Dillapiol
Structural formula | |||||||||||||||||||
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General | |||||||||||||||||||
Surname | Dillapiol | ||||||||||||||||||
other names |
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Molecular formula | C 12 H 14 O 4 | ||||||||||||||||||
Brief description |
yellow-green color |
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External identifiers / databases | |||||||||||||||||||
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properties | |||||||||||||||||||
Molar mass | 222.24 g · mol -1 | ||||||||||||||||||
Physical state |
firmly |
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density |
1.16 g cm −3 |
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Melting point |
29.5 ° C |
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boiling point |
285 ° C |
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safety instructions | |||||||||||||||||||
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Toxicological data | |||||||||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Dillapiol is a natural product from the group of phenylpropanoids .
Occurrence
It is found in essential oils and the like. a. in fennel and dill and is an isomer of apiol . It is obtained by isolating it from the Brazilian medicinal plant Heckeria umbellata ( Piperaceae ).
Individual evidence
- ↑ a b c d Dillapiole data sheet at Sigma-Aldrich , accessed on October 16, 2016 ( PDF ).
- ↑ a b c Entry on dillapiol in the ChemIDplus database of the United States National Library of Medicine (NLM) .
- ↑ Entry on Dill-Apiol. In: Römpp Online . Georg Thieme Verlag, accessed on March 13, 2013.
literature
- Shulgin, Alexander (1967): Psychotropic Phenylisopropylamines derived from Apiole and Dillapiole. In: Nature . Vol. 215, pp. 1494-1495. PMID 4861200 HTML