Chemical Properties of Dicyclohexyl suberate

Dicyclohexyl suberate

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InChI
InChI=1S/C20H34O4/c21-19(23-17-11-5-3-6-12-17)15-9-1-2-10-16-20(22)24-18-13-7-4-8-14-18/h17-18H,1-16H2
InChI Key
VBSJUCDAWVFYNG-UHFFFAOYSA-N
Formula
C20H34O4
SMILES
O=C(CCCCCCC(=O)OC1CCCCC1)OC1CCCCC1
Molecular Weight1
338.48
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Physical Properties

Property Value Unit Source
Δf -301.42 kJ/mol Joback Calculated Property
Δfgas -837.09 kJ/mol Joback Calculated Property
Δfus 36.80 kJ/mol Joback Calculated Property
Δvap 79.28 kJ/mol Joback Calculated Property
log10WS -5.93 Crippen Calculated Property
logPoct/wat 5.079 Crippen Calculated Property
McVol 285.820 ml/mol McGowan Calculated Property
Pc 1439.16 kPa Joback Calculated Property
Inp 2446.00 NIST
Tboil 848.68 K Joback Calculated Property
Tc 1062.77 K Joback Calculated Property
Tfus 474.24 K Joback Calculated Property
Vc 1.069 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [963.36; 1058.24] J/mol×K [848.68; 1062.77] Show Hide
Cp,gas 963.36 J/mol×K 848.68 Joback Calculated Property
Cp,gas 983.22 J/mol×K 884.36 Joback Calculated Property
Cp,gas 1001.42 J/mol×K 920.04 Joback Calculated Property
Cp,gas 1017.99 J/mol×K 955.73 Joback Calculated Property
Cp,gas 1032.97 J/mol×K 991.41 Joback Calculated Property
Cp,gas 1046.37 J/mol×K 1027.09 Joback Calculated Property
Cp,gas 1058.24 J/mol×K 1062.77 Joback Calculated Property
η [0.0000568; 0.0010931] Pa×s [474.24; 848.68] Show Hide
η 0.0010931 Pa×s 474.24 Joback Calculated Property
η 0.0005014 Pa×s 536.65 Joback Calculated Property
η 0.0002705 Pa×s 599.05 Joback Calculated Property
η 0.0001640 Pa×s 661.46 Joback Calculated Property
η 0.0001083 Pa×s 723.87 Joback Calculated Property
η 0.0000765 Pa×s 786.27 Joback Calculated Property
η 0.0000568 Pa×s 848.68 Joback Calculated Property

Similar Compounds

Dicyclohexyl azelate. Dicyclohexyl pimelate. Hexanedioic acid, dicyclohexyl ester. Octanoic acid, cyclohexyl ester. Cyclohexyl pentadecanoate. Decanoic acid, cyclohexyl ester. Hexadecanoic acid, cyclohexyl ester. Cyclohexyl myristate. Cyclohexyl undecanoate. Nonanoic acid, cyclohexyl ester. Cyclohexyl tridecanoate. Cyclohexyl nonadecanoate. Cyclohexyl stearate. Cyclohexyl heptadecanoate. Cyclohexyl heptanoate.

Find more compounds similar to Dicyclohexyl suberate.

Sources

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