CH100862A - Process for the preparation of an acidic monoazo dye. - Google Patents
Process for the preparation of an acidic monoazo dye.Info
- Publication number
- CH100862A CH100862A CH100862DA CH100862A CH 100862 A CH100862 A CH 100862A CH 100862D A CH100862D A CH 100862DA CH 100862 A CH100862 A CH 100862A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- red
- monoazo dye
- acidic
- blue
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23G—COCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
- A23G1/00—Cocoa; Cocoa products, e.g. chocolate; Substitutes therefor
- A23G1/04—Apparatus specially adapted for manufacture or treatment of cocoa or cocoa products
- A23G1/042—Manufacture or treatment of liquid, cream, paste, granule, shred or powder
-
- 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
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines sauren 1Vlonoazofar bstoffes. Es wurde gefunden, dass man einen sau ren Monoazofarbstof f.' herstellen kann, wenn ivan die Diazoverbindung des 2-Amino-4- äulfo-4'-chlor-1,1'-diphenylsulfons mit Äthyl ss-naphtylamin kuppelt.
Der neue Farbstoff hildet ein braunrotes Pulver, das sich in Nasser mit blauroter, in konzentrierter Schwefelsäure mit brauner Farbe löst und \Volle aus essigsaurem Bade in sehr gleich- niiissigen, lebhaften, vollen, licht- und wasch echten, blauroten Tönen färbt.
<I>Beispiel:</I> 88,4 Teile der Dia.zoverbindung des ?- Ainino--l-sulfo-4'-clilor-1,1'-diphexiylstclfons (erhalten zum Beispiel durch Kondensieren der p-Clilorbenzolsulfinsäure mit 1-Chlor-2- iiiti-ijl)en7ol-4-sulfos < iure, Reduzieren und DI- azotieren des Kondensationsproduktes) wer- den in 500 Teilen Wasser verteilt und mit einer Lösung von 20,
7 Teilen Xthyl-ss-naph- tylamin-ehlorhydrat versetzt. Die Kupplung tritt sehr bald ein; sie wird durch vorsich tiges Abstumpfen der freien Mineralsäure ge fördert. Der gebildete Farbstoff wird alka lisch ausgesalzen und abfiltriert.
Process for the production of an acidic 1-vlonoazo dye. It has been found that an acidic monoazo dye can be used. can produce if ivan couples the diazo compound of 2-amino-4-sulfo-4'-chloro-1,1'-diphenylsulfone with ethyl ss-naphthylamine.
The new dye forms a brownish-red powder which dissolves in water with blue-red color, in concentrated sulfuric acid with brown color, and turns full from acetic acid bath in very indifferent, lively, full, light and washable, blue-red tones.
<I> Example: </I> 88.4 parts of the dia.zo compound of? - ainino - l-sulfo-4'-clilor-1,1'-diphexylstclfons (obtained for example by condensing p-clilobenzenesulfinic acid with 1 -Chlor-2- iiiti-ijl) en7ol-4-sulfos <iure, reducing and diazotizing the condensation product) are distributed in 500 parts of water and mixed with a solution of 20,
7 parts of ethyl-ss-naphthylamine-chlorohydrate are added. The clutch occurs very soon; it is promoted by carefully blunting the free mineral acid. The dye formed is salted out alkali and filtered off.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH90093T | 1918-12-14 | ||
CH100862T | 1922-04-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH100862A true CH100862A (en) | 1923-08-16 |
Family
ID=25704113
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH100862D CH100862A (en) | 1918-12-14 | 1922-04-29 | Process for the preparation of an acidic monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH100862A (en) |
-
1922
- 1922-04-29 CH CH100862D patent/CH100862A/en unknown
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