DE698926C - Process for the production of a water-insoluble azo dye on vegetable fibers - Google Patents

Process for the production of a water-insoluble azo dye on vegetable fibers

Info

Publication number
DE698926C
DE698926C DE1937I0058589 DEI0058589D DE698926C DE 698926 C DE698926 C DE 698926C DE 1937I0058589 DE1937I0058589 DE 1937I0058589 DE I0058589 D DEI0058589 D DE I0058589D DE 698926 C DE698926 C DE 698926C
Authority
DE
Germany
Prior art keywords
water
vegetable fibers
azo dye
insoluble azo
production
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
DE1937I0058589
Other languages
German (de)
Inventor
Dr Ernst Heinrich
Dr Werner Zerweck
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
IG Farbenindustrie AG
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
Priority to DE1937I0058589 priority Critical patent/DE698926C/en
Application granted granted Critical
Publication of DE698926C publication Critical patent/DE698926C/en
Expired legal-status Critical Current

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
    • C09B29/10—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
    • C09B29/18—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides
    • C09B29/20—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides of the naphthalene series

Landscapes

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

Description

Verfahren zur Herstellung eines wasserunlöslichen Azofarbstoffs auf pflanzlichen Fasern Es wurde gefunden, daß man lebhafte rüte Färbungen auf pflan#zli#lilen Fasern erhält, wenn man- 2- (2, 3'-Oxynaphi.thoylamino) -naphthalin mit diazotiertem i-Amino-2-m#eihoxybeilzol-5-stilfonsäure-n-bu,tylamid nach Eisfarbdnart vereinigt.Process for the preparation of a water-insoluble azo dye Vegetable Fibers It has been found that vivid, dark colorations can be found on vegetable fibers Fibers are obtained when 2- (2, 3'-Oxynaphi.thoylamino) naphthalene is diazotized i-Amino-2-m # eihoxybeilzol-5-stilfonsäure-n-bu, tylamide combined according to ice color.

Man erhält im Gegensatz zu den Angaben in der Patetitschlift 604 135 eine gut naßechte sowie sehr gut lichtechte lebhafte rote Färbung, die der bekannten, durch Kuippeln vo-ndiazotiertem i-Amin0-2-Ä.thoxybenz,ul-5-s-ulfo,n,säuredim,eth.ylanud mit der gleich-en Azokomponente erhältlichen Färbung in der Lebhaftigkeit des Farbtons und in der Lichtechtheit überlegen ist. Beispiel 50 g abgekochtes Baumwollgarn werden in dem nachstehenden Grundierungsbad a 1/2 Stunde behandelt, durch Abwinden, Ab- quetschen oder Schleudern gut entm,ässert und in nachstehendem Entwicklungsbad b 1/2 Stunde entwickelt.In contrast to the information in Patetitschlift 604 135, the result is a good wetfast and very good lightfast vivid red coloration, similar to the known i-amin0-2-Ä.thoxybenz, ul-5-s-ulfo, n, säuredim, eth.ylanud with the same azo component available coloring is superior in the vividness of the hue and in the lightfastness. Example 50 g of boiled cotton are treated in the following Grundierungsbad a 1/2 hour, by unwinding, squeezing off or spinning entm well ässert and indicated in the following developing bath b 1/2 hour developed.

a. Grundierungsbad 2 9 2-(2', 3'-Oxynaphthoylamino)-iiaphthalin, 4 ccm Soprozentiges Türkischrotöl, 6 - Natronlauge von 34' B6, 2 - 3oprozentige Formaldehydlösung, 5oo. - siedendes Wasser, dann -mit Wasser aufgefüllt auf 1 1. b. Entwicklungsbad 2,6 g i-Amino-2-methoxybenzol-5-sulfonsäuren-butylarnid vom F. i:o3' C werden mit 2#,8 ccm Salzsäure von 22' B6 und o,7 g in etwas Wasser gelöstem Natriumnitrit unter Eiszusatz diazotiert. Nach Beendigung der Diazotierung stumpft man die Lösung mit etwa - 2,5 g Natriumacetat ab, setzt eine Lösung von 25,0 g Natriumchlorid in Wasser zu und füllt mit Wasser auf 11 auf. Dann wird Idas Färbegut gespült, kocIiend geseift, nochmals gespült und getrocknet.a. Primer bath 2 9 2- (2 ', 3'-Oxynaphthoylamino) -iiaphthalin, 4 ccm 5% Turkish red oil, 6 - caustic soda from 34' B6, 2 - 3% formaldehyde solution, 500. - boiling water, then -filled with water to 1 1. b. Development bath 2.6 g of i-amino-2-methoxybenzene-5-sulfonic acid butyl amide from F. i: o3 ' C are mixed with 2 #, 8 ccm of hydrochloric acid from 22' B6 and 0.7 g of sodium nitrite dissolved in a little water with the addition of ice diazotized. After completion of the diazotisation blunts the solution of about - 2.5 g of sodium acetate from a solution is of 25.0 g of sodium chloride in water and made up to 1 1 with water. Then Idas dyed material is rinsed, soaped with coconut oil, rinsed again and dried.

Man erhält so einelebhafte roteFärbungvon gu-#ten Naßechtheiten und sehr guter Lichtechtheit.This gives a vivid red coloration with good wet fastness properties and very good lightfastness.

Claims (1)

PATENTANSPRUCII'. Verfahren zur Herstellung eines wasserunlöslichen Azofarbstoffes auf pflanzlichen Fasern, dadurch, gekennzeichnet, d,aß man 2-(2', 3'-Oxynaphtho-ylaniiino)-nap-ii,thaliii mit diazotiertem i-Amino-2-methoxybenzol-5-sulfonsäure-n-butylamid nach Eisfarbenart vereinigt.PATENT CLAIM '. Process for the preparation of a water-insoluble Azo dye on vegetable fibers, characterized in that d, one ate 2- (2 ', 3'-Oxynaphtho-ylaniiino) -nap-ii, thaliii with diazotized i-amino-2-methoxybenzene-5-sulfonic acid-n-butylamide united in the manner of ice color.
DE1937I0058589 1937-07-20 1937-07-20 Process for the production of a water-insoluble azo dye on vegetable fibers Expired DE698926C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DE1937I0058589 DE698926C (en) 1937-07-20 1937-07-20 Process for the production of a water-insoluble azo dye on vegetable fibers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE1937I0058589 DE698926C (en) 1937-07-20 1937-07-20 Process for the production of a water-insoluble azo dye on vegetable fibers

Publications (1)

Publication Number Publication Date
DE698926C true DE698926C (en) 1940-11-20

Family

ID=7194809

Family Applications (1)

Application Number Title Priority Date Filing Date
DE1937I0058589 Expired DE698926C (en) 1937-07-20 1937-07-20 Process for the production of a water-insoluble azo dye on vegetable fibers

Country Status (1)

Country Link
DE (1) DE698926C (en)

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