Alanine
- Formula: C3H7NO2
- Molecular weight: 89.0932
- IUPAC Standard InChIKey: QNAYBMKLOCPYGJ-UWTATZPHSA-N
- CAS Registry Number: 56-41-7
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
The 3d structure may be viewed using Java or Javascript. - Stereoisomers:
- Other names: L-Alanine; Alanine, L-; α-Alanine; α-Aminopropionic acid; (S)-Alanine; L-α-Alanine; L-α-Aminopropionic acid; L-(+)-Alanine; L-2-Aminopropanoic acid; L-2-Aminopropionic acid; Propanoic acid, 2-amino-; Propanoic acid, 2-amino-, (S)-; L-CH3CH(NH2)COOH; (S)-2-Aminopropanoic acid; 2-Aminopropanoic acid; 2-Aminopropionic acid; Ala; Ritalanine; NSC 206315; 2-Aminopropanoic acid, L-
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Gas phase ion energetics data
Go To: Top, Ion clustering data, Mass spectrum (electron ionization), UV/Visible spectrum, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data evaluated as indicated in comments:
HL - Edward P. Hunter and Sharon G. Lias
L - Sharon G. Lias
Data compiled as indicated in comments:
B - John E. Bartmess
MM - Michael M. Meot-Ner (Mautner)
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi
RDSH - Henry M. Rosenstock, Keith Draxl, Bruce W. Steiner, and John T. Herron
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
IE (evaluated) | 8.88 | eV | N/A | N/A | L |
Quantity | Value | Units | Method | Reference | Comment |
Proton affinity (review) | 901.6 | kJ/mol | N/A | Hunter and Lias, 1998 | HL |
Quantity | Value | Units | Method | Reference | Comment |
Gas basicity | 867.7 | kJ/mol | N/A | Hunter and Lias, 1998 | HL |
Proton affinity at 298K
Proton affinity (kJ/mol) | Reference | Comment |
---|---|---|
894.5 ± 0.4 | Bouchoux and Salpin, 2003 | T = 298K; MM |
902. ± 4. | Hahn and Wesdemiotis, 2003 | MM |
Gas basicity at 298K
Gas basicity (review) (kJ/mol) | Reference | Comment |
---|---|---|
865.4 ± 0.4 | Bouchoux and Salpin, 2003 | T = 298K; MM |
864.0 ± 6.3 | Cassady, Carr, et al., 1995 | T = 298K; GB> dimethylformamide, ≈ 3-methylaniline, < 3-fluropyridine; MM |
863.6 ± 6.7 | Wu and Lebrilla, 1995 | T = 300K; MM |
Ionization energy determinations
IE (eV) | Method | Reference | Comment |
---|---|---|---|
8.88 | PE | Klasinc, 1976 | LLK |
8.8 | PE | Debies and Rabalais, 1974 | LLK |
9.63 | CTS | Slifkin and Allison, 1967 | RDSH |
De-protonation reactions
C3H6NO2- + =
By formula: C3H6NO2- + H+ = C3H7NO2
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1430. ± 7.9 | kJ/mol | CIDC | Jones, Bernier, et al., 2007 | gas phase; B |
ΔrH° | 1425. ± 8.8 | kJ/mol | G+TS | Locke and McIver, 1983 | gas phase; B |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | 1401. ± 8.4 | kJ/mol | H-TS | Jones, Bernier, et al., 2007 | gas phase; B |
ΔrG° | 1396. ± 8.4 | kJ/mol | IMRE | Locke and McIver, 1983 | gas phase; B |
Ion clustering data
Go To: Top, Gas phase ion energetics data, Mass spectrum (electron ionization), UV/Visible spectrum, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: Robert C. Dunbar
Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. Searches may be limited to ion clustering reactions. A general reaction search form is also available.
Clustering reactions
By formula: Na+ + C3H7NO2 = (Na+ • C3H7NO2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 169. ± 13. | kJ/mol | IMRE | Gapeev and Dunbar, 2003 | Anchor glycine=38.5+-2.0 |
ΔrH° | 167. | kJ/mol | CIDC | Kish, Ohanessian, et al., 2003 | Anchor alanine=39.89 |
Mass spectrum (electron ionization)
Go To: Top, Gas phase ion energetics data, Ion clustering data, UV/Visible spectrum, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director
Spectrum
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Additional Data
View image of digitized spectrum (can be printed in landscape orientation).
Due to licensing restrictions, this spectrum cannot be downloaded.
Owner | NIST Mass Spectrometry Data Center Collection (C) 2014 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. All rights reserved. |
---|---|
Origin | Japan AIST/NIMC Database- Spectrum MS-NW- 301 |
NIST MS number | 228084 |
UV/Visible spectrum
Go To: Top, Gas phase ion energetics data, Ion clustering data, Mass spectrum (electron ionization), References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Spectrum
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Additional Data
View image of digitized spectrum (can be printed in landscape orientation).
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Download spectrum in JCAMP-DX format.
Source | Abu-Eittah, et al., 1988 |
---|---|
Owner | INEP CP RAS, NIST OSRD Collection (C) 2007 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. All rights reserved. |
Origin | INSTITUTE OF ENERGY PROBLEMS OF CHEMICAL PHYSICS, RAS |
Source reference | RAS UV No. 17326 |
Instrument | unknown |
Melting point | 300 dec. |
References
Go To: Top, Gas phase ion energetics data, Ion clustering data, Mass spectrum (electron ionization), UV/Visible spectrum, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Hunter and Lias, 1998
Hunter, E.P.; Lias, S.G.,
Evaluated Gas Phase Basicities and Proton Affinities of Molecules: An Update,
J. Phys. Chem. Ref. Data, 1998, 27, 3, 413-656, https://doi.org/10.1063/1.556018
. [all data]
Bouchoux and Salpin, 2003
Bouchoux, G.; Salpin, J.Y.,
Gas-phase basicity of glycine, alanine, proline, serine, lysine, histidine and some of their peptides by the thermokinetic method,
European J. Mass Spectrometry, 2003, 9, 391-402. [all data]
Hahn and Wesdemiotis, 2003
Hahn, I.S.; Wesdemiotis, C.,
Protonation Thermochemistry of beta-Alanine. An Evaluation of Proton Affinities and Entropies Determined by the Extended Kinetic Method,
Int. J. Mass Spectrometry, 2003, 222, 465. [all data]
Cassady, Carr, et al., 1995
Cassady, C.J.; Carr, S.R.; Zhang, K.; Chung-Phillips, C.,
Experimental and Ab Intio Studies of Protonations of Alanine and Samll Peptides of Alanine and Glycine,
J. Org. Chem., 1995, 60, 1704. [all data]
Wu and Lebrilla, 1995
Wu, J.; Lebrilla, C.B.,
Intrinsic Basicity of Oligomeric Peptides that Contain Glycine, Alanine, and Valine - The Effects of the Alkyl Side Chain on Proton Transfer Reactions,
J. Am. Soc. Mass Spectrom., 1995, 6, 91. [all data]
Klasinc, 1976
Klasinc, L.,
Application of photoelectron spectroscopy to biologically active molecules and their constituent parts,
J. Electron Spectrosc. Relat. Phenom., 1976, 8, 161. [all data]
Debies and Rabalais, 1974
Debies, T.P.; Rabalais, J.W.,
Electronic structure of amino acids and ureas,
J. Electron Spectrosc. Relat. Phenom., 1974, 3, 315. [all data]
Slifkin and Allison, 1967
Slifkin, M.A.; Allison, A.C.,
Measurement of ionization potentials from contact charge transfer spectra,
Nature, 1967, 215, 949. [all data]
Jones, Bernier, et al., 2007
Jones, C.M.; Bernier, M.; Carson, E.; Colyer, K.E.; Metz, R.; Pawlow, A.; Wischow, E.D.; Webb, I.; Andriole, E.J.; Poutsma, J.C.,
Gas-phase Acities of the 20 Protein Amino Acids,
Int. J. Mass Spectrom., 2007, 267, 1-3, 54-62, https://doi.org/10.1016/j.ijms.2007.02.018
. [all data]
Locke and McIver, 1983
Locke, M.J.; McIver, R.T., Jr.,
Effect of Solvation on the Acid/Base Properties of Glycine,
J. Am. Chem. Soc., 1983, 105, 4226. [all data]
Gapeev and Dunbar, 2003
Gapeev, A.; Dunbar, R.C.,
Na+ Affinities of Gas-Phase Amino Acids by Ligand Exchange Equilibrium,
Int. J. Mass Spectrom., 2003, 228, 2-3, 825, https://doi.org/10.1016/S1387-3806(03)00242-2
. [all data]
Kish, Ohanessian, et al., 2003
Kish, M.M.; Ohanessian, G.; Wesdemiotis, C.,
The Na+ affinities of a-amino acids: side-chain substituent effects,
Int. J. Mass Spectrom., 2003, 227, 3, 509, https://doi.org/10.1016/S1387-3806(03)00082-4
. [all data]
Abu-Eittah, et al., 1988
Abu-Eittah, R., et al.,
Bull. Chem. Soc. Japan., 1988, 61, 2609. [all data]
Notes
Go To: Top, Gas phase ion energetics data, Ion clustering data, Mass spectrum (electron ionization), UV/Visible spectrum, References
- Symbols used in this document:
IE (evaluated) Recommended ionization energy ΔrG° Free energy of reaction at standard conditions ΔrH° Enthalpy of reaction at standard conditions - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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