
83-46-5
- Product Name:beta-Sitosterol
- Molecular Formula:C29H50O
- Purity:99%
- Molecular Weight:414.715
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
Ramaiah, Parimi Atchuta,Lavie, David,Budhiraja, Ramji D.,Sudhir, Sharan,Garg, Kailash N.
, p. 143 - 150 (1984)
The structure of a new withanolide was e...
Leonurosides A-D: Steroid N-acetylglucosaminides from the fruits of Leonurus japonicus
Ye, Miao,Ma, Guang-Lei,Su, Jing-Jing,Xiong, Juan,Hu, Jin-Feng
, p. 287 - 290 (2014)
Four new naturally occurring steroidal g...
Biosynthesis of Sitosterol in Tissue Cultures of Rabdosia japonica Hara and Ergosterol in Yeast from Acetate
Seo, Shujiro,Sankawa, Ushio,Seto, Haruo,Uomori, Atsuko,Yoshimura, Yohko,et al.
, p. 1139 - 1141 (1986)
The fate of the hydrogen atoms originati...
New compounds from the Red Sea marine sponge Echinoclathria gibbosa
Mohamed, Gamal A.,Abd-Elrazek, Ali E.E.,Hassanean, Hashim A.,Youssef, Diaa T.A.,Van Soest, Rob
, p. 51 - 58 (2014)
Three new compounds; β-sitosterol-3-O-(3...
Sitosterol 3-O-α-riburonofuranoside from Bauhinia candicans
M. Iribarren, Adolfo,B. Pomilio, Alicia
, p. 360 - 361 (1985)
From the aerial parts of Bauhinia candic...
New n-nonadecanoyl-β-sitosterol and other constituents from the stem-bark of Anacardium occidentale
Shehu, Abdullahi,Ponnapalli, Mangala Gowri,Mahboob,Prabhakar,Olatunji, Gabriel Ademola
, p. 1357 - 1363 (2019/08/22)
A new steroidal ester bearing n-nonadeca...
Chemical constituents of the aerial parts of Algerian Galium brunneum: Isolation of new hydroperoxy sterol glucosyl derivatives
Bertella, Anis,Bitam, Fatma,Carbone, Marianna,Ciavatta, Maria Letizia,Gavagnin, Margherita,Smadi, Abla
, p. 39 - 45 (2020/05/25)
The liposoluble extract of Galium brunne...
Chemical Constituents of Astragalus falcatus
Alaniya,Sutiashvili,Kavtaradze, N. Sh.,Skhirtladze
, p. 1202 - 1203 (2017/11/27)
-
Nurotoxic sterol glycosides
-
, (2017/03/14)
The invention relates to compositions fo...
83-46-5 Process route
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C54H96O7

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

-
-
83-46-5
β-sitosterol

-
-
57-10-3
1-hexadecylcarboxylic acid
Conditions | Yield |
---|---|
With
sulfuric acid;
In
water;
for 0.5h;
Heating;
|
-
-
1236770-07-2
stigmast-5-en-3β-ol-3β-D-glucopyranosyl-4'-eicosanoate

-
-
492-61-5
β-D-glucose

-
-
506-30-9
Arachidic acid

-
-
83-46-5
β-sitosterol
Conditions | Yield |
---|---|
With
water; sodium hydroxide;
In
ethanol;
for 1h;
Heating;
|
83-46-5 Upstream products
-
(24R)-3β-chlorostigmast-5-ene
-
methyl-(3α.5α-cyclo-stigmasten-(22t)-yl-(6β))-ether
-
acetic acid stigmasteryl ester
-
(10R)-3c-Acetoxy-10r.13c-dimethyl-17c-((R)-1-methyl-4-isopropyl-hexen-(4t)-yl)-(8cH.9tH.14tH)-Δ5-tetradecahydro-1H-cyclopenta[a]phenanthren
83-46-5 Downstream products
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stigmast-5-en-3-ol, oleate
-
dehydroepiandrosterone
-
Stigmastanol
-
stigmast-4-ene-3,6-dione
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