Melezitose
Title: Melezitose
CAS Registry Number: 597-12-6
CAS Name: O-a-D-Glucopyranosyl-(1®3)-b-D-fructofuranosyl-a-D-glucopyranoside
Molecular Formula: C18H32O16
Molecular Weight: 504.44
Percent Composition: C 42.86%, H 6.39%, O 50.75%
Literature References: Trisaccharide built from 2 mols glucose and 1 mol fructose. Acid hydrolysis yields at first glucose and turanose. Occurs in a manna that forms upon the Douglas fir, jack pine (Pinus virginiana Mill., Pinaceae) and other trees. During periods of drought, bees collect it from the manna in sufficient quantity to change the character of the honey, making it unsuitable for maintaining the bees, but providing a source of melezitose: Hudson, Sherwood, J. Am. Chem. Soc. 42, 116 (1920). Procedure: Bates, Natl. Bur. Std. Circ. C440, p 472 (1942). Structure: Hehre, Carlson, Arch. Biochem. Biophys. 36, 158 (1952); Hehre, Adv. Carbohydr. Chem. 8, 277 (1953). Review: E. B. Rathbone, Dev. Food Carbohydr. 2, 145-185 (1980).
 
Derivative Type: Dihydrate
Properties: Crystals from water. The water of crystn is given up at 110°. When anhydr, mp 153-154°. [a]D20 +88° (c = 4). Sol in water, very sparingly sol in alc. Not fermented by baker's yeast; does not reduce Fehling's soln.
Melting point: mp 153-154°
Optical Rotation: [a]D20 +88° (c = 4)

Others monographs:
ArecaOxyclozanideSenecioRacecadotril
SyringaldehydeAllopregnane-3β,11β,17α,21-tetrol-20-oneKetorolacSpiroxamine
Potassium Tetraiodomercurate(II)DoxorubicinMethyl BromideMeperidine
AbataceptCreosol5-Methylpyrazole-3-carboxylic AcidMetyrosine
©2016 DrugLead US FDA&EMEA