[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

CH288427A - Process for the preparation of a new trisazo dye. - Google Patents

Process for the preparation of a new trisazo dye.

Info

Publication number
CH288427A
CH288427A CH288427DA CH288427A CH 288427 A CH288427 A CH 288427A CH 288427D A CH288427D A CH 288427DA CH 288427 A CH288427 A CH 288427A
Authority
CH
Switzerland
Prior art keywords
compound
new
parts
coupled
preparation
Prior art date
Application number
Other languages
German (de)
Inventor
Limited Imperial Ch Industries
Original Assignee
Ici Ltd
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 Ici Ltd filed Critical Ici Ltd
Publication of CH288427A publication Critical patent/CH288427A/en

Links

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
    • C09B35/00Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
    • C09B35/38Trisazo dyes ot the type
    • C09B35/44Trisazo dyes ot the type the component K being a hydroxy amine
    • C09B35/46Trisazo dyes ot the type the component K being a hydroxy amine the component K being an amino naphthol

Landscapes

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

Description

  

  Verfahren zur Herstellung eines neuen     Trisazofarbstoffes.       Die     vorliegende    Erfindung bezieht sich       aiif    ein Verfahren zur     Herstellung    eines neuen       '1'risazofai:

  #bstoffes,    welcher volle     seliwarze     Farbtöne auf Leder in jedem      < gegerbten        Zii-          5tand    liefert, wobei die ei-zielten Farbtöne       -(#gen        Säuren        beständi-    sind und      < 111#e1    Ein-         wirkeng    von Alkalien kaum wesentlich ver  ändert werden.  



  Erfindungsgemäss wird ein neuer schwar  zer     Trisazofarbstoff    für Leder gemäss     fol-          (yeRder    Formel:  
EMI0001.0018     
         dadurch    erhalten,     da.ss    man     4,4'-Diaminostil-          ben        tetrazotiert    und 1     Mol.    der so     gebildeten          Tetrazoverbindung    in saurein Medium mit.

         111o1        1,8-Aminoiiaplitliol-a,6-disulfonsäure          kuppelt,    die     dureb        Diazotierung    von     Sulfanil-          @üure    Gebildete     Diazoverbindurig    in alkalischem       J-lediuni        finit    der so gebildeten     Diazoazover-          bindung    kuppelt und schliesslich die- so ge  bildete     Diazodisazov        erbindung    in     alkaliseheni     Medium mit 1.

       Mol        in-Aininophenol    kuppelt.  



  Die Erfindung sei durch das folgende Bei  spiel, in welchem die Teile Gewichtsteile be  deuten, erläutert.  



  <I>Beispiel:</I>  14 Teile     Natriumnitrit    werden einer Lö  sung von 21 Teilen     4,4'-Diaminostilben    in  einem     Gemisch    von 400 Teilen Wasser und  50 Teilen einer 36%igen     wässrigen    Lösung  von Chlorwasserstoff zugesetzt. Hierauf ver  setzt man dieses Gemisch innerhalb von 30     Mi-          nnten    bei Zimmertemperatur mit einer Lö-         sung        von    36,6 Teilen des     Dinatriumsalzes    der  1,8-     Aminonaphthol-3,6-disulfonsäure    in 250  Teilen Wasser und rührt das Gemisch wäh  rend 12 Stunden.

   Dann versetzt man langsam  mit     Natriumbiearbonat,        und    zwar in genügen  den Mengen, um das Gemisch zu neutralisie  ren. Das Gemisch wird auf 10  C gekühlt und  hierauf     finit    einer     wässrigen    Suspension des       Diazoniumchlorids,    welches aus 17,3 Teilen       Sulfanilsäure    erhalten wird, versetzt. Hierauf  fügt man dem Gemisch genügend Natrium  carbonat hinzu,     iun    es     lackmusalkalisch    zu  stellen, worauf man es während 1     Stunde    bei  10  C rührt.

   Eine Lösung von 10,9 Teilen       ni-Aminophenol    und 4 Teilen     Ätznatron    in  150 Teilen Wasser wird dann hinzugegeben  und das Gemisch während 4 Stunden bei 10  C  gerührt. Dann wird es durch Zugabe von  Salzsäure gerade sauer gestellt, worauf der  ausgefällte Farbstoff     abfiltriert,    gewaschen,  getrocknet und gemahlen wird. Das so er-           haltene    schwarze Pulver ist in Wasser löslich,  und die Lösung färbt Leder in neutralen  grauen bis schwarzen Farbtönen von guter  Echtheit.



  Process for the preparation of a new trisazo dye. The present invention relates to a process for the preparation of a new '1'risazofai:

  # Substance, which delivers full black color tones on leather in every tanned condition, whereby the specific color tones - (# are resistant to acids and <111 # e1 the action of alkalis are hardly changed significantly.



  According to the invention, a new black trisazo dye is used for leather according to the following formula:
EMI0001.0018
         obtained by tetrazotizing 4,4'-diaminostilbene and adding 1 mol of the tetrazo compound thus formed in an acidic medium.

         111o1 1,8-Aminoiiaplitliol-a, 6-disulfonic acid couples, the diazo compound formed by the diazotization of sulfanilic acid in alkaline J-lediuni finitely couples the diazoazo compound thus formed and finally the so formed diazodisazo compound in an alkali metal compound 1.

       Mol in-amino phenol couples.



  The invention is illustrated by the following example, in which the parts are parts by weight.



  <I> Example: </I> 14 parts of sodium nitrite are added to a solution of 21 parts of 4,4'-diaminostilbene in a mixture of 400 parts of water and 50 parts of a 36% strength aqueous solution of hydrogen chloride. This mixture is then added within 30 minutes at room temperature to a solution of 36.6 parts of the disodium salt of 1,8-aminonaphthol-3,6-disulfonic acid in 250 parts of water and the mixture is stirred for 12 hours .

   Sodium carbonate is then slowly added, in sufficient quantities to neutralize the mixture. The mixture is cooled to 10 ° C. and an aqueous suspension of diazonium chloride, which is obtained from 17.3 parts of sulfanilic acid, is added. Sufficient sodium carbonate is then added to the mixture to make it litmus-alkaline, whereupon it is stirred at 10 ° C. for 1 hour.

   A solution of 10.9 parts of ni-aminophenol and 4 parts of caustic soda in 150 parts of water is then added and the mixture is stirred at 10 ° C. for 4 hours. Then it is just acidified by adding hydrochloric acid, whereupon the precipitated dye is filtered off, washed, dried and ground. The black powder obtained in this way is soluble in water, and the solution dyes leather in neutral gray to black shades of good fastness.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines neuen schwarzen Trisazofarbstoffes für Leder der allgemeinen Formel: EMI0002.0004 dadurch gekennzeichnet; dass man 4,4'-Di- aminostilben tetrazotiert und 1 Mol der so gebildeten Tetrazoverbindung in saurem Me dium mit 1 1M1 1,8-Aminonaphthol-3,6-disul- fonsäure kuppelt, PATENT CLAIM: Process for the production of a new black trisazo dye for leather of the general formula: EMI0002.0004 characterized; that 4,4'-di-aminostilbene is tetrazotized and 1 mol of the tetrazo compound thus formed is coupled in acidic medium with 1 1M1 1,8-aminonaphthol-3,6-disulfonic acid, worauf man die durch Di- azotierung von Sulfanilsäure gebildete Diazo- v erbindung in alkalischem Medium mit der so gebildeten Diazoazoverbindung kuppelt und schliesslich die so gebildete Diazodisa.zoverbin- dung in alkalischem Medium mit 1 Mol m Aminophenolkuppelt. Der neue Farbstoff ist ein schwarzes Pul ver, welches in Wasser löslich ist und Leder in neutralen grauen bis schwarzen Farbtönen von guter Echtheit färbt. whereupon the diazo compound formed by diazotization of sulfanilic acid is coupled in an alkaline medium with the diazoazo compound thus formed and finally the diazodiszo compound thus formed is coupled in an alkaline medium with 1 mol m of aminophenol. The new dye is a black powder that is soluble in water and dyes leather in neutral gray to black shades of good fastness.
CH288427D 1949-07-27 1950-07-27 Process for the preparation of a new trisazo dye. CH288427A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB288427X 1949-07-27

Publications (1)

Publication Number Publication Date
CH288427A true CH288427A (en) 1953-01-31

Family

ID=10282037

Family Applications (1)

Application Number Title Priority Date Filing Date
CH288427D CH288427A (en) 1949-07-27 1950-07-27 Process for the preparation of a new trisazo dye.

Country Status (1)

Country Link
CH (1) CH288427A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4006130A (en) * 1973-12-06 1977-02-01 Bayer Aktiengesellschaft Triaszo dyestuffs containing etherified or esterified hydroxyl groups

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4006130A (en) * 1973-12-06 1977-02-01 Bayer Aktiengesellschaft Triaszo dyestuffs containing etherified or esterified hydroxyl groups

Similar Documents

Publication Publication Date Title
CH288427A (en) Process for the preparation of a new trisazo dye.
DE868034C (en) Process for the preparation of new trisazo dyes
DE926385C (en) Process for the preparation of a new copper-containing disazo dye
DE843452C (en) Process for the preparation of a new trisazo dye
CH251878A (en) Process for the production of a new azo dye.
CH292650A (en) Process for the preparation of a trisazo dye.
CH239328A (en) Process for the preparation of a disazo dye.
CH249545A (en) Process for the preparation of a trisazo dye.
CH190620A (en) Process for the preparation of an azo dye.
CH239326A (en) Process for the preparation of a disazo dye.
CH90837A (en) Process for the preparation of a substantive o-oxyazo dye.
CH239325A (en) Process for the preparation of a disazo dye.
CH292649A (en) Process for the preparation of a trisazo dye.
CH284265A (en) Process for the preparation of a monoazo dye.
CH249547A (en) Process for the preparation of a trisazo dye.
CH292651A (en) Process for the preparation of a trisazo dye.
CH191735A (en) Process for the production of a new copper-containing azo dye.
CH249544A (en) Process for the preparation of a trisazo dye.
CH299709A (en) Process for the preparation of a trisazo dye.
CH292648A (en) Process for the preparation of a trisazo dye.
CH218817A (en) Process for the preparation of a disazo dye.
CH249543A (en) Process for the preparation of a trisazo dye.
CH249546A (en) Process for the preparation of a trisazo dye.
CH239322A (en) Process for the preparation of a disazo dye.
CH239331A (en) Process for the preparation of a disazo dye.