The coagel and gel phases formed by the D and L diastereoisomers of ascorbyl-dodecanoate (ASC12) in deuterated water were studied through solid-state NMR techniques In particular the dynamic properties of water and surfactant chains were investigated by H-2 and C-13 NMR static spectra, respectively Two fractions of water with very different dynamics were found in the coagel phases, one solidlike and one liquidlike, assigned to water strongly bound to the surfactant polar heads and bulk water, respectively Only one kind of "intermediate' water was instead detected in the gel phase suggesting that the merging of the two types of water in the interlayers between the surfactant lamellae occurs at the coagel-to-gel transition Moreover, the surfactant chains, very rigid in the coagel phase give rise to fast trans-gauche interconformational jumps in the gel phase where almost isotropic reorientations of the whole aggregates also occur A different dynamic behavior was found for the two diastereoisomers in particular for what concerns the surfactant molecules in the gel phase and the water molecules in the coagel presumably ascribable to different inter-and intramolecular interactions that involve the polar heads