CH211018A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH211018A CH211018A CH211018DA CH211018A CH 211018 A CH211018 A CH 211018A CH 211018D A CH211018D A CH 211018DA CH 211018 A CH211018 A CH 211018A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- production
- new azo
- new
- water
- Prior art date
Links
- 239000000987 azo dye Substances 0.000 title claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- XTTIQGSLJBWVIV-UHFFFAOYSA-N 2-methyl-4-nitroaniline Chemical compound CC1=CC([N+]([O-])=O)=CC=C1N XTTIQGSLJBWVIV-UHFFFAOYSA-N 0.000 claims description 3
- 239000000975 dye Substances 0.000 claims description 3
- 244000299507 Gossypium hirsutum Species 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- 239000000758 substrate Substances 0.000 claims description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 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
- C09B29/10—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
- C09B29/12—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group of the benzene series
-
- 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 neuen Azofarüstoffes. Es wurde gefunden, dass ein neuer Azo- farbstoff hergestellt werden kann, wenn man dia.zotiertes 1-Amino-2-methyl-4-nitro- benzol mit 2,3-Oxynaphthoesäure-3'-pyrenolid vereinigt.
Der neue Azofarbstoff bildet ein corinth- rotes, in Wasser unlösliches Pulver. Auf geeigneten Substraten, wie z. B. Baumwolle, hergestellt, färbt er diese in sehr echten, insbesondere auch lichtechten, corinthroten Tönen.
<I>Beispiel</I> 1.ä,9 Teile 1-Amino-2-methyl-4-nitro- benzol (1/1a 142o1) werden wie üblich diazo- tiert und in eine Lösung von 38,8 Teilen 2,3-Oxynaphthoesäure-3'-pyrenolid ('/1o Hol), <B>100</B> Teilen Natriumhydroxydlösung von 36 <I> </I> Be, <B>15</B> Teilen Natriumacetat und 2000 Teilen Wasser eingetragen. Der gebildete Farbstoff fällt sofort aus.
Er wird abfil- triert, mit Wasser gewaschen und getrocknet.
Process for the production of a new azo fuel. It has been found that a new azo dye can be produced by combining dia.zotierter 1-amino-2-methyl-4-nitro-benzene with 2,3-oxynaphthoic acid-3'-pyrenolide.
The new azo dye forms a corinth-red powder that is insoluble in water. On suitable substrates, such as. B. cotton, produced, he dyes them in very real, especially lightfast, corin-red tones.
<I> Example </I> 1.ä, 9 parts of 1-amino-2-methyl-4-nitrobenzene (1 / 1a 142o1) are diazotized as usual and in a solution of 38.8 parts of 3-oxynaphthoic acid-3'-pyrenolide ('/ 1o Hol), <B> 100 </B> parts of sodium hydroxide solution of 36 <I> </I> Be, <B> 15 </B> parts of sodium acetate and 2000 parts of water registered. The dye formed precipitates immediately.
It is filtered off, washed with water and dried.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH211018T | 1937-06-02 | ||
| CH208951T | 1937-06-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH211018A true CH211018A (en) | 1940-08-15 |
Family
ID=25724632
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH211018D CH211018A (en) | 1937-06-02 | 1937-06-02 | Process for the production of a new azo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH211018A (en) |
-
1937
- 1937-06-02 CH CH211018D patent/CH211018A/en unknown
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