Chemical Properties of Pimelic acid, di(2-methylpropyl) ester

Pimelic acid, di(2-methylpropyl) ester

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InChI
InChI=1S/C15H28O4/c1-12(2)10-18-14(16)8-6-5-7-9-15(17)19-11-13(3)4/h12-13H,5-11H2,1-4H3
InChI Key
XHJWIYQAARIEMU-UHFFFAOYSA-N
Formula
C15H28O4
SMILES
CC(C)COC(=O)CCCCCC(=O)OCC(C)C
Molecular Weight1
272.38
Other Names
  • Diisobutyl pimelate
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Physical Properties

Property Value Unit Source
Δf -397.30 kJ/mol Joback Calculated Property
Δfgas -853.09 kJ/mol Joback Calculated Property
Δfus 33.13 kJ/mol Joback Calculated Property
Δvap 66.52 kJ/mol Joback Calculated Property
log10WS -3.34 Crippen Calculated Property
logPoct/wat 3.335 Crippen Calculated Property
McVol 237.090 ml/mol McGowan Calculated Property
Pc 1537.87 kPa Joback Calculated Property
Inp [1751.00; 1810.00]   Show Hide
Inp 1810.00 NIST
Inp 1751.00 NIST
Inp 1751.00 NIST
Inp 1810.00 NIST
Tboil 694.30 K Joback Calculated Property
Tc 874.56 K Joback Calculated Property
Tfus 373.13 K Joback Calculated Property
Vc 0.911 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [678.23; 765.47] J/mol×K [694.30; 874.56] Show Hide
Cp,gas 678.23 J/mol×K 694.30 Joback Calculated Property
Cp,gas 694.81 J/mol×K 724.34 Joback Calculated Property
Cp,gas 710.56 J/mol×K 754.39 Joback Calculated Property
Cp,gas 725.49 J/mol×K 784.43 Joback Calculated Property
Cp,gas 739.62 J/mol×K 814.47 Joback Calculated Property
Cp,gas 752.95 J/mol×K 844.52 Joback Calculated Property
Cp,gas 765.47 J/mol×K 874.56 Joback Calculated Property
η [0.0000905; 0.0020958] Pa×s [373.13; 694.30] Show Hide
η 0.0020958 Pa×s 373.13 Joback Calculated Property
η 0.0008937 Pa×s 426.66 Joback Calculated Property
η 0.0004608 Pa×s 480.19 Joback Calculated Property
η 0.0002714 Pa×s 533.71 Joback Calculated Property
η 0.0001760 Pa×s 587.24 Joback Calculated Property
η 0.0001227 Pa×s 640.77 Joback Calculated Property
η 0.0000905 Pa×s 694.30 Joback Calculated Property

Similar Compounds

Suberic acid, diisobutyl ester. Sebacic acid, diisobutyl ester. Nonanedioic acid, bis(2-methylpropyl) ester. Heptanoic acid, 2-methylpropyl ester. Eicosanoic acid, isobutyl ester. Isobutyl pentadecanoate. Isobutyl nonadecanoate. n-Caprylic acid isobutyl ester. n-Capric acid isobutyl ester. Myristic acid isobutyl ester. Undecanoic acid, isobutyl ester. Isobutyl laurate. Heptadecanoic acid, isobutyl ester. Hexadecanoic acid, 2-methylpropyl ester. Heneicosanoic acid, isobutyl ester.

Find more compounds similar to Pimelic acid, di(2-methylpropyl) ester.

Sources

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