The leishmanicidal drug, meglumine antimoniate (MA), has been synthesized b
y the reaction of antimony oxyhydrated and N-methyl glucamine. Infrared and
solid state NMR C-13 analysis of MA and the ligand strongly suggests that
antimony binds to N-methyl glucamine through the oxygen of C-3 carbon. Pote
ntiometric titration indicated that, between pH 4.5 and 7.5, MA exists in t
he zwitterionic form.