Quinic acid
Structural formula | |||||||||||||||||||
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D - (-) - quinic acid | |||||||||||||||||||
General | |||||||||||||||||||
Surname | D -quinic acid | ||||||||||||||||||
other names |
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Molecular formula | C 7 H 12 O 6 | ||||||||||||||||||
Brief description |
white, crystalline powder with a sour taste |
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properties | |||||||||||||||||||
Molar mass | 192.17 g mol −1 | ||||||||||||||||||
Physical state |
firmly |
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density |
1.64 g cm −3 (20 ° C) |
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Melting point |
165 ° C |
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solubility |
290 g l −1 in water (at 9 ° C) |
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safety instructions | |||||||||||||||||||
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Quinic acid is a hydroxycarboxylic acid . It can be found in many fruits, for example in star anise .
Quinic acid was first isolated from the cinchona bark in 1790 by the pharmacist Friedrich Christian Hofmann in Leer (East Friesland) . Its ester with caffeic acid , in which quinic acid functions as an alcoholic component, is found as chlorogenic acid in coffee .
Quinic acid is an intermediate product of the shikimic acid pathway .
Web links
Wiktionary: Quinic acid - explanations of meanings, word origins, synonyms, translations
Individual evidence
- ↑ a b c d Data sheet D - (-) - Quinic acid from Sigma-Aldrich , accessed on October 22, 2016 ( PDF ).
- ↑ a b Entry on quinic acid. In: Römpp Online . Georg Thieme Verlag, accessed on August 18, 2011.
- ↑ a b Data sheet quinic acid (PDF) from Merck , accessed on January 19, 2011.
- ^ Hofmann: Crell's chemical annal. 1790 , II, p. 314, quoted in S. Baup: About quinic acid and some of its compounds . In: Annalen der Physik und Chemie 1833 , pp. 64–70 ( limited preview in Google book search).