Chemical Properties of Sucrose monopalmitate

Sucrose monopalmitate

InChI
InChI=1S/C28H52O12/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-21(31)37-17-20-22(32)24(34)25(35)27(38-20)40-28(18-30)26(36)23(33)19(16-29)39-28/h19-20,22-27,29-30,32-36H,2-18H2,1H3
InChI Key
XYFGTTCGHCGTDZ-UHFFFAOYSA-N
Formula
C28H52O12
SMILES
CCCCCCCCCCCCCCCC(=O)OCC1OC(OC2(CO)OC(CO)C(O)C2O)C(O)C(O)C1O
Molecular Weight1
580.71
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Physical Properties

Property Value Unit Source
ΔfusH° 105.38 kJ/mol Joback Calculated Property
log10WS -4.47 Relay (1.0) Calculated Property
logPoct/wat 0.637 Crippen Calculated Property
McVol 449.800 ml/mol McGowan Calculated Property
Tfus 421.66 K Relay (1.0) Calculated Property

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 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 [694.02; 1682.54] 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-3.44830e+01
Coefficient B3.13802e+00
Coefficient C-1.83200e-03
Coefficient D4.11000e-07
Coefficient E0.00000e+00
Temperature range, min.273.00
Temperature range, max.1000.00
Cp,gas 694.02 J/mol×K 273.00 Calculated Property
Cp,gas 864.59 J/mol×K 353.78 Calculated Property
Cp,gas 1016.94 J/mol×K 434.56 Calculated Property
Cp,gas 1152.37 J/mol×K 515.33 Calculated Property
Cp,gas 1272.19 J/mol×K 596.11 Calculated Property
Cp,gas 1377.69 J/mol×K 676.89 Calculated Property
Cp,gas 1470.18 J/mol×K 757.67 Calculated Property
Cp,gas 1550.95 J/mol×K 838.44 Calculated Property
Cp,gas 1621.30 J/mol×K 919.22 Calculated Property
Cp,gas 1682.54 J/mol×K 1000.00 Calculated Property

Similar Compounds

Sucrose dipalmitate. D-Raffinose. Melezitose, monohydrate. Sucrose. Methyl salicylate, Rut, TFA. N-Acetylnornarcotine. 9H-purine-6(1h)-thione, 9-beta-d-ribofuranosyl-, 3',5'-cyclic phosphate. 5'-Inosinic acid, dibutyl ester. 4H,6h-m-dioxino[4',5':5,6]pyrano[4,3-d]-4-oxazolin-2-one, hexahydro-4-methoxy-1,8-diphenyl-. 1,2,3,4-Tetrahydroanthracene-cis-1,2-diol, ferrocenylboronate. Adenosine, N-(trimethylsilyl)-2',3'-bis-O-(trimethylsilyl)-, 5'-[bis(trimethylsilyl) phosphate]. Eruciflorine. Thymidine, 3'-O-cyclotetramethylene-tertbutylsilyl, 5'-O-acetyl. Hydrastine. 1-Alpha-2-methyl-8-methoxy-6,7-methylenedioxy-1-(6,7-dimethoxy-3-phthalidyl)-1,2,3,4-tetrahydroisoquinoline.

Find more compounds similar to Sucrose monopalmitate.

Sources

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