CH116738A - Process for the production of a new dye. - Google Patents

Process for the production of a new dye.

Info

Publication number
CH116738A
CH116738A CH116738DA CH116738A CH 116738 A CH116738 A CH 116738A CH 116738D A CH116738D A CH 116738DA CH 116738 A CH116738 A CH 116738A
Authority
CH
Switzerland
Prior art keywords
new dye
production
acid
violet
green
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 CH116738A publication Critical patent/CH116738A/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
    • C09B29/095Amino naphthalenes
    • C09B29/0955Amino naphthalenes containing water solubilizing groups
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
  • Coloring (AREA)
  • Paper (AREA)

Description

  

  Verfahren zur Herstellung eines neuen Farbstoffes.    Es wurde gefunden, dass man einen neuen  Farbstoff erhält, wenn . man     diazotierte        6-          Nitro-2-amino-l-phenol-4-sulfosäure    mit     3-          Aminonaphthalin-1,8-dikarbonsäure    vereinigt.  Der neue Farbstoff bildet ein schwarzes  Pulver, das sich in Wasser mit     violettroter,     in Schwefelsäure mit grüngelber Farbe löst.  Er färbt Wolle aus saurem Bade in     violett-          braunen    Tönen, welche beim     Nachchromieren     nach olive umschlagen. Im Chromdruck auf  Baumwolle erzeugt er grüne Töne.

           Beispiel:       10,7 Teile     3-Aminonaphthalin-1,8-dikar-          bonsäureanhydrid    werden mit Hilfe von 10  Teilen 30     %iger    Natronlauge in 150 Teilen  Wasser heiss gelöst, mit 10 Teilen Soda ver  setzt, abgekühlt und mit der aus 11,7 Teilen       6-Nitro-2-amino-l-phenol-4-sulfosäure    herge-    stellten     Diazoverbindung    versetzt. Nach er  folgter Kupplung     wird    der     Farbstoff        ausge-          salzen,    filtriert und getrocknet.



  Process for the production of a new dye. It has been found that a new dye is obtained when. diazotized 6-nitro-2-amino-1-phenol-4-sulfonic acid is combined with 3-aminonaphthalene-1,8-dicarboxylic acid. The new dye forms a black powder that dissolves in water with a purple-red color and in sulfuric acid with a green-yellow color. He dyes wool from an acid bath in violet-brown tones, which turn to olive when they are chromed. In the chrome print on cotton it creates green tones.

           Example: 10.7 parts of 3-aminonaphthalene-1,8-dicarboxylic anhydride are dissolved in 150 parts of hot water using 10 parts of 30% strength sodium hydroxide solution, 10 parts of soda are added, the mixture is cooled and the 11.7 parts are added 6-nitro-2-amino-1-phenol-4-sulfonic acid produced diazo compound was added. After coupling has taken place, the dye is salted out, filtered and dried.

 

Claims (1)

PATENTANSPRUCH Verfahren zur Herstellung eines neuen Farbstoffes, dadurch gekennzeichnet, dass man diazotierte 6-Nitro-2-amino:l-phenol-4- sulfosäure mit 3-Aminonaphthalin-1,8-dikar- bonsäure vereinigt. Der neue Farbstoff bil det ein schwarzes Pulver, das sich in Was ser mit violettroter, in Schwefelsäure mit grüngelber Farbe löst. Er färbt Wolle aus saurem Bade in violettbraunen Tönen, wel che beim Nachchromieren nach olive um schlagen. Im. Chromdruck auf Baumwolle erzeugt er grüne Töne. PATENT CLAIM Process for the production of a new dye, characterized in that diazotized 6-nitro-2-amino: 1-phenol-4-sulfonic acid is combined with 3-aminonaphthalene-1,8-dicarboxylic acid. The new dye forms a black powder that dissolves in water with a violet-red color and in sulfuric acid with a green-yellow color. It dyes wool from an acid bath in violet-brown tones, which turn olive when they are chromed. In the chrome print on cotton it creates green tones.
CH116738D 1923-12-28 1924-08-16 Process for the production of a new dye. CH116738A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH110287T 1923-12-28
CH116738T 1924-08-16

Publications (1)

Publication Number Publication Date
CH116738A true CH116738A (en) 1926-09-16

Family

ID=25707687

Family Applications (1)

Application Number Title Priority Date Filing Date
CH116738D CH116738A (en) 1923-12-28 1924-08-16 Process for the production of a new dye.

Country Status (1)

Country Link
CH (1) CH116738A (en)

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