Reinvestigation of the crystal structure of β‐alanine
- 1 November 1986
- journal article
- Published by Wiley in International Journal of Peptide and Protein Research
- Vol. 28 (5) , 525-528
- https://doi.org/10.1111/j.1399-3011.1986.tb03287.x
Abstract
A reinvestigation of the crystal structure of β‐alanine was carried out. The structure is orthorhombic, space group Pbca, with eight molecules per unit cell. Cell parameters were a = 9.882 (2), b = 13.807 (2), and c = 6.086 (2) Å. Three‐dimensional intensity data collected in a CAD‐4 diffractometer using Cu K α radiation was used in the least‐squares refinement leading to a final R value of 0.038. The average standard deviations in bond lengths and angles were 0.002 Å and 0.2°, respectively. The corresponding values in the earlier work of José & Pant (1965) were 0.01 Å and 0.6°, respectively. The positions of all the hydrogen atoms were located in the present study. The amino nitrogen forms three hydrogen bonds of nearly equal bond lengths and angles, with the oxygen atoms. The β‐alanine molecules exist in the crystal as zwitterions.Keywords
This publication has 2 references indexed in Scilit:
- Precision neutron diffraction structure determination of protein and nucleic acid components. I. Crystal and molecular structure of the amino acid L-alanineJournal of the American Chemical Society, 1972
- The crystal and molecular structure of β-alanineActa Crystallographica, 1965