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Lotaustralin structure.svg
Lotaustralin 3D sticks.png
IUPAC name
534-67-8 YesY
ChemSpider 390193 N
Jmol-3D images Image
PubChem 441467
Molar mass 261.27 g·mol−1
Appearance colorless needles
Density 1.36 g·cm−3
Melting point 139 °C (282 °F; 412 K)[1]
good, also good in Ethyl acetate [1]
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
 N verify (what isYesY/N?)
Infobox references

Lotaustralin is a cyanogenic glucoside found in small amounts in Fabaceae Austral Trefoil (Lotus australis),[1] cassava (Manihot esculenta), lima bean (Phaseolus lunatus),[2] roseroot (Rhodiola rosea)[3] and white clover (Trifolium repens),[4] among other plants. Lotaustralin is the glucoside of methyl ethyl ketone cyanohydrin and is structurally related to linamarin, the acetone cyanohydrin glucoside also found in these plants. Both lotaustralin and linamarin may be hydrolyzed by the enzyme linamarase to form glucose and a precursor to the toxic compound hydrogen cyanide.


  1. ^ a b c Shmuel Yannai: Dictionary of Food Compounds with CD-ROM: Additives, Flavors, and Ingredients. CRC Press, 2003, ISBN 978-1-58488-416-3, p. 688
  2. ^ Frehner M, Scalet M, Conn EE (1990). "Pattern of the Cyanide-Potential in Developing Fruits : Implications for Plants Accumulating Cyanogenic Monoglucosides (Phaseolus lunatus) or Cyanogenic Diglucosides in Their Seeds (Linum usitatissimum, Prunus amygdalus)". Plant Physiol 94 (1): 28–34. doi:10.1104/pp.94.1.28. PMC 1077184. PMID 16667698. 
  3. ^ Akgul Y, Ferreira D, Abourashed E, Khan I (2004). "Lotaustralin from Rhodiola rosea roots". Fitoterapia 75 (6): 612–4. doi:10.1016/j.fitote.2004.06.002. PMID 15351122. 
  4. ^ "Notes on poisoning: Trifolium repens". Canadian Poisonous Plants Information System. May 30, 2006. Retrieved 2007-02-11.