Triphenylmethan

Bezeichnung:Triphenylmethan

CAS-Nr519-73-3

Englisch Name:Triphenylmethane

CBNumberCB5689132

SummenformelC19H16

Molgewicht244.33

MOL-Datei519-73-3.mol

Synonyma

Triphenylmethan

Triphenylmethan physikalisch-chemischer Eigenschaften

Schmelzpunkt	92-94 °C(lit.)
Siedepunkt	358-359 °C754 mm Hg(lit.)
Dichte	1.014 g/mL at 25 °C(lit.)
Brechungsindex	nD100 1.59546
Flammpunkt	358-359°C
storage temp.	Store below +30°C.
Löslichkeit	dioxane: 0.1 g/mL, clear
Aggregatzustand	Powder
pka	31.5(at 25℃)
Farbe	Faint yellow
Wichte	1.014
Wasserlöslichkeit	INSOLUBLE
Merck	14,9741
BRN	1909753
Dielectric constant	3.6（65℃）
Stabilität	Stable; combustible. Incompatible with strong oxidizing agents.
CAS Datenbank	519-73-3(CAS DataBase Reference)
NIST chemische Informationen	Triphenylmethane(519-73-3)
EPA chemische Informationen	Benzene, 1,1',1''-methylidynetris- (519-73-3)

Sicherheit

Kennzeichnung gefährlicher	Xi
R-Sätze:	36/37/38
S-Sätze:	22-24/25-36-26
WGK Germany	3
Hazard Note	Irritant
TSCA	Yes
HS Code	29029080

Gefahreninformationscode (GHS)

Triphenylmethane Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
S-Sätze Betriebsanweisung:
S22:Staub nicht einatmen.
S24/25:Berührung mit den Augen und der Haut vermeiden.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
Chemische Eigenschaften
colorless or light brown powder. soluble in nonpolar organic solvents and not in water. Triphenylmethane is the basic skeleton of many synthetic dyes called triarylmethane dyes, many of them are pH indicators, and some display fluorescence. A trityl group in organic chemistry is a triphenylmethyl group Ph3C, e.g. triphenylmethyl chloride (trityl chloride) and the triphenylmethyl radical (trityl radical).
Verwenden
Triphenylmethane is a triarylmethane compound used as the backbone of synthetic dyes. Triphenylmethane has also been shown to inhibit 3-methylcholanthrene-induced neoplastic transformation of 10T1/2 cells.
Definition
ChEBI: Triphenylmethane is a triarylmethane in which the three aryl groups are phenyl. It forms the basic skeleton of several synthetic dyes. It has a role as a xenobiotic and an environmental contaminant.
synthetische
Triphenylmethane can be synthesized by Friedel–Crafts reaction from benzene and chloroform with aluminium chloride catalyst:
3 C6H6 + CHCl3 → Ph3CH + 3 HCl
Synthesis Reference(s)
Journal of the American Chemical Society, 73, p. 5846, 1951 DOI: 10.1021/ja01156a116
Organic Syntheses, Coll. Vol. 1, p. 548, 1941
Tetrahedron Letters, 21, p. 801, 1980 DOI: 10.1016/S0040-4039(00)71509-7
läuterung methode
Crystallise triphenylmethane from EtOH or *benzene (with one molecule of *benzene of crystallisation which is lost on exposure to air or by heating on a water bath). It can also be sublimed under vacuum. It has been given a preliminary purification by refluxing with tin and glacial acetic acid, then filtered hot through a glass sinter disc, and precipitated by addition of cold water. [Beilstein 5 H 698, 5 IV 2495.]

Triphenylmethane Upstream-Materialien And Downstream Produkte

Triphenylmethan Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

519-73-3, Triphenylmethane Verwandte Suche:

Send Inquriy