Chemical Properties of Lanosterol (CAS 79-63-0)

Lanosterol

InChI
InChI=1S/C30H50O/c1-20(2)10-9-11-21(3)22-14-18-30(8)24-12-13-25-27(4,5)26(31)16-17-28(25,6)23(24)15-19-29(22,30)7/h10,21-22,25-26,31H,9,11-19H2,1-8H3/t21?,22?,25-,26-,28?,29?,30?/m1/s1
InChI Key
CAHGCLMLTWQZNJ-HGYRDELPSA-N
Formula
C30H50O
SMILES
CC(C)=CCCC(C)C1CCC2(C)C3=C(CCC12C)C1(C)CCC(O)C(C)(C)C1CC3
Molecular Weight1
426.72
CAS
79-63-0
Other Names
  • (3«beta»)-Lanosta-8,24-dien-3-ol
  • Botalan base 138
  • Cholesta-8,24-dien-3-ol, 4,4,14-trimethyl-, (3«beta»,5«alpha»)-
  • Lanosta-8,24-dien-3-ol, (3«beta»)-
  • Lanosta-8,24-dien-3«beta»-ol
  • Lanosta-8,24-dienol
  • Lanosterin
  • Lanster
  • NSC 60677
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Physical Properties

Property Value Unit Source
ΔfusH° 33.42 kJ/mol Joback Calculated Property
logPoct/wat 8.479 Crippen Calculated Property
McVol 387.390 ml/mol McGowan Calculated Property
Inp [3300.00; 3300.00]   Show Hide
Inp 3300.00 NIST
Inp 3300.00 NIST
Tfus 413.65 K Jean-Claude Bradley Open Melting Point Dataset (2014, CC0) Compiled value

Cheméo can also estimate Normal Boiling Point Temperature, Critical Temperature, Critical Pressure, Critical Volume, Enthalpy of formation at standard conditions, Enthalpy of vaporization at standard conditions, Standard Gibbs free energy of formation, Acentric Factor, Ionization energy, Log10 of Water solubility in mol/l for this compound, but they fall outside the models' validated range, so they are not shown here. Open the prediction tool to compute them on demand.

Correlations

Property Value Unit Temperature (K) Source
Cp,gas [511.71; 1495.17] J/mol×K [273.00; 1000.00] Joback Predicted correlation Show Hide
EquationY = A + B·T + C·T² + D·T³ + E·T⁴
Y is Cp,gas in J/mol×K, T in K
Coefficient A-4.06988e+02
Coefficient B4.38246e+00
Coefficient C-4.19410e-03
Coefficient D1.71380e-06
Coefficient E0.00000e+00
Temperature range, min.273.00
Temperature range, max.1000.00
Cp,gas 511.71 J/mol×K 273.00 Calculated Property
Cp,gas 694.39 J/mol×K 353.78 Calculated Property
Cp,gas 846.06 J/mol×K 434.56 Calculated Property
Cp,gas 972.16 J/mol×K 515.33 Calculated Property
Cp,gas 1078.11 J/mol×K 596.11 Calculated Property
Cp,gas 1169.31 J/mol×K 676.89 Calculated Property
Cp,gas 1251.21 J/mol×K 757.67 Calculated Property
Cp,gas 1329.20 J/mol×K 838.44 Calculated Property
Cp,gas 1408.71 J/mol×K 919.22 Calculated Property
Cp,gas 1495.17 J/mol×K 1000.00 Calculated Property

Similar Compounds

Cholesta-8,24-dien-3-ol, (3«beta»,5«alpha»)-. 4,4,14-«alpha»-Trimethyl-5-«alpha»-cholest-8-en-3-«beta»-ol. 4,4,14-«alpha»-Trimethyl-5-«alpha»-cholest-9(11)-en-3-«beta»-ol. 4,4,14-.alpha.-Trimethyl-5-.alpha.-cholest-7-en-3-.beta.-ol. «alpha»-Amyrin. 4-.alpha.-Methyl-24-ethylcholest-8-en-3-.beta.-ol. 4-.alpha.,24-Dimethylcholest-8-en-3-.beta.-ol. 8-Dehydro DHEA. 4-.alpha.,24-Dimethylcholest-8,24(28)-dien-3-.beta.-ol. Olean-12-en-3-ol, (3.beta.)-. Podocarp-7-en-3.beta.-ol, 13.beta.-methyl-13-vinyl-. Cholest-7-en-3-ol, 4-methyl-, (3«beta»,4«alpha»,5«alpha»)-. Lophenol. Uvaol. 7-Dehydro DHEA.

Find more compounds similar to Lanosterol.

Sources

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Calculated This icon marks a calculated value or equation: a prediction, not a measurement.
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