Bisabolene
α-Bisabolene | |
β-Bisabolene | |
β-Bisabolene | |
γ-Bisabolene | |
Names | |
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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 interactive 3D | (α): Image (β): Image (γ): Image |
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Properties | |
C15H24 | |
Molar mass | 204.36 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 | |
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
- ↑ 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.
- ↑ 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.
- ↑ Bisabolene derived sesquiterpenoid biosynthesis
- ↑ (−)-β-bisabolene, flavornet.org
External links
- Beta-bisabolene, NIST Chemistry WebBook listing
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