“…Of course, attractive nonionic glycosurfactants could be widely used in cosmetics, pesticide delivery, household and industrial applications, degumming agents, and adhesives and nanoreactors owing to their remarkable surface activity and extraordinary environmental comparative advantage. Importantly, in terms of their amphiphilic structure, renewable origin, and multifunctional features, owing mostly to the corresponding autoadapted microphase separation, self-organization, and self-assembly based on the repulsive interaction between the polar portion and nonpolar portion each other in a specific temperature range, a lot of glycosurfactants would preferentially exhibit intriguing thermotropic or lyotropic liquid crystal structures, − namely Maltese crosses, smetic (SmA, SmA*, SmA 1 *, SmA 2 *, SmA c *, SmA d *, SmX), columnar (fan texture), reversed micellar (L 2 ), hexagonal (H 1 ), reversed hexagonal (H 2 ), , cubic (I 1 , V 1 ), reversed cubic (I 2 , V 2 ), inverse bicontinuous cubic (V II , i.e., V II G (Ia3d), V II D (Pn3m), and V II (Im3m)), , lamellar (L α ), − sponge (L 3 ), ,, micellar (L 1 ), and Gel (L β ) . All investigation involving phase formation, stability, and transformation could be useful to formulate specific self-assembly materials for practical applications.…”