CH138224A - 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
CH138224A
CH138224A CH138224DA CH138224A CH 138224 A CH138224 A CH 138224A CH 138224D A CH138224D A CH 138224DA CH 138224 A CH138224 A CH 138224A
Authority
CH
Switzerland
Prior art keywords
dye
amino
chromium
production
containing 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 CH138224A publication Critical patent/CH138224A/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
    • 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Coloring (AREA)

Description

  

  Zusatzpatent zum Hauptpatent     Nr.    136649.    Verfahren zur Herstellung eines neuen     ehromhaltigen    Farbstoffes.    Es wurde gefunden,     dass    man einen  neuen wertvollen     ehromhaltigen    Farbstoff  erhält, wenn man den     Azofarbstoff    aus     di-          azotierter        2--Amino-l-oxyna.pihthalin-4,8-di-          sulfosäure    und     2-Amino-5-oxynaphthalin-7-          sulfosäure    mit chromabgebenden Mitteln  und mit einem Oxydationsmittel behandelt,  wobei diese beiden Operationen nicht gleich  zeitig,

   sondern nacheinander durchgeführt       21     werden.  Der erhaltene     chromhaltige    Farbstoff  bildet getrocknet ein dunkles     P-Ltlv'er,    welches  in Wasser und in verdünnter     Sodalösung        mii     blauer und in konzentrierter Schwefelsäure  mit     rötlichschwarzer    Farbe löslich ist.  Er färbt     vegetabile    Fasern aus neutralem       Glaubersalzbade    in echten grünblauen Tö  nen an.  



  <I>Beispiel:</I>  Die<B>7</B> Teilen     Natriumnitrit    entsprechende       Menge        Diazoverbindung        der        2-Amino-1.-ox-        ,v-          naphthalin-4,8-disuliosäure    wird in Gegen  wart von Soda oder     Ammüniak    mit<B>23,9</B>    Teilen     2-Amino-5-oxynaphthalin-7-sulfosäure     kombiniert und der gebildete Farbstoff durch  Kochen mit einer     Fluorchromlösung,        entspre-          o'hend   <B>15</B> Teilen     Cr#01"    in die Chromverbin  dung übergeführt.

   Diese wird mit Soda. alka  lisch gestellt und vom     Chromsc'hlamm    durch  Filtrieren befreit. Die     Farbstofflösung    wird  darauf mit einer     Alkaliliypoehloritlösung,     entsprechend<B>1,0</B> bis<B>15</B> Teilen aktivem Chlor,  versetzt und nach beendeter Reaktion der  neue Farbstoff durch Eindampfen gewonnen.



  Additional patent to main patent No. 136649. Process for the production of a new Ehrom-containing dye. It has been found that a new valuable Ehrom-containing dye is obtained if the azo dye is obtained from diacotized 2 - amino-1-oxyna.phthalene-4,8-disulfonic acid and 2-amino-5-oxynaphthalene-7- sulfonic acid treated with chromium-releasing agents and with an oxidizing agent, these two operations not being carried out simultaneously,

   but be carried out one after the other 21. When dried, the chromium-containing dye obtained forms a dark P-Ltlv'er, which is soluble in water and in dilute soda solution with blue and in concentrated sulfuric acid with a reddish black color. It colors vegetable fibers from neutral Glauber's salt bath in real green-blue tones.



  <I> Example: </I> The <B> 7 </B> parts of sodium nitrite corresponding amount of diazo compound of 2-amino-1.-ox-, v-naphthalene-4,8-disulioic acid is in the presence of soda or Ammüniak combined with <B> 23.9 </B> parts of 2-amino-5-oxynaphthalene-7-sulfonic acid and the dye formed by boiling with a fluorochrome solution, corresponding to <B> 15 </B> parts of Cr # 01 "transferred to the chrome compound.

   This is made with soda. alkaline and freed from chrome lamb by filtering. The dye solution is then mixed with an alkali metal polypolorite solution, corresponding to <B> 1.0 </B> to <B> 15 </B> parts of active chlorine, and after the reaction has ended, the new dye is obtained by evaporation.

 

Claims (1)

PATENTANSPRUCH: -Verfahren zur Herstellung eines neuen chromhaltigen Farbstoffes, dadurch gekenn zeichnet, dass man den Azofarbstoff aus di- azetierter 2-Amino-l-oxynap,hthalin-4,8-di- sulfos#ä,ure und 9--Amino-5-oxynaplitliaJin-7- sulfosäure mit chromabgebenden Mitteln und mit einem Oxydationsmittel behandelt, wobei diese beiden Operationen nicht gleich zeitig, sondern nacheinander durchgeführt werden. PATENT CLAIM: -Process for the production of a new chromium-containing dye, characterized in that the azo dye from diacetated 2-amino-1-oxynap, hthalene-4,8-disulfos # ä, ure and 9 - amino 5-oxynaplitliaJin-7-sulfonic acid treated with chromium-releasing agents and with an oxidizing agent, these two operations not being carried out simultaneously but one after the other. Der erhaltene ehromhaItige Farbstoff bildet getrocknet ein dunkles Pulver, welches in Wasser und in verdünnter Sodalösung mit blauer und in konzentrierter Schwefelsäure mit rötlichschwarzer Farbe löslich ist. Er färbt vegetabile Fasern aus neutralem Gla.ubersa17,bade in echten grünblauen Tö nen an. When dried, the honest dye obtained forms a dark powder which is soluble in water and in dilute soda solution with blue and in concentrated sulfuric acid with a reddish black color. He dyes vegetable fibers from neutral glaze cover17, bathe in real green-blue tones.
CH138224D 1928-07-13 1928-07-13 Process for the production of a new chromium-containing dye. CH138224A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH136649T 1928-07-13
CH138224T 1928-07-13

Publications (1)

Publication Number Publication Date
CH138224A true CH138224A (en) 1930-02-15

Family

ID=25712778

Family Applications (1)

Application Number Title Priority Date Filing Date
CH138224D CH138224A (en) 1928-07-13 1928-07-13 Process for the production of a new chromium-containing dye.

Country Status (1)

Country Link
CH (1) CH138224A (en)

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