Chemical Properties of 2-Propenoic acid, oxiranylmethyl ester (CAS 106-90-1)

InChI

InChI=1S/C6H8O3/c1-2-6(7)9-4-5-3-8-5/h2,5H,1,3-4H2

InChI Key

RPQRDASANLAFCM-UHFFFAOYSA-N

Formula

C6H8O3

SMILES

C=CC(=O)OCC1CO1

Molecular Weight¹

128.13

CAS

106-90-1

Other Names

• 1-Propanol, 2,3-epoxy-, acrylate
• 2,3-Epoxypropanol acrylate
• 2,3-Epoxypropyl acrylate
• 2-Propenoic acid, 2-oxiranylmethyl ester
• Acrylic acid glycidyl ester
• Acrylic acid, 2,3-epoxypropyl ester
• Glycidyl acrylate
• Glycidyl propenate
• Glycidylester kyseliny akrylove
• M 581
• Methacyclic acid, 2,3-epoxypropyl ester
• NSC 24151

• ω : Acentric Factor.
• 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).
• log₁₀WS : Log10 of Water solubility in mol/l.
• 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_boilr : Boiling point at reduced pressure (K).
• T_c : Critical Temperature (K).
• T_fus : Normal melting (fusion) point (K).
• V_c : Critical Volume (m³/kmol).
• ¹: Molecular weight from the IUPAC atomic weights tables.

Physical Properties

Cheméo can also estimate Standard Gibbs free energy of formation for this compound, but it falls outside the models' validated range, so it is not shown here. Open the prediction tool to compute it on demand.

Pressure Dependent Properties

Correlations

Property	Value	Unit	Temperature (K)	Source
Cp,gas	[133.21; 307.73]	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			-1.30690e+01
Coefficient B			6.46900e-01
Coefficient C			-4.37200e-04
Coefficient D			1.11100e-07
Coefficient E			0.00000e+00
Temperature range, min.			273.00
Temperature range, max.			1000.00
Cp,gas	133.21	J/mol×K	273.00	Calculated Property
Cp,gas	165.99	J/mol×K	353.78	Calculated Property
Cp,gas	194.60	J/mol×K	434.56	Calculated Property
Cp,gas	219.40	J/mol×K	515.33	Calculated Property
Cp,gas	240.73	J/mol×K	596.11	Calculated Property
Cp,gas	258.95	J/mol×K	676.89	Calculated Property
Cp,gas	274.41	J/mol×K	757.67	Calculated Property
Cp,gas	287.46	J/mol×K	838.44	Calculated Property
Cp,gas	298.45	J/mol×K	919.22	Calculated Property
Cp,gas	307.73	J/mol×K	1000.00	Calculated Property

Property	Value	Unit	Temperature (K)	Source
η	[0.0023870; 0.0004567]	Pa×s	[242.46; 433.07]	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			-9.79498e+00
Coefficient B			9.10990e+02
Coefficient C			0.00000e+00
Coefficient D			0.00000e+00
Coefficient E			0.00000e+00
Temperature range, min.			242.46
Temperature range, max.			433.07
η	0.0023870	Pa×s	242.46	Calculated Property
η	0.0017651	Pa×s	263.64	Calculated Property
η	0.0013652	Pa×s	284.82	Calculated Property
η	0.0010941	Pa×s	306.00	Calculated Property
η	0.0009023	Pa×s	327.18	Calculated Property
η	0.0007618	Pa×s	348.36	Calculated Property
η	0.0006557	Pa×s	369.54	Calculated Property
η	0.0005737	Pa×s	390.72	Calculated Property
η	0.0005089	Pa×s	411.89	Calculated Property
η	0.0004567	Pa×s	433.07	Calculated Property

Similar Compounds

Find more compounds similar to 2-Propenoic acid, oxiranylmethyl ester.

Sources

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

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