Cholest-5-en-3-β-ylacetat

Bezeichnung:Cholest-5-en-3-β-ylacetat

CAS-Nr604-35-3

Englisch Name:Cholesteryl acetate

CBNumberCB1346745

SummenformelC29H48O2

Molgewicht428.69

MOL-Datei604-35-3.mol

Synonyma

Cholest-5-en-3-β-ylacetat

Cholest-5-en-3-β-ylacetat physikalisch-chemischer Eigenschaften

Schmelzpunkt	112-114 °C (lit.)
alpha	-44 º (c=2, CHCl3)
Siedepunkt	483.49°C (rough estimate)
Dichte	0.9935 (rough estimate)
Brechungsindex	1.5045 (estimate)
storage temp.	Sealed in dry,Room Temperature
Löslichkeit	insoluble
Aggregatzustand	Solid
Farbe	White to Off-White
Optische Aktivität	[α]24/D 44°, c = 2 in chloroform
Wasserlöslichkeit	insoluble
Merck	14,2201
BRN	2064235
Stabilität	Hygroscopic
LogP	10.542 (est)
CAS Datenbank	604-35-3(CAS DataBase Reference)
NIST chemische Informationen	Cholesteryl acetate(604-35-3)
EPA chemische Informationen	Cholest-5-en-3-ol (3.beta.)-, acetate (604-35-3)

Sicherheit

Kennzeichnung gefährlicher	Xi
R-Sätze:	36/37/38
S-Sätze:	22-24/25-36-26
WGK Germany	3
TSCA	Yes

Gefahreninformationscode (GHS)

Cholesteryl acetate 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
white fine crystalline powder or needles
Verwenden
Cholesteryl acetate is used in cosmetics, wrist watches, thermometers, propane tank volume indicators, video displays, pharmaceuticals.
Verwenden
Cholesteryl acetate is derived from cholesterol, which is a major component of all biological membranes. Approximately 25% of total brain lipid is made up of cholesterol, which is the principal sterol of higher animals. Cholesterol is found in all body tissues, with particularly high concentrations in the brain, spinal cord, and animal fats or oils. Additionally, cholesterol is the main constituent of gallstones.
synthetische
Cholesteryl acetate can be synthesized by the reaction of cholesterol with acetic anhydride in the presence of a catalyst such as pyridine or sulfuric acid. The reaction proceeds as follows:
Cholesterol + Acetic anhydride → Cholesteryl acetate + Acetic acid
The reaction is typically carried out at room temperature or slightly elevated temperatures for several hours. The resulting cholesteryl acetate can be purified by recrystallization from a suitable solvent such as ethanol or acetone.
Definition
ChEBI: Cholesteryl acetate is a cholesterol ester obtained by formal acylation of the hydroxy group of cholesterol by acetic acid. It has a role as a human metabolite. It is a cholesteryl ester and an acetate ester.
läuterung methode
Crystallise the acetate from n-pentanol or Me2CO. Also purify it by chromatography through silica gel and eluting with MeOH. [Beilstein 6 III 2607, 6 IV 4004.]

Cholesteryl acetate Upstream-Materialien And Downstream Produkte

Cholest-5-en-3-β-ylacetat Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

604-35-3, Cholesteryl acetate Verwandte Suche:

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