83-46-5

  • Product Name:beta-Sitosterol
  • Molecular Formula:C29H50O
  • Purity:99%
  • Molecular Weight:414.715
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Product Details;

CasNo: 83-46-5

Molecular Formula: C29H50O

Appearance: white solid

Chinese Manufacturer supply beta-Sitosterol 83-46-5 in stock with high standard

  • Molecular Formula:C29H50O
  • Molecular Weight:414.715
  • Appearance/Colour:white solid 
  • Vapor Pressure:3.53E-12mmHg at 25°C 
  • Melting Point:136-140 °C(lit.) 
  • Refractive Index:1.521 
  • Boiling Point:501.9 °C at 760 mmHg 
  • PKA:15.03±0.70(Predicted) 
  • Flash Point:220.4 °C 
  • PSA:20.23000 
  • Density:0.97 g/cm3 
  • LogP:8.02480 

beta-Sitosterol(Cas 83-46-5) Usage

Biochem/physiol Actions

Sitosterol promotes the antioxidant levels and is used as an effective anti-inflammatory, antiapoptotic and anticancer agent in medicinal preparations. It acts as a neutralizing agent for the venom from viper and cobra. Sitosterol acts on protein kinase C (PKC) and in the sphingomyelin cycle to mediate tumor progression inhibition.

Purification Methods

Crystallise -sitosterol from EtOH, MeOH, Me2CO, Me2CO/EtOH or Me2CO/MeOH. It has also been purified by zone melting. The acetate crystallises from MeOH or EtOH as plates with m 127128o and [] D 20 -41o (c 2, CHCl3). The benzoate crystallises from EtOH as needles with m 146-147o and [] D 20 –13.8o (c 2, CHCl3). [Fujimoto & Jacobson J Org Chem 29 3377, 3381 1964, Shoppee J Chem Soc 10431948, Heilbron et al. J Chem Soc 344, 347 1941, Beilstein 6 III 2696.]

Definition

A steroid with long aliphatic side chains (8–10 carbons) and at least one hydroxyl group. They are lipidsoluble and often occur in membranes. Examples are cholesterol and ergosterol.

General Description

Sitosterol, also called as β-sitosterol, is synthesized through the mevalonate and deoxy xylulose pathways. Synthetically, it is synthesized from stigmasterol by Δ22–23 alkene group hydrogenation. Structurally sitosterol differ from cholesterol with ethyl (sitosterol) group in C24 position of side chain(65). Sitosterol is a lipid component of membranes. It corresponds to a molecular mass of 414.71 g/mol).

InChI:InChI=1/C29H50O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h10,19-21,23-27,30H,7-9,11-18H2,1-6H3/t20?,21?,23-,24?,25+,26?,27?,28-,29+/m0/s1

83-46-5 Relevant articles

SPECTROSCOPIC STUDIES ON A WITHANOLIDE FROM WITHANIA COAGULANS

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The structure of a new withanolide was e...

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, p. 1139 - 1141 (1986)

The fate of the hydrogen atoms originati...

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Three new compounds; β-sitosterol-3-O-(3...

Sitosterol 3-O-α-riburonofuranoside from Bauhinia candicans

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, p. 360 - 361 (1985)

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A new steroidal ester bearing n-nonadeca...

Chemical constituents of the aerial parts of Algerian Galium brunneum: Isolation of new hydroperoxy sterol glucosyl derivatives

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Chemical Constituents of Astragalus falcatus

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, p. 1202 - 1203 (2017/11/27)

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83-46-5 Process route

C<sub>54</sub>H<sub>96</sub>O<sub>7</sub>

C54H96O7

2,3,4-tri-O-methyl-D-glucose
4060-09-7

2,3,4-tri-O-methyl-D-glucose

β-sitosterol
83-46-5

β-sitosterol

1-hexadecylcarboxylic acid
57-10-3

1-hexadecylcarboxylic acid

Conditions
Conditions Yield
With sulfuric acid; In water; for 0.5h; Heating;
stigmast-5-en-3β-ol-3β-D-glucopyranosyl-4'-eicosanoate
1236770-07-2

stigmast-5-en-3β-ol-3β-D-glucopyranosyl-4'-eicosanoate

β-D-glucose
492-61-5

β-D-glucose

Arachidic acid
506-30-9

Arachidic acid

β-sitosterol
83-46-5

β-sitosterol

Conditions
Conditions Yield
With water; sodium hydroxide; In ethanol; for 1h; Heating;

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