CH133097A - Process for the production of a new dye. - Google Patents

Process for the production of a new dye.

Info

Publication number
CH133097A
CH133097A CH133097DA CH133097A CH 133097 A CH133097 A CH 133097A CH 133097D A CH133097D A CH 133097DA CH 133097 A CH133097 A CH 133097A
Authority
CH
Switzerland
Prior art keywords
sulfur
dye
new
production
chromium
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
Priority claimed from CH128228T external-priority patent/CH128228A/en
Publication of CH133097A publication Critical patent/CH133097A/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
    • C09B45/48Preparation from other complex metal compounds of azo dyes
    • 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
    • C09B56/00Azo dyes containing other chromophoric systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)

Description

  

  Verfahren zur Herstellung eines neuen Farbstoffes.    Es wurde gefunden, dass man einen neuen,  gleichzeitig     Chrom-    und schwefelhaltigen Farb  stoff erhält, wenn man die Chromverbindung  des durch Kupplung der nitrierten     Diazover-          bindung    der     1-Amino-2-oxynaphtalin-4-sulfo-          säure    und     a-Naphthol    und     nachlierige    Reduk  tion der Nitrogruppe erhaltenen     Azofarbstoffes     mit Schwefel abgebenden Mitteln in Gegen  wart von Äthylalkohol behandelt.  



  Der so erhaltene neue Farbstoff stellt ein  blauschwarzes Pulver dar, er ist in Wasser  unlöslich, in     Schwefelalkalien    mit blauer  Farbe löslich und färbt aus     schwefelnatrium-          haltigem    Bade Baumwolle     iti    grauen, gut  wasch- und lichtechten Tönen an.  



       Beispiel:     In 60 Teilen     Ätzkali    werden 72,5 Teile       Chromhydroxydpaste        mit        11,8        %        Cra0s        vor-          sichtig    gelöst. Dann werden 45 Teile des  reduzierten Farbstoffes aus nitrierter     Diazo-          verbindung    der     1.2-Aminonaphthol-4-sulfo-          säure    und     a-Naphthol    eingetragen.

   Die dicke    Masse wird 16 Stunden bei 75-80 0 gerührt,  wonach die fertige Chromverbindung durch  Verdünnen,     Neutralstellen    mit verdünnter  Schwefelsäure und     Aussalzen    abgeschieden  wird.  



  55 Teile dieses getrockneten     Farbstoffes     trägt man in eine alkoholische Polysulfid  lösung ein, hergestellt aus 120 Teilen     kalzi-          niertem    Schwefelnatrium, 96 Teilen Schwefel  und 400 Teilen Alkohol. Die Masse wird  110 Stunden in einem mit     Rückfluss        ver-          sehenen    Gefäss gekocht, dann wird die Haupt  menge des Alkohols     abdestilliert    und der  Schwefelfarbstoff durch Verdünnen mit einer  20 % Kochsalz enthaltenden wässerigen Lö  sung gefällt.

   Er wird hierauf filtriert, mit       einer        Kochsalzlösung        von    3     %        gewaschen        und     getrocknet.



  Process for the production of a new dye. It has been found that a new, at the same time chromium and sulfur-containing dye is obtained if the chromium compound of the 1-amino-2-oxynaphthalene-4-sulfonic acid and α-naphthol and subsequent ones is obtained by coupling the nitrated diazo compound Reduction of the nitro group obtained azo dye with sulfur-releasing agents in the presence of ethyl alcohol treated.



  The new dye obtained in this way is a blue-black powder, it is insoluble in water, soluble in alkaline sulfur with a blue color, and from bath cotton containing sulfur sodium it stains gray, washable and lightfast shades.



       Example: 72.5 parts of chromium hydroxide paste with 11.8% CraOs are carefully dissolved in 60 parts of caustic potash. Then 45 parts of the reduced dye from nitrated diazo compound of 1,2-aminonaphthol-4-sulfonic acid and α-naphthol are introduced.

   The thick mass is stirred for 16 hours at 75-80 °, after which the finished chromium compound is deposited by dilution, neutralization with dilute sulfuric acid and salting out.



  55 parts of this dried dye are introduced into an alcoholic polysulphide solution made from 120 parts of calcined sodium sulphide, 96 parts of sulfur and 400 parts of alcohol. The mass is boiled for 110 hours in a refluxing vessel, then most of the alcohol is distilled off and the sulfur dye is precipitated by dilution with an aqueous solution containing 20% sodium chloride.

   It is then filtered, washed with a 3% saline solution and dried.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines neuen, gleichzeitig chrom- und schwefelhaltigen Farb stoffes, dadurch gekennzeichnet, dass man die Chromverbindung des durch Kupplung der nitrierten Diazoverbindung der 1-Amino- 2-oxynaphtalin-4-sulfosäure und a-Naphthol und nachherige Reduktion der Nitrogruppe erhaltenen Azofarbatoffes mit Schwefel abge benden Mitteln in Gegenwart von Äthyl- alkohol behandelt. PATENT CLAIM: A process for the production of a new, at the same time chromium and sulfur-containing dye, characterized in that the chromium compound of the 1-amino-2-oxynaphthalene-4-sulfonic acid and α-naphthol and subsequent reduction of the nitro group by coupling the nitrated diazo compound Azofarbatoffes obtained treated with sulfur abending agents in the presence of ethyl alcohol. Der so erhaltene neue Farbstoff stellt ein blauschwarzes Pulver dar, er ist in Wasser unlöslich, in Schwefelalkalien mit blauer Farbe löslich und färbt aus schwefelnatriumhaltigen Bade Baumwolle in grauen, gut wasch- und lichtechten Tönen an. The new dye obtained in this way is a blue-black powder, it is insoluble in water, soluble in alkaline sulfur with a blue color and stains cotton in gray, washable and lightfast shades from baths containing sodium sulphide.
CH133097D 1927-05-07 1927-05-07 Process for the production of a new dye. CH133097A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH133097T 1927-05-07
CH128228T CH128228A (en) 1927-05-07 1927-05-07 Process for the production of a new dye.

Publications (1)

Publication Number Publication Date
CH133097A true CH133097A (en) 1929-05-15

Family

ID=25711065

Family Applications (1)

Application Number Title Priority Date Filing Date
CH133097D CH133097A (en) 1927-05-07 1927-05-07 Process for the production of a new dye.

Country Status (1)

Country Link
CH (1) CH133097A (en)

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