CH128007A - Process for the production of a vat dye of the pyranthrone series. - Google Patents

Process for the production of a vat dye of the pyranthrone series.

Info

Publication number
CH128007A
CH128007A CH128007DA CH128007A CH 128007 A CH128007 A CH 128007A CH 128007D A CH128007D A CH 128007DA CH 128007 A CH128007 A CH 128007A
Authority
CH
Switzerland
Prior art keywords
red
orange
production
color
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 CH128007A publication Critical patent/CH128007A/en

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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
    • C09B3/00Dyes with an anthracene nucleus condensed with one or more carbocyclic rings
    • C09B3/40Pyranthrones
    • C09B3/44Preparation from starting materials already containing the pyranthrone nucleus
    • C09B3/46Preparation from starting materials already containing the pyranthrone nucleus by halogenation

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)
  • Coloring (AREA)
  • Cosmetics (AREA)

Description

  

  Verfahren zur Herstellung eines     Küpenfarbstoffes    der     Pyranthronreihe.       Es wurde gefunden,     dass    man einen neuen       Küpenfarbstoff    der     Pyranthronreihe    erhält,  wenn man das     Trichlorpyrantliron,    das er  halten werden kann nach den Angaben des  Beispiels<B>3</B> des<B>D.</B>     R.    P.     Nr.        2181#62,    mit  Phenol in Gegenwart von     Alkalikarbonat     kondensiert.  



  Der erhaltene Farbstoff bildet ein orange  rotes Pulver, welches Baumwolle aus schar  lachroter     Küpe    in echten, sehr reinen, feu  rigen, roten Tönen färbt. Das neue Produkt  löst sich mit blauroter Farbe in konzentrier  ter Schwefelsäure, in Wasser gegossen schei  den aus dieser Lösung orangerote Flocken  aus. In siedendem     Xylol    löst es sich mit gel  ber Farbe und schwacher gelbgrüner Fluo  reszenz; in siedendem Nitrobenzol orange  rot mit schwach gelbgrüner Fluoreszenz; in  Anilin mit orangeroter Farbe.    <I>Beispiel:</I>    <B>100</B> Teile Phenol werden mit<B>5</B> Teilen  Natriumkarbonat versetzt und zum Vertrei  ben des Wassers aus der Mischung 'kurze Zeit  im Sieden erhalten.

   Hierauf     lässt    man ab-    kühlen, versetzt mit<B>5</B> Teilen     Trielilorpyr-          anthron    (welches zweckmässig nach Beispiel  <B>3</B> des<B>D.</B>     R.    P.     Nr.   <B>2,18162</B> hergestellt worden  ist) und erhitzt einige Stunden -zum Sieden.  Während des     Siedeus    tritt langsam Farben  umschlag von orange nach orangerot ein und  der neue Farbstoff scheidet sich aus. Hier  auf     lässt    man abkühlen, versetzt mit 200 Tei  len Alkohol,     filtriert    den     ausgesehiedenen     Farbstoff ab,     wäselit    ihn mit heissem Wasser  und trocknet ihn.



  Process for the production of a vat dye of the pyranthrone series. It has been found that a new vat dye of the pyranthrone series is obtained if the trichloropyrantlirone, which it can be obtained from, is obtained according to the information in Example 3 of the D. RP No. 2181 # 62, condensed with phenol in the presence of alkali carbonate.



  The dye obtained forms an orange-red powder which dyes cotton from a sharp, laugh-red vat in real, very pure, fiery red tones. The new product dissolves in concentrated sulfuric acid with a blue-red color; when poured into water, orange-red flakes separate from this solution. It dissolves in boiling xylene with a yellow color and a weak yellow-green fluorescence; in boiling nitrobenzene orange red with pale yellow-green fluorescence; in aniline with an orange-red color. <I> Example: </I> <B> 100 </B> parts of phenol are mixed with <B> 5 </B> parts of sodium carbonate and boiled for a short time to drive the water out of the mixture.

   It is then allowed to cool, mixed with <B> 5 </B> parts of Trielilorpyranthron (which is expediently according to example <B> 3 </B> of <B> D. </B> RP No. <B> 2,18162 </B>) and heated to boiling for a few hours. During the boiling process, the color slowly changes from orange to orange-red and the new dye separates out. Here it is allowed to cool, 200 parts of alcohol are added, the dye that has separated out is filtered off, washed with hot water and dried.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines neuen Küpenfarbstoffes der Pyranthronreille, da durch gekennzeichnet, dass man das Tri- chlorpyranthron, das erhalten werden kann nach den Angaben des Beispiels<B>3</B> des<B>D.</B> R. P. Nr. <B>218162,</B> mit Plienol in Gegenwart von Alkalikarbonat kondensiert. Der erhaltene Farbstoff bildet ein orange rotes Pulver, welches Baumwolle aus schar lachroter Küpe in echten, sehr reinen, feu rigen, roten Tönen färbt. PATENT CLAIM: Process for the production of a new vat dye of the Pyranthronreille, characterized in that the trichloropyranthrone, which can be obtained according to the information in Example 3 of the D. RP No. <B> 218162, </B> condensed with plienol in the presence of alkali carbonate. The dye obtained forms an orange-red powder which dyes cotton from a sharp, laugh-red vat in real, very pure, fiery red tones. Das neue Produkt löst sieh mit blauroter Farbe in konzentrier ter Schwefelsäure, in Wasser gegossen seliei- den aus dieser Lösung orangerote Flocken aus. In siedendem Xylol löst es sich mit gelber Farbe und schwacher gelbgrüner Fluoreszenz; in siedendem Nitrobenzol orangerot mit schwach gelbgrüner Fluores zenz<B>;</B> in Anilin mit orangeroter Farbe. The new product dissolves in concentrated sulfuric acid with a blue-red color, and when poured into water, this solution produces orange-red flakes. In boiling xylene, it dissolves with a yellow color and weak yellow-green fluorescence; in boiling nitrobenzene orange-red with pale yellow-green fluorescence <B>; </B> in aniline with orange-red color.
CH128007D 1927-04-01 1927-04-01 Process for the production of a vat dye of the pyranthrone series. CH128007A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH128007T 1927-04-01

Publications (1)

Publication Number Publication Date
CH128007A true CH128007A (en) 1928-10-01

Family

ID=4386516

Family Applications (1)

Application Number Title Priority Date Filing Date
CH128007D CH128007A (en) 1927-04-01 1927-04-01 Process for the production of a vat dye of the pyranthrone series.

Country Status (1)

Country Link
CH (1) CH128007A (en)

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