CH111925A - Process for the preparation of a new dye. - Google Patents

Process for the preparation of a new dye.

Info

Publication number
CH111925A
CH111925A CH111925DA CH111925A CH 111925 A CH111925 A CH 111925A CH 111925D A CH111925D A CH 111925DA CH 111925 A CH111925 A CH 111925A
Authority
CH
Switzerland
Prior art keywords
dye
preparation
new dye
parts
greenish blue
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 CH111925A publication Critical patent/CH111925A/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
    • C09B45/00Complex metal compounds of azo dyes
    • C09B45/02Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
    • C09B45/14Monoazo compounds
    • C09B45/16Monoazo compounds containing chromium

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

  

  Verfahren zur Darstellung eines neuen     Farbstoffes.       Es wurde gefunden,     .dass    man einen neuen   Farbstoff erhält, wenn man das     5,8-Dichlor-a-          naphthol    mit :der     Diazoverbindung    aus     1-          Oxy        naphthalin-8-sulfamid-2    -     amino    - 4     -sulf        o-          säure    kuppelt und .den so erhaltenen Farb  stoff mit     Alkalichromit    behandelt.

   Der neue  Farbstoff bildet ein schwärzliches Pulver,  das sich in Wasser mit grünstickig blauer,  in verdünnter Natronlauge mit violetter     Farbe     löst. Er färbt Wolle aus saurem Bade in sehr  egalen, echten grünstickig blauen Tönen an.       Beispiel:

       In ein Gemisch von 60 Teilen Kalihydrat,  46 Teilen Wasser und 21,3 Teilen     5,8-Di-          chlor-a-naphthol    trägt man unter Rühren bei  mittlerer Temperatur     (ca.    50  ) 32,9 Teile der       Diazoverbindung    aus     1-Oxynaphthalin-8-sul-          famid-2-amino-4-sulfosäure    in Form einer       ca.    30     %igen    Paste ein. Man rührt noch län  gere Zeit bei dieser Temperatur, bis die     Di-          azoverbin.dung    verschwunden ist.

   Hierauf  verdünnt man mit 350 Teilen Wasser, stellt  mit nicht     zii    verdünnter Mineralsäure neu-         tral    und     f6.llt    den gebildeten Farbstoff mit  Kochsalz aus.  



  In 54 Teile einer 16,2 %     Cr203    enthalten  den     Cliromoxydhydratpaste    werden     nassh    und  nach 60 Teile festes     Ätzkali    eingetragen, bis  sämtliches     Cr203    in Lösung gegangen ist:  Hierauf setzt man 54,2 Teile des Farbstof  fes aus     5,8-Dichlor-a-naphthol    und     1-Oxy-          naphthalin-8-sulfamid-2-a,mino    - 4 -     sulfosäure     hinzu und erhitzt die Masse so lange auf  80  , bis sämtliches Chrom vom Farbstoff  aufgenommen ist. Dann verdünnt man das  Reaktionsgemisch mit Wasser, stellt mit  Mineralsäure neutral und salzt den erhaltenen  Farbstoff mit Kochsalz aus.



  Process for the preparation of a new dye. It has been found that .that a new dye is obtained if the 5,8-dichloro-anaphthol is coupled with: the diazo compound of 1-oxynaphthalene-8-sulfamide-2-amino-4-sulfo acid and . Treated the dye thus obtained with alkali chromite.

   The new dye forms a blackish powder that dissolves in water with a greenish blue color and in dilute caustic soda with a purple color. He dyes wool from an acid bath in very even, genuine greenish blue tones. Example:

       32.9 parts of the diazo compound from 1-oxynaphthalene are added to a mixture of 60 parts of potassium hydrate, 46 parts of water and 21.3 parts of 5,8-dichloro-a-naphthol with stirring at medium temperature (approx. 50) 8-sulphamide-2-amino-4-sulphonic acid in the form of an approx. 30% paste. The mixture is stirred for a longer time at this temperature until the diazo compound has disappeared.

   It is then diluted with 350 parts of water, neutralized with mineral acid that is not dilute, and the dye formed is precipitated with sodium chloride.



  In 54 parts of a 16.2% Cr203 containing the Cliromoxydhydratpaste wet and after 60 parts solid caustic potash, until all the Cr203 has gone into solution: 54.2 parts of the dye are then put from 5,8-dichloro-a-naphthol and 1-oxynaphthalene-8-sulfamid-2-a, mino - 4 - sulfonic acid and heat the mass to 80 until all the chromium has been absorbed by the dye. The reaction mixture is then diluted with water, made neutral with mineral acid and the dye obtained is salted out with sodium chloride.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Darstellung eines neuen Farbstoffes, dadurch gekennzeichnet, dass man das 5,8-Dichlor-a-naphthol mit der Di- azoverbindung aus 1-Oxynaphthalin-8-sul- fami,d-2-amino-4-sulfosäure kuppelt und den so erhaltenen Farbstoff mit Alkalichromit behandelt. Der neue Farbstoff bildet ein schwärzliches Pulver, das sich in Nasser mit grünstiohig blauer, in verdünnter Natron lauge mit violetter Farbe löst. Er färbt Wolle aus saurem Bade in sehr egalen, ech ten grünstichig blauen Tönen an. PATENT CLAIM: Process for the preparation of a new dye, characterized in that the 5,8-dichloro-a-naphthol is coupled with the di-azo compound from 1-oxynaphthalene-8-sulphami, d-2-amino-4-sulphonic acid and treating the dye thus obtained with alkali chromite. The new dye forms a blackish powder that dissolves in water with a greenish blue color, in dilute caustic soda with a purple color. He dyes wool from an acid bath in very even, genuine greenish blue tones.
CH111925D 1924-03-20 1924-03-20 Process for the preparation of a new dye. CH111925A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH111925T 1924-03-20
CH111565T 1924-03-20

Publications (1)

Publication Number Publication Date
CH111925A true CH111925A (en) 1925-09-16

Family

ID=25707883

Family Applications (1)

Application Number Title Priority Date Filing Date
CH111925D CH111925A (en) 1924-03-20 1924-03-20 Process for the preparation of a new dye.

Country Status (1)

Country Link
CH (1) CH111925A (en)

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