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(2E,6E)-Farnesyl acetate

CAS# 4128-17-0

(2E,6E)-Farnesyl acetate

Catalog No. BCX0390----Order now to get a substantial discount!

Product Name & Size Price Stock
(2E,6E)-Farnesyl acetate: 5mg Please Inquire In Stock
(2E,6E)-Farnesyl acetate: 10mg Please Inquire In Stock
(2E,6E)-Farnesyl acetate: 20mg Please Inquire Please Inquire
(2E,6E)-Farnesyl acetate: 50mg Please Inquire Please Inquire
(2E,6E)-Farnesyl acetate: 100mg Please Inquire Please Inquire
(2E,6E)-Farnesyl acetate: 200mg Please Inquire Please Inquire
(2E,6E)-Farnesyl acetate: 500mg Please Inquire Please Inquire
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Chemical structure

(2E,6E)-Farnesyl acetate

3D structure

Chemical Properties of (2E,6E)-Farnesyl acetate

Cas No. 4128-17-0 SDF Download SDF
PubChem ID 638500 Appearance Liquid
Formula C17H28O2 M.Wt 264.4
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name [(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl] acetate
SMILES CC(=CCCC(=CCCC(=CCOC(=O)C)C)C)C
Standard InChIKey ZGIGZINMAOQWLX-NCZFFCEISA-N
Standard InChI InChI=1S/C17H28O2/c1-14(2)8-6-9-15(3)10-7-11-16(4)12-13-19-17(5)18/h8,10,12H,6-7,9,11,13H2,1-5H3/b15-10+,16-12+
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

(2E,6E)-Farnesyl acetate Dilution Calculator

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(2E,6E)-Farnesyl acetate Molarity Calculator

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Preparing Stock Solutions of (2E,6E)-Farnesyl acetate

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.7821 mL 18.9107 mL 37.8215 mL 75.643 mL 94.5537 mL
5 mM 0.7564 mL 3.7821 mL 7.5643 mL 15.1286 mL 18.9107 mL
10 mM 0.3782 mL 1.8911 mL 3.7821 mL 7.5643 mL 9.4554 mL
50 mM 0.0756 mL 0.3782 mL 0.7564 mL 1.5129 mL 1.8911 mL
100 mM 0.0378 mL 0.1891 mL 0.3782 mL 0.7564 mL 0.9455 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on (2E,6E)-Farnesyl acetate

The male-produced aggregation pheromone of the bean flower thrips Megalurothrips usitatus in China: identification and attraction of conspecifics in the laboratory and field.[Pubmed:32246573]

Pest Manag Sci. 2020 Sep;76(9):2986-2993.

BACKGROUND: Thrips, Megalurothrips usitatus, usually display aggregation behavior, which is probably mediated by a male-produced aggregation pheromone. Aggregation pheromones are species-specific, and can be used to develop commercial lures for monitoring and mass-trapping of pests. The active components of the aggregation pheromone for four thrips species have been identified. However, the components of M. usitatus-produced aggregation pheromone are still not clear. RESULT: Y-tube olfactometer assays showed that both male and virgin female M. usitatus were significantly attracted to male but not female volatiles. This was additionally supported by electroantennogram (EAG) assays. Coupled gas chromatography-electroantennogram detection (GC-EAD) showed that one component of male-specific odors elicited a significant electrophysiological response. This compound was characterized as (2E,6E)-Farnesyl acetate, which is structurally different from the active components of the aggregation pheromones of other reported thrips species. Electroantennal responses of M. usitatus increased with increasing doses of synthetic (2E,6E)-Farnesyl acetate. Additionally, this compound significantly attracted adults in laboratory behavioral bioassays. Under field conditions, sticky traps with synthetic (2E,6E)-Farnesyl acetate caught 1.5-7-fold more M. usitatus than controls, and this effect of the compound at a dose of 60 mug lasted at least 6 days. CONCLUSION: (2E,6E)-Farnesyl acetate was identified as the male-produced aggregation pheromone of M. usitatus. It could attract this thrips species under laboratory and field conditions, suggesting considerable potential as a commercial application to control M. usitatus populations. (c) 2020 Society of Chemical Industry.

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