Quassin
From Wikipedia, the free encyclopedia
Quassin | |
---|---|
IUPAC name | (3aS,6aR,7aS,8S,11aS,11bS,11cS)1,3a,4,5,6a,7,7a,8,11,11a,11b,11c-dodecahydro-
2,10dimethoxy-3,8,11a,11c-tetramethyldibenzo[de,g]chromene1,5,11-trione |
EINECS number | |
Identifiers | |
CAS number | [76-78-8] |
PubChem | |
SMILES | CC1C=C(C(=O)C2(C1CC3C4(C2C(=O)C(=C(C4CC(=O)O3)C)OC)C)C)OC |
InChI key | IOSXSVZRTUWBHC-LBTVDEKVBB |
Properties | |
Molecular formula | C22H28O6 |
Molar mass | 388.454 g/mol |
Appearance | White crystalline substance |
Melting point |
200-222°C |
Boiling point |
586°C |
Solubility in water | Insoluble |
Vapor pressure | 13 mmHg (@ 25°C) |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
Quassin is a white bitter, crystalline substance extracted from the quassia tree. It is the bitterest substance found in nature with a bitter threshold of 0.08ppm and it is 50 times more bitter than quinine.[1]
Quassin is used as a medicine in traditional Chinese medicine.
Extracts of the Bitter tree (or bitter wood) (Quassia amara L. or Picrasma excelsa) are also used as additives in soft drinks.[1]
Although its skeleton possesses 20 carbon atoms Quassin is not a diterpene but a triterpene lactone, which derives from euphol by loss of 10 carbon atoms including C4.
[edit] References
- ^ a b Scientific Committee on Food Opinion of the Scientific Committee on Food on quassin (expressed on 2 July 2002). SCF/CS/FLAV/FLAVOUR/29 Final