Methods for purifying steviol glycosides and uses of the same
US-9169285-B2 · Oct 27, 2015 · US
US10626136B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10626136-B2 |
| Application number | US-201615171400-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 2, 2016 |
| Priority date | Dec 19, 2012 |
| Publication date | Apr 21, 2020 |
| Grant date | Apr 21, 2020 |
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Polymorphic and amorphous forms of Rebaudioside X and methods for preparing the same are provided herein. Also provided herein are Rebaudioside X complexes and methods for preparing the same. Sweetener compositions and sweetened compositions comprising Rebaudioside X forms and Rebaudioside X complexes are described, as well as and methods of their preparation. Methods of improving the flavor and/or temporal profile of sweetenable compositions, such as beverages, are also provided herein.
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What Is Claimed Is: 1. A method for preparing amorphous Rebaudioside X comprising: (i) heating a mixture consisting of water and a steviol glycoside mixture comprising Rebaudioside X in an amount greater than about 80% by weight on a dry basis, wherein the Rebaudioside X is in substantially pure crystalline form, to a temperature between about 100° C. to about 130° C.; (ii) cooling the mixture; and (iii) removing the water from the mixture to provide a steviol glycoside mixture comprising Rebaudioside X in an amount greater than about 80% by weight on a dry basis, wherein the Rebaudioside X is in substantially pure amorphous form. 2. The method of claim 1 , wherein the Rebaudioside X in (i) is Form A Rebaudioside X. 3. The method of claim 1 , wherein the mixture is heated to a temperature from about 120° C. to about 125° C. 4. The method of claim 1 , wherein the mixture in (ii) is cooled to room temperature such that crash precipitation does not occur. 5. The method of claim 4 , wherein the mixture is cooled at a rate of about 1° C. per minute. 6. The method of claim 1 , wherein the water is removed by a process selected from the group consisting of decantation, centrifugation, filtration, evaporation, vacuum, spray-drying and a combination thereof. 7. The method of claim 6 , wherein the water is removed by spray-drying. 8. The method of claim 1 , wherein the amorphous Rebaudioside X has a solubility of about 0.3% or greater. 9. The method of claim 1 , wherein the amorphous Rebaudioside X has a solubility of about 1.0% or greater. 10. A method for preparing amorphous Rebaudioside X comprising: (i) heating a mixture consisting of ethanol and a steviol glycoside mixture comprising Rebaudioside X in an amount greater than about 80% by weight on a dry basis, wherein the Rebaudioside X is in substantially pure crystalline form, to a temperature between about 70 ° C. to about 120 ° C.; (ii) cooling the mixture; and (iii) removing the ethanol from the mixture to provide a steviol glycoside mixture comprising Rebaudioside X in an amount greater than about 80% by weight on a dry basis wherein the Rebaudioside X is in substantially pure amorphous form. 11. The method of claim 10 , wherein the Rebaudioside X in (i) is Form A Rebaudioside X. 12. The method of claim 10 , wherein the mixture is heated to a temperature between about 80° C. and about 85° C. 13. The method of claim 10 , wherein the mixture in (ii) is cooled to about room temperature such that crash precipitation does not occur. 14. The method of claim 10 , wherein the ethanol is removed by a process selected from the group consisting of decantation, centrifugation, filtration, evaporation, vacuum, spray-drying and a combination thereof. 15. The method of claim 14 , wherein the ethanol is removed by vacuum. 16. The method of claim 10 , wherein the amorphous Rebaudioside X has a solubility of about 0.3% or greater. 17. The method of claim 10 , wherein the amorphous Rebaudioside X has a solubility of about 1.0% or greater.
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