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
- 238000000034 method Methods 0.000 title claims description 3
- 239000000975 dye Substances 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 238000004382 potting Methods 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- 210000002268 wool Anatomy 0.000 claims description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- OKAUOXITMZTUOJ-UHFFFAOYSA-N 7-aminonaphthalene-2-sulfonic acid Chemical compound C1=CC(S(O)(=O)=O)=CC2=CC(N)=CC=C21 OKAUOXITMZTUOJ-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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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