Hydroxydanaidal

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Hydroxydanaidal
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Names
IUPAC name
7-Hydroxy-6,7-dihydro-5H-pyrrolizin-1-carboxaldehyde
Identifiers
34199-35-4
Jmol 3D model Interactive image
  • OC1CCN2ccc(C=O)c12
Properties
C8H9NO2
Molar mass 151.17 g·mol−1
Appearance Solid
Melting point 55 °C (131 °F; 328 K) [1]
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Hydroxydanaidal is an insect pheromone synthesized by some species of moth from pyrrolizidine alkaloids found in their diet.

Use by insects

The caterpillars of several kinds of arctiid moth ingest pyrrolizidine alkaloids - substances which plants produce to deter herbivores - and use them as protection against insectivores. The larva converts the alkaloid into an N-oxide for storage; on metamorphosis, the alkaloid is retained and used by the adult. This was discovered after the observation that Utetheisa ornatrix moths caught in spider-webs were cut loose by the spider.

Many insects that carry pyrrolizidine alkaloids are brightly-colored to signal their toxicity.

Male tiger moths convert the alkaloid through various intermediate stages[2] into the pheromone hydroxydanaidal;[3] female moth prefer males with more pheromone, since the alkaloid will be transferred by the male into her eggs and will protect them from predation.

References

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