As models of naturally occurring glycolipids, structurally well-determined amphiphilic compounds were prepared. The synthetic molecules have beta-D-galactopyranosyl or alpha-D-mannopyranosyl and two dodecyl groups as terminal hydrophilic sugar and hydrophobic hydrocarbon moieties, respectively. The two long alkyl chains are connected by 3,5-dioxybenzamide through ether linkages to give a lipid analog purified easily due to its absorbance of ultraviolet light. In the synthetic glycolipids, the glycoside and lipid parts are covalently bound via an oligomethylene spacer. The glycolipids could be easily incorporated into liposomes of L-alpha-phosphatidylcholine. The monoglycosyl moiety of the synthetic glycolipids possessing a hexamethylene spacer was present on the surface of the liposomes and interacted specifically with a lectin to give liposomal assemblies. Such agglutination of these liposomes induced by lectins was determined by analyses of turbidity and particle size based on dynamic light scattering and laser diffraction methods. The other liposomes possessing a shorter ethylene or longer decamethylene linker gave few lectin-induced agglutinates, indicating that these spacers were not effective for the presentation of the galacto-terminal on the liposomal surfaces. Similar spacer-dependent recognition of ricin with a galactolipid-incorporated phospholipid monolayer was confirmed by surface plasmon resonance technique on a substrate.