CH193343A - Process for the preparation of an azo dye. - Google Patents

Process for the preparation of an azo dye.

Info

Publication number
CH193343A
CH193343A CH193343DA CH193343A CH 193343 A CH193343 A CH 193343A CH 193343D A CH193343D A CH 193343DA CH 193343 A CH193343 A CH 193343A
Authority
CH
Switzerland
Prior art keywords
dye
azo dye
blue
preparation
formula
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 CH193343A publication Critical patent/CH193343A/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
    • C09B43/00Preparation of azo dyes from other azo compounds
    • C09B43/08Preparation of azo dyes from other azo compounds by reduction

Landscapes

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

Description

  

  Verfahren zur Herstellung eines     Azofarbstoffes.       Es wurde     gefunden,        dass    ein     Polyazofarbstoff        hergestellt    werden kann,     wenn    man auf  den     Azofarbstoff,der        Formel     
EMI0001.0009     
    alkalische reduzierende     Mittel        bis    zur     Ver-          kettung    zweier     Azofarbstoffmoleküle    durch  die bei der Reduktion der     Nitrogruppen    ent  stehende     Stiekstoffbrückeeinwirken    lässt.

    



  Der Farbstoff     stellt    in trockenem     Zu-          stande        ein        dunkles        Pulver    dar, das :sich in       verdünnter        Sodalösung,    sowie in     konzentrier-          ter    Schwefelsäure mit blauer Farbe löst und  Baumwolle aus     glaubersalzhaltigem    Bade     in     blaugrauen Tönen färbt, die beim Nach  kupfern in ein     eehtes    Grünblau     übergehen.     



  Als reduzierende Mittel, die     in    alka  lischem Medium     (z.    B.     Natronlauge    oder       Kalilauge)    verwendet werden,     kommen    bei-         spielsweise    Glukose, Schwefelalkalien oder       Stannit    in     Betracht.     



  <I>Beispiel:</I>       Man        diazotiert    1,7 Teile     5-Nitro-29-amino-          1-ogybenzol        und    kuppelt auf     übliche        Weise     mit 4,1 Teilen :des     Imidazols    der     Formel     
EMI0001.0048     
      Der abgeschiedene Farbstoff wird     unter    Zu  satz von 11,8 Teilen 80     %        iger    Natronlauge in  80 Teilen Wasser bei 60   gelöst.

   Hierauf  gibt man 1, 6 Teile Traubenzucker     als    10     %        ige     Lösung hinzu und rührt     während    etwa.     einer     Stunde bei 55 bis<B>60'.</B>     Durch    Zurückstellen  mit Säure bis zur schwach alkalischen Reak  tion und Beigabe von Kochsalz     wird    der    Farbstoff     abgeschieden;        zwecks        Reinigung          kann    er in verdünnter Soda gelöst und mit  Kochsalz wieder ausgefällt werden.



  Process for the preparation of an azo dye. It has been found that a polyazo dye can be made by referring to the azo dye of the formula
EMI0001.0009
    allows alkaline reducing agents to act until two azo dye molecules are linked by the nitrogen bridge formed during the reduction of the nitro groups.

    



  When dry, the dye is a dark powder which: dissolves in a dilute soda solution and in concentrated sulfuric acid with a blue color and colors cotton from a bath containing Glauber's salt in blue-gray tones, which turn into a deep green-blue when copper is applied.



  Possible reducing agents which are used in an alkaline medium (for example sodium hydroxide or potassium hydroxide) are, for example, glucose, alkaline sulfur or stannite.



  <I> Example: </I> 1.7 parts of 5-nitro-29-amino-1-ogybenzene are diazotized and coupled with 4.1 parts in the usual way: of the imidazole of the formula
EMI0001.0048
      The deposited dye is dissolved in 80 parts of water at 60 with the addition of 11.8 parts of 80% strength sodium hydroxide solution.

   Then add 1.6 parts of glucose as a 10% solution and stir for about. one hour at 55 to <B> 60 '. </B> By setting back with acid until the reaction is weakly alkaline and adding sodium chloride, the dye is deposited; For cleaning purposes, it can be dissolved in diluted soda and precipitated with table salt.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines Poly- azofarbstoffes, dadurch ,gekennzeichnet, dass man auf .den Azofarbstoff der Formel EMI0002.0020 alkalische reduzierende .Mittel bis zur Ver kettung zweier Farbstoffmoleküle durch die bei der Reduktion der Nitrogruppen ent- stehende Stickstoffbrücke, einwirken lässt. PATENT CLAIM: Process for the production of a poly azo dye, characterized in that the azo dye of the formula EMI0002.0020 alkaline reducing agents until two dye molecules are linked by the nitrogen bridge formed during the reduction of the nitro groups. Der Farbstoff stellt in trockenem Zu stande ein dunkles Pulver dar, das sich in verdünnter Sodalösung, sowie in konzentrier- ter Schwefelsäure mit blauer Farbe löst und Baumwolle aus glaubersalzhaltigem Bade in blaugrauen Tönen färbt, die beim Nach kupfern in ein echtes Grünblau übergehen. When dry, the dye is a dark powder that dissolves in a dilute soda solution and in concentrated sulfuric acid with a blue color and dyes cotton from a bath containing Glauber's salt in blue-gray tones, which turn into a true green-blue when copper is added.
CH193343D 1936-06-17 1936-06-17 Process for the preparation of an azo dye. CH193343A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH193343T 1936-06-17

Publications (1)

Publication Number Publication Date
CH193343A true CH193343A (en) 1937-10-15

Family

ID=4438797

Family Applications (1)

Application Number Title Priority Date Filing Date
CH193343D CH193343A (en) 1936-06-17 1936-06-17 Process for the preparation of an azo dye.

Country Status (1)

Country Link
CH (1) CH193343A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6727351B1 (en) 1999-03-13 2004-04-27 Basf Aktiengesellschaft Azoxy dyes and their Cu complexes

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6727351B1 (en) 1999-03-13 2004-04-27 Basf Aktiengesellschaft Azoxy dyes and their Cu complexes
US6903197B2 (en) 1999-03-13 2005-06-07 Basf Aktiengesellschaft Azoxy dyes and copper complexes thereof

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