Lactaroviolin
Structural formula | |||||||||||||
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General | |||||||||||||
Surname | Lactaroviolin | ||||||||||||
other names |
7-isopropenyl-4-methyl-1-azulene carbaldehyde ( IUPAC ) |
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Molecular formula | C 15 H 14 O | ||||||||||||
Brief description |
purple crystals |
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properties | |||||||||||||
Molar mass | 210.28 g mol −1 | ||||||||||||
Physical state |
firmly |
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Melting point |
58 ° 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 . |
Lactaroviolin is a chemical compound - more precisely a sesquiterpene - and contains the functional group of an aldehyde . The natural substance was first isolated by Willstaedt in the 1930s and is one of the Reizker dyes .
Occurrence
Lactaroviolin is a derivative of the orange-red dye (7-isopropenyl-4-methyl-6,7-dihydroazulen-1-yl) methyl stearate contained in the milk sap of the noble irritant ( Lactarius delicious ).
Individual evidence
- ↑ a b c Entry on lactaroviolin. In: Römpp Online . Georg Thieme Verlag, accessed on May 16, 2015.
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
- ↑ E. Heilbronner, RW Schmid: On the knowledge of the sesquiterpenes and azulenes. Communication 113. Azulene aldehydes and azulene ketones: The structure of lactaroviolin . In: Helvetica Chimica Acta . tape 37 , no. 7 , 1954, pp. 2018 , doi : 10.1002 / hlca.19540370715 ( PDF ).
- ↑ Albert Gossauer: Structure and reactivity of biomolecules . Helvetica Chimica Acta, Zurich 2006, ISBN 978-3-906390-29-1 , p. 167.