Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Malic Acid | HCID 525 | — |
| Reactant | Sorbitol | HCID 5780 | — |
| Reactant | Neohesperidin dihydrochalcone | HCID 30231 | — |
| Reactant | HCID 178508931 | HCID 178508931 | — |
| Reactant | HCID 178526002 | HCID 178526002 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178518214 | HCID 178518214 | — |
Reaction Steps
Neohesperidin dihydrochalcone (10 g) and sorbitol (50 g) were mixed together and were heated to 140° C. to 170° C. (water or alcohol in appropriate quantities may be used to assist dissolution of the starting material). The liquified mixture was cooled to about 60° C. to 70° C., and the pH of the solution was adjusted to 5.5 to 6.0 by the addition of citric acid or malic acid. Then a mixture of disodium 5'--inosinate and disodium 5'--guanylate (0.016 g), which is commercially obtained as ribotide, was added and the entire mixture was dried by conventional methods. The dried mixture was ground into a fine powder. The resulting composition had excellent solubility in aqueous solution and gave an immediate sweet taste with no methanol-like aftertaste. This composition may be used to sweeten beverages and other food products.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04254155 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-ce44b1806a0949bbbe4a6081be05a341 |
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| Source note | uspto-grants-1981_03 |
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