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Title: Alternative Sweeteners

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284 Kato and Moskowitz<br />

cation and concentration, is hydrogenated by means of a nickel or other transition<br />

metal catalyst. After additional purification steps to remove the starting materials<br />

and catalyst, the solution is concentrated to syrup, then crystallized (3). Maltitol<br />

may also contain trace or quite low levels of sorbitol, maltotriitol, and higher<br />

hydrogenated oligosaccharides. Currently, there are two kinds of crystalline maltitol<br />

powders on the market with minimum maltitol contents of 92.5% and 98%<br />

that are produced and marketed worldwide.<br />

III. PHYSICAL CHARACTERISTICS<br />

The structure of maltitol (alpha(1-4)-glucosylsorbibtol) has been confirmed by<br />

nuclear magnetic resonance and infrared absorption studies as a crystalline polyhydric<br />

alcohol obtained by the catalytic hydrogenation of maltose, a disaccharide<br />

consisting of two glucose units linked by means of an alpha(1-4) bond (Fig. 1).<br />

Crystallographic studies have also demonstrated that the molecular structure is<br />

a fully extended conformation with no intramolecular hydrogen bonding; all nine<br />

hydroxyl groups are involved in intermolecular hydrogen bonds and in bifurcated,<br />

finite chains (3).<br />

Maltitol exhibits a negligible cooling effect in the mouth given its negative<br />

heat of solution (23 kJ/kg), which is close to that of sucrose (18 kJ/kg),<br />

and much less than that of other carbohydrates: xylitol (153 kJ/kg), mannitol<br />

(121 kJ/kg), sorbitol (111 kJ/kg), isomalt (39 kJ/kg), and dextrose<br />

(104.6 kJ/kg).<br />

Figure 1 (a) Chemical structure for maltose. (b) Chemical structure for maltitol.

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