CH118628A - Process for the preparation of a basic dye of the malachite green series. - Google Patents
Process for the preparation of a basic dye of the malachite green series.Info
- Publication number
- CH118628A CH118628A CH118628DA CH118628A CH 118628 A CH118628 A CH 118628A CH 118628D A CH118628D A CH 118628DA CH 118628 A CH118628 A CH 118628A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- basic dye
- green series
- malachite green
- dye
- 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
- C09B11/00—Diaryl- or thriarylmethane dyes
- C09B11/04—Diaryl- or thriarylmethane dyes derived from triarylmethanes, i.e. central C-atom is substituted by amino, cyano, alkyl
- C09B11/10—Amino derivatives of triarylmethanes
- C09B11/12—Amino derivatives of triarylmethanes without any OH group bound to an aryl nucleus
- C09B11/14—Preparation from aromatic aldehydes, aromatic carboxylic acids or derivatives thereof and aromatic amines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. <B>116995.</B> Verfahren zur Darstellung eines basischen Farbstoffes der )la.lachitgrünreihe. Es wurde gefunden, dass man zu einem neuen basischen Farbstoff der Malachit- grünreihe gelangt, wenn man<B>1</B> Molekül 2.3.6-Trichlorberizaldehyd mit 2 Molekülen *#lorioaethyl-o-toluidin kondensiert und die so entstandene Leukobase oxydiert.
Trocken -ist der Farbstoff ein graublaues Pulver, löslich in Wasser mit prachtvoll blauer Farbe, und färbt Baumwolle, Seide und Kunstseide in egalen und reinen blauen Tönen an. Bemerkenswert ist seine über raschend grosse Affinität zur Kunstseide.
<I>Beispiel:</I> <B>10,5 kg.</B> 2.3.5-Trichlorbenzaldebyd vom Schmelzpunkt<B>75</B> bis<B>76'</B> und 14,8<B>kg</B> Mono- aethyl-o-tolLiidin werden mit<B>6</B> Liter Schwefel säure 47' BA<B>30</B> Stunden bei<B>105</B> bis<B>110 0</B> gerührt. Nach dem Übersättigen mit Soda- lösung wird die überschüssige Base mit Dampf abgetrieben, und die in der Kälte harte Leuko- base abfiltriert und getrocknet.
Die erhaltene Leukobase wird in 200 Liter Wasser mit<B>13,9</B> Liter Salzsäure<B>221)</B> B6 und<B>3 kg</B> Eisessig ge löst, und die kalte Lösung durch Zugeben von 31 kg Bleisuperoxydpaste mit 49,4%Pb02 unter Rühren oxydiert. Nach einer halben Stunde wird das Blei mit<B>7,8 kg</B> Natrium sulfat ausgefällt.
Nach Erwärmen auf 70') und Zugabe von so viel heissem Wasser, dass aller Farbstoff in Lösung geht, wird abgesaugt, und aus dem Filtrat der Farbstoff mit Kochsalz ausge- salzen, wobei er in grünschillernden Flittern sich ausscheidet. Er wird filtriert und getrocknet.
Additional patent to main patent no. <B> 116995. </B> Process for the preparation of a basic dye of the) la.lachite green series. It has been found that a new basic dye of the malachite green series is obtained if <B> 1 </B> molecule 2,3,6-trichlorberizaldehyde is condensed with 2 molecules * # lorioaethyl-o-toluidine and the leuco base thus formed is oxidized .
When dry, the dye is a gray-blue powder, soluble in water with a splendid blue color, and stains cotton, silk and rayon in even and pure blue tones. Its surprisingly high affinity for artificial silk is remarkable.
<I> Example: </I> <B> 10.5 kg. </B> 2.3.5-Trichlorobenzaldehyde with a melting point of <B> 75 </B> to <B> 76 '</B> and 14.8 <B> kg </B> Mono-ethyl-o-tolLiidine are mixed with <B> 6 </B> liters of sulfuric acid for 47 'BA <B> 30 </B> hours at <B> 105 </B> to <B> 110 0 </B> stirred. After supersaturation with soda solution, the excess base is driven off with steam, and the leuco base, which is hard in the cold, is filtered off and dried.
The leuco base obtained is dissolved in 200 liters of water with <B> 13.9 </B> liters of hydrochloric acid <B> 221) </B> B6 and <B> 3 kg </B> glacial acetic acid, and the cold solution through Adding 31 kg of lead peroxide paste with 49.4% Pb02 oxidized with stirring. After half an hour, the lead is precipitated with <B> 7.8 kg </B> sodium sulfate.
After heating to 70 ') and adding enough hot water that all the dye dissolves, it is filtered off with suction and the dye is salted out of the filtrate with common salt, where it is precipitated in shimmering green flakes. It is filtered and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH116995T | 1925-09-03 | ||
CH118628T | 1925-09-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH118628A true CH118628A (en) | 1927-01-17 |
Family
ID=25708772
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH118628D CH118628A (en) | 1925-09-03 | 1925-09-03 | Process for the preparation of a basic dye of the malachite green series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH118628A (en) |
-
1925
- 1925-09-03 CH CH118628D patent/CH118628A/en unknown
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