Selected ATcT [1, 2] enthalpy of formation based on version 1.130 of the Thermochemical Network [3]

This version of ATcT results[4] was generated by additional expansion of version 1.128 [5,6] to include with the calculations provided in reference [4].

Methanimine

Formula: CH2NH (g)

CAS RN: 2053-29-4

ATcT ID: 2053-29-4*0

SMILES: C=N

InChI: InChI=1S/CH3N/c1-2/h2H,1H2

InChIKey: WDWDWGRYHDPSDS-UHFFFAOYSA-N

Hills Formula: C1H3N1

2D Image:

Aliases: CH2NH; Methanimine; Methylenimine; Azomethine; Formaldehyde imine; Formaldimine; Iminomethane; Methyleneamine; Methyleneimine; Methylimide; N-Methylenamine; H2CNH; H2C=NH; CH2=NH; NHCH2; HNCH2; HN=CH2

Relative Molecular Mass: 29.04126 ± 0.00083

Δ_fH°(0 K)	Δ_fH°(298.15 K)	Uncertainty	Units
96.38	88.47	± 0.34	kJ/mol

3D Image of CH2NH (g)

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Top contributors to the provenance of Δ_fH° of CH2NH (g)

The 20 contributors listed below account only for 74.2% of the provenance of Δ_fH° of CH2NH (g).
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
34.7	2600.14	CH2NH (g) → C (g) + 3 H (g) + N (g)	Δ_rH°(0 K) = 1733.46 ± 0.56 kJ/mol	Gratzfeld 2017
6.9	2600.13	CH2NH (g) → C (g) + 3 H (g) + N (g)	Δ_rH°(0 K) = 414.41 ± 0.30 kcal/mol	Karton 2008
6.9	2600.12	CH2NH (g) → C (g) + 3 H (g) + N (g)	Δ_rH°(0 K) = 414.41 ± 0.30 kcal/mol	Karton 2011
5.0	2606.3	CH2NH2 (g) → CH2NH (g) + H (g)	Δ_rH°(0 K) = 36.62 ± 0.30 kcal/mol	Karton 2011
4.9	2605.1	CH4 (g) + NH3 (g) → CH2NH (g) + 2 H2 (g)	Δ_rH°(0 K) = 201.41 ± 1.5 kJ/mol	Klippenstein 2017
3.5	2606.4	CH2NH2 (g) → CH2NH (g) + H (g)	Δ_rH°(0 K) = 152.90 ± 1.5 kJ/mol	Klippenstein 2017
1.9	2600.11	CH2NH (g) → C (g) + 3 H (g) + N (g)	Δ_rH°(0 K) = 414.37 ± 0.56 kcal/mol	Karton 2011
1.4	2606.2	CH2NH2 (g) → CH2NH (g) + H (g)	Δ_rH°(0 K) = 36.74 ± 0.56 kcal/mol	Karton 2011
1.2	5077.6	CH3NCH2 (g) + NH3 (g) → CH2NH (g) + CH3NH2 (g)	Δ_rH°(0 K) = 33.41 ± 2.0 kJ/mol	Klippenstein 2017
1.0	2619.1	CH4 (g) + NH3 (g) → CH3N (g) + 2 H2 (g)	Δ_rH°(0 K) = 427.99 ± 2.0 kJ/mol	Klippenstein 2017
0.7	2621.10	CH3N (g) → CH2NH (g)	Δ_rH°(0 K) = -226.58 ± 1.5 kJ/mol	Klippenstein 2017
0.7	5083.6	CH3CHNH (g, trans) + CH2CH2 (g) → CH2NH (g) + CH3CHCH2 (g)	Δ_rH°(0 K) = 14.63 ± 2.0 kJ/mol	Klippenstein 2017
0.7	5561.5	HNCNH (g) → NH2CN (g)	Δ_rH°(0 K) = -2.70 ± 1.2 kcal/mol	Ruscic W1RO
0.6	6927.5	N(CHCHCHCHCH) (g) + CH2CH2 (g) → C6H6 (g) + CH2NH (g)	Δ_rH°(0 K) = -5.11 ± 0.9 kcal/mol	Ruscic W1RO
0.6	5092.6	CH3CHNH (g, trans) → CH3CHN (g) + H (g)	Δ_rH°(0 K) = 370.92 ± 2.0 kJ/mol	Klippenstein 2017
0.6	5093.6	CH3CHNH (g, trans) + CH2N (g) → CH3CHN (g) + CH2NH (g)	Δ_rH°(0 K) = 8.24 ± 1.5 kJ/mol	Klippenstein 2017
0.6	5080.1	2 CH4 (g) + NH3 (g) → CH3CHNH (g, trans) + 3 H2 (g)	Δ_rH°(0 K) = 227.55 ± 2.0 kJ/mol	Klippenstein 2017
0.6	5561.2	HNCNH (g) → NH2CN (g)	Δ_rH°(0 K) = -2.99 ± 1.3 kcal/mol	Ruscic G4
0.6	5561.4	HNCNH (g) → NH2CN (g)	Δ_rH°(0 K) = -2.10 ± 1.3 kcal/mol	Ruscic CBS-n
0.5	6927.4	N(CHCHCHCHCH) (g) + CH2CH2 (g) → C6H6 (g) + CH2NH (g)	Δ_rH°(0 K) = -5.07 ± 1.0 kcal/mol	Ruscic CBS-n

Top 10 species with enthalpies of formation correlated to the Δ_fH° of CH2NH (g)

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
37.1	Methanediimine	HNCNH (g)	153.1	146.4	± 1.3	kJ/mol	42.04006 ± 0.00082	151-51-9*0
23.0	(1E)-Ethanimine	CH3CHNH (g, trans)	55.74	39.53	± 0.72	kJ/mol	43.0678 ± 0.0016	56003-81-7*0
23.0	Ethanimine	CH3CHNH (g)	55.74	41.11	± 0.72	kJ/mol	43.0678 ± 0.0016	20729-41-3*0
20.9	Methylimidogen	CH3N (g)	323.0	315.3	± 1.0	kJ/mol	29.04126 ± 0.00083	27770-42-9*0
19.4	(1Z)-Ethanimine	CH3CHNH (g, cis)	58.8	44.2	± 1.4	kJ/mol	43.0678 ± 0.0016	56003-82-8*0
18.8	N-Methylenemethanamine	CH3NCH2 (g)	94.55	79.64	± 0.67	kJ/mol	43.0678 ± 0.0016	1761-67-7*0
15.6	Aminomethyl	CH2NH2 (g)	159.40	149.56	± 0.35	kJ/mol	30.04920 ± 0.00085	10507-29-6*0
15.5	Methylimidogen anion	[CH3N]- (g)	321.1	313.4	± 1.3	kJ/mol	29.04181 ± 0.00083	82539-34-2*0
14.1	Methyliumylamino	[CH2NH]+ (g)	1056.1	1049.2	± 1.7	kJ/mol	29.04071 ± 0.00083	65130-65-6*0
12.6	Methanediimine cation	[HNCNH]+ (g, cis)	1137.8	1133.1	± 2.2	kJ/mol	42.03951 ± 0.00082	1189338-16-6*2

Most Influential reactions involving CH2NH (g)

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
0.427	2621.10	CH3N (g) → CH2NH (g)	Δ_rH°(0 K) = -226.58 ± 1.5 kJ/mol	Klippenstein 2017
0.354	2600.14	CH2NH (g) → C (g) + 3 H (g) + N (g)	Δ_rH°(0 K) = 1733.46 ± 0.56 kJ/mol	Gratzfeld 2017
0.301	5093.6	CH3CHNH (g, trans) + CH2N (g) → CH3CHN (g) + CH2NH (g)	Δ_rH°(0 K) = 8.24 ± 1.5 kJ/mol	Klippenstein 2017
0.207	5183.6	CH3NCH2 (g) + HCNH (g, trans) → CH3NCH (g, trans) + CH2NH (g)	Δ_rH°(0 K) = 4.18 ± 2.0 kJ/mol	Klippenstein 2017
0.201	2602.8	[CH2NH]- (g) → CH2NH (g)	Δ_rH°(0 K) = -1.284 ± 0.050 eV	Ruscic W1RO
0.191	2601.12	CH2NH (g) → [CH2NH]+ (g)	Δ_rH°(0 K) = 9.943 ± 0.040 eV	Ruscic W1RO
0.136	5084.5	CH3CHNH (g, cis) + CH2CH2 (g) → CH2NH (g) + CH3CHCH2 (g)	Δ_rH°(0 K) = 2.82 ± 0.85 kcal/mol	Ruscic W1RO
0.135	2602.4	[CH2NH]- (g) → CH2NH (g)	Δ_rH°(0 K) = -1.339 ± 0.061 eV	Ruscic G4
0.128	5083.6	CH3CHNH (g, trans) + CH2CH2 (g) → CH2NH (g) + CH3CHCH2 (g)	Δ_rH°(0 K) = 14.63 ± 2.0 kJ/mol	Klippenstein 2017
0.125	2606.3	CH2NH2 (g) → CH2NH (g) + H (g)	Δ_rH°(0 K) = 36.62 ± 0.30 kcal/mol	Karton 2011
0.122	2601.1	CH2NH (g) → [CH2NH]+ (g)	Δ_rH°(0 K) = 9.97 ± 0.05 eV	Bock 1987a, est unc, as quoted by NIST WebBook, Bock 1987
0.122	2601.4	CH2NH (g) → [CH2NH]+ (g)	Δ_rH°(0 K) = 9.99 ± 0.05 eV	Holzmeier 2013, est unc
0.121	5084.4	CH3CHNH (g, cis) + CH2CH2 (g) → CH2NH (g) + CH3CHCH2 (g)	Δ_rH°(0 K) = 2.79 ± 0.90 kcal/mol	Ruscic CBS-n
0.121	5084.2	CH3CHNH (g, cis) + CH2CH2 (g) → CH2NH (g) + CH3CHCH2 (g)	Δ_rH°(0 K) = 2.60 ± 0.90 kcal/mol	Ruscic G4
0.121	5084.1	CH3CHNH (g, cis) + CH2CH2 (g) → CH2NH (g) + CH3CHCH2 (g)	Δ_rH°(0 K) = 2.69 ± 0.90 kcal/mol	Ruscic G3X
0.120	5077.6	CH3NCH2 (g) + NH3 (g) → CH2NH (g) + CH3NH2 (g)	Δ_rH°(0 K) = 33.41 ± 2.0 kJ/mol	Klippenstein 2017
0.104	5560.5	HNCNH (g) + 2 CH2CH2 (g) → CH2CCH2 (g) + 2 CH2NH (g)	Δ_rH°(0 K) = 27.47 ± 0.9 kcal/mol	Ruscic W1RO
0.103	5559.5	HNCNH (g) + CH4 (g) → 2 CH2NH (g)	Δ_rH°(0 K) = 25.18 ± 0.9 kcal/mol	Ruscic W1RO
0.098	5084.3	CH3CHNH (g, cis) + CH2CH2 (g) → CH2NH (g) + CH3CHCH2 (g)	Δ_rH°(0 K) = 2.68 ± 1.00 kcal/mol	Ruscic CBS-n
0.088	2606.4	CH2NH2 (g) → CH2NH (g) + H (g)	Δ_rH°(0 K) = 152.90 ± 1.5 kJ/mol	Klippenstein 2017

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. 1.130 of the Thermochemical Network. Argonne National Laboratory, Lemont, Illinois 2023; available at ATcT.anl.gov [DOI: 10.17038/CSE/1997229]
4		N. Genossar, P. B. Changala, B. Gans, J.-C. Loison, S. Hartweg, M.-A. Martin-Drumel, G. A. Garcia, J. F. Stanton, B. Ruscic, and J. H. Baraban Ring-Opening Dynamics of the Cyclopropyl Radical and Cation: the Transition State Nature of the Cyclopropyl Cation J. Am. Chem. Soc. 144, 18518-18525 (2022) [DOI: 10.1021/jacs.2c07740]
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		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]
8		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 [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.