Campesterol

Base Information Edit

Chemical Name:Campesterol
CAS No.:474-62-4
Molecular Formula:C28H48O
Molecular Weight:400.689
Hs Code.:29061990
European Community (EC) Number:207-484-4
UNII:5L5O665639
DSSTox Substance ID:DTXSID801009891
Nikkaji Number:J5.962E
Wikipedia:Campesterol
Wikidata:Q2756479
NCI Thesaurus Code:C68328
Metabolomics Workbench ID:34760
ChEMBL ID:CHEMBL520535
Mol file:474-62-4.mol

Synonyms:22,23-dihydrobrassicasterol;24 alpha-methylcholest-5-en-3 beta-ol;24-methylcholesterol;campesterol;campesterol, (3beta)-isomer;campesterol, (3beta,24xi)-isomer;ergost-5-en-3 beta- ol, 24 epimer

Suppliers and Price of Campesterol

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Usbiological
Campesterol
10mg
$ 490.00

TRC
Campesterol
10mg
$ 425.00

Sigma-Aldrich
Campesterol ~65%
10mg
$ 481.00

Sigma-Aldrich
Campesterol ~65%
5mg
$ 288.00

Sigma-Aldrich
Campesterol ~65%
1mg
$ 108.00

Medical Isotopes, Inc.
Campesterol(24-methyl-d3)
5 mg
$ 190.00

Labseeker
CAMPESTEROL 98
1g
$ 1662.00

DC Chemicals
Campesterol >98%
1 g
$ 3600.00

Crysdot
(8R,9S,10S,13R,14S,17R)-17-((2R,5R)-5,6-Dimethylheptan-2-yl)-10,13-dimethyl-4,5,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol 95+%
25mg
$ 700.00

Crysdot
(8R,9S,10S,13R,14S,17R)-17-((2R,5R)-5,6-Dimethylheptan-2-yl)-10,13-dimethyl-4,5,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol 95+%
10mg
$ 350.00

Total 63 raw suppliers

Chemical Property of Campesterol Edit

Chemical Property:

Melting Point:156-160 °C
Refractive Index:1.522
Boiling Point:489.5 °C at 760 mmHg
PKA:15.03±0.70(Predicted)
Flash Point:214.3 °C
PSA：20.23000
Density:0.98 g/cm³
LogP:8.40550
Storage Temp.:−20°C
Solubility.:Chloroform (Sparingly), Methanol (Slightly, Sonicated)
XLogP3:8.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:400.370516150
Heavy Atom Count:29
Complexity:620

Purity/Quality:

95%-98% ^*data from raw suppliers

Campesterol ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xn,T
Hazard Codes:Xn,T
Statements: 20/21/22-36/37/38-48/20/22-40-38-22
Safety Statements: 26-36-45-36/37/39-23

MSDS Files:

Useful:

Chemical Classes:Biological Agents -> Plant Oils and Extracts
Canonical SMILES:CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C
Isomeric SMILES:C[C@H](CC[C@@H](C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC[C@@H](C4)O)C)C
Description 24α-methyl Cholesterol is a phytosterol found in vegetables, fruits, nuts, and seeds that competitively inhibits the absorption of intestinal cholesterol and decreases the transcription of genes important for cholesterol metabolism. The cholesterol lowering effects of phytosterols, such as 24α-methyl cholesterol, have been reported to be beneficial for lowering the incidence of atherosclerotic plaques. 24α-methyl Cholesterol can also act as an agonist at liver X receptors (LXR) and, through activation of LXR signaling, has been shown to suppress the proliferation of prostate and breast cancer cells.
Uses A phytosterol, which may inhibit the intestinal absorption of cholesterol. Campesterol may be used as a plant sterol to test its effect on the transcriptional activation of liver X receptor α (LXRA) in breast cancer cells. It may also be used as a sterol standard for calibration curve generation in liquid chromatography multiple reaction monitoring (LC-MRM) analysis.

Technology Process of Campesterol

There total 33 articles about Campesterol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 81.0%