Bisabolene

Bisabolenes

α-Bisabolene

β-Bisabolene

β-Bisabolene

γ-Bisabolene
Names
IUPAC names
(α): (E)-1-Methyl-4-(6-methylhepta-2,5-dien-2-yl)cyclohex-1-ene
(β): (S)-1-Methyl-4-(6-methylhepta-1,5-dien-2-yl)cyclohex-1-ene
(γ): (Z)-1-Methyl-4-(6-methylhept-5-en-2-ylidene)cyclohex-1-ene
Identifiers
17627-44-0 (α) 
495-61-4 (β) 
495-62-5 (γ) 
ChemSpider 4509521 (α)
8279897 (β)
2298446 (γ)
Jmol-3D images Image

(α)
Image (β)
Image (γ)

Properties
Molecular formula
C15H24
Molar mass 204.35 g·mol−1
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

Bisabolenes are a group of closely related natural chemical compounds which are classified as sesquiterpenes. Bisabolenes are present in the essential oils of a wide variety of plants including cubeb, lemon and oregano. Various derivates also function as pheromones in different insects, such as stink bugs[1] and fruit flies.[2]

Uses

Bisabolenes are intermediates in the biosynthesis of many other natural chemical compounds,[3] including hernandulcin, a natural sweetener. β-Bisabolene has a balsamic odor[4] and is approved in Europe as a food additive.

References

  1. Aldrich, J.R.; Numata, H.; Borges, M.; Bin, F.; Waite, G.K.; Lusby, W.R. (1993). "Artifacts and pheromone blends from Nezara spp. and other stink bug (Heteroptera: Pentatomidae)". Zeitschrift für Naturforschung 48C: 73–79.
  2. Lu, F.; Teal, P.E. (2001). "Sex pheromone components in oral secretions and crop of male Caribbean fruit flies, Anastrepha suspensa (Loew)". Arch Insect Biochem Physiol 48 (3): 144–154. doi:10.1002/arch.1067.
  3. Bisabolene derived sesquiterpenoid biosynthesis
  4. (−)-β-bisabolene, flavornet.org

External links