CH100860A - Process for the preparation of an acidic monoazo dye. - Google Patents
Process for the preparation of an acidic monoazo dye.Info
- Publication number
- CH100860A CH100860A CH100860DA CH100860A CH 100860 A CH100860 A CH 100860A CH 100860D A CH100860D A CH 100860DA CH 100860 A CH100860 A CH 100860A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- monoazo dye
- red
- 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 Nonoazofarbstoffes. Es wurde gefunden, dass man einen sauren Monoazofarbstoff herstellen kann, wenn man die Diazoverbindung des 2-Amino- 4-sulfo-4'-methyl-1,1'-dipheiiylsulfons mit Äthyl-ss-naphtylamin kuppelt. Der neue Farbstoff bildet ein braunrotes Pulver, das sich in Wasser mit blauroter, in konzen trierter Schwefelsäure mit brauner Farbe löst und Wolle aus essigsaurem Bade in sehr gleichmässigen, lebhaften, vollen, licht- und waschechten, blauroten Tönen färbt.
Beispiel: 35,6 Teile der Diazoverbindung des ?-Amino -4 -sulfo -4'-methyl -1,1'- diphenylsul- fons (erhalteri zum Beispiel durch Kon densieren der p-Toluolsulfinsäure mit 1- Clilor-2-nitrobenzol-4-sulfosätire, Reduzieren und Diazotieren des Kondensationsproduktes) werden in 500 Teilen Wasser verteilt und mit einer Lösung von 20,7 Teilen Äthyl-ss- naphtylaminchlorhydrat versetzt.
Die Kupp lung tritt sehr bald ein; sie wird durch vor sichtiges Abstumpfen der freien Mineralsäure gefördert. Der gebildete Farbstoff wird al kalisch ausgesalzen und abfiltriert.
Process for the preparation of an acidic nonoazo dye. It has been found that an acidic monoazo dye can be produced if the diazo compound of 2-amino-4-sulfo-4'-methyl-1,1'-dipheiiylsulfone is coupled with ethyl-ß-naphthylamine. The new dye forms a brownish-red powder that dissolves in water with blue-red, in concentrated sulfuric acid with brown color and colors wool from acetic acid bath in very even, lively, full, light- and washfast, blue-red tones.
Example: 35.6 parts of the diazo compound of? -Amino -4 -sulfo -4'-methyl -1,1'-diphenyl sulfone (obtained, for example, by condensing p-toluenesulfinic acid with 1- Clilor-2-nitrobenzene- 4-sulfosätire, 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.
The coupling occurs very soon; it is promoted by careful blunting of the free mineral acid. The dye formed is salted out and filtered off.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH90093T | 1918-12-14 | ||
CH100860T | 1922-04-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH100860A true CH100860A (en) | 1923-08-16 |
Family
ID=25704111
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH100860D CH100860A (en) | 1918-12-14 | 1922-04-29 | Process for the preparation of an acidic monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH100860A (en) |
-
1922
- 1922-04-29 CH CH100860D patent/CH100860A/en unknown
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