Selected ATcT [1, 2] enthalpy of formation based on version 1.124 of the Thermochemical Network [3]

This version of ATcT results was generated by additional expansion of version 1.122x [4] to include additional information relevant to the study of thermophysical and thermochemical properties of CH2 and CH3 using nonrigid rotor anharmonic oscillator (NRRAO) partition functions [5], the development and benchmarking of a state-of-the-art computational approach that aims to reproduce total atomization energies of small molecules within 10–15 cm^-1 [6], as well as the study of the reversible reaction C₂H₃ + H₂ ⇌ C₂H₄ + H ⇌ C₂H₅ [7]

Ammonia

Formula: NH3 (aq, undissoc)

CAS RN: 7664-41-7

ATcT ID: 7664-41-7*1000

SMILES: N

InChI: InChI=1S/H3N/h1H3

InChIKey: QGZKDVFQNNGYKY-UHFFFAOYSA-N

Hills Formula: H3N1

2D Image:

Aliases: NH3; Ammonia; Azane; Lambda1-azane; Nitrogen hydride; Nitrogen trihydride; Spirit of Hartshorn; Nitro-Sil; R717; UN1005; UN2073; UN2672

Relative Molecular Mass: 17.03056 ± 0.00022

Δ_fH°(0 K)	Δ_fH°(298.15 K)	Uncertainty	Units
	-80.882	± 0.053	kJ/mol

Top contributors to the provenance of Δ_fH° of NH3 (aq, undissoc)

The 13 contributors listed below account for 90.3% of the provenance of Δ_fH° of NH3 (aq, undissoc).

Please note: The list is limited to 20 most important contributors or, if less, a number sufficient to account for 90% of the provenance. The Reference acts as a further link to the relevant references and notes for the measurement. The Measured Quantity is normaly given in the original units; in cases where we have reinterpreted the original measurement, the listed value may differ from that given by the authors. The quoted uncertainty is the a priori uncertainty used as input when constructing the initial Thermochemical Network, and corresponds either to the value proposed by the original authors or to our estimate; if an additional multiplier is given in parentheses immediately after the prior uncertainty, it corresponds to the factor by which the prior uncertainty needed to be multiplied during the ATcT analysis in order to make that particular measurement consistent with the prevailing knowledge contained in the Thermochemical Network.

Contribution (%)	TN ID	Reaction	Measured Quantity	Reference
37.2	1663.1	NH3 (g) → NH3 (aq, undissoc)	Δ_rH°(298.15 K) = -8.448 ± 0.015 kcal/mol	Vanderzee 1972
12.6	1602.1	1/2 N2 (g) + 3/2 H2 (g) → NH3 (g)	Δ_rH°(298.15 K) = -10.885 ± 0.010 kcal/mol	Larson 1923, Vanderzee 1972
9.3	1663.2	NH3 (g) → NH3 (aq, undissoc)	Δ_rH°(298.15 K) = -8.456 ± 0.030 kcal/mol	Stavaley 1971, Vanderzee 1972, as quoted by CODATA Key Vals
9.3	1663.7	NH3 (g) → NH3 (aq, undissoc)	Δ_rH°(298.15 K) = -8.456 ± 0.030 kcal/mol	Staveley 1971, Vanderzee 1972
6.4	1601.5	1/2 N2 (g) + 3/2 H2 (g) → NH3 (g)	Δ_rH°(298.15 K) = -10.875 ± 0.014 kcal/mol	Schulz 1966, Vanderzee 1972
4.0	1668.1	N2 (g) + 3 H2O (cr,l) + 2 H+ (aq) → 3/2 O2 (g) + 2 [NH4]+ (aq)	Δ_rH°(298.15 K) = 141.292 ± 0.119 kcal/mol	Vanderzee 1972c
3.3	1663.3	NH3 (g) → NH3 (aq, undissoc)	Δ_rH°(298.15 K) = -8.442 ± 0.050 kcal/mol	Thomsen 1873, Vanderzee 1972
2.5	1601.4	1/2 N2 (g) + 3/2 H2 (g) → NH3 (g)	Δ_rH°(298.15 K) = -10.910 ± 0.015 (×1.477) kcal/mol	Larson 1924, Vanderzee 1972
1.6	1667.1	NH3 (g) + HON(O)O (aq) → [NH4]+ (aq) + [ON(O)O]- (aq)	Δ_rH°(298.15 K) = -87.23 ± 0.25 (×1.164) kJ/mol	Becker 1934, Vanderzee 1972a, as quoted by CODATA Key Vals
1.0	1662.3	(NH4)NO3 (cr,l) → N2 (g) + 1/2 O2 (g) + 2 H2O (cr,l)	Δ_rH°(293.65 K) = -49.44 ± 0.06 kcal/mol	Becker 1934
0.9	1668.3	N2 (g) + 3 H2O (cr,l) + 2 H+ (aq) → 3/2 O2 (g) + 2 [NH4]+ (aq)	Δ_rH°(298.15 K) = 141.226 ± 0.239 kcal/mol	Becker 1934, as quoted by CODATA Key Vals
0.8	1602.8	1/2 N2 (g) + 3/2 H2 (g) → NH3 (g)	Δ_rG°(635 K) = 20.084 ± 0.157 kJ/mol	Schulz 1966, 3rd Law
0.8	1663.4	NH3 (g) → NH3 (aq, undissoc)	Δ_rH°(298.15 K) = -8.475 ± 0.100 kcal/mol	Baud 1909, Vanderzee 1972

Top 10 species with enthalpies of formation correlated to the Δ_fH° of NH3 (aq, undissoc)

Please note: The correlation coefficients are obtained by renormalizing the off-diagonal elements of the covariance matrix by the corresponding variances.
The correlation coefficient is a number from -1 to 1, with 1 representing perfectly correlated species, -1 representing perfectly anti-correlated species, and 0 representing perfectly uncorrelated species.

Correlation Coefficent (%)	Species Name	Formula	Δ_fH°(0 K)	Δ_fH°(298.15 K)	Uncertainty	Units	Relative Molecular Mass	ATcT ID
95.3	Ammonium	[NH4]+ (aq)		-133.074	± 0.056	kJ/mol	18.03795 ± 0.00029	14798-03-9*800
95.1	Ammonia	NH3 (aq)		-77.030	± 0.056	kJ/mol	17.03056 ± 0.00022	7664-41-7*800
91.5	Ammonium hydroxide	NH4OH (aq, undissoc)		-366.678	± 0.061	kJ/mol	35.04584 ± 0.00047	1336-21-6*1000
87.6	Ammonium hydroxide	NH4OH (aq)		-362.826	± 0.062	kJ/mol	35.04584 ± 0.00047	1336-21-6*800
83.8	Ammonium chloride	(NH4)Cl (cr)	-311.553	-314.714	± 0.062	kJ/mol	53.49120 ± 0.00095	12125-02-9*510
51.3	Ammonia	NH3 (g)	-38.563	-45.556	± 0.029	kJ/mol	17.03056 ± 0.00022	7664-41-7*0
51.3	Azanylium	[NH3]+ (g)	944.274	937.319	± 0.029	kJ/mol	17.03001 ± 0.00022	19496-55-0*0
34.3	Ammonium bromide	(NH4)Br (cr)	-253.64	-270.22	± 0.15	kJ/mol	97.9425 ± 0.0010	12124-97-9*510
16.5	Ammonium nitrate	(NH4)NO3 (cr,l)	-350.21	-365.17	± 0.18	kJ/mol	80.04344 ± 0.00095	6484-52-2*500
13.3	Ammonium hydroxide	NH4OH (aq, 1000 H2O)		-366.37	± 0.41	kJ/mol	35.04584 ± 0.00047	1336-21-6*839

Most Influential reactions involving NH3 (aq, undissoc)

Please note: The list, which is based on a hat (projection) matrix analysis, is limited to no more than 20 largest influences.

Influence Coefficient	TN ID	Reaction	Measured Quantity	Reference
1.000	1664.1	NH3 (aq, undissoc) + H2O (cr,l) → NH4OH (aq, undissoc)	Δ_rH°(298.15 K) = 0.000 ± 0.000 kJ/mol	triv
0.687	1665.1	[NH4]+ (aq) → NH3 (aq, undissoc) + H+ (aq)	Δ_rG°(298.15 K) = 52.771 ± 0.020 kJ/mol	Bates 1950, Bates 1950, Bates 1949, Bates 1943, Bates 1946
0.529	1663.1	NH3 (g) → NH3 (aq, undissoc)	Δ_rH°(298.15 K) = -8.448 ± 0.015 kcal/mol	Vanderzee 1972
0.423	1849.2	3 NH2OH (aq, undissoc) → N2 (g) + NH3 (aq, undissoc) + 3 H2O (cr,l)	Δ_rH°(298.15 K) = -154.2 ± 2.4 kcal/mol	Thomsen 1882, Ellingson 1915, Berthelot 1877, Lumme 1965, Muhammad 1957, Svyentoslavskii 1909, Berthelot 1890, as quoted by NBS Tables
0.423	1849.1	3 NH2OH (aq, undissoc) → N2 (g) + NH3 (aq, undissoc) + 3 H2O (cr,l)	Δ_rH°(298.15 K) = -153.7 ± 2.4 kcal/mol	Thomsen 1882, Ellingson 1915, Berthelot 1877, Lumme 1965, Muhammad 1957, Svyentoslavskii 1909, Berthelot 1890, as quoted by NBS Tables
0.162	1666.3	NH3 (aq, undissoc) + H2O (cr,l) → [NH4]+ (aq) + [OH]- (aq)	Δ_rH°(298.15 K) = 0.920 ± 0.010 kcal/mol	Vanderzee 1972a
0.132	1663.7	NH3 (g) → NH3 (aq, undissoc)	Δ_rH°(298.15 K) = -8.456 ± 0.030 kcal/mol	Staveley 1971, Vanderzee 1972
0.132	1663.2	NH3 (g) → NH3 (aq, undissoc)	Δ_rH°(298.15 K) = -8.456 ± 0.030 kcal/mol	Stavaley 1971, Vanderzee 1972, as quoted by CODATA Key Vals
0.109	1665.5	[NH4]+ (aq) → NH3 (aq, undissoc) + H+ (aq)	Δ_rG°(298.15 K) = 52.732 ± 0.050 kJ/mol	Everett 1954, Olofsson 1975a, as quoted by CODATA Key Vals
0.047	1663.3	NH3 (g) → NH3 (aq, undissoc)	Δ_rH°(298.15 K) = -8.442 ± 0.050 kcal/mol	Thomsen 1873, Vanderzee 1972
0.019	1665.2	[NH4]+ (aq) → NH3 (aq, undissoc) + H+ (aq)	Δ_rH°(298.15 K) = 52.201 ± 0.118 kJ/mol	Bates 1950, Bates 1950, Bates 1949, Bates 1943, Bates 1946
0.011	1663.4	NH3 (g) → NH3 (aq, undissoc)	Δ_rH°(298.15 K) = -8.475 ± 0.100 kcal/mol	Baud 1909, Vanderzee 1972
0.005	1663.5	NH3 (g) → NH3 (aq, undissoc)	Δ_rH°(298.15 K) = -8.320 ± 0.150 kcal/mol	Wrewsky 1924, Vanderzee 1972
0.005	1666.2	NH3 (aq, undissoc) + H2O (cr,l) → [NH4]+ (aq) + [OH]- (aq)	Δ_rH°(298.15 K) = 0.865 ± 0.030 (×1.874) kcal/mol	Pitzer 1937
0.003	1665.6	[NH4]+ (aq) → NH3 (aq, undissoc) + H+ (aq)	Δ_rH°(298.15 K) = 51.92 ± 0.11 (×2.484) kJ/mol	Olofsson 1975a, Parker 1965, as quoted by CODATA Key Vals
0.001	1665.8	[NH4]+ (aq) → NH3 (aq, undissoc) + H+ (aq)	Δ_rH°(298.15 K) = 51.798 ± 0.314 (×1.269) kJ/mol	Everett 1954
0.001	1663.6	NH3 (g) → NH3 (aq, undissoc)	Δ_rH°(298.15 K) = -8.160 ± 0.150 (×1.915) kcal/mol	Ramstetter 1931, Vanderzee 1972
0.001	1666.1	NH3 (aq, undissoc) + H2O (cr,l) → [NH4]+ (aq) + [OH]- (aq)	Δ_rH°(298.15 K) = 0.800 ± 0.030 (×4.088) kcal/mol	Pitzer 1937, Vanderzee 1972a

References

1		B. Ruscic, R. E. Pinzon, M. L. Morton, G. von Laszewski, S. Bittner, S. G. Nijsure, K. A. Amin, M. Minkoff, and A. F. Wagner, Introduction to Active Thermochemical Tables: Several "Key" Enthalpies of Formation Revisited. J. Phys. Chem. A 108, 9979-9997 (2004) [DOI: 10.1021/jp047912y]
2		B. Ruscic, R. E. Pinzon, G. von Laszewski, D. Kodeboyina, A. Burcat, D. Leahy, D. Montoya, and A. F. Wagner, Active Thermochemical Tables: Thermochemistry for the 21^st Century. J. Phys. Conf. Ser. 16, 561-570 (2005) [DOI: 10.1088/1742-6596/16/1/078]
3		B. Ruscic and D. H. Bross, Active Thermochemical Tables (ATcT) values based on ver. 1.124 of the Thermochemical Network, Argonne National Laboratory, Lemont, Illinois 2022; available at ATcT.anl.gov [DOI: 10.17038/CSE/1885923]
4		Y. Ren, L. Zhou, A. Mellouki, V. Daële, M. Idir, S. S. Brown, B. Ruscic, Robert S. Paton, M. R. McGillen, and A. R. Ravishankara, Reactions of NO3 with Aromatic Aldehydes: Gas-Phase Kinetics and Insights into the Mechanism of the Reaction. Atmos. Chem. Phys. 21, 13537-13551 (2021) [DOI: 10.5194/acp2021-228]
5		B. Ruscic and D. H. Bross, Active Thermochemical Tables: The Thermophysical and Thermochemical Properties of Methyl, CH3, and Methylene, CH2, Corrected for Nonrigid Rotor and Anharmonic Oscillator Effects. Mol. Phys. e1969046 (2021) [DOI: 10.1080/00268976.2021.1969046]
6		J. H. Thorpe, J. L. Kilburn, D. Feller, P. B. Changala, D. H. Bross, B. Ruscic, and J. F. Stanton, Elaborated Thermochemical Treatment of HF, CO, N2, and H2O: Insight into HEAT and Its Extensions J. Chem. Phys. 155, 184109 (2021) [DOI: 10.1063/5.0069322]
7		T. L. Nguyen, D. H. Bross, B. Ruscic, G. B. Ellison, and J. F. Stanton, Mechanism, Thermochemistry, and Kinetics of the Reversible Reactions: C2H3 + H2 ⇌ C2H4 + H ⇌ C2H5. Faraday Discuss. , (Advance Article) (2022) [DOI: 10.1039/D1FD00124H]
8		B. Ruscic, Uncertainty Quantification in Thermochemistry, Benchmarking Electronic Structure Computations, and Active Thermochemical Tables. Int. J. Quantum Chem. 114, 1097-1101 (2014) [DOI: 10.1002/qua.24605]
9		B. Ruscic and D. H. Bross, Thermochemistry Computer Aided Chem. Eng. 45, 3-114 (2019) [DOI: 10.1016/B978-0-444-64087-1.00001-2]

Formula

The aggregate state is given in parentheses following the formula, such as: g - gas-phase, cr - crystal, l - liquid, etc.

Uncertainties

The listed uncertainties correspond to estimated 95% confidence limits, as customary in thermochemistry (see, for example, Ruscic [8,9]).
Note that an uncertainty of ± 0.000 kJ/mol indicates that the estimated uncertainty is < ± 0.000₅ kJ/mol.

Website Functionality Credits

The reorganization of the website was developed and implemented by David H. Bross (ANL).
The find function is based on the complete Species Dictionary entries for the appropriate version of the ATcT TN.
The molecule images are rendered by Indigo-depict.
The XYZ renderings are based on Jmol: an open-source Java viewer for chemical structures in 3D. http://www.jmol.org/.

Acknowledgement

This work was supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences and Biosciences under Contract No. DE-AC02-06CH11357.