CH100859A - Process for the preparation of an acidic monoazo dye. - Google Patents
Process for the preparation of an acidic monoazo dye.Info
- Publication number
- CH100859A CH100859A CH100859DA CH100859A CH 100859 A CH100859 A CH 100859A CH 100859D A CH100859D A CH 100859DA CH 100859 A CH100859 A CH 100859A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- acidic
- red
- dye
- brick
- 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
-
- 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
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines sauren Honoazofarbstoffes. <B><I>EI</I></B> s wurde gefunden, dass man einen sauren 111onoazofarbstoff herstellen kann, wenn man die Diazoverbindung des 2-Amino-4-sulfo-4'- inethyl-1,1'-diplienylsulfons mit ss-Naphtyl- amin kuppelt. Der neue Farbstoff bildet ein ziegelrotes Pulver, das sich in Wasser mit roter, in konzentrierter Schwefelsäure mit gelbbrauner Farbe löst und Wolle aus essig saurem Lade in sehr gleichmässigen, lebhaf ten, vollen, licht- und waschechten, ziegel roten Tönen färbt.
Beispiel: <B>35,6</B> Teile der Diazoverbindung des 2 A mino-4-sulf o-4'-methy l-1,1'-diphenylsulfons (erhalten zum Beispiel durch Kondensieren der p-Toluolsulfinsäure mit 1-Chlor-2-nitro- beiizol-4-sulfosä.ure, Reduzieren und Diazo- t.ieren des Kondensationsproduktes) werden in 500 Teilen Wasser verteilt und mit einer Lösung von 17,9 Teilen ss-Naphi.ylamin- chlorhydrat versetzt.
Die Kupplung tritt sehr bald ein; sie wird durch vorsichtiges Ab stumpfen der freien Mineralsäure gefördert. Der gebildete Farbstoff wird alkalisch aus gesalzen und abfiltriert.
Process for the preparation of an acidic honoazo dye. <B><I>EI</I> </B> It has been found that an acidic 111onoazo dye can be produced if the diazo compound of 2-amino-4-sulfo-4'-ynethyl-1,1'- diplienylsulfons coupled with ss-naphthylamine. The new dye forms a brick-red powder, which dissolves in water with red, in concentrated sulfuric acid with a yellow-brown color and dyes wool from acetic acid ark in very even, vivid, full, light- and washfast, brick-red shades.
Example: <B> 35.6 </B> parts of the diazo compound of 2 A mino-4-sulfo-4'-methy l-1,1'-diphenyl sulfone (obtained for example by condensing p-toluenesulfinic acid with 1- Chlor-2-nitro-beiizol-4-sulfosä.ure, reducing and diazo- t.ieren the condensation product) are distributed in 500 parts of water and treated with a solution of 17.9 parts of β-naphthylamine chlorohydrate.
The clutch occurs very soon; it is promoted by carefully blunting the free mineral acid. The dye formed is alkaline, salted out and filtered off.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH90093T | 1918-12-14 | ||
CH100859T | 1922-04-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH100859A true CH100859A (en) | 1923-08-16 |
Family
ID=25704110
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH100859D CH100859A (en) | 1918-12-14 | 1922-04-29 | Process for the preparation of an acidic monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH100859A (en) |
-
1922
- 1922-04-29 CH CH100859D patent/CH100859A/en unknown
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