Chrysanthemic acid

Chrysanthemic acid
IUPAC name
2,2-Dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylic acid
4638-92-0 (1R,3R) or (+)-trans
3D model (Jmol) Interactive image
ChEMBL ChEMBL1437285
ChemSpider 15876 (+)-trans
19543 (−)-cis
ECHA InfoCard 100.022.788
PubChem 16747 (1R,3R) or (+)-trans
33607 (1S,3S) or (−)-trans
33606 (1R,3S) or (+)-cis
20755 (1S,3R) or (−)-cis
Molar mass 168.24 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Chrysanthemic acid is an organic compound that is related to a variety of natural and synthetic insecticides. It is related to the pyrethrin I and II, as well as the pyrethroids. One of the four stereoisomers, (1R,3R)- or (+)-trans-chrysanthemic acid (pictured), is the acid part of the ester pyrethrin I, which occurs naturally in the seed cases of Chrysanthemum cinerariaefolium. Many synthetic pyrethroids, for example the allethrins, are esters of all four stereoisomers.


Chrysanthemic acid is derived from its pyrophosphate ester, which in turn is produced naturally from two molecules of dimethylallyl diphosphate.[1]

Industrial synthesis

Chrysanthemic acid is produced industrially in a cyclopropanation reaction of a diene as a mixture of cis- and trans isomers, followed by hydrolysis of the ester:[2]

Many pyrethroids are accessible by re-esterification of chrysanthemic acid ethylester.


  1. Shattuck-Eidens DM, Wrobel WM, Peiser GD, Poulter CD (2001). "Chrysanthemyl diphosphate synthase: isolation of the gene and characterization of the recombinant non-head-to-tail monoterpene synthase from Chrysanthemum cinerariaefolium". Proc. Natl. Acad. Sci. U.S.A. 98 (8): 43738. doi:10.1073/pnas.071543598. PMC 31842Freely accessible. PMID 11287653.
  2. Kelly Lawrence F (1987). "A synthesis of chrysanthemic ester: An undergraduate experiment". J. Chem. Educ. 64 (12): 1061. doi:10.1021/ed064p1061.

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