Quassin

From Wikipedia, the free encyclopedia

Quassin
(+)-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 200-985-9
Identifiers
CAS number [76-78-8]
PubChem 10971
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

  1. ^ 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
Languages