Selected ATcT [1, 2] enthalpy of formation based on version 1.172 of the Thermochemical Network [3]

This version of ATcT results[3] was generated by additional expansion of version 1.156 to include species relevant to a study of photodissociation of formamide[4].

Ammonium bromide

Formula: (NH4)Br (cr)

CAS RN: 12124-97-9

ATcT ID: 12124-97-9*510

SMILES: [NH4+].[Br-]

InChI: InChI=1S/BrH.H3N/h1H;1H3

InChIKey: SWLVFNYSXGMGBS-UHFFFAOYSA-N

Hills Formula: Br1H4N1

2D Image:

Aliases: (NH4)Br; Ammonium bromide; NH4Br; FR-1; FR-11

Relative Molecular Mass: 97.9425 ± 0.0010

Δ_fH°(0 K)	Δ_fH°(298.15 K)	Uncertainty	Units
-253.27	-269.84	± 0.14	kJ/mol

Top contributors to the provenance of Δ_fH° of (NH4)Br (cr)

The 20 contributors listed below account only for 69.9% of the provenance of Δ_fH° of (NH4)Br (cr).
A total of 102 contributors would be needed to account for 90% of the provenance.

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
16.3	9631.1	S(O)(OH)2 (aq, 2500 H2O) + Br2 (cr,l) + H2O (cr,l) → OS(O)(OH)2 (aq, 2500 H2O) + 2 HBr (aq, 1250 H2O)	Δ_rH°(298.15 K) = -55.47 ± 0.11 kcal/mol	Johnson 1963
8.6	1209.1	[HBr]+ (g) → H (g) + Br+ (g)	Δ_rH°(0 K) = 31394.5 ± 20 cm-1	Haugh 1971, Norling 1935
7.0	1108.2	Br2 (cr,l) → Br2 (g)	Δ_rH°(298.15 K) = 7.386 ± 0.027 kcal/mol	Hildenbrand 1958
6.0	1142.1	HBr (aq, 3000 H2O) → HBr (aq)	Δ_rH°(298.15 K) = -0.239 ± 0.040 kJ/mol	NBS Tables 1989, Parker 1965, NBS TN270
5.1	1726.1	NH3 (g) → NH3 (aq, undissoc)	Δ_rH°(298.15 K) = -8.448 ± 0.015 kcal/mol	Vanderzee 1972
5.0	1733.5	(NH4)Br (cr) → [NH4]+ (aq) + Br- (aq)	Δ_rG°(298.15 K) = -7.849 ± 0.040 kJ/mol	CODATA Key Vals
4.6	1138.1	HBr (g) → HBr (aq, 2570 H2O)	Δ_rH°(298.15 K) = -20.286 ± 0.012 kcal/mol	Vanderzee 1963
1.8	1662.1	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
1.7	1135.1	1/2 H2 (g) + 1/2 Br2 (cr,l) → HBr (aq)	Δ_rG°(298.15 K) = -102.81 ± 0.80 kJ/mol	Jones 1934, as quoted by CODATA Key Vals
1.6	1209.3	[HBr]+ (g) → H (g) + Br+ (g)	Δ_rH°(0 K) = 31358 ± 15 (×3.018) cm-1	Penno 1998, Norling 1935, est unc
1.5	1199.1	Cl2 (g) + 2 Br- (aq) → Br2 (cr,l) + 2 Cl- (aq)	Δ_rH°(298.15 K) = -91.29 ± 0.40 (×4.269) kJ/mol	Johnson 1963, as quoted by CODATA Key Vals
1.5	1199.2	Cl2 (g) + 2 Br- (aq) → Br2 (cr,l) + 2 Cl- (aq)	Δ_rH°(298.15 K) = -91.29 ± 0.80 (×2.134) kJ/mol	Sunner 1964, as quoted by CODATA Key Vals
1.2	1726.7	NH3 (g) → NH3 (aq, undissoc)	Δ_rH°(298.15 K) = -8.456 ± 0.030 kcal/mol	Staveley 1971, Vanderzee 1972
1.2	1726.2	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
1.2	1733.3	(NH4)Br (cr) → [NH4]+ (aq) + Br- (aq)	Δ_rG°(298.15 K) = -1.883 ± 0.019 kcal/mol	Shults 1966, Stephenson 1968, est unc
1.1	1199.3	Cl2 (g) + 2 Br- (aq) → Br2 (cr,l) + 2 Cl- (aq)	Δ_rH°(298.15 K) = -91.55 ± 2.00 kJ/mol	Thomsen 1882, as quoted by CODATA Key Vals
1.0	1356.1	Br2 (cr,l) + 3 I- (aq) → [I3]- (aq) + 2 Br- (aq)	Δ_rH°(298.15 K) = -29.355 ± 0.364 kcal/mol	Wu 1963
0.9	1661.5	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
0.8	6252.1	CH3Br (g) → [CH3]+ (g) + Br (g)	Δ_rH°(0 K) = 12.834 ± 0.002 (×2.828) eV	Song 2001
0.7	3106.2	HCO (g) + HBr (g) → CH2O (g) + Br (g)	Δ_rG°(385 K) = 6.79 ± 0.64 (×1.297) kJ/mol	Becerra 1997, Nava 1981, 3rd Law, note unc

Top 10 species with enthalpies of formation correlated to the Δ_fH° of (NH4)Br (cr)

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°(298.15 K)	Uncertainty	Units	Relative Molecular Mass	ATcT ID
87.9	Bromide	Br- (aq)	-120.50	± 0.12	kJ/mol	79.90455 ± 0.00100	24959-67-9*800
87.9	Hydrogen bromide	HBr (aq)	-120.50	± 0.12	kJ/mol	80.9119 ± 0.0010	10035-10-6*800
83.3	Hydrogen bromide	HBr (aq, 3000 H2O)	-120.26	± 0.12	kJ/mol	80.9119 ± 0.0010	10035-10-6*842
83.2	Hydrogen bromide	HBr (aq, 700 H2O)	-120.04	± 0.12	kJ/mol	80.9119 ± 0.0010	10035-10-6*835
83.2	Hydrogen bromide	HBr (aq, 20000 H2O)	-120.40	± 0.12	kJ/mol	80.9119 ± 0.0010	10035-10-6*852
83.2	Hydrogen bromide	HBr (aq, 20 H2O)	-118.02	± 0.12	kJ/mol	80.9119 ± 0.0010	10035-10-6*818
83.2	Hydrogen bromide	HBr (aq, 100000 H2O)	-120.44	± 0.12	kJ/mol	80.9119 ± 0.0010	10035-10-6*861
83.2	Hydrogen bromide	HBr (aq, 600 H2O)	-120.01	± 0.12	kJ/mol	80.9119 ± 0.0010	10035-10-6*834
83.2	Hydrogen bromide	HBr (aq, 5000 H2O)	-120.31	± 0.12	kJ/mol	80.9119 ± 0.0010	10035-10-6*844
83.2	Hydrogen bromide	HBr (aq, 1000 H2O)	-120.11	± 0.12	kJ/mol	80.9119 ± 0.0010	10035-10-6*839

Most Influential reactions involving (NH4)Br (cr)

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
0.786	1733.5	(NH4)Br (cr) → [NH4]+ (aq) + Br- (aq)	Δ_rG°(298.15 K) = -7.849 ± 0.040 kJ/mol	CODATA Key Vals
0.199	1733.3	(NH4)Br (cr) → [NH4]+ (aq) + Br- (aq)	Δ_rG°(298.15 K) = -1.883 ± 0.019 kcal/mol	Shults 1966, Stephenson 1968, est unc
0.014	1724.4	(NH4)Br (cr) → NH3 (g) + HBr (g)	Δ_rH°(298.15 K) = 45.08 ± 0.17 kcal/mol	Smits 1928, JANAF 3, 3rd Law
0.013	1724.2	(NH4)Br (cr) → NH3 (g) + HBr (g)	Δ_rG°(643.3 K) = 3.316 ± 0.035 (×5.076) kcal/mol	Smith 1914, 3rd Law
0.004	1733.2	(NH4)Br (cr) → [NH4]+ (aq) + Br- (aq)	Δ_rH°(298.15 K) = 4.007 ± 0.015 (×8.175) kcal/mol	Stephenson 1968
0.004	1733.4	(NH4)Br (cr) → [NH4]+ (aq) + Br- (aq)	Δ_rH°(298.15 K) = 4.01 ± 0.10 (×1.242) kcal/mol	Parker 1965, as quoted by CODATA Key Vals
0.003	1724.3	(NH4)Br (cr) → NH3 (g) + HBr (g)	Δ_rH°(298.15 K) = 45.50 ± 0.17 (×2.044) kcal/mol	Smits 1928, JANAF 3, 2nd Law
0.001	1724.7	(NH4)Br (cr) → NH3 (g) + HBr (g)	Δ_rG°(589.4 K) = 28.72 ± 2.13 kJ/mol	Johnson 1909, 3rd Law
0.000	1724.1	(NH4)Br (cr) → NH3 (g) + HBr (g)	Δ_rH°(643.3 K) = 42.77 ± 0.78 kcal/mol	Smith 1914, 2nd Law
0.000	1724.8	(NH4)Br (cr) → NH3 (g) + HBr (g)	Δ_rH°(589.4 K) = 197.44 ± 7.16 (×2.43) kJ/mol	Johnson 1909, 2nd Law

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. 1.172 of the Thermochemical Network (2024); available at ATcT.anl.gov
4		K. L. Caster, N. A. Seifert, B. Ruscic, A. W. Jasper, and K. Prozument, Dynamics of HCN, NHC, and HNCO Formation in the 193 nm Photodissociation of Formamide J. Phys. Chem. A (in press) (2024) [DOI: 10.1021/acs.jpca.4c02232]
5		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]
6		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 [5] and Ruscic and Bross[6]).
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.