Dolphin
Structural formula | |||||||||||||||||||
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General | |||||||||||||||||||
Surname | Dolphin | ||||||||||||||||||
other names |
Staphysagrin |
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Molecular formula | C 33 H 45 NO 9 | ||||||||||||||||||
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properties | |||||||||||||||||||
Molar mass | 599.70 g mol −1 | ||||||||||||||||||
Physical state |
firmly |
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Melting point |
198-200 ° C |
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solubility | |||||||||||||||||||
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 . |
Delphinine is a poisonous alkaloid that is particularly known as an ingredient in delphinium . The specific rotation [α] D is + 25 ° (ethanol).
Occurrence
Delphinin is found in larkspurs such as Delphinium consolida L. Field Larkspur , Delphinium staphisagria L. St. Stephen's Herb, and Delphinium elatum L. High Larkspur .
effect
It is similar to aconitine and produces flaccid paralysis of the heart muscles , but has no effect on the eye. According to Serck, the influence on the vessels is much stronger than that of aconitine and is based on an effect on the spinal cord or the peripheral vascular nerves , but is independent of the vasomotor center . Delphinin can cause severe inflammation on the skin.
Individual evidence
- ↑ a b c d Entry on Delphinin. In: Römpp Online . Georg Thieme Verlag, accessed on September 23, 2014.
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
- ↑ Lutz Roth, Max Daunderer , Kurt Kormann: Poison plants plant poisons. Occurrence, effect, therapy. Allergic and phototoxic reactions. 4th, revised and significantly expanded edition. ecomed, Landsberg / Lech 1994, ISBN 3-609-64810-4 .