CH135219A - Process for the production of a new chromium-containing dye. - Google Patents

Process for the production of a new chromium-containing dye.

Info

Publication number
CH135219A
CH135219A CH135219DA CH135219A CH 135219 A CH135219 A CH 135219A CH 135219D A CH135219D A CH 135219DA CH 135219 A CH135219 A CH 135219A
Authority
CH
Switzerland
Prior art keywords
yellow
acid
production
dye
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 CH135219A publication Critical patent/CH135219A/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B45/00—Complex metal compounds of azo dyes
    • C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
    • C09B45/14—Monoazo compounds
    • C09B45/16—Monoazo compounds containing chromium

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)
  • Paper (AREA)

Description

  

  Verfahren zur Herstellung eines neuen     ehromhaltigen    Farbstoffes.    Es wurde gefunden,     dass    man einen neuen  wertvollen     ehromhaltigen    Farbstoff erhält,  wenn man     diazotierte        2-Amitio-l-oxybenzol-          4,6-disulfosäure    mit     1-Phenyl-3-methyl-5-          pyrazolon    vereinigt und den erhaltenen     Azo-          farbstoff    mit     ehromabgebenden    Mitteln be  handelt.  



  Der erhaltene     ehromhaltige    Farbstoff stellt  getrocknet ein gelbbraunes Pulver dar, löst  sich in Wasser mit     gelboranger,        in    wässeriger  Natronlauge mit     gelboranger,    in konzentrierter  Schwefelsäure mit gelber Farbe und färbt  Wolle in     schwefelsaurern    Färbebade in sehr  gleichmässigen     Orangetönen    von sehr guten  Echtheitseigenschaften.  



  <I>Beispiel:</I>  <B>26,9</B> Teile     2-Ainino-l-oxybenzol-4,6-disulfo-          säure    werden in 200 Teilen Wasser gelöst  beziehungsweise suspendiert und nach Zusatz  von<B>30</B> Teilen Salzsäure und Eis bei<B>0-5 0</B>  wie üblich mit<B>7</B> Teilen     Natriumnitrit        diazo-          tiert.    Man     lässt    nun die     Diazolbsung    unter    Rühren einlaufen in eine eiskalte Auflösung  von     17,4Teilei)        1-Phenyl-3-methyl-5-pyi-azolon     und<B>30</B> Teilen     Natriumcarbonat    in<B>300</B> Teilen  Wasser.

   Nach beendigter Kupplung wärmt  man auf<B>60 0</B> an, salzt den Farbstoff mit  Kochsalz aus, filtriert,     presst    und trocknet.  Er bildet ein     gelbstithig    rotes Pulver, das  sich in Wasser orangerot, in konzentrierter  Schwefelsäure rein gelb löst. Wolle wird aus  saurem Bade gelbbraun angefärbt; die Farbe  schlägt beim     Nachchromieren    nach Orange  rot um.  



  <B>95,2</B> Teile des so erhaltenen Farbstoffes  werden in 2000 Teilen Wasser kochend ge  löst, hernach mit 30,4 Teilen Chromoxyd,  in Form einer     Fluorchromlösung,    versetzt  und längere Zeit     rückfliessend    gekocht. Durch  Eindampfen- und     Kristallisierenlassen    wird  der Farbstoff gewonnen.



  Process for the preparation of a new Ehrom-containing dye. It has been found that a new valuable Ehrom-containing dye is obtained if diazotized 2-amino-1-oxybenzene-4,6-disulfonic acid is combined with 1-phenyl-3-methyl-5-pyrazolone and the resulting azo dye with Ehrom-donating Funds treated.



  The dyestuff containing Ehrom is a yellow-brown powder when dried, dissolves in water with yellow-orange, in aqueous sodium hydroxide solution with yellow-orange, in concentrated sulfuric acid with yellow color and dyes wool in a sulfuric-acid dyebath in very even orange tones with very good fastness properties.



  <I> Example: </I> <B> 26.9 </B> parts of 2-amino-1-oxybenzene-4,6-disulphonic acid are dissolved or suspended in 200 parts of water and, after the addition of <B> 30 parts hydrochloric acid and ice at <B> 0-5 0 </B> as usual with <B> 7 </B> parts sodium nitrite diazotized. The diazole solution is now allowed to run into an ice-cold solution of 17.4 parts of 1-phenyl-3-methyl-5-pyi-azolone and 30 parts of sodium carbonate in 300 parts Share water.

   When the coupling is complete, the mixture is warmed to <B> 60 0 </B>, the dye is salted out with sodium chloride, filtered, pressed and dried. It forms a yellowish red powder that dissolves orange-red in water and pure yellow in concentrated sulfuric acid. Wool is dyed yellow-brown from an acid bath; the color changes to orange red when chromium plating.



  95.2 parts of the dye thus obtained are dissolved at the boil in 2000 parts of water, 30.4 parts of chromium oxide, in the form of a fluorochrome solution, are then added and the mixture is refluxed for a long time. The dye is obtained by allowing it to evaporate and crystallize.

Claims (1)

PAT.ENTANSPRUCH: Verfahren zur Herstellung eines neuen chromhaltigen Farbstoffes, dadurch gekenn- zeichnet, dass man diazotierte 2-Amino-l- oxybenzol-4,6-disulfosäure mit 1-Phenyl-3- methyl-5-pyrazolon vereinigt und den er haltenen Azofarbstoff mit ehromabgebenden Mitteln behandelt. PATENT CLAIM: Process for the production of a new chromium-containing dye, characterized in that diazotized 2-amino-l-oxybenzene-4,6-disulfonic acid is combined with 1-phenyl-3-methyl-5-pyrazolone and obtained Azo dye treated with Ehroma donating agents. Der erhaltene ehromhaltige Farbstoff stellt getrocknet ein gelbbraunes Pulver dar, löst sich in Wasser und in wässeriger Natron- lauge mit gelboranger, in konzentrierter Schwefelsäure mit gelber Farbe und färbt Wolle in schwefelsaurem Färbebade- in schi- gleichmässigen Orangetönen von sehr guten Echtheitseigenschaften. The dyestuff containing Ehrom is a yellow-brown powder when dried, dissolves in water and in aqueous sodium hydroxide solution with yellow-orange color, in concentrated sulfuric acid with yellow color and dyes wool in a sulfuric-acid dyebath in uniform orange tones with very good fastness properties.
CH135219D 1928-04-19 1928-04-19 Process for the production of a new chromium-containing dye. CH135219A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH135219T 1928-04-19

Publications (1)

Publication Number Publication Date
CH135219A true CH135219A (en) 1929-09-15

Family

ID=4393130

Family Applications (1)

Application Number Title Priority Date Filing Date
CH135219D CH135219A (en) 1928-04-19 1928-04-19 Process for the production of a new chromium-containing dye.

Country Status (1)

Country Link
CH (1) CH135219A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998058025A1 (en) * 1997-06-14 1998-12-23 Clariant Finance (Bvi) Limited Method for dying aluminum oxide layers

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998058025A1 (en) * 1997-06-14 1998-12-23 Clariant Finance (Bvi) Limited Method for dying aluminum oxide layers
US6309427B1 (en) * 1997-06-14 2001-10-30 Clariant Finance (Bvi) Limited Method of coloring aluminum oxide layers

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