It was found that methyl-4,6-O-p-nitrobenzylidene-alpha -D-galactopyranosid
e (1) and methyl-4,6-O-benzylidene-alpha -D-mannopyranoside (2), which are
scarcely soluble in apolar solvents, act as "supergelators" when they are e
nforcedly dissolved above their bp's in a sealed tube. The minimum gelator
concentrations (C-min) were 0.03-0.07% [g mL(-1)] which are one of the lowe
st concentrations achieved so far. The coupled study of TEM observation wit
h partial solvent exchange established that the organogel stability is rela
ted to the superstructure in the fibril network constructed in specific sol
vents.