Chemical Properties of l-camphoronic acid

l-camphoronic acid

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InChI
InChI=1S/C9H14O6/c1-8(2,6(12)13)9(3,7(14)15)4-5(10)11/h4H2,1-3H3,(H,10,11)(H,12,13)(H,14,15)
InChI Key
MJCJFUJXVGIUOD-UHFFFAOYSA-N
Formula
C9H14O6
SMILES
CC(C)(C(=O)O)C(C)(CC(=O)O)C(=O)O
Molecular Weight1
218.21
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Physical Properties

Property Value Unit Source
Δf -766.64 kJ/mol Joback Calculated Property
Δfgas -1041.02 kJ/mol Joback Calculated Property
Δfus 21.30 kJ/mol Joback Calculated Property
Δvap 103.31 kJ/mol Joback Calculated Property
log10WS -0.29 Aq. Sol...
logPoct/wat 0.663 Crippen Calculated Property
McVol 159.990 ml/mol McGowan Calculated Property
Pc 4010.84 kPa Joback Calculated Property
Tboil 837.01 K Joback Calculated Property
Tc 1031.21 K Joback Calculated Property
Tfus 528.28 K Joback Calculated Property
Vc 0.593 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [478.50; 514.70] J/mol×K [837.01; 1031.21] Show Hide
Cp,gas 478.50 J/mol×K 837.01 Joback Calculated Property
Cp,gas 485.48 J/mol×K 869.38 Joback Calculated Property
Cp,gas 492.03 J/mol×K 901.74 Joback Calculated Property
Cp,gas 498.17 J/mol×K 934.11 Joback Calculated Property
Cp,gas 503.96 J/mol×K 966.47 Joback Calculated Property
Cp,gas 509.46 J/mol×K 998.84 Joback Calculated Property
Cp,gas 514.70 J/mol×K 1031.21 Joback Calculated Property
η [0.0000010; 0.0002007] Pa×s [528.28; 837.01] Show Hide
η 0.0002007 Pa×s 528.28 Joback Calculated Property
η 0.0000566 Pa×s 579.74 Joback Calculated Property
η 0.0000196 Pa×s 631.19 Joback Calculated Property
η 0.0000080 Pa×s 682.64 Joback Calculated Property
η 0.0000037 Pa×s 734.10 Joback Calculated Property
η 0.0000019 Pa×s 785.56 Joback Calculated Property
η 0.0000010 Pa×s 837.01 Joback Calculated Property

Similar Compounds

2,2-Dimethylglutaric acid. 1,3-Cyclopentanedicarboxylic acid, 1,2,2-trimethyl-, (1R-cis)-. Succinic acid, isopropyl-. 2,2-Dimethylbutanedioic acid. D-Campholic acid. 1-Methylcyclohexylcarboxylic acid. Meso-2,3-diethylbutanedioic acid. Cyclopentanecarboxylic acid, 1-methyl-. Bicyclo[2.2.2]octane-1-carboxylic acid, 4-methyl-. ethyl succinic acid. 4a(2H)-naphthalenecarboxylic acid, octahydro-, trans-. Cyclohexanecarboxylic acid, 1-cyclohexyl-. 4a(2H)-Naphthalenecarboxylic acid, octahydro-, cis-. 1,2-Cyclohexanedicarboxylic acid, cis-. 1,2-Cyclohexanedicarboxylic acid, trans-.

Find more compounds similar to l-camphoronic acid.

Sources

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