Chemical Properties of Stearamide, m-hydroxyphenol (CAS 103-99-1)

Stearamide, m-hydroxyphenol

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InChI
InChI=1S/C24H41NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-24(27)25-22-18-20-23(26)21-19-22/h18-21,26H,2-17H2,1H3,(H,25,27)
InChI Key
YASWBJXTHOXPGK-UHFFFAOYSA-N
Formula
C24H41NO2
SMILES
CCCCCCCCCCCCCCCCCC(=O)Nc1ccc(O)cc1
Molecular Weight1
375.59
CAS
103-99-1
Other Names
  • N-4-hydroxyphenylstearamide
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Physical Properties

Property Value Unit Source
Δf 69.46 kJ/mol Joback Calculated Property
Δfgas -538.58 kJ/mol Joback Calculated Property
Δfus 64.44 kJ/mol Joback Calculated Property
Δvap 97.49 kJ/mol Joback Calculated Property
log10WS -7.92 Crippen Calculated Property
logPoct/wat 7.592 Crippen Calculated Property
McVol 342.680 ml/mol McGowan Calculated Property
Pc 1136.73 kPa Joback Calculated Property
Tboil 959.86 K Joback Calculated Property
Tc 1175.38 K Joback Calculated Property
Tfus 600.97 K Joback Calculated Property
Vc 1.278 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [1166.24; 1270.46] J/mol×K [959.86; 1175.38] Show Hide
Cp,gas 1166.24 J/mol×K 959.86 Joback Calculated Property
Cp,gas 1185.15 J/mol×K 995.78 Joback Calculated Property
Cp,gas 1203.28 J/mol×K 1031.70 Joback Calculated Property
Cp,gas 1220.76 J/mol×K 1067.62 Joback Calculated Property
Cp,gas 1237.70 J/mol×K 1103.54 Joback Calculated Property
Cp,gas 1254.23 J/mol×K 1139.46 Joback Calculated Property
Cp,gas 1270.46 J/mol×K 1175.38 Joback Calculated Property

Similar Compounds

N-stearoyl p-amino phenol. Octanamide, N-(4-methoxyphenyl)-. Hexanamide, N-(4-methoxyphenyl)-. Pentanamide, N-(4-methoxyphenyl)-. Octanamide, N-(4-bromophenyl)-. Hexanamide, N-phenyl-. Hexanamide, N-(4-bromophenyl)-. Octanamide, N-(4-fluorophenyl)-. Octanamide, N-(3-chlorophenyl)-. Hexanamide, N-(4-fluorophenyl)-. Pentanamide, N-phenyl-. Pentanamide, N-(4-bromophenyl)-. 3',4'-Dichloroenanthoanilide. 3',4'-Dichlorocapryloanilide. 3',4'-Dichlorocaproanilide.

Find more compounds similar to Stearamide, m-hydroxyphenol.

Sources

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