CH166790A - Process for the preparation of a new dye of the anthraquinone series. - Google Patents
Process for the preparation of a new dye of the anthraquinone series.Info
- Publication number
- CH166790A CH166790A CH166790DA CH166790A CH 166790 A CH166790 A CH 166790A CH 166790D A CH166790D A CH 166790DA CH 166790 A CH166790 A CH 166790A
- Authority
- CH
- Switzerland
- Prior art keywords
- gray
- acid
- preparation
- new dye
- anthraquinone series
- 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
- C09B1/32—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
- C09B1/34—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated
- C09B1/343—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated only sulfonated in the anthracene nucleus
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Darstellung eines neuen Farbstoffes der Anthrachinonreihe. Es wurde gefunden, dass man in vorzüg licher Ausbeute neue Anthrachinonderivate von hohem technischem Wert erhält, wenn man Aminoarylaminoanthrachinone, sowie deren Substitutions- und Umwandlungspro- dukte, bezw. deren Sulfonsäuren mit Salpe tersäure behandelt. Die so erhaltenen Pro dukte liefern, soweit sie als Sulfosäuren vorliegen, auf tierischen Fasern Färbungen, die sich durch wertvolle Nuancen und ausge zeichnete Echtheitseigenschaften auszeichnen.
Zur Ausführung des vorliegenden Verfah rens verfährt man am besten so, dass man die Aminoarylaminoanthrachinone in Schwe felsäure geeigneter Konzentration löst oder suspendiert und der erhaltenen Lösung oder Suspension Salpetersäure oder ein Gemisch aus Salpetersäure und Schwefelsäure oder ein Nitrat zusetzt.
Das vorliegende Patent betrifft ein Ver fahren zur Darstellung eines neuen Farb stoffes der Anthrachinonreihe, nach welchem man 1-Acnino-4-p-toluidoanthrachinon-2-sul- fosäure mit Salpetersäure behandelt.
<I>Beispiel:</I> 8,6 Teile 1-Amino-4-p-toluidoanthrachi- non-2-sulfosaures Natrium werden in der 4fachen Menge Monohydrat (resp. conc. 112S04) gelöst und bei - 5 bis -E-5 0 lang sam mit 2,
6 Teilen Salpeterschwefelsäure von 50% versetzt. Dann hält man noch einige Zeit auf 0 0 und lässt dann bei Zim mertemperatur weiterrühren (zur raschen Be endigung kann die Temperatur auch unbe denklich auf 50-60 0 gesteigert werden). Zur Isolierung des Farbstoffes wird die Schmelze auf Eis gegossen.
Der so erhaltene Farbstoff ist ein grau schwarzer Körper, der sich in Wasser mit grauvioletter, in Schwefelsäure mit braun gelber Farbe löst. Er färbt Wolle aus saurem Bade in schönen, grauen Tönen an. Chargierte und unchargierte Seide wird sowohl aus saurem wie neutralem Bade grau angefärbt. Ebenso wird Leder in wertvollen grauen Tönen angefärbt.
Process for the preparation of a new dye of the anthraquinone series. It has been found that new anthraquinone derivatives of high technical value are obtained in excellent yield if aminoarylaminoanthraquinones, and their substitution and conversion products, respectively. their sulfonic acids treated with nitric acid. The products thus obtained, in so far as they are present as sulfonic acids, provide dyeings on animal fibers that are distinguished by valuable nuances and excellent fastness properties.
The best way to carry out the present method is to dissolve or suspend the aminoarylaminoanthraquinones in sulfuric acid of suitable concentration and add nitric acid or a mixture of nitric acid and sulfuric acid or a nitrate to the resulting solution or suspension.
The present patent relates to a process for the preparation of a new dye of the anthraquinone series, according to which 1-acnino-4-p-toluidoanthraquinone-2-sulphonic acid is treated with nitric acid.
<I> Example: </I> 8.6 parts of 1-amino-4-p-toluidoanthraquinone-2-sulfonic acid sodium are dissolved in 4 times the amount of monohydrate (or conc. 112S04) and at -5 to -E -5 0 slow sam with 2,
6 parts of 50% nitric sulfuric acid are added. Then hold at 0 0 for some time and then continue stirring at room temperature (to finish quickly, the temperature can be safely increased to 50-60 0). To isolate the dye, the melt is poured onto ice.
The dye obtained in this way is a gray-black body that dissolves in water with a gray-violet color and in sulfuric acid with a brown-yellow color. He dyes wool from an acid bath in beautiful gray tones. Charged and uncharged silk is dyed gray from both acid and neutral baths. Leather is also dyed in valuable gray tones.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH166790T | 1932-11-04 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH166790A true CH166790A (en) | 1934-01-31 |
Family
ID=4419315
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH166790D CH166790A (en) | 1932-11-04 | 1932-11-04 | Process for the preparation of a new dye of the anthraquinone series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH166790A (en) |
-
1932
- 1932-11-04 CH CH166790D patent/CH166790A/en unknown
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