CH224874A - Process for the preparation of a new, water-soluble dye of the anthraquinone series. - Google Patents
Process for the preparation of a new, water-soluble dye of the anthraquinone series.Info
- Publication number
- CH224874A CH224874A CH224874DA CH224874A CH 224874 A CH224874 A CH 224874A CH 224874D A CH224874D A CH 224874DA CH 224874 A CH224874 A CH 224874A
- Authority
- CH
- Switzerland
- Prior art keywords
- water
- new
- preparation
- soluble dye
- mol
- 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
- C09B1/28—Dyes with amino groups substituted by hydrocarbon radicals substituted by alkyl, aralkyl or cyclo alkyl groups
- C09B1/30—Dyes with amino groups substituted by hydrocarbon radicals substituted by alkyl, aralkyl or cyclo alkyl groups sulfonated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 210608. Verfahren zur Darstellung eines neuen, wasserlöslichen Farbstoffes der Anthrachinonreihe. Das vorliegende Patent betrifft ein Ver fahren zur Darstellung eines neuen, wasser löslichen Farbstoffes der Anthrachinonreihe und ist dadurch gekennzeichnet, dass man 1 711o1 1,4-Diaminoanthraehinon, 2 Mol Phenol und 2 Mol Formaldehyd aufeinander einwir ken lässt und das erhaltene Produkt sulfoniert.
Der neue Farbstoff enthält zwei Sulfogrup- pen und löst sich in konzentrierter Schwefelsäure mit blassgelber, in Wasser mit rotstichig blauer Farbe. Er soll zum Färben von Acetatseide, acetylierter Baumwolle und von Acetylcel- lulosefolien verwendet werden. Das Färbegut wird in der wässerigen Lösung in rotvioletten Tönen gefärbt.
<I>Beispiel:</I> 100 kg Phenol werden mit 15 kg Form aldehyd von 40 Vol.-% geschmolzen, bei 40 C werden 20 kg 1,4-Diaminoanthrachinon ein getragen und vier Stunden weiter gerührt. Die Schmelze wird nun in 1000 Liter Wasser ge drückt, das 50 kg Natriumchlorid und 45 kg Natriumhydroxyd gelöst enthält. Das ausge fallene Kondensationsprodukt wird. abfiltriert, in Wasser aufgenommen und mit Schwefel säure neutral gestellt. Man filtriert, wäscht und trocknet.
Durch Sulfonieren bei 20 C in Schwefel säuremonohydrat erhält man einen Farbstoff, der sich in Wasser mit rotstichigblauer, in konzentrierter Schwefelsäure mit blassgelber Farbe löst. Er soll zum Färben von Acetat seide, acetylierter Baumwolle und von Acetyl- cellulosefolien verwendet werden. Das Färbe gut wird in der wässerigen Lösung in rot violetten Tönen gefärbt.
<B> Additional patent </B> to main patent no. 210608. Process for the preparation of a new, water-soluble dye from the anthraquinone series. The present patent relates to a process for the preparation of a new, water-soluble dye of the anthraquinone series and is characterized in that 1,711o1 1,4-diaminoanthraehinone, 2 moles of phenol and 2 moles of formaldehyde are allowed to act on one another and the product obtained is sulfonated.
The new dye contains two sulfo groups and dissolves in concentrated sulfuric acid with a pale yellow color, in water with a reddish blue color. It is said to be used for dyeing acetate silk, acetylated cotton and acetyl cellulose films. The dyed goods are dyed in the aqueous solution in red-violet tones.
<I> Example: </I> 100 kg of phenol are melted with 15 kg of formaldehyde of 40% by volume, at 40 ° C. 20 kg of 1,4-diaminoanthraquinone are introduced and the mixture is stirred for another four hours. The melt is then pressed into 1000 liters of water containing 50 kg of sodium chloride and 45 kg of sodium hydroxide dissolved. The precipitated condensation product is. filtered off, taken up in water and made neutral with sulfuric acid. It is filtered, washed and dried.
By sulfonating at 20 C in sulfuric acid monohydrate, a dye is obtained which dissolves in water with a reddish blue color, in concentrated sulfuric acid with a pale yellow color. It is said to be used for dyeing acetate silk, acetylated cotton and acetyl cellulose films. The dye well is colored in an aqueous solution in red violet shades.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH536303X | 1938-12-19 | ||
CH224874T | 1939-04-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH224874A true CH224874A (en) | 1942-12-15 |
Family
ID=25726799
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH224874D CH224874A (en) | 1938-12-19 | 1939-04-22 | Process for the preparation of a new, water-soluble dye of the anthraquinone series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH224874A (en) |
-
1939
- 1939-04-22 CH CH224874D patent/CH224874A/en unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CH224874A (en) | Process for the preparation of a new, water-soluble dye of the anthraquinone series. | |
CH224876A (en) | Process for the preparation of a new, water-soluble dye of the anthraquinone series. | |
CH224877A (en) | Process for the preparation of a new, water-soluble dye of the anthraquinone series. | |
CH224875A (en) | Process for the preparation of a new, water-soluble dye of the anthraquinone series. | |
DE746839C (en) | Process for the preparation of metal-containing dye mixtures | |
CH224879A (en) | Process for the preparation of a new, water-soluble dye of the anthraquinone series. | |
CH224878A (en) | Process for the preparation of a new, water-soluble dye of the anthraquinone series. | |
AT156582B (en) | Process for the preparation of o-oxyazo dyes. | |
DE673024C (en) | Process for the production of azo dyes | |
CH137637A (en) | Process for the production of a new metal-containing dye. | |
CH191160A (en) | Process for the preparation of a new monoazo dye. | |
CH199664A (en) | Process for the preparation of an anthraquinone dye. | |
CH224548A (en) | Process for the preparation of a new dye of the anthraquinone series. | |
CH219415A (en) | Process for the preparation of a halogen-containing dye of the anthraquinone series. | |
CH224347A (en) | Process for the preparation of an azo dye. | |
CH199663A (en) | Process for the preparation of an anthraquinone dye. | |
CH180293A (en) | Process for the production of a new dye. | |
CH222155A (en) | Process for the preparation of a new dye of the anthraquinone series. | |
CH222151A (en) | Process for the preparation of a new dye of the anthraquinone series. | |
CH182279A (en) | Process for the preparation of an azo dye. | |
CH182277A (en) | Process for the preparation of an azo dye. | |
CH182276A (en) | Process for the preparation of an azo dye. | |
CH199662A (en) | Process for the preparation of an anthraquinone dye. | |
CH184016A (en) | Process for the production of a new anthraquinone dye. | |
CH199660A (en) | Process for the preparation of an anthraquinone dye. |