Chemical Properties of Methyltestosterone, HFB

Methyltestosterone, HFB

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InChI Key
Molecular Weight1
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Physical Properties

Property Value Unit Source
Δf -1389.52 kJ/mol Joback Calculated Property
Δfgas -2008.46 kJ/mol Joback Calculated Property
Δfus 25.65 kJ/mol Joback Calculated Property
Δvap 70.21 kJ/mol Joback Calculated Property
log10WS -7.64 Crippen Calculated Property
logPoct/wat 6.653 Crippen Calculated Property
McVol 322.680 ml/mol McGowan Calculated Property
Pc 1138.27 kPa Joback Calculated Property
Inp 2272.00 NIST
Tboil 921.66 K Joback Calculated Property
Tc 1144.56 K Joback Calculated Property
Tfus 642.67 K Joback Calculated Property
Vc 1.270 m3/kmol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas [1186.79; 1381.93] J/mol×K [921.66; 1144.56] Show Hide
Cp,gas 1186.79 J/mol×K 921.66 Joback Calculated Property
Cp,gas 1214.54 J/mol×K 958.81 Joback Calculated Property
Cp,gas 1243.61 J/mol×K 995.96 Joback Calculated Property
Cp,gas 1274.45 J/mol×K 1033.11 Joback Calculated Property
Cp,gas 1307.49 J/mol×K 1070.26 Joback Calculated Property
Cp,gas 1343.17 J/mol×K 1107.41 Joback Calculated Property
Cp,gas 1381.93 J/mol×K 1144.56 Joback Calculated Property

Similar Compounds

Testosterone, HFB. Nortestosterone, HFB. methyltestosterone acetate. 5-«alpha»-Androst-9(11)-ene-3-«alpha»,17-«beta»-diol, HFB. 10A,12a-dimethyl-3,4,4a,5,6,9,10,10a,10b,11,12,12a-dodecahydro-2h-naphtho[2,1-f]chromene-2,8(4bh)-dione. Hydroxyprogesterone Caproate. 5-Androsten-3-«beta»,17-«beta»-diol, HFB. 5-Androsten-3-«alpha»,17-«beta»-diol, HFB. 5-Androsten-3-«beta»,17-«alpha»-diol, HFB. 5-Pregnen-3-«beta»,20-«beta»-diol, HFB. 5-Pregnen-3-«beta»,20-«alpha»-diol, HFB. 17Alpha-acetoxy-6alpha-methyl-pregn-4-ene-3,20-dione. Medroxyprogesterone acetate. Testosterone acetate. Norethindrone Acetate.

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