AT57136B - Process for the preparation of leuco compounds from the dyes obtainable according to the process of Patent No. 55688. - Google Patents

Process for the preparation of leuco compounds from the dyes obtainable according to the process of Patent No. 55688.

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Publication number
AT57136B
AT57136B AT57136DA AT57136B AT 57136 B AT57136 B AT 57136B AT 57136D A AT57136D A AT 57136DA AT 57136 B AT57136 B AT 57136B
Authority
AT
Austria
Prior art keywords
preparation
leuco compounds
obtainable according
dyes obtainable
dyes
Prior art date
Application number
Other languages
German (de)
Original Assignee
Farbenfab Vorm Bayer F & Co
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 Farbenfab Vorm Bayer F & Co filed Critical Farbenfab Vorm Bayer F & Co
Application granted granted Critical
Publication of AT57136B publication Critical patent/AT57136B/en

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  • Coloring (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Investigating Or Analysing Biological Materials (AREA)

Description

  

   <Desc/Clms Page number 1> 
 



  Verfahren zur Darstellung von Leukoverbindungen aus den gemäss dem Verfahren des
Patentes   Nr.   55688 erhältlichen Farbstoffen. 



   Durch das Patent Nr. 55688 ist ein Verfahren zur Darstellung von Oxazinfarbstoffen, die aus   Pyrogallolderivaten   und   p-Nitrosophenolen   oder   Chinonch1orimiden   erhalten werden, 
 EMI1.1 
 Farbstoffe mit Salzen   der schwefligen Säure behandelt. Dies ist um   so überraschender, als man bei der Reduktion mit freier schwefliger Säure nur Leuliokörper von der gleichen Nuance erhält, wie sie die mit anderen gebräuchlichen Reduktionsmitteln erhältlichen Produkte liefern. 



   In dem Britischen Patente Nr. 11556 A. D.   18 ! J3   und in der amerikanischen Patent- 
 EMI1.2 
 weise aus p-Nitrosophenolen entsprechend, die Hydroxylgruppe des   Nitrosophenols   nicht zur   Ringbildung herangezogen wird, sondern   als solche in dem entstandenen Farbstoff beziehungsweise seiner Leukoverbindung unverändert enthalten ist Im ersteren Fall ist also 
 EMI1.3 
 Kerne Hydroxylgruppen. 



    Beispiel 1.   



   30 Teile des Farbstoffes aus Gallaminsäure und Nitrosophenol oder die äquivalente 
 EMI1.4 
   mehr enthalt, saugt man ab ; das Produkt kann direkt   als Paste für Druckereizwecke Verwendung tinden. Die Nuance des chromlackes ist ein   rötliches   Korinth und bedeutend brauner als die mit dem Ausgangsmaterial erhältliche. Der Chromalck zeichnet sich ebenfalls durch chlor- und Seifenechtheit aus. 



   Beispiel 2. 

**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.



   <Desc / Clms Page number 1>
 



  Method for the preparation of leuco compounds from the according to the method of
U.S. Patent No. 55688.



   Patent No. 55688 describes a process for the preparation of oxazine dyes which are obtained from pyrogallol derivatives and p-nitrosophenols or quinone chlorimides,
 EMI1.1
 Dyes treated with salts of sulphurous acid. This is all the more surprising since the reduction with free sulphurous acid only gives Leulio bodies of the same shade as the products obtainable with other common reducing agents.



   In British Patent No. 11556 A.D. 18! J3 and in the American patent
 EMI1.2
 wise from p-nitrosophenols accordingly, the hydroxyl group of the nitrosophenol is not used for ring formation, but as such is contained unchanged in the resulting dye or its leuco compound. In the first case is therefore
 EMI1.3
 Nuclei hydroxyl groups.



    Example 1.



   30 parts of the dye from gallamic acid and nitrosophenol or the equivalent
 EMI1.4
   contains more, one sucks off; the product can be used directly as a paste for printing purposes. The shade of the chrome lacquer is a reddish Corinth and significantly more brown than that available with the original material. The Chromalck is also characterized by its resistance to chlorine and soap.



   Example 2.

** WARNING ** End of DESC field may overlap beginning of CLMS **.

 

Claims (1)

3 l'eile des Farbstoffes aus Gallaminsaure und Nitrosopheuol oder die äquivalente EMI1.5 von 30 Teilen Natriumsulfit verrührt. Sobald die Reduktion beendigt ist, gibt man Koch- salz LU und saugt ab, PATENT-ANSPRÜCHE: Verfahren zur Darstellung von Leukoverbindungen aus den gemäss dem Verfahren des EMI1.6 **WARNUNG** Ende CLMS Feld Kannt Anfang DESC uberlappen**. 3 l'eile of the dye from gallamic acid and nitrosopheuene or the equivalent EMI1.5 stirred by 30 parts of sodium sulfite. As soon as the reduction is over, you give table salt LU and suck off, PATENT CLAIMS: Method for the preparation of leuco compounds from the according to the method of EMI1.6 ** WARNING ** End of CLMS field may overlap beginning of DESC **.
AT57136D 1910-08-27 1911-08-18 Process for the preparation of leuco compounds from the dyes obtainable according to the process of Patent No. 55688. AT57136B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE57136X 1910-08-27

Publications (1)

Publication Number Publication Date
AT57136B true AT57136B (en) 1913-01-10

Family

ID=5629039

Family Applications (1)

Application Number Title Priority Date Filing Date
AT57136D AT57136B (en) 1910-08-27 1911-08-18 Process for the preparation of leuco compounds from the dyes obtainable according to the process of Patent No. 55688.

Country Status (1)

Country Link
AT (1) AT57136B (en)

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