CH309447A - Process for the preparation of a water-soluble and licensing azophthalocyanine dye. - Google Patents

Process for the preparation of a water-soluble and licensing azophthalocyanine dye.

Info

Publication number
CH309447A
CH309447A CH309447DA CH309447A CH 309447 A CH309447 A CH 309447A CH 309447D A CH309447D A CH 309447DA CH 309447 A CH309447 A CH 309447A
Authority
CH
Switzerland
Prior art keywords
water
dye
azophthalocyanine
soluble
blue
Prior art date
Application number
Other languages
German (de)
Inventor
Ag Durand Huguenin
Original Assignee
Durand & Huguenin 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 Durand & Huguenin Ag filed Critical Durand & Huguenin Ag
Publication of CH309447A publication Critical patent/CH309447A/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
    • C09B43/12Preparation of azo dyes from other azo compounds by acylation of amino groups

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

Description

  

  Zusatzpatent zum Hauptpatent Nr. 307327.    Verfahren zur Herstellung eines wasserlöslichen<B>und</B>     beizenziehenden          Azophthalocyaninfarbstofes.       Die vorliegende Erfindung betrifft ein  Verfahren zur Herstellung eines     wasserlösli-          cüen    und     beizenziehenden        Azophthalocy        anin-          farbstoffes,    welches dadurch gekennzeichnet  ist, dass man 1     Mol        Nickelpllthalocyanin-3,3',          3",

  3"'-tetrasltlfochlorid    mit 1     Mol        4-Amino-          2-chlor-4'-oxy-1,1'-azobenzol-5'-carbonsäure    in  Gegenwart einer Mineralsäure neutralisieren  den Substanz zur Umsetzung bringt. Im übri  gen wird man sich von den im Hauptpatent       memachten    Ausführungen leiten lassen.  



  Das nachstehende Beispiel erläutert das  neue Verfahren. Die angegebenen Teile be  deuten Gewichtsteile.  



       Beispiel:     29 Teile     (3/10o        12o1)        Nickelphthalocyanin-          3,3"'    -     t.etrasulfochlorid,    erhalten durch       Einwirkung    von     Chlorsulfonsäure    auf     Nik-          helphthaloey        anin,    werden auf Eis ausgeladen  und     (las    abgetrennte Reaktionsprodukt als  feuchte Paste mit.

   150 Teilen zerkleinertem  Isis vermischt und eine Lösung von 9,4 Tei  len     (a/100        31o1)    des     Natriumsalzes    der     4-          Aniino-''-chlor-4'-oxy-1,1'-        azobenzol-5'-ca.rbon-          säure    in 100 Teilen Wasser und 15 Teilen       Cal.ciumcarbonat    zugegeben.

   Man lässt wäh  rend 24 Stunden bei 0-5 C rühren, stellt       das    Reaktionsgemisch mit     Natriumcarbonat     sehwach alkalisch, erwärmt auf 60  C, filtriert    vom     Calciumcarbonat    ab und isoliert den  Farbstoff durch     Aussalzen    mit     Natriumchlo-          rid.     



  Der so erhaltene Farbstoff stellt ein dun  kelblaugraues Pulver dar, das sich in Wasser  mit grünstickig blauer und in     konz.    Schwefel  säure mit gelbbrauner Farbe löst. Im Chrom  druck auf Baumwolle liefert der Farbstoff  blaugrüne Farbtöne von guten Echtheits  eigenschaften.



  Additional patent to main patent no. 307327. Process for the production of a water-soluble <B> and </B> associated azophthalocyanine dye. The present invention relates to a process for the production of a water-soluble azophthalocyanine dye, which is characterized in that 1 mol of nickel-3,3 ', 3 ",

  3 "'- tetrasltlfochlorid with 1 mole of 4-amino-2-chloro-4'-oxy-1,1'-azobenzene-5'-carboxylic acid in the presence of a mineral acid will neutralize the substance be guided by the statements made in the main patent.



  The following example illustrates the new procedure. The parts indicated are parts by weight.



       Example: 29 parts (3 / 10o 12o1) nickel phthalocyanine 3.3 "'- tetrasulphochloride, obtained by the action of chlorosulphonic acid on nickel phthalocyanine, are unloaded onto ice and the separated reaction product as a moist paste.

   150 parts of crushed Isis mixed and a solution of 9.4 Tei len (a / 100 31o1) of the sodium salt of 4-Aniino -''-chloro-4'-oxy-1,1'-azobenzene-5'-carbon - Acid in 100 parts of water and 15 parts of calcium carbonate were added.

   The mixture is stirred for 24 hours at 0-5 ° C., the reaction mixture is made slightly alkaline with sodium carbonate, heated to 60 ° C., calcium carbonate is filtered off and the dye is isolated by salting out with sodium chloride.



  The dye obtained in this way is a dark blue-gray powder that turns greenish blue in water and in conc. Sulfuric acid dissolves with a yellow-brown color. In chrome printing on cotton, the dye provides blue-green shades with good fastness properties.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines wasser löslichen und beizenziehenden Azophthalo- cyaninfarbstoffes, dadurch gekennzeichnet, dass man 1 111o1 Nickelphthalocyanin-3,3', 3",3"'-tetrasulfochlorid mit 1 Mol 4 Amino- 2-ehlor-4'-oxy-1,1'-azobenzol-5'-carbonsäure in Gegenwart einer Mineralsäure neutralisieren den Substanz zur Umsetzung bringt. PATENT CLAIM: A process for the production of a water-soluble azophthalocyanine dye, characterized in that 1 111o1 nickel phthalocyanine-3,3 ', 3 ", 3"' - tetrasulfochloride with 1 mol of 4-amino-2-chloro-4'-oxy -1,1'-azobenzene-5'-carboxylic acid in the presence of a mineral acid neutralize the substance and reacts. Der neue, so erhaltene Farbstoff stellt ein dunkelblaugraues Pulver dar, das sich in Wasser mit grünstickig blauer und in konz. Schwefelsäure mit gelbbrauner Farbe löst und im Chromdruck auf Baumwolle blaugrüne Farbtöne von guten Echtheitseigenschaften liefert. The new dye obtained in this way is a dark blue-gray powder, which in water turns green with a blue and in conc. Sulfuric acid dissolves with a yellow-brown color and, in chrome printing on cotton, provides blue-green shades with good fastness properties.
CH309447D 1952-07-31 1952-07-31 Process for the preparation of a water-soluble and licensing azophthalocyanine dye. CH309447A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH309447T 1952-07-31
CH307327T 1955-05-31

Publications (1)

Publication Number Publication Date
CH309447A true CH309447A (en) 1955-08-31

Family

ID=25735273

Family Applications (1)

Application Number Title Priority Date Filing Date
CH309447D CH309447A (en) 1952-07-31 1952-07-31 Process for the preparation of a water-soluble and licensing azophthalocyanine dye.

Country Status (1)

Country Link
CH (1) CH309447A (en)

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