CH110882A - Process for the production of a new dye. - Google Patents

Process for the production of a new dye.

Info

Publication number
CH110882A
CH110882A CH110882DA CH110882A CH 110882 A CH110882 A CH 110882A CH 110882D A CH110882D A CH 110882DA CH 110882 A CH110882 A CH 110882A
Authority
CH
Switzerland
Prior art keywords
dye
new dye
parts
production
new
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 CH110882A publication Critical patent/CH110882A/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

  

  <B>Zusatzpatent</B> zum Hauptpatent Nr. 110287.    Verfahren zur Herstellung eines neuen     Farbstoffes.       Es wurde gefunden, dass man einen neuen  Farbstoff erhält, wenn man die     3-Oxynaph-          thalin-1,8-dikarbonsäure    mit     diazotierter    4  Chlor-2-a.mino-1=phenol-6-sulfosäure kuppelt  und den so erhaltenen Farbstoff mit     Alkali-          chromit    behandelt. Der neue     Farbstoff    bil  det ein schwärzliches Pulver, löst sich in  Wasser     unter    Zusatz von Natronlauge mit  rotvioletter Farbe und erzeugt im Chrom  ,druck auf Baumwolle sehr echte violette  Töne.  



       Beispiel:     22,3 Teile     4-Clilor-2-,amino-l-ph@enol-6-          sulfosäure    werden wie üblich     diazotiert    und  in eine Lösung von     21.,6    Teilen     3-Oxynaph-          thalin-1,8-dik        @anbons.äureanhydrid,    8 Teilen  Natronlauge und 40 Teilen Soda in 500 Tei  len     Wasser    eingetragen. Man rührt, bis die       Diazoverbindung    verschwunden ist. Hierauf  salzt man mit     go:chsalz    aus und filtriert     Iden     ausgeschiedenen Farbstoff.  



  26,7 Teile dieses Farbstoffes werden in  eine kochende Lösung, enthaltend 8,5 Teile         Cr-#Os,    100 Teile Wasser, 28 Teile     Ätzkali     und 10 Teile Glyzerin eingetragen und län  gere Zeit gekocht. Nach dem     Verdünnen    mit  zirka 200 Teilen Wasser wird filtriert und  aus dem Filtrate der neue Farbstoff durch  Neutralisieren und     Aussalzen    isoliert.



  <B> Additional patent </B> to main patent no. 110287. Process for the production of a new dye. It has been found that a new dye is obtained if the 3-oxynaphthalene-1,8-dicarboxylic acid is coupled with diazotized 4-chloro-2-a.mino-1 = phenol-6-sulfonic acid and the dye thus obtained is coupled with it Treated with alkali chromite. The new dye forms a blackish powder, dissolves in water with the addition of caustic soda with a red-violet color and produces very real violet tones in the chrome print on cotton.



       Example: 22.3 parts of 4-Clilor-2-, amino-l-ph @ enol-6-sulfonic acid are diazotized as usual and converted into a solution of 21.6 parts of 3-oxynaphthalin-1,8-dik @ Anbons.äureanhydrid, 8 parts of sodium hydroxide solution and 40 parts of soda in 500 parts of water entered. Stir until the diazo compound has disappeared. It is then salted out with salt and the precipitated dye is filtered off.



  26.7 parts of this dye are added to a boiling solution containing 8.5 parts of Cr- # Os, 100 parts of water, 28 parts of caustic potash and 10 parts of glycerol and boiled for a longer time. After dilution with about 200 parts of water, the mixture is filtered and the new dye is isolated from the filtrate by neutralization and salting out.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines neuen Farbstoffes, dadurch gekennzeichnet, dass mau die 3-Oxynaphthalin-1,8-dikarbonsäure mit diazotierter 4-Chlor-2-amino-l-phenol-6- sulfosäure kuppelt und den so erhaltenen Farbstoff mit Alkalichromit behandelt. Der neue Farbstoff bildet ein schwärzliches Pul ver, löst sich in Wasser unter Zusatz von Natronlauge mit rotvioletter Farbe und er zeugt im Chromdruck auf Baumwolle sehr echte violette Töne. PATENT CLAIM: Process for the production of a new dye, characterized in that the 3-oxynaphthalene-1,8-dicarboxylic acid is coupled with diazotized 4-chloro-2-amino-1-phenol-6-sulfonic acid and the dye thus obtained is treated with alkali chromite . The new dye forms a blackish powder, dissolves in water with the addition of caustic soda with a red-violet color and it produces very real violet tones in the chrome print on cotton.
CH110882D 1923-12-28 1923-12-28 Process for the production of a new dye. CH110882A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH110882T 1923-12-28
CH110287T 1923-12-28

Publications (1)

Publication Number Publication Date
CH110882A true CH110882A (en) 1925-07-01

Family

ID=25707673

Family Applications (1)

Application Number Title Priority Date Filing Date
CH110882D CH110882A (en) 1923-12-28 1923-12-28 Process for the production of a new dye.

Country Status (1)

Country Link
CH (1) CH110882A (en)

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