CH110877A - Process for the production of a new dye. - Google Patents

Process for the production of a new dye.

Info

Publication number
CH110877A
CH110877A CH110877DA CH110877A CH 110877 A CH110877 A CH 110877A CH 110877D A CH110877D A CH 110877DA CH 110877 A CH110877 A CH 110877A
Authority
CH
Switzerland
Prior art keywords
dye
new dye
production
dissolves
parts
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 CH110877A publication Critical patent/CH110877A/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

  

  Zusatzpatent     zum    Hauptpatent     Nr.   <B>110287.</B>    Verfahren zur Herstellung eines neuen     Farbstoffes.       Es wurde gefunden,     dass    man einen neuen  Farbstoff erhält, wenn man die     3-Oxytiaph-          thalin-1,8-dikarbonsäure    mit     diazotierter        4-Me-          thyl-2-amitio-l-phenol-6-sulfosätii,e    kuppelt und  den so erhaltenen Farbstoff mit     Chromformiat     behandelt.

   Der neue Farbstoff bildet ein  schwärzliches Pulver, löst sich in Wasser  unter Zusatz von Natronlauge mit rotvioletter  Farbe und erzeugt im Chromdruck auf Baum  wolle sehr echte violette Töne.    <I>Beispiel:</I>  <B>25</B> Teile     4-Methyl-2-amino-l-phenol-6-sulfo-          säure    werden wie üblich     diazotiert    und in  eine Lösung von<B>21,6</B> Teilen     3-Oxynaphtbaliii-          1,8-dikarbonsäureanhydrid,   <B>8</B> Teilen     Natron-          lange    und 40 Teilen Soda in<B>500</B> Teilen  Wasser eingetragen. Man rührt, bis die     Diazo-          verbindung    verschwunden ist.

   Hierauf salzt       man    mit Kochsalz aus und filtriert den aus  geschiedenen Farbstoff.    <B>25,6</B> Teile dieses     Farbstoffes    werden in  <B>500</B> Teilen Wasser heiss gelöst Lind mit einer       Chromformiatmenge,    entsprechend 12,5 Teilen       C'r20s,    versetzt. Man kocht einige Zeit und  filtriert den durch     Kochsalzzusatz    abgeschie  denen Farbstoff.



  Additional patent to main patent no. <B> 110287. </B> Process for the production of a new dye. It has been found that a new dye is obtained if the 3-oxytiaphthalene-1,8-dicarboxylic acid is coupled with diazotized 4-methyl-2-amitio-1-phenol-6-sulfosätii, e and the like obtained dye treated with chromium formate.

   The new dye forms a blackish powder, dissolves in water with the addition of caustic soda with a red-violet color and creates very real violet tones when printed with chrome on cotton. <I> Example: </I> <B> 25 </B> parts of 4-methyl-2-amino-1-phenol-6-sulfonic acid are diazotized as usual and converted into a solution of <B> 21.6 Parts 3-Oxynaphtbaliii- 1,8-dikarbonsäureanhydrid, <B> 8 </B> parts of long soda and 40 parts of soda in <B> 500 </B> parts of water. Stir until the diazo compound has disappeared.

   It is then salted out with common salt and the dye which has separated out is filtered off. <B> 25.6 </B> parts of this dye are dissolved in <B> 500 </B> parts of hot water and an amount of chromium formate corresponding to 12.5 parts of C'r20s is added. It is boiled for some time and the dye separated by the addition of common salt is filtered off.

 

Claims (1)

<B>PATENTANSPRUCH:</B> Verfahren zur Herstellung eines neuen Farbstoffes, dadurch gekennzeichnet, dass man die S-Oxynaphthalin-1,8-dikarbonsätire mit di- azotierter 4-Methyl-2-amino-l-phenol-6-sulfo- säure kuppelt Lind den so erhaltenen Farb stoff mit Chromformiat behandelt. Der neue Farbstoff bildet ein schwärzliches Pulver, löst ,sich in Wasser unter Zusatz von Natronlauge mit rotvioletter Farbe und ei-zeugt im Chrom druck auf Baumwolle sehrechte violette Töne. <B> PATENT CLAIM: </B> Process for the preparation of a new dye, characterized in that the S-oxynaphthalene-1,8-dicarboxylic acids are mixed with azotized 4-methyl-2-amino-1-phenol-6-sulfo - Acid couples and the dye obtained is treated with chromium formate. The new dye forms a blackish powder, dissolves, dissolves in water with the addition of caustic soda with a red-violet color and, in the chrome print on cotton, creates vertical violet tones.
CH110877D 1923-12-28 1923-12-28 Process for the production of a new dye. CH110877A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH110287T 1923-12-28
CH110877T 1923-12-28

Publications (1)

Publication Number Publication Date
CH110877A true CH110877A (en) 1925-07-01

Family

ID=25707668

Family Applications (1)

Application Number Title Priority Date Filing Date
CH110877D CH110877A (en) 1923-12-28 1923-12-28 Process for the production of a new dye.

Country Status (1)

Country Link
CH (1) CH110877A (en)

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