Chemical Properties of p-Cresyl glycidyl ether

InChI

InChI=1S/C10H12O2/c1-8-2-4-9(5-3-8)11-6-10-7-12-10/h2-5,10H,6-7H2,1H3

InChI Key

CUFXMPWHOWYNSO-UHFFFAOYSA-N

Formula

C10H12O2

SMILES

Cc1ccc(OCC2CO2)cc1

Molecular Weight¹

164.20

Other Names

• 2,3-Epoxypropyl p-tolyl ether
• Oxirane, [(4-methylphenoxy)methyl]-
• Propane, 1,2-epoxy-3-(p-tolyloxy)-
• p-Cresol glycidyl ether
• 1,2-Epoxy-3-(p-tolyloxy)propane
• Glycidyl 4-methylphenyl ether
• Glycidyl p-tolyl ether
• 2-[(4-Methylphenoxy)methyl]oxirane
• ((4-Methylphenoxy)methyl)oxirane
• NSC 112255
• p-Methylphenol glycidyl ether
• [(p-tolyloxy)methyl]oxirane

• C_p,gas : Ideal gas heat capacity (J/mol×K).
• η : Dynamic viscosity (Pa×s).
• Δ_fH°_gas : Enthalpy of formation at standard conditions (kJ/mol).
• Δ_fusH° : Enthalpy of fusion at standard conditions (kJ/mol).
• Δ_vapH° : Enthalpy of vaporization at standard conditions (kJ/mol).
• IE : Ionization energy (eV).
• logP_oct/wat : Octanol/Water partition coefficient.
• McVol : McGowan's characteristic volume (ml/mol).
• P_c : Critical Pressure (kPa).
• T_boil : Normal Boiling Point Temperature (K).
• T_c : Critical Temperature (K).
• T_fus : Normal melting (fusion) point (K).
• ¹: Molecular weight from the IUPAC atomic weights tables.

Physical Properties

Cheméo can also estimate Critical Volume, Standard Gibbs free energy of formation, Acentric Factor, 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.

Correlations

Property	Value	Unit	Temperature (K)	Source
Cp,gas	[172.24; 431.43]	J/mol×K	[273.00; 1000.00]	Joback Predicted correlation
Equation			Y = A + B·T + C·T² + D·T³ + E·T⁴ Y is Cp,gas in J/mol×K, T in K
Coefficient A			-3.32290e+01
Coefficient B			9.00120e-01
Coefficient C			-5.79660e-04
Coefficient D			1.44200e-07
Coefficient E			0.00000e+00
Temperature range, min.			273.00
Temperature range, max.			1000.00
Cp,gas	172.24	J/mol×K	273.00	Calculated Property
Cp,gas	219.05	J/mol×K	353.78	Calculated Property
Cp,gas	260.29	J/mol×K	434.56	Calculated Property
Cp,gas	296.43	J/mol×K	515.33	Calculated Property
Cp,gas	327.91	J/mol×K	596.11	Calculated Property
Cp,gas	355.19	J/mol×K	676.89	Calculated Property
Cp,gas	378.72	J/mol×K	757.67	Calculated Property
Cp,gas	398.97	J/mol×K	838.44	Calculated Property
Cp,gas	416.39	J/mol×K	919.22	Calculated Property
Cp,gas	431.43	J/mol×K	1000.00	Calculated Property

Property	Value	Unit	Temperature (K)	Source
η	[0.0016203; 0.0004032]	Pa×s	[308.14; 514.93]	Joback Predicted correlation
Equation			Y = exp(A + B/T + C·ln(T) + D·T^E) Y is η in Pa×s, T in K
Coefficient A			-9.88889e+00
Coefficient B			1.06732e+03
Coefficient C			0.00000e+00
Coefficient D			0.00000e+00
Coefficient E			0.00000e+00
Temperature range, min.			308.14
Temperature range, max.			514.93
η	0.0016203	Pa×s	308.14	Calculated Property
η	0.0012741	Pa×s	331.12	Calculated Property
η	0.0010336	Pa×s	354.09	Calculated Property
η	0.0008602	Pa×s	377.07	Calculated Property
η	0.0007311	Pa×s	400.05	Calculated Property
η	0.0006325	Pa×s	423.02	Calculated Property
η	0.0005554	Pa×s	446.00	Calculated Property
η	0.0004940	Pa×s	468.98	Calculated Property
η	0.0004442	Pa×s	491.96	Calculated Property
η	0.0004032	Pa×s	514.93	Calculated Property

Similar Compounds

Find more compounds similar to p-Cresyl glycidyl ether.

Sources

• Cheméo Relay (1.0)
• Crippen Method
• Crippen Method
• Joback Method
• McGowan Method
• NIST Webbook

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