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

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

• 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.

Temperature Dependent Properties

Property	Value	Unit	Temperature (K)	Source
Cp,gas	[296.78; 372.64]	J/mol×K	[516.17; 735.62]
Cp,gas	296.78	J/mol×K	516.17	Joback Calculated Property
Cp,gas	311.56	J/mol×K	552.74	Joback Calculated Property
Cp,gas	325.43	J/mol×K	589.32	Joback Calculated Property
Cp,gas	338.43	J/mol×K	625.89	Joback Calculated Property
Cp,gas	350.60	J/mol×K	662.47	Joback Calculated Property
Cp,gas	361.99	J/mol×K	699.04	Joback Calculated Property
Cp,gas	372.64	J/mol×K	735.62	Joback Calculated Property
η	[0.0004012; 0.0016203]	Pa×s	[308.14; 516.17]
η	0.0016203	Pa×s	308.14	Joback Calculated Property
η	0.0011414	Pa×s	342.81	Joback Calculated Property
η	0.0008576	Pa×s	377.48	Joback Calculated Property
η	0.0006760	Pa×s	412.15	Joback Calculated Property
η	0.0005530	Pa×s	446.83	Joback Calculated Property
η	0.0004656	Pa×s	481.50	Joback Calculated Property
η	0.0004012	Pa×s	516.17	Joback 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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