Callicarpenal

Callicarpenal

Names
IUPAC name [(1S,2R,4aR,8aR)-1,2,4a,5-Tetramethyl-1,2,3,4,4a,7,8,8a-octahydro-1-naphthalenyl]acetaldehyde
Other names (−)-Callicarpenal; 13,14,15,16-Tetranor-3-cleroden-12-al
Identifiers
CAS Number	161105-12-0
ChemSpider	9282422
Jmol interactive 3D	Image
PubChem	11107286
InChI InChI=1S/C16H26O/c1-12-6-5-7-14-15(12,3)9-8-13(2)16(14,4)10-11-17/h6,11,13-14H,5,7-10H2,1-4H3/t13-,14+,15+,16+/m1/s1 Key: MPWIIQYWQOBNKS-UGUYLWEFSA-N InChI=1/C16H26O/c1-12-6-5-7-14-15(12,3)9-8-13(2)16(14,4)10-11-17/h6,11,13-14H,5,7-10H2,1-4H3/t13-,14+,15+,16+/m1/s1 Key: MPWIIQYWQOBNKS-UGUYLWEFBV
SMILES O=CC[C@@]2([C@@H]1[C@](/C(=C\CC1)C)(CC[C@H]2C)C)C
Properties
Chemical formula	C16H26O
Molar mass	234.38 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

Callicarpenal is a terpenoid that has been isolated from plants of the genus Callicarpa (beautyberry).^[1] It acts as an insect repellent against mosquitoes (Aedes aegypti and Anopheles stephensi) and fire ants.^[1][2] It also has activity against ticks (Ixodes scapularis and Amblyomma americanum).^[3]

In comparison to the most commonly used insect repellent, DEET, callicarpenal is less effective against mosquitoes.^[4]

Callicapenal was discovered by scientists at the United States Department of Agriculture's Agricultural Research Service who were inspired by reports that Callicarpa americana (American beautyberry) was used as a folk remedy to prevent mosquito bites.^[5]

References

1. Cantrell, C. L.; Klun, J. A.; Bryson, C. T.; Kobaisy, M.; Duke, S. O. (2005). "Isolation and Identification of Mosquito Bite Deterrent Terpenoids from Leaves of American (Callicarpa americana) and Japanese (Callicarpa japonica) Beautyberry". Journal of Agricultural and Food Chemistry 53 (15): 5948–53. doi:10.1021/jf0509308. PMID 16028979.
2. Chen, J; Cantrell, CL; Duke, SO; Allen, ML (2008). "Repellency of callicarpenal and intermedeol against workers of imported fire ants (Hymenoptera: Formicidae)". Journal of economic entomology 101 (2): 265–71. doi:10.1603/0022-0493(2008)101[265:ROCAIA]2.0.CO;2. PMID 18459387.
3. Carroll, JF; Cantrell, CL; Klun, JA; Kramer, M (2007). "Repellency of two terpenoid compounds isolated from Callicarpa americana (Lamiaceae) against Ixodes scapularis and Amblyomma americanum ticks". Experimental & applied acarology 41 (3): 215–24. doi:10.1007/s10493-007-9057-2. PMID 17380408.
4. Ling, Taotao; Xu, Jing; Smith, Ryan; Ali, Abbas; Cantrell, Charles L.; Theodorakis, Emmanuel A. (2011). "Synthesis of (−)-callicarpenal, a potent arthropod repellent". Tetrahedron 67 (17): 3023–3029. doi:10.1016/j.tet.2011.02.078. PMC 3105892. PMID 21643472.
5. Luis Pons (February 2006). "Folk Remedy Yields Mosquito-Thwarting Compound". Agricultural Research Magazine (U.S. Department of Agriculture) 54 (2).

External links

• "Scientists Confirm Folk Remedy Repels Mosquitoes". ScienceDaily. July 3, 2006.