Chemical Properties of Citronellic acid, 4,4-Dimethyloxazoline (DMOX) derivative

Citronellic acid, 4,4-Dimethyloxazoline (DMOX) derivative

InChI
InChI=1S/C14H25NO/c1-11(2)7-6-8-12(3)9-13-15-14(4,5)10-16-13/h7,12H,6,8-10H2,1-5H3
InChI Key
MEMKUNKVVADDCW-UHFFFAOYSA-N
Formula
C14H25NO
SMILES
CC(C)=CCCC(C)CC1=NC(C)(C)CO1
Molecular Weight1
223.36
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Physical Properties

Property Value Unit Source
Δfus 28.97 kJ/mol Joback Calculated Property
Δvap 64.04 kJ/mol Relay (1.0) Calculated Property
logPoct/wat 3.966 Crippen Calculated Property
McVol 204.510 ml/mol McGowan Calculated Property
Inp [1452.20; 1452.20]   Show Hide
Inp 1452.20 NIST
Inp 1452.20 NIST
Tboil 525.93 K Relay (1.0) Calculated Property

Cheméo can also estimate Normal melting (fusion) point, Critical Temperature, Critical Pressure, Critical Volume, Enthalpy of formation at standard conditions, Standard Gibbs free energy of formation, Acentric Factor, Ionization energy, Log10 of Water solubility in mol/l 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.

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [566.32; 672.91] J/mol×K [623.63; 836.81] Show Hide
Cp,gas 566.32 J/mol×K 623.63 Joback Calculated Property
Cp,gas 586.37 J/mol×K 659.16 Joback Calculated Property
Cp,gas 605.34 J/mol×K 694.69 Joback Calculated Property
Cp,gas 623.36 J/mol×K 730.22 Joback Calculated Property
Cp,gas 640.55 J/mol×K 765.75 Joback Calculated Property
Cp,gas 657.02 J/mol×K 801.28 Joback Calculated Property
Cp,gas 672.91 J/mol×K 836.81 Joback Calculated Property

Similar Compounds

(R)-(+)-Citronellic acid, 4,4-dimethyloxazoline (dmox) derivative. (S)-(-)-Citronellic acid, 4,4-Dimethyloxazoline (DMOX) derivative. cis-6-Octadecenoic acid, 4,4-dimethyloxazoline (dmox) derivative. trans-Vaccenic acid, 4,4-dimethyloxazoline (dmox) derivative. cis-Vaccenic acid, 4,4-dimethyloxazoline (dmox) derivative. cis-11-Eicosenoic acid, 4,4-Dimethyloxazoline (DMOX) derivative. cis-13-Docosenoic acid, 4,4-dimethyloxazoline (dmox) derivative. cis-9-Octadecenoic acid, 4,4-Dimethyloxazoline (DMOX) derivative. trans-9-Octadecenoic acid, 4,4-dimethyloxazoline (dmox) derivative. cis-10-Nonadecenoic acid, 4,4-Dimethyloxazoline (DMOX) derivative. cis-13-Eicosenoic acid, 4,4-dimethyloxazoline (dmox) derivative. cis-15-Tetracosenoic acid, 4,4-dimethyloxazoline (dmox) derivative. cis-13-Octadecenoic acid, 4,4-dimethyloxazoline (dmox) derivative. cis-10-Heptadecenoic acid, 4,4-dimethyloxazoline (dmox) derivative. Trans-13-octadecenoic acid, 4,4-dimethyloxazoline (dmox) derivative.

Find more compounds similar to Citronellic acid, 4,4-Dimethyloxazoline (DMOX) derivative.

Sources

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