azo dye.

Country Status (1)

Country Link
CH (1) CH123736A (en)

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