Chemical Properties of 2-Methoxyethyl undecanoate

2-Methoxyethyl undecanoate

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InChI
InChI=1S/C14H28O3/c1-3-4-5-6-7-8-9-10-11-14(15)17-13-12-16-2/h3-13H2,1-2H3
InChI Key
MFGPWSRSAOCJRL-UHFFFAOYSA-N
Formula
C14H28O3
SMILES
CCCCCCCCCCC(=O)OCCOC
Molecular Weight1
244.37
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Physical Properties

Property Value Unit Source
Δf -271.92 kJ/mol Joback Calculated Property
Δfgas -709.31 kJ/mol Joback Calculated Property
Δfus 35.99 kJ/mol Joback Calculated Property
Δvap 58.32 kJ/mol Joback Calculated Property
log10WS -3.63 Crippen Calculated Property
logPoct/wat 3.707 Crippen Calculated Property
McVol 221.430 ml/mol McGowan Calculated Property
Pc 1558.58 kPa Joback Calculated Property
Inp 1676.00 NIST
Tboil 618.43 K Joback Calculated Property
Tc 786.56 K Joback Calculated Property
Tfus 341.93 K Joback Calculated Property
Vc 0.862 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [596.50; 686.56] J/mol×K [618.43; 786.56] Show Hide
Cp,gas 596.50 J/mol×K 618.43 Joback Calculated Property
Cp,gas 613.16 J/mol×K 646.45 Joback Calculated Property
Cp,gas 629.16 J/mol×K 674.47 Joback Calculated Property
Cp,gas 644.50 J/mol×K 702.49 Joback Calculated Property
Cp,gas 659.17 J/mol×K 730.51 Joback Calculated Property
Cp,gas 673.19 J/mol×K 758.53 Joback Calculated Property
Cp,gas 686.56 J/mol×K 786.56 Joback Calculated Property
η [0.0001203; 0.0019209] Pa×s [341.93; 618.43] Show Hide
η 0.0019209 Pa×s 341.93 Joback Calculated Property
η 0.0009201 Pa×s 388.01 Joback Calculated Property
η 0.0005153 Pa×s 434.10 Joback Calculated Property
η 0.0003225 Pa×s 480.18 Joback Calculated Property
η 0.0002192 Pa×s 526.26 Joback Calculated Property
η 0.0001585 Pa×s 572.35 Joback Calculated Property
η 0.0001203 Pa×s 618.43 Joback Calculated Property

Similar Compounds

Octanoic acid, 2-methoxyethyl ester. 2-Methoxyethyl palmitate. 2-Methoxyethyl nonadecanoate. 2-Methoxyethyl tridecanoate. 2-Methoxyethyl pentadecanoate. heptadecanoic acid, 2-methoxyethyl ester. 2-Methoxyethyl arachidate. 2-Methoxyethyl myristate. 2-Methoxyethyl nonanoate. 2-Methoxyethyl stearate. 2-Methoxyethyl caprate. 2-Methoxyethyl heptanoate. Hexanoic acid, 2-methoxyethyl ester. 2-(2-Methoxyethoxy)ethyl nonanoate. Sebacic acid, di(2-methoxyethyl) ester.

Find more compounds similar to 2-Methoxyethyl undecanoate.

Sources

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