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Title: Alternative Sweeteners

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Aspartame-Acesulfame: Twinsweet 483<br />

aldehyde attack, and the salt can be used successfully to create products of acceptable<br />

shelf-life.<br />

It will be apparent, however, that the advantages of aspartame-acesulfame<br />

are not confined to its physicochemical properties as a solid. Because it provides<br />

two sweetening components in each molecule of the crystalline material, the salt<br />

represents a saving on the number of raw materials to be purchased, stored, and<br />

handled. In addition, the salt is a more concentrated source of sweetness than<br />

the blend because it is free of potassium and lower in moisture content. As a<br />

result, the sweetener-sweetener salt provides 11% more sweetness on a weightfor-weight<br />

basis than the corresponding equimolar blend, which is a modest but<br />

real advantage to those handling large quantities of low-calorie sweeteners.<br />

Finally, aspartame-acesulfame poses no new toxicological issues. The<br />

sweetener-sweetener salt dissociates immediately on solution in water. In doing<br />

so it releases the same sweetener molecules that would be present were a mere<br />

mixture of aspartame and acesulfame-K to have been used. Consequently, the<br />

consumer is exposed only to known, permitted sweeteners.<br />

For all the above reasons, aspartame-acesulfame was the sweetenersweetener<br />

salt preferred for commercial development, and these and other attributes<br />

of Twinsweet are discussed further below.<br />

II. PRODUCTION<br />

In the patented process (2), aspartame-acesulfame is made by combining aspartame<br />

and acesulfame-K in an aqueous acid solution. The trans-salification reaction<br />

is depicted in Fig. 1. The sweetener-sweetener salt is subsequently crystallized,<br />

separated, washed, and dried.<br />

All the components used are commercially available and of food grade. No<br />

unusual forms of the sweeteners and no organic solvents are used. No additional<br />

purification of the salt is necessary. This is because, as is apparent from Figure<br />

1, the preparation of the salt is, in effect, also a recrystallization of the starting<br />

materials. As might be expected of such a process, the resultant aspartameacesulfame<br />

has a higher degree of purity than even the food-grade raw materials.<br />

Moreover, the process introduces no new impurities, and so neatly combines<br />

synthesis with purification.<br />

III. PHYSICAL AND OTHER DATA<br />

Table 1 lists the main characteristics of aspartame-acesulfame.

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