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'''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 0.08 ppm and it is 50 times more bitter than [[quinine]].<ref name=ooscf-2002>Scientific Committee on Food [http://ec.europa.eu/food/fs/sc/scf/out134_en.pdf Opinion of the Scientific Committee on Food on quassin (expressed on 2 July 2002).] SCF/CS/FLAV/FLAVOUR/29 Final </ref>
'''Quassin''' is a white bitter, crystalline substance extracted from the [[quassia]] tree. It is one of the most bitter substances found in nature with a bitter threshold of 0.08 ppm and it is 50 times more bitter than [[quinine]].<ref name=ooscf-2002>Scientific Committee on Food [http://ec.europa.eu/food/fs/sc/scf/out134_en.pdf Opinion of the Scientific Committee on Food on quassin (expressed on 2 July 2002).] SCF/CS/FLAV/FLAVOUR/29 Final </ref>


Quassin is used as a [[medicine]] in [[traditional Chinese medicine]].
Quassin is used as a [[medicine]] in [[traditional Chinese medicine]].

Revision as of 00:28, 4 April 2011

Template:Chembox Identifiers2
Quassin
(+)-Quassin
Names
IUPAC name
2,12-dimethoxypicrasa-2,12-diene-1,11,16-trione
Other names
(3aS,6aR,7aS,8S,11aS,11bS,11cS) -1,3a,4,5,6a,7,7a,8,11,11a,11b,11c-dodecahydro-2,10-dimethoxy-3,8,11a,11c- tetramethyldibenzo[de,g]chromene-1,5,11-trione
Properties
C22H28O6
Molar mass 388.460 g·mol−1
Appearance White crystalline substance
Melting point 200-222 °C
Boiling point 586 °C
Insoluble
Vapor pressure 13 mmHg (@25 °C)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Quassin is a white bitter, crystalline substance extracted from the quassia tree. It is one of the most bitter substances found in nature with a bitter threshold of 0.08 ppm 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 rather a triterpene lactone, which derives from euphol by loss of 10 carbon atoms including C4.

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