CH88130A - Process for the preparation of a new chromable orthoxyazo dye. - Google Patents
Process for the preparation of a new chromable orthoxyazo dye.Info
- Publication number
- CH88130A CH88130A CH88130DA CH88130A CH 88130 A CH88130 A CH 88130A CH 88130D A CH88130D A CH 88130DA CH 88130 A CH88130 A CH 88130A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- new
- chromable
- orthoxyazo
- preparation
- Prior art date
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
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/095—Amino naphthalenes
- C09B29/0955—Amino naphthalenes containing water solubilizing groups
-
- 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
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
-
- 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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/14—Monoazo compounds
- C09B45/16—Monoazo compounds containing chromium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
Description
Verfahren zur Herstellung eines neuen chrofnierbaren Orthoozyazofarbstof%s. Es wurde gefunden, dass mau durch Kup peln von diazotiertem 5-Nitro-4-ehlor-2-atnitio- 1-oxybenzol mit der N-Methyleiisulfosäitre der 2-Amittonaphtalin-7-sulfosäure einen neuen chromierbaren Orthooxyazofarbstoff herstellen kann.
Dieser Farbstoff bildet ein dunkel violettes Pulver und färbt Wolle aus saurem Bade in blaustichig bordeauxroten Tönen an, welche beim Nachehromieren in ein grüii- stichiges Blau von guter Walk- und Potting- echtheit übergehen.
Beispiel 18,8 kg 5-Nitro-4-eltlor-2-atnino-l-oxyben- zol werden mit 30 kg Salzsäure von<B>30'</B> ;'o und 7,2 kg technischem Natriumnitrit wie üblich diazotiert. Die Diazolösung lässt man einlaufen in eine Lösung von 32 kg der N-Methylensulfosäure der 2-Aminonaphtaliir 7-sulfosäure (dargestellt durch Einwirkung von Formaldehyd und Natriumbisulfit ;
tuf 2-aminottaphtalin-7-sulfosaures Natron) gelöst in 100 Liter Wasser. Die Kupplung ist bei gewöhnlicher Temperatur innerhalb einiger Stunden beendigt, dann wird der Farbstoff durch Aassalzen abgeschieden.
Process for the production of a new chromable orthozyazo dye% s. It has been found that by coupling diazotized 5-nitro-4-chloro-2-atnitio-1-oxybenzene with the N-methyleiisulfosäitre of 2-amittonaphthalene-7-sulfonic acid, a new chromable orthooxyazo dye can be produced.
This dye forms a dark violet powder and dyes wool from an acid bath in bluish, burgundy-red tones, which, when retouched, turn into a greenish blue of good milled and potting fastness.
Example 18.8 kg of 5-nitro-4-eltloro-2-atnino-1-oxybenzene are diazotized as usual with 30 kg of hydrochloric acid of 30 ';' o and 7.2 kg of technical grade sodium nitrite . The diazo solution is allowed to run into a solution of 32 kg of N-methylene sulfonic acid, 2-aminonaphthalene 7-sulfonic acid (produced by the action of formaldehyde and sodium bisulfite;
tuf 2-aminottaphthalene-7-sulphonic acid soda) dissolved in 100 liters of water. The coupling is completed within a few hours at ordinary temperature, then the dye is deposited by carrion salts.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH88130T | 1917-08-08 | ||
CH86851T | 1917-08-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH88130A true CH88130A (en) | 1921-02-01 |
Family
ID=25703650
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH88130D CH88130A (en) | 1917-08-08 | 1917-08-08 | Process for the preparation of a new chromable orthoxyazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH88130A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1006988B (en) * | 1954-03-05 | 1957-04-25 | Geigy Ag J R | Process for the production of chromium-containing azo dyes |
-
1917
- 1917-08-08 CH CH88130D patent/CH88130A/en unknown
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1006988B (en) * | 1954-03-05 | 1957-04-25 | Geigy Ag J R | Process for the production of chromium-containing azo dyes |
DE1006988C2 (en) * | 1954-03-05 | 1957-10-03 | Geigy Ag J R | Process for the production of chromium-containing azo dyes |
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