CH117270A - Process for the production of a new dye. - Google Patents

Process for the production of a new dye.

Info

Publication number
CH117270A
CH117270A CH117270DA CH117270A CH 117270 A CH117270 A CH 117270A CH 117270D A CH117270D A CH 117270DA CH 117270 A CH117270 A CH 117270A
Authority
CH
Switzerland
Prior art keywords
acid
new dye
green
production
dye
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 CH117270A publication Critical patent/CH117270A/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)
  • Coloring (AREA)

Description

  

  Verfahren zur     Herstellung    eines neuen Farbstoffes.    Es wurde gefunden, dass man einen neuen       Farbstoff    erhält, wenn man dianotierte     6-Nitro-          2-amino-l-phenol-4-sulfosäure    mit     3-Amino-          naphthalin-1,8-dikarbonsäurevereinigt    und den  so erhaltenen     Azofarbstoff    mit chromabgeben  den Mitteln behandelt. Der neue Farbstoff stellt  ein schwärzliches Pulver dar und löst sich  in Wasser mit grüner, in konzentrierter Schwe  felsäure mit rotbrauner Farbe.

   Er färbt Wolle  aus saurem Bade in grünen Tönen von vor  züglichen Echtheitseigenschaften und gibt im       Baumwolldruck,        vorzugsweise    in Gegenwart  von Chrombeizen, echte, grüne Färbungen.  <I>Beispiel:</I>  10,7 Teile     3-Aminonaphthaliri-1,8-dikar-          borisäureanhydrid        werden    mit Hilfe von 10  Teilen 30     %iger    Natronlauge in 160 Teilen  Wasser heiss gelöst, mit 10 Teilen Soda ver  setzt, abgekühlt und mit der aus 11,7 Teilen       6-Nitro-2-ainino-l-phenol-4-sulfosäure    herge  stellten     Diazoverbindung    versetzt.

   Nach er  folgter Kupplung wird der Farbstoff     ausge-          salzen,        filtriert    und getrocknet,    47,6 Teile des so erhaltenen     Azofarbstoffes     werden in 950 Teilen Wasser kochend ge  löst, mit einer     Ohromformiatlösung    entspre  chend 22,6 Teilen     Or20s    versetzt und längere  Zeit am     Rückflusskühler    gekocht.     Hierauf    wird  die Chromverbindung durch     Aussalzen    ge  wonnen.



  Process for the production of a new dye. It has been found that a new dye is obtained if dianotated 6-nitro-2-amino-1-phenol-4-sulfonic acid is combined with 3-amino-naphthalene-1,8-dicarboxylic acid and the azo dye thus obtained is combined with chromium-releasing agents treated. The new dye is a blackish powder and dissolves in water with green, in concentrated sulfuric acid with red-brown color.

   It dyes wool from acid baths in green shades with excellent fastness properties and gives real green dyeings in cotton printing, preferably in the presence of chrome stains. <I> Example: </I> 10.7 parts of 3-aminonaphthalen-1,8-dicarboric anhydride are dissolved in 160 parts of hot water using 10 parts of 30% strength sodium hydroxide solution, 10 parts of soda are added, the mixture is cooled and with the diazo compound produced from 11.7 parts of 6-nitro-2-ainino-1-phenol-4-sulfonic acid.

   After coupling, the dyestuff is salted out, filtered and dried, 47.6 parts of the azo dyestuff obtained in this way are dissolved in 950 parts of boiling water, an odor formate solution corresponding to 22.6 parts of Or20s is added and the mixture is refluxed for a long time. The chromium compound is then obtained by salting out.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines neuen Farbstoffes, dadurch gekennzeichnet, dass man dianotierte 6-Nitro-2-amino-l-phenol-4-sulfo- säure mit 3-Aminonaphthalin-1,8-dikarbori- säure vereinizt und den so erhaltenen Azo- farbstoff mit chromabgebenden Mitteln be handelt. Der neue Farbstoff stellt ein schwärz liches Pulver dar und löst sich in Wasser mit grüner, in konzentrierter Schwefelsäure mit rotbrauner Farbe. Claim: process for the production of a new dye, characterized in that dianotized 6-nitro-2-amino-1-phenol-4-sulfonic acid is combined with 3-aminonaphthalene-1,8-dicarboric acid and the azo thus obtained - Dye treated with chromium-releasing agents. The new dye is a blackish powder and dissolves in water with green, in concentrated sulfuric acid with red-brown color. Er färbt Wolle aus saurem Bade in grünen Tönen von vorzüg lichen Echtheitseigenschaften und gibt im Baumwolldruck, vorzugsweise in Gegenwart von Chrombeizen, echte, grüne Färbungen. It dyes wool from acid baths in green shades with excellent fastness properties and gives real green dyeings in cotton printing, preferably in the presence of chrome stains.
CH117270D 1923-12-28 1925-07-31 Process for the production of a new dye. CH117270A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH110287T 1923-12-28
CH117270T 1925-07-31

Publications (1)

Publication Number Publication Date
CH117270A true CH117270A (en) 1926-10-16

Family

ID=25707695

Family Applications (1)

Application Number Title Priority Date Filing Date
CH117270D CH117270A (en) 1923-12-28 1925-07-31 Process for the production of a new dye.

Country Status (1)

Country Link
CH (1) CH117270A (en)

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