“…2 The latter form, which may represent as much as 90% of the total, has a varied composition, although the phosphate esters are certainly a major component. 3 The bound form may be freed completely by strong acid hydrolysis, and partly by the action of phosphatases and glycosidases. Structural studies on inositol containing phosphatides indicate that the myoinositol is chemically fixed in these substances through glycosidic bonds, phosphate ester links, and possibly esterification with carboxylic acids.4• 6 Brown and Serró6 have recently described a glycoside of myoinositol which they found to occur free in the juice of the sugar beet, and which they isolated in a pure crystalline form.…”