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. Author manuscript; available in PMC: 2024 Oct 4.
Published in final edited form as: J Phys Chem A. 2024 Feb 7;128(7):1339–1357. doi: 10.1021/acs.jpca.3c04937

Table 4:

Standard enthalpies of formation for the liquid phase ΔfHm(l) and the ideal gas ΔfHm(g) for auxiliary compounds at the reference temperature T=298.15Ka

Compound CASRN ΔfHm(l)kJmol1 ΔfHm(g)kJmol1 Referencea
hydrogen atom 12385-13-6 217.998 ± 0.006  38
water 7732-18-5 −(285.83 ± 0.04) −(241.83 ± 0.04)  38
carbon dioxide 124-38-9 −(393.51 ± 0.13)  38
bromine atom 10097-32-2 111.85 ± 0.06  39
hydrogen bromide 10035-10-6 −(35.69 ± 0.13)  39
HBrxH2O 10035-10-6  39,61
dibromine 7726-95-6 0 30.91 ± 0.11  38
hydrogen iodide 10034-85-2 26.47 ± 0.04  39
iodine bromide 7789-33-5 40.80 ± 0.14  67
ethane 74-98-6 −(93.6 ± 2.5)  8
propane 74-98-6 −(120.9 ± 2.5)  8
butane 106-97-8 −(147.3 ± 2.5)  8
2-methylpropane 75-28-5 −(154.2 ± 1.2)  8
2-methylbut-2-ene 75-28-5 −(41.7 ± 1.0)  8
propene 115-07-1 4.0 ± 2.5 20.02 ± 0.18  8; 39
but-1-ene 106-98-9 −20.8 ± 1.0 0.19 ± 0.34  8; 39
Compound CASRN ΔfHm(l)kJmol1 ΔfHm(g)kJmol1 Referenceb

propan-1-ol 71-23-8 −(255.11 ± 0.24)  39
allyl alcohol 107-18-6 −(169.5 ± 1.6) −(124.5 ± 1.3)  40; 68
difluoromethane 75-10-5 −(452.3 ± 1.0)  69
trifluoromethane 75-46-7 −(696.6 ± 2.8)  69
tetrafluoroethylene 116-14-3 −(673.2 ± 3.0)  24
trichloromethane 67-66-3 −(134.1 ± 2.5)  70
2-chloropropane 75-29-6 −(144.9 ± 1.3)  8
a

For hydrocarbons, only the sources different from ATcT v.1.13039 are listed.

b

Sources of ΔfHm for the liquid and gas phases (if different) are separated by semicolon.