z-logo
open-access-imgOpen Access
Calorimetric Investigation ofN-Acyl Amino Acids
Author(s) -
Shigeyoshi Miyagishi,
Seiichi Matsumura,
Kazuhiko Murata,
Tsuyoshi Asakawa,
Morie Nishida
Publication year - 1985
Publication title -
bulletin of the chemical society of japan
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.145
H-Index - 99
eISSN - 1348-0634
pISSN - 0009-2673
DOI - 10.1246/bcsj.58.1019
Subject(s) - chemistry , amino acid , organic chemistry , biochemistry
The melting characteristics of N-acyl amino acids were examined using a differential scanning calorimeter (DSC). The melting-point temperature of N-dodecanoyl L-amino acid increased with the size of its amino acid residue, while the order was opposite for the DL-amino acids. The racemic derivatives formed racemic compounds in their solid states. Each N-dodecanoyl L-amino acid had a larger enthalpy and entropy-of-fusion than its racemic isomer. Differences in the thermodynamic quantities between the optically active and racemic isomers were larger for N-dodecanoylvaline and -leucine compared with those of N-dodecanoylalanine. A mixture of these molecules were also studied. Each racemic isomer of N-dodecanoylalanine and -leucine partly formed a racemic pair in the liquid state

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom