1058600-85-3Relevant articles and documents
Endocyclic double bond isomers and by-products from rebaudioside A and stevioside formed under acid conditions
Perera, Wilmer H.,Docampo, Maite L.,Wiggers, Frank T.,Hufford, Charles D.,Fronczek, Frank R.,Avula, Bharathi,Khan, Ikhlas A.,McChesney, James D.
, p. 163 - 170 (2018/04/20)
The hydrolysis reaction of rebaudioside A and stevioside was studied under mild and strong acidic conditions at different temperatures and times. Exposure of rebaudioside A to vigorous acid conditions yielded three different aglycone cores which were puri
STEVIOL GLYCOSIDE ISOMERS
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Page/Page column 21-26, (2009/04/25)
Steviol glycoside isomers are provided having the formula (II): wherein R1 may be hydrogen, 1-β-D-glucopyranosyl, or 2-(1-β-D-glucopyranosyl)-1-β-D- glucopyranosyl, and R2 may be hydrogen, 1-β-D-glucopyranosyl, 2-(1-β-D-glucopyranosyl)- 1-β-D-glucopyranosyl, 2,3 -bis(1-β-D-glucopyranosyl)-1-β-D-glucopyranosyl, 2-(1-α-L- rhamnopyranosyl)-1-β-D-glucopyranosyl, 2-(1-α-L-rhamnopyranosyl)-3 -(1-β-D- glucopyranosyl)-1-β-D-glucopyranosyl, or 2-(1-β-D-xylopyranosyl)-3 -(1-β-D- glucopyranosyl)-1-β-D-glucopyranosyl. Methods for making steviol glycoside isomers are also disclosed. These compounds may be present in food and beverage products as non- nutritive sweeteners.
