DE409280C - Process for the preparation of monoazo dyes for wool - Google Patents
Process for the preparation of monoazo dyes for woolInfo
- Publication number
- DE409280C DE409280C DEF51649D DEF0051649D DE409280C DE 409280 C DE409280 C DE 409280C DE F51649 D DEF51649 D DE F51649D DE F0051649 D DEF0051649 D DE F0051649D DE 409280 C DE409280 C DE 409280C
- Authority
- DE
- Germany
- Prior art keywords
- wool
- preparation
- weight
- monoazo dyes
- parts
- 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
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
- C09B29/24—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 Darstellung von blonoazofarbstoffen für Wolle. Es wurde gefunden, daß wertvolle Wollfarbstoffe dadurch erhalten werden, daß man Diazoverbindungen der Benzolreihe, die eine Alk-vlacet laminogruppe enthalten, mit Aryly b aininonaphtholstilfosätiren und ihrenDerivaten kuppelt.Process for the preparation of blonoazo dyes for wool. It has been found that valuable wool dyes are obtained by reacting diazo compounds of the benzene series, which contain a vlacet Alk-laminogruppe, aininonaphtholstilfosätiren with Aryly b and coupling their derivatives.
Die so erhältlichen Farbstoffe sind dadurch besonders wertvoll, daß sie gut egalisieren, sehr leicht löslich sind und trotz ihrer leichten Löslichkeit gute Walkechtheit zeigen.The dyes obtainable in this way are particularly valuable in that they level well, are very easily soluble and despite their easy solubility show good flexing fastness.
Beispiel i.Example i.
17,8 Gewichtsteile p-Ai-ninoät-hylacetan#ilid iverden, wie üblich, diazotiert und die Diazoverbindung zu einer sodaalkalischen Lösung Von 35 Gewichtsteilen o-Methoxyphenyl-2-amino-8-naphthol-6-stilfosätire (iooprozentig) gegeben.17.8 parts by weight of p-aminoeth-hylacetanilide are diazotized, as usual, and the diazo compound is added to a soda-alkaline solution of 35 parts by weight of o-methoxyphenyl-2-amino-8-naphthol-6-stilfosätire (10%).
Der ausgesalzene Farbstoff färbt Wolle in braunen Tönen an.The salted-out dye stains wool in brown tones.
Beispiel 19,2 Gewichtsteile 2-Äthylacetylamiilo-4-toluidiii werden, wie üblich, diazotiert und die Diazoverbindung zu einer sodaalkalischen Lösung von 32 Gewichtsteilen Phenyl-2-amino-8-naphtliol-6-stilfosätire (iooprozentig) gegeben.Example 1 9.2 parts by weight of 2-ethylacetylamiilo-4-toluidiii are diazotized as usual and the diazo compound is added to an alkaline soda solution of 32 parts by weight of phenyl-2-amino-8-naphthol-6-stilfosätire (10%).
Der ausgesalzene Farbstoff färbt Wolle braun an. Beispiel 3. The salted-out dye stains wool brown. Example 3.
19,2 Gewichtsteile 5-Äthylacetylainino-2-toluidin werden, wie üblich, diazotiert und die Diazoverbindung zu einer sodaallzalischen Lösung von 4o Gewichtsteilen p-Ätliylacetyl--irninophenyl-2-amiiio-S-naphtliol-6-stilfosätire (iooprozentig) gegeben.19.2 parts by weight of 5-Äthylacetylainino-2-toluidine are, as usual, diazotized and the diazo compound to a sodaallzalischen solution of 40 parts by weight p-Ätliylacetyl - iminophenyl-2-amiiio-S-naphthiol-6-stilfosätire (100 percent) given.
Der ausgesalzene Farbstoff färbt Wolle in Bordeauxtönen an.The salted-out dye stains wool in shades of Bordeaux.
Beispiel 4, 19,2 Gewichtsteile 4-Äthylacetylamilioo-toluidin werden, wie üblich, diazotiert und die Diazoverbindung zu einer sodaalkalischen Lösung von 35 Gewichtsteilen p-Methoxyphenyl-2-amino-8-naphthol-6-stilfosäure (iooprozentig) gegeben.Example 4, 19.2 parts by weight of 4-ethylacetylamilio-toluidine are diazotized as usual and the diazo compound is added to an alkaline soda solution of 35 parts by weight of p-methoxyphenyl-2-amino-8-naphthol-6-stilfonic acid (10%).
Der ausgesalzene Farbstoff färbt Wolle ge g lbstichigbraun an.The salted-out dye stains wool in a yellowish brown.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF51649D DE409280C (en) | 1922-04-26 | 1922-04-26 | Process for the preparation of monoazo dyes for wool |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF51649D DE409280C (en) | 1922-04-26 | 1922-04-26 | Process for the preparation of monoazo dyes for wool |
Publications (1)
Publication Number | Publication Date |
---|---|
DE409280C true DE409280C (en) | 1925-01-31 |
Family
ID=7104785
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEF51649D Expired DE409280C (en) | 1922-04-26 | 1922-04-26 | Process for the preparation of monoazo dyes for wool |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE409280C (en) |
-
1922
- 1922-04-26 DE DEF51649D patent/DE409280C/en not_active Expired
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