Tyrosine

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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 as indicated in comments:
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
DH - Eugene S. Domalski and Elizabeth D. Hearing

Quantity Value Units Method Reference Comment
Δfsolid-163.86 ± 0.37kcal/molCcbHuffman, Fox, et al., 1937Author's hf298=-165.54 kcal/mol; ALS
Quantity Value Units Method Reference Comment
Δcsolid-1058.34 ± 0.37kcal/molCcbHuffman, Fox, et al., 1937Author's hf298=-165.54 kcal/mol; ALS
Δcsolid-1071.2kcal/molCcbEmery and Benedict, 1911ALS
Quantity Value Units Method Reference Comment
solid,1 bar51.150cal/mol*KN/ACole, Hutchens, et al., 1963DH
solid,1 bar53.01cal/mol*KN/AHuffman and Ellis, 1937Extrapolation below 90 K. 64.56 J/mol*K.; DH

Constant pressure heat capacity of solid

Cp,solid (cal/mol*K) Temperature (K) Reference Comment
51.730298.15Cole, Hutchens, et al., 1963DH
51.219294.6Huffman and Ellis, 1937T = 87 to 295 K. Value is unsmoothed experimental datum.; DH

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

ΔsubH (kcal/mol) Temperature (K) Method Reference Comment
24. ± 2.462.LEGaffney, Pierce, et al., 1977Based on data from 412. to 512. K.

Reaction 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: John E. Bartmess

Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. A general reaction search form is also available. Future versions of this site may rely on reaction search pages in place of the enumerated reaction displays seen below.

Individual Reactions

L-Tyrosine anion + Hydrogen cation = Tyrosine

By formula: C9H10NO3- + H+ = C9H11NO3

Quantity Value Units Method Reference Comment
Δr340.6 ± 1.8kcal/molG+TSTian, Wang, et al., 2009gas phase; Probes indicate 70% phenoxide, 30% carboxylate (0.5 kcal/mol). dSacid calc at B3LYP, mixture of anions
Δr337.7 ± 2.6kcal/molCIDCJones, Bernier, et al., 2007gas phase
Δr337.6 ± 3.1kcal/molG+TSO'Hair, Bowie, et al., 1992gas phase
Quantity Value Units Method Reference Comment
Δr332.5 ± 1.5kcal/molN/ATian, Wang, et al., 2009gas phase; Probes indicate 70% phenoxide, 30% carboxylate (0.5 kcal/mol). dSacid calc at B3LYP, mixture of anions
Δr329.5 ± 3.0kcal/molCIDCO'Hair, Bowie, et al., 1992gas phase

References

Go To: Top, Condensed phase thermochemistry data, Phase change data, Reaction thermochemistry data, Notes

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

Huffman, Fox, et al., 1937
Huffman, H.M.; Fox, S.W.; Ellis, E.L., Thermal data. VII. The heats of combustion of seven amino acids, J. Am. Chem. Soc., 1937, 59, 2144-21. [all data]

Emery and Benedict, 1911
Emery, A.G.; Benedict, F.G., The heat of combustion of compounds of physiological importance, Am. J. Physiol., 1911, 28, 301-307. [all data]

Cole, Hutchens, et al., 1963
Cole, A.G.; Hutchens, J.O.; Stout, J.W., Heat capacities from 11 to 305°K. and entropies of L-phenylalanine, L-proline, L-tryptophane, and L-tyrosine. Some free energies of formation, J. Phys. Chem., 1963, 67, 1852-1855. [all data]

Huffman and Ellis, 1937
Huffman, H.M.; Ellis, E.L., Thermal data. VIII. The heat capacities, entropies and free energies of some amino acids, J. Am. Chem. Soc., 1937, 59, 2150-2152. [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]

Tian, Wang, et al., 2009
Tian, Z.X.; Wang, X.B.; Wang, L.S.; Kass, S.R., Are Carboxyl Groups the Most Acidic Sites in Amino Acids? Gas-Phase Acidities, Photoelectron Spectra, and Computations on Tyrosine, p-Hydroxybenzoic Acid, and Their Conjugate Bases, J. Am. Chem. Soc., 2009, 131, 3, 1174-1181, https://doi.org/10.1021/ja807982k . [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]

O'Hair, Bowie, et al., 1992
O'Hair, R.J.; Bowie, J.H.; Gronert, S., Gas Phase Acidity of the alpha-Amino Acids, Int. J. Mass Spectrom. Ion Proc., 1992, 117, 23, https://doi.org/10.1016/0168-1176(92)80083-D . [all data]


Notes

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