CH123644A - Process for the production of a diazo salt preparation for dyeing and printing. - Google Patents

Process for the production of a diazo salt preparation for dyeing and printing.

Info

Publication number
CH123644A
CH123644A CH123644DA CH123644A CH 123644 A CH123644 A CH 123644A CH 123644D A CH123644D A CH 123644DA CH 123644 A CH123644 A CH 123644A
Authority
CH
Switzerland
Prior art keywords
dyeing
diazo salt
ended
added
reaction
Prior art date
Application number
Other languages
German (de)
Inventor
Aktiengesellsc Farbenindustrie
Original Assignee
Ig Farbenindustrie Ag
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 Ig Farbenindustrie Ag filed Critical Ig Farbenindustrie Ag
Publication of CH123644A publication Critical patent/CH123644A/en

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

  

  Verfahren zur Herstellung eines     Diazosalzpräparates    für Färberei und     Druclcerei.       Es wurde gefunden, dass man ein gut  haltbares     Diazosalzpräparat    für Färberei und  Druckerei erhält, wenn man die wie üblich  hergestellte mineralsaure     Diazosalzlösung    von       4-Chlor-2-amino-l-anisol    mit einem     1.5-naph-          talindisulfosauren    Metallsalz umsetzt.  



  Das so erhaltene neutrale     1.5-Naphtalin-          disulfonat    des dianotierten     Chloraminoanisols          von        zum        Beispiel        32        %        Gehalt        an        Chlor-          aminoanisolbase    bildet ein fast weisses, gut  haltbares, lösliches, unmittelbar zum Aus  färben grundierter Baumwolle geeignetes     Di-          azosalzpräparat,    das zweckmässig mit geeig  neten, die Ausfärbungen,

   die Löslichkeit und  die Haltbarkeit günstig beeinflussenden Zu  sätzen und     Färbereihilfsmitteln,    wie zum  Beispiel Aluminiumsulfat oder Alaun,     aryl-          sulfosauren    Metallsalzen und dergleichen noch  auf 'einen handelsüblichen     Diazogehalt    einge  stellt wird.  



       Beispiel     Eine aus 158 Teilen     4-Chlor-2-amino-l-          anisol    in üblicher Weise hergestellte konzen-         trierte    Lösung des     Diazochlorids    wird mit  185 Teilen     1.5-naphtalindisulfosaurem    Na  trium,     Molekulargewicht    332; bis zur völligen  Umsetzung verrührt- dann wird     abfiltriert     und das     Diazosalz    bei mässiger Temperatur  getrocknet und unter Umständen durch Ver  mischen mit -geeigneten     Färbereihilfsstoffen     in handelsfertige Form gebracht.

   Diese Zu  sätze können auch dem noch feuchten     Diazo-          salz    zugemischt werden.



  Process for the production of a diazo salt preparation for dyeing and printing. It has been found that a diazo salt preparation with good stability for dyeing and printing is obtained if the conventionally prepared mineral acid diazo salt solution of 4-chloro-2-amino-1-anisole is reacted with a 1,5-naphthalenedisulfonic acid metal salt.



  The neutral 1,5-naphthalene disulfonate of the dianotized chloraminoanisole obtained in this way, for example 32% chloroaminoanisole content, forms an almost white, well-preserved, soluble, diazo salt preparation suitable for dyeing primed cotton, which is conveniently mixed with the Discoloration,

   the solubility and shelf life of additives and dyeing auxiliaries, such as aluminum sulfate or alum, aryl sulfonic acid metal salts and the like, which have a beneficial effect on the shelf life, are still set to a commercial diazo content.



       EXAMPLE A concentrated solution of the diazo chloride prepared in a conventional manner from 158 parts of 4-chloro-2-amino-l-anisole is trium with 185 parts of 1.5-naphthalene disulfonic acid, molecular weight 332; Stirred until complete conversion - then it is filtered off and the diazo salt is dried at a moderate temperature and, under certain circumstances, brought into commercial form by mixing it with suitable dyeing auxiliaries.

   These additives can also be added to the still moist diazo salt.

 

Claims (1)

PATENTANSPRUCH: ' Verfahren zur Herstellung eines Diazo- salzpräparates für Färberei und Druckerei, dadurch gekennzeichnet, dass man die wie üblich hergestellte mineralsaure Diazosalz- lösung von 4-Chlor-2-amino-l-anisol mit einem 1.5-naphtalindisulfosauren Metallsalz um setzt. PATENT CLAIM: A process for the production of a diazo salt preparation for dyeing and printing, characterized in that the normally produced mineral acid diazo salt solution of 4-chloro-2-amino-1-anisole is converted with a 1.5-naphthalene disulphonic acid metal salt. Das so erhaltene neutrale 1.5-Naphtalin- disulfonat des dianotierten Chloraminoanisols bildet ein fast weisses, gut haltbares, lösli ches, unmittelbar zum Ausfärben grundierter Baumwolle geeignetes Diazosalzpräparat. UNTERANSPRüCHE r. Verfahren nach Patentanspruch, dadurch gekennzeichnet, dass man nach beendeter Reaktion noch einen Färbereihilfsstoff zu setzt. \?. Verfahren nach Patentanspruch, dadurch gekennzeichnet, dass man nach beendeter Reaktion noch Aluminiumsulfat zusetzt. 3. The neutral 1,5-naphthalene disulfonate of the dianotized chloraminoanisole obtained in this way forms an almost white, easily durable, soluble diazo salt preparation that is immediately suitable for coloring primed cotton. SUBClaims r. Process according to patent claim, characterized in that after the reaction has ended, a dyeing auxiliary is also added. \ ?. Process according to claim, characterized in that after the reaction has ended, aluminum sulfate is also added. 3. Verfahren nach Patentanspruch, dadurch gekennzeichnet, dass man nach beendeter Reaktion noch Alaun zusetzt. 4. Verfahren nach Patentanspruch, dadurch gekennzeichnet, dass man nach beendeter Reaktion noch ein ary1sulfonsaures Metall salz zusetzt. Process according to patent claim, characterized in that alum is also added after the reaction has ended. 4. The method according to claim, characterized in that, after the reaction has ended, an ary1sulfonic acid metal salt is added.
CH123644D 1925-01-19 1926-01-18 Process for the production of a diazo salt preparation for dyeing and printing. CH123644A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE123644X 1925-01-19
CH121789T 1926-01-18

Publications (1)

Publication Number Publication Date
CH123644A true CH123644A (en) 1927-12-01

Family

ID=25709761

Family Applications (1)

Application Number Title Priority Date Filing Date
CH123644D CH123644A (en) 1925-01-19 1926-01-18 Process for the production of a diazo salt preparation for dyeing and printing.

Country Status (1)

Country Link
CH (1) CH123644A (en)

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