CH203594A - Process for the preparation of a water-soluble azo dye. - Google Patents

Process for the preparation of a water-soluble azo dye.

Info

Publication number
CH203594A
CH203594A CH203594DA CH203594A CH 203594 A CH203594 A CH 203594A CH 203594D A CH203594D A CH 203594DA CH 203594 A CH203594 A CH 203594A
Authority
CH
Switzerland
Prior art keywords
water
soluble azo
azo dye
preparation
brown
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 CH203594A publication Critical patent/CH203594A/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
    • C09B29/00—Monoazo dyes prepared by diazotising and coupling
    • 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
    • C09B29/00—Monoazo dyes prepared by diazotising and coupling
    • C09B29/24—Monoazo dyes prepared by diazotising and coupling from coupling components containing both hydroxyl and amino directing groups
    • C09B29/28—Amino naphthols
    • C09B29/30—Amino naphtholsulfonic acid

Landscapes

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

Description

  

  Verfahren zur Herstellung eines wasserlöslichen     Azofarbstoffes.       Gegenstand des vorliegenden Zusatz  patentes ist ein Verfahren zur Herstellung  eines wasserlöslichen     Azofarbstoffes,    welches  dadurch gekennzeichnet ist, dass man diano  tierte     p-Aminobenzolmonosulfonsäure    mit 2  (Sulfoäthylamino)-8-naphtol-6-sulfonsäure in  alkalischem Medium vereinigt.  



  <I>Beispiel:</I>  29,9 Gewichtsteile     p-aminobenzolmono-          sulfonsaures    Natrium     (Mol.        Gew.    299) wer  den in 400     Volumteilen    Wässer bei 65   C  gelöst, unter Rühren auf<B>10'</B> C gekühlt und  mit     gesättigter        Natriumchloridlösung    so weit  ausgefällt, dass der Auslauf auf Filtrier  papier nur noch gering ist. Dann wird mit  6,9 Gewichtsteilen     Natriumnitrit    versetzt,  10 Minuten nachgerührt, und 30     Volumteile     roher Salzsäure von 20'     B6        werden    schnell  hinzugefügt.

   Nach beendeter Dianotierung  wird bei 0   C langsam in eine     sodaalkalische     Lösung von 41 Gewichtsteilen des Dinatrium-         salzes    der     2-(Sulfoäthylamino)-8-naphtol-6-          sulfonsäure    gegeben. Die Endreaktion muss       sodaalkalisch    sein. Der gebildete Farbstoff  wird wie üblich isoliert und getrocknet.  



  Er bildet ein braunes Pulver, das sich in  Wasser mit brauner Farbe löst und Leder  in tiefbraunen Tönen einfärbt.



  Process for the preparation of a water-soluble azo dye. The subject of the present additional patent is a process for the production of a water-soluble azo dye, which is characterized in that diano-oriented p-aminobenzene monosulfonic acid is combined with 2 (sulfoethylamino) -8-naphthol-6-sulfonic acid in an alkaline medium.



  <I> Example: </I> 29.9 parts by weight of p-aminobenzene monosulfonic acid sodium (mol. Wt. 299) are dissolved in 400 parts by volume of water at 65 ° C., with stirring to <B> 10 '</B> C cooled and precipitated with saturated sodium chloride solution so far that the leakage on filter paper is only slight. Then 6.9 parts by weight of sodium nitrite are added, stirring is continued for 10 minutes, and 30 parts by volume of crude hydrochloric acid of 20 'B6 are quickly added.

   When the dianotization is complete, it is slowly added at 0 ° C. to a soda-alkaline solution of 41 parts by weight of the disodium salt of 2- (sulfoethylamino) -8-naphthol-6-sulfonic acid. The end reaction must be soda-alkaline. The dye formed is isolated as usual and dried.



  It forms a brown powder that dissolves in water with a brown color and dyes leather in deep brown tones.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines wasser löslichen Azofarbstoffes, dadurch gekenn zeichnet, dass man dianotierte p-Aminobenzol- monosulfonsäure mit 2-(Sulfoäthylamino)-8- naphtol-6-sulfonsäure in alkalischem Medium vereinigt. Der so erhaltene Farbstoff bildet ein braunes Pulver, das sich in Wasser mit brau ner Farbe löst und Leder in tiefbraunen Tönen einfärbt. PATENT CLAIM: A process for the production of a water-soluble azo dye, characterized in that dianotated p-aminobenzene-monosulfonic acid is combined with 2- (sulfoethylamino) -8-naphthol-6-sulfonic acid in an alkaline medium. The dye thus obtained forms a brown powder which dissolves in water with a brown color and dyes leather in deep brown shades.
CH203594D 1935-10-15 1936-10-09 Process for the preparation of a water-soluble azo dye. CH203594A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE203594X 1935-10-15
CH199460T 1938-08-31

Publications (1)

Publication Number Publication Date
CH203594A true CH203594A (en) 1939-03-15

Family

ID=25723291

Family Applications (1)

Application Number Title Priority Date Filing Date
CH203594D CH203594A (en) 1935-10-15 1936-10-09 Process for the preparation of a water-soluble azo dye.

Country Status (1)

Country Link
CH (1) CH203594A (en)

Similar Documents

Publication Publication Date Title
CH203597A (en) Process for the preparation of a water-soluble azo dye.
CH204145A (en) Process for the preparation of a water-soluble disazo dye.
CH202429A (en) Process for the preparation of a water-soluble monoazo dye.
CH204147A (en) Process for the preparation of a water-soluble disazo dye.
CH203596A (en) Process for the preparation of a water-soluble azo dye.
CH202437A (en) Process for the preparation of a water-soluble monoazo dye.
CH210495A (en) Process for the preparation of a water-soluble azo dye.
CH202430A (en) Process for the preparation of a water-soluble monoazo dye.
CH214806A (en) Process for the preparation of an azo dye.
CH211662A (en) Process for the preparation of an azo dye.
CH199964A (en) Process for the preparation of an azo dye.
CH204148A (en) Process for the preparation of a water-soluble disazo dye.
CH204141A (en) Process for the preparation of a water-soluble disazo dye.
CH183455A (en) Process for the preparation of an azo dye.
CH203599A (en) Process for the preparation of a water-soluble azo dye.
CH199963A (en) Process for the preparation of an azo dye.
CH187020A (en) Process for the preparation of an azo dye.
CH202173A (en) Process for the preparation of a nitro dye.
CH202435A (en) Process for the preparation of a water-soluble monoazo dye.
CH203619A (en) Process for the preparation of an azo dye.
CH209560A (en) Process for the preparation of a water-soluble azo dye.
CH202431A (en) Process for the preparation of a water-soluble monoazo dye.
CH187019A (en) Process for the preparation of an azo dye.
CH204139A (en) Process for the preparation of a water-soluble disazo dye.
CH203593A (en) Process for the preparation of a water-soluble azo dye.