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534-73-6

534-73-6 structural image
Product Name: 6-O-ALPHA-D-GLUCOPYRANOSYL-D-GLUCITOL
Formula: C12H24O11
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CHEMICAL AND PHYSICAL PROPERTIES

Physical Description Odourless, white, slightly hygroscopic, crystalline mass.
Taste Pure sweet taste (sweetening power =0.45 relative to sucrose in about a 10% solution)
Solubility Soluble in water, very slightly soluble in ethanol.
Stability/Shelf Life Isomalt has very good thermal and chemical stability. When it is melted, no changes in the molecular structure are observed.
Optical Rotation Specific rotation: +89.8 deg to +92.2 deg
Decomposition /Isomalt/ exhibits considerable resistance to acids and microbial influences. ... Isomalt does not undrego browning reactions; it has no reducing groups, and therefore it does not react with other ingredients in a formulation.
Viscosity In the melt, has a lower viscosity, higher specific heat capacity, and higher boiling-point elevation than sucrose
Other Experimental Properties Water content <7% ... has a lower viscosity, higher specific heat capacity, and higher boiling-point elevation than sucrose ... The components are hydrolyzed to give 1 mol each of glucose and sorbitol or mannitol

COMPUTED DESCRIPTORS

Molecular Weight 344.31 g/mol
XLogP3 -5.2
Hydrogen Bond Donor Count 9
Hydrogen Bond Acceptor Count 11
Rotatable Bond Count 8
Exact Mass 344.13186158 g/mol
Monoisotopic Mass 344.13186158 g/mol
Topological Polar Surface Area 201 Ų
Heavy Atom Count 23
Formal Charge 0
Complexity 343
Isotope Atom Count 0
Defined Atom Stereocenter Count 9
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
Covalently-Bonded Unit Count 1
Compound Is Canonicalized Yes

PRODUCT INTRODUCTION

description

6-O-alpha-D-glucopyranosyl-D-glucitol is a glycosyl alditol consisting of alpha-D-glucopyranose and D-glucitol residues joined in sequence by a (1->6)-glycosidic bond. It is an O-acyl carbohydrate and a glycosyl alditol. It is functionally related to a beta-D-glucose and a D-glucitol.