Chemical Properties of 2-hydroxypropyl acrylate

2-hydroxypropyl acrylate

InChI
InChI=1S/C6H10O3/c1-3-6(8)9-4-5(2)7/h3,5,7H,1,4H2,2H3
InChI Key
GWZMWHWAWHPNHN-UHFFFAOYSA-N
Formula
C6H10O3
SMILES
C=CC(=O)OCC(C)O
Molecular Weight1
130.14
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Physical Properties

Property Value Unit Source
ω 0.6439 Relay (1.0) Calculated Property
Δfgas -562.11 kJ/mol Relay (1.0) Calculated Property
Δfus 14.95 kJ/mol Joback Calculated Property
Δvap 60.83 kJ/mol Relay (1.0) Calculated Property
IE 10.45 eV Relay (1.0) Calculated Property
log10WS 0.30 Relay (1.0) Calculated Property
logPoct/wat 0.096 Crippen Calculated Property
McVol 104.410 ml/mol McGowan Calculated Property
Pc 3686.49 kPa Joback Calculated Property
Tboil 449.68 K Relay (1.0) Calculated Property
Tc 636.77 K Relay (1.0) Calculated Property
Tfus 272.44 K Relay (1.0) Calculated Property
Vc 0.387 m3/kmol Relay (1.0) Calculated Property

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.

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [225.57; 272.09] J/mol×K [483.52; 658.20] Show Hide
Cp,gas 225.57 J/mol×K 483.52 Joback Calculated Property
Cp,gas 234.24 J/mol×K 512.63 Joback Calculated Property
Cp,gas 242.53 J/mol×K 541.75 Joback Calculated Property
Cp,gas 250.46 J/mol×K 570.86 Joback Calculated Property
Cp,gas 258.02 J/mol×K 599.97 Joback Calculated Property
Cp,gas 265.23 J/mol×K 629.09 Joback Calculated Property
Cp,gas 272.09 J/mol×K 658.20 Joback Calculated Property
η [0.0001581; 0.0647927] Pa×s [243.77; 483.52] Show Hide
η 0.0647927 Pa×s 243.77 Joback Calculated Property
η 0.0117357 Pa×s 283.73 Joback Calculated Property
η 0.0032411 Pa×s 323.69 Joback Calculated Property
η 0.0011876 Pa×s 363.64 Joback Calculated Property
η 0.0005309 Pa×s 403.60 Joback Calculated Property
η 0.0002744 Pa×s 443.56 Joback Calculated Property
η 0.0001581 Pa×s 483.52 Joback Calculated Property

Similar Compounds

1,2-Propanediol diacrylate. 2-Propenoic acid, 2-methyl-, 2-hydroxypropyl ester. 1,2-propanediol, 1-acetate. diacrylate of tri-propoxylated glycerol (Acrylic acid 2-{2-acryloyloxy-3-[2-(2-hydroxy-propoxy)-propoxy]-propoxy}-1-methyl-ethyl ester). dipropoxylated glycerol diacrylate (Acrylic acid 2-acryloyloxy-3-[2-(2-hydroxy-propoxy)-propoxy]-propyl ester). dipropoxylated glycerol diacrylate (Acrylic acid 3-[2-(2-acryloyloxy-propoxy)-propoxy]-2-hydroxy-propyl ester). 2-Propenoic acid, oxiranylmethyl ester. Tripropylene glycol diacrylate. dipropoxylated glycerol diacrylate (Acrylic acid 2-[2-acryloyloxy-3-(2-hydroxy-propoxy)-propoxy]-1-methyl-ethyl ester). dipropoxylated glycerol diacrylate (Acrylic acid 2-[3-(2-acryloyloxy-propoxy)-2-hydroxy-propoxy]-1-methyl-ethyl ester). Propionic acid, 2-methyl-2-hydroxy propyl ester. diacrylate of tri-propoxylated glycerol (Acrylic acid 1-[2-(2-acryloyloxy-propoxy)-propoxymethyl]-2-(2-hydroxy-propoxy)-ethyl ester). diacrylate of tetra-propoxylated glycerol (Acrylic acid 2-(2-acryloyloxy-3-{2-[2-(2-hydroxy-propoxy)-propoxy]-propoxy}-propoxy)-1-methyl-ethyl ester). diacrylate of tetra-propoxylated glycerol (Acrylic acid 2-[2-(2-acryloyloxy-propoxy)-propoxy]-1-[2-(2-hydroxy-propoxy)-propoxymethyl]-ethyl ester). Propylene glycol monobutyrate (p).

Find more compounds similar to 2-hydroxypropyl acrylate.

Mixtures

Sources

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