Histidine

• Formula: C₆H₉N₃O₂
• Molecular weight: 155.1546
• IUPAC Standard InChI: InChI=1S/C6H9N3O2/c7-5(6(10)11)1-4-2-8-3-9-4/h2-3,5H,1,7H2,(H,8,9)(H,10,11)/t5-/m1/s1 Copy

  
• IUPAC Standard InChIKey: HNDVDQJCIGZPNO-RXMQYKEDSA-N Copy
• CAS Registry Number: 71-00-1
• Chemical structure:
  This structure is also available as a 2d Mol file
• Other names: L-Histidine; Histidine, L-; Glyoxaline-5-alanine; L-(-)-Histidine; 1H-Imidazole-4-propanoic acid, α-amino-, (S)-; 4-(2-Amino-2-carboxyethyl)imidazole; Anti-rheuma
• Permanent link for this species. Use this link for bookmarking this species for future reference.
• Information on this page:
  • Condensed phase thermochemistry data
  • Phase change data
  • Ion clustering data
  • References
  • Notes
• Other data available:
  • Reaction thermochemistry data
  • Gas phase ion energetics data
  • IR Spectrum
  • Mass spectrum (electron ionization)
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Condensed phase thermochemistry data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Phase change data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: William E. Acree, Jr., James S. Chickos

Enthalpy of sublimation

Ion clustering data

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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⁺ + C₆H₉N₃O₂ = (Na⁺ • C₆H₉N₃O₂)

References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Vasilev, Borodin, et al., 1989
Vasilev, V.P.; Borodin, V.A.; Kopnyshev, S.B., Standard enthalpies of formation of L-histidine and L-proline, Russ. J. Phys. Chem. (Engl. Transl.), 1989, 63, 891-892. [all data]

Wilson, Watson, et al., 1979
Wilson, S.R.; Watson, I.D.; Malcolm, G.N., Enthalpies of formation of solid cytosine, L-histidine, and uracil, J. Chem. Thermodyn., 1979, 11, 911-912. [all data]

Gaffney, Pierce, et al., 1977
Gaffney, Jeffrey S.; Pierce, Robert C.; Friedman, Lewis, Mass spectrometer study of evaporation of .alpha.-amino acids, J. Am. Chem. Soc., 1977, 99, 13, 4293-4298, https://doi.org/10.1021/ja00455a015 . [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]

Notes

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• Symbols used in this document:
  

  ΔcH°solid	Enthalpy of combustion of solid at standard conditions
  ΔfH°solid	Enthalpy of formation of solid at standard conditions
  ΔrH°	Enthalpy of reaction at standard conditions
  ΔsubH	Enthalpy of sublimation

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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