73492
trans-β-Farnesene
analytical standard
Sinónimos:
trans-7,11-Dimethyl-3-methylene-1,6,10-dodecatriene
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About This Item
Fórmula empírica (notación de Hill):
C15H24
Número de CAS:
Peso molecular:
204.35
EC Number:
MDL number:
UNSPSC Code:
85151701
PubChem Substance ID:
NACRES:
NA.24
Productos recomendados
grade
analytical standard
Quality Level
assay
≥90% (GC)
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
application(s)
food and beverages
format
neat
storage temp.
−20°C
SMILES string
[H]\C(CCC(=C)C=C)=C(\C)CC\C=C(\C)C
InChI
1S/C15H24/c1-6-14(4)10-8-12-15(5)11-7-9-13(2)3/h6,9,12H,1,4,7-8,10-11H2,2-3,5H3/b15-12+
InChI key
JSNRRGGBADWTMC-NTCAYCPXSA-N
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General description
trans-β-Farnesene is the main active constituent of the alarm pheromone in the aphid species. It causes behavioral responses, such as kicking, discontinuation of feeding, moving away, or dropping down among them.
Application
This analytical standard can also be used as follows:
- Secondary metabolite profiling of various plant parts collected from 82 plants belonging to 21 different cannabis strains using gas chromatography-mass spectrometry (GC-MS) for sterols and terpenoids (mono-, sesqui-, tri-), and high-performance liquid chromatography (HPLC) with UV and mass spectrometric (MS) detection for flavonoids
- Gas chromatographic analysis of a total of 163 compounds in the essential oil samples extracted from the leaves and flowers of Lantana camara, in combination with detection techniques of mass spectrometry (MS) and flame ionization detection (FID)
- Simultaneous determination of 49 compounds from the essential oil samples obtained from the methanolic extracts of dried leaves and flowers of C. macropodum by GC-FID and GC-MS methods
- Identification and quantification of 31 volatile organic compounds from the flowers of P. Nobby’s Pacific Sunset using DVB/CAR/PDMS fibers in the solid-phase microextraction (SPME) technique for the sample enrichment followed by their GC-MS analysis
Other Notes
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
signalword
Danger
hcodes
Hazard Classifications
Asp. Tox. 1
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
230.0 °F
flash_point_c
110 °C
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Los clientes también vieron
Martin de Vos et al.
Proceedings of the National Academy of Sciences of the United States of America, 107(33), 14673-14678 (2010-08-04)
In most aphid species, facultative parthenogenetic reproduction allows rapid growth and formation of large single-genotype colonies. Upon predator attack, individual aphids emit an alarm pheromone to warn the colony of this danger. (E)-beta-farnesene (EBF) is the predominant constituent of the
James D Blande et al.
Environmental pollution (Barking, Essex : 1987), 157(1), 174-180 (2008-09-09)
Plants can respond physiologically to damaging ultraviolet-B radiation by altering leaf chemistry, especially UV absorbing phenolic compounds. However, the effects on terpene emissions have received little attention. We conducted two field trials in plots with supplemented UV-B radiation and assessed
Eduardo Hatano et al.
Journal of chemical ecology, 34(9), 1149-1152 (2008-08-16)
When aphids are attacked by natural enemies, they emit alarm pheromone to alert conspecifics. For most aphids tested, (E)-beta-farnesene (EBF) is the main, or only, constituent of the alarm pheromone. In response to alarm pheromone, alerted aphids drop off the
Stéphanie Heuskin et al.
Pest management science, 68(1), 127-136 (2011-07-05)
Optimisation of alginate formulations is described in order to develop semiochemical (E-β-farnesene and E-β-caryophyllene) slow-release devices in biological control approaches by attracting predators and parasitoids of aphids. Various formulation criteria were optimised with respect to semiochemical encapsulation capacity. Moreover, the
Tao Zhong et al.
Journal of insect physiology, 58(6), 771-781 (2012-02-07)
Odorant-binding proteins (OBPs) are important parts of insect olfactory systems, and sensitive olfaction is vital for phytophagous insects in host foraging. Electrophysiological studies are helpful in understanding olfactory sensing in Sitobion avenae (Hemiptera: Aphididae), but the functions of odorant-binding proteins
Protocolos
-β-Farnesene; α-Huµlene; Germacrene D; (+)-Valencene; Bicyclogermacrene; (+)-δ-Cadinene
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