| Weight | 331.438 g/mol |
|---|---|
| Formula | C14H25N3O4S |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 6 |
Alitame (80863-62-3)
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LabBot
- Alitame stability in chewing gum by encapsulation (1989)
- Evolution of the Sweetness Receptor in Primates. I. Why Does Alitame Taste Sweet in all Prosimians and Simians, and Aspartame only in Old World Simians? (Chemical Senses, 1995)
- Stability and degradation of the highintensity sweeteners: Aspartame, Alitame, and Sucralose (Food Reviews International, 1999)
- Conformational analysis of the dipeptide sweetener alitame and two stereoisomers by proton NMR, computer simulations, and X-ray crystallography (Journal of the American Chemical Society, 1991)
- Sweetening cakes and cake mixes with alitame (Cereal Foods World, 1989)
- Storage stable chewing gum containing alitame (1990)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C(=O)NC1C(SC1(C)C)(C)C)NC(=O)C(CC(=O)O)N
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- Pubchem - Alitame
- Wikipedia - alitame anhydrous
Alitame is an aspartic acid-containing dipeptide sweetener. It was developed by Pfizer in the early 1980s and currently marketed in some countries under the brand name Aclame. Most dipeptides are not sweet, but the unexpected discovery of aspartame in 1965 led to a search for similar compounds that shared its sweetness.
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