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Title: Alternative Sweeteners

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318 Le and Mulderrig<br />

out and the solution is purified. It is then evaporated to 70% solids and sold as<br />

sorbitol solution (1).<br />

Crystalline sorbitol is made by further evaporating the sorbitol solution into<br />

molten syrup containing at least 99% solids. The molten syrup is crystallized<br />

into a stable crystalline polymorph that has one single melting point (99–101°C)<br />

and heat of fusion (42 cal/g, assuming 44 cal/g represents a fully crystallized<br />

crystalline sorbitol). The stable polymorph of sorbitol is known as gamma (γ)<br />

sorbitol and was determined from the work of Atlas Powder Company and University<br />

of Pittsburgh researchers in the early 1960s. Most commercially available<br />

crystalline sorbitol is the gamma polymorph (2, 3).<br />

When hydrogenated invert sugar is the raw material, both sorbitol and mannitol<br />

are produced in the solution because they are isomers. The mannitol and<br />

sorbitol are separated on the basis of their different solubilities. Mannitol is crystallized<br />

from the solution because of its lower solubility than sorbitol in water.<br />

The resulting product is the most stable polymorph, the β-polymorph (4). Mannitol<br />

is then filtered, dried, and sold as white powder or free-flowing granules (directly<br />

compressible material).<br />

III. PHYSICAL AND CHEMICAL PROPERTIES OF<br />

SORBITOL AND MANNITOL<br />

Sorbitol and mannitol are six-carbon, straight-chain polyhydric alcohols, meaning<br />

they have more than one hydroxyl group. Both sorbitol and mannitol have six<br />

hydroxyl groups and the same molecular formula, C 6H 14O 6. They are isomers of<br />

one another and have different molecular configurations. The difference between<br />

sorbitol and mannitol occurs in the planar orientation of the hydroxyl group on<br />

the second carbon atom (Figs. 1 and 2). This dissimilarity has a powerful influence<br />

and results in an individual set of properties for each isomer.<br />

Figure 1 The chemical structures of sorbitol and mannitol.

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