| Title:  b-Carboxyaspartic Acid CAS Registry Number:  75898-26-9 CAS Name:  2-Amino-1,1,2-ethanetricarboxylic acid Additional Names:  Asa Molecular Formula:  C5H7NO6 Molecular Weight:  177.11 Percent Composition:  C 33.91%, H 3.98%, N 7.91%, O 54.20% Literature References:  Amino acid found in ribosomal proteins of E. coli; homolog of g-carboxyglutamic acid.  Isoln and synthesis of DL-form:  M. R. Christy et al., J. Am. Chem. Soc. 103, 3935 (1981).  Synthesis of DL-form:  E. B. Henson et al., Tetrahedron 37, 2561 (1981); N. E. Dixon, A. M. Sargeson, J. Am. Chem. Soc. 104, 6716 (1982).  Quantitative analysis method:  P. V. Hauschka et al., Anal. Biochem. 108, 57 (1980).  Chemical reactivity:  M. R. Christy, T. H. Koch, J. Am. Chem. Soc. 104, 1771 (1982).  Crystal structure and pKa values of DL-zwitterion:  B. Richey et al., Biochemistry 21, 4819 (1982).  Asymmetric synthesis of D-form:  R. M. Williams et al., J. Am. Chem. Soc. 110, 482 (1988).  Review:  T. H. Koch et al., Methods Enzymol. 107, 563-575 (1984).   Derivative Type:  DL-Form hydrochloride  CAS Registry Number:  81156-58-3 Molecular Formula:  C5H7NO6.HCl Molecular Weight:  213.57 Percent Composition:  C 28.12%, H 3.78%, N 6.56%, O 44.95%, Cl 16.60% Properties:  White crystalline powder.  pK1 0.8 ±0.2, pK2 2.5 ±0.1, pK3 4.7 ±0.1, pK4 10.9 ±0.1. pKa:  pK1 0.8 ±0.2, pK2 2.5 ±0.1, pK3 4.7 ±0.1, pK4 10.9 ±0.1   Derivative Type:  D-Form hydrochloride  CAS Registry Number:  111934-05-5 Molecular Formula:  C5H7NO6.HCl Molecular Weight:  213.57 Percent Composition:  C 28.12%, H 3.78%, N 6.56%, O 44.95%, Cl 16.60% Properties:  White solid, [a]D25 -13.25° (c = 0.8 in H2O, pH 2.56). Optical Rotation:  [a]D25 -13.25° (c = 0.8 in H2O, pH 2.56)     Status:  This monograph has been retired and is no longer subject to revision or update.  |