1. Others
  2. Insecticide
  3. (E)-11-Tetradecenyl acetate

(E)-11-Tetradecenyl acetate is a monounsaturated 14-carbon acetate insecticide and a component of the sex pheromone of the currant shoot borer. (E)-11-Tetradecenyl acetate triggers strong antennal responses in males and is used in combination with (Z)-11-tetradecenyl acetate to produce an attracting effect. (E)-11-Tetradecenyl acetate has important application value in the sustainable control of pests, and can be used to monitor population dynamics and implement mating disruption. (E)-11-Tetradecenyl acetate is highly species-specific, triggering only extremely weak responses and showing no attracting activity towards Melanotus communis beetles. (E)-11-Tetradecenyl acetate can be used in studies related to the currant shoot borer and targeted pest control.

For research use only. We do not sell to patients.

(E)-11-Tetradecenyl acetate

(E)-11-Tetradecenyl acetate Chemical Structure

CAS No. : 33189-72-9

Size Stock
50 mg   Get quote  
100 mg   Get quote  
250 mg   Get quote  

* Please select Quantity before adding items.

This product is a controlled substance and not for sale in your territory.

Other Forms of (E)-11-Tetradecenyl acetate:

Top Publications Citing Use of Products
  • Biological Activity

  • Purity & Documentation

  • References

  • Customer Review

Description

(E)-11-Tetradecenyl acetate is a monounsaturated 14-carbon acetate insecticide and a component of the sex pheromone of the currant shoot borer. (E)-11-Tetradecenyl acetate triggers strong antennal responses in males and is used in combination with (Z)-11-tetradecenyl acetate to produce an attracting effect. (E)-11-Tetradecenyl acetate has important application value in the sustainable control of pests, and can be used to monitor population dynamics and implement mating disruption. (E)-11-Tetradecenyl acetate is highly species-specific, triggering only extremely weak responses and showing no attracting activity towards Melanotus communis beetles. (E)-11-Tetradecenyl acetate can be used in studies related to the currant shoot borer and targeted pest control[1][2].

In Vitro

(E)-11-tetradecenyl acetate shows almost no effect on the antennae of male Melanotus communis beetles[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Mixing (E)-11-Tetradecenyl acetate (10-100 μg; field trapping lure; single loading) with (Z)-11-Tetradecenyl acetate attracts male Euhyponomeutoides albithoracellus[1].
(E)-11-Tetradecenyl acetate (1 ng; single exposure) triggers a strong and stable electrophysiological response in the antennae of male Euhyponomeutoides albithoracellus[1].
When (E)-11-Tetradecenyl acetate and (E)-11-Tetradecenol are formulated at a 2:1 ratio, or when formulated into a multi-component mixture at a 1:1:1:1 ratio for testing, they only trigger negligible antennal responses and show no attractant activity towards male Melanotus communis in field bioassays[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Euhyponomeutoides albithoracellus (male adults)[1]
Dosage: 10-90 μg (in (E):(Z) blends); 100 μg (in 1:1 (E):(Z) blend with/without tetradecyl acetate)
Administration: field trap bait; single load
Result: Captured high numbers of male moths when in 1:1 blend with (Z)-11-tetradecenyl acetate.
Showed numerically >60% higher trap catches when 100 μg tetradecyl acetate was added to 1:1 blend, though difference was not statistically significant.
Captured very few male moths when used alone.
Captured large numbers of male moths when in 25:75 or 50:50 (E):(Z) blends, with 25:75 blend having the highest mean trap catch.
Captured significantly fewer male moths when in 10:90, 75:25, or 90:10 (E):(Z) blends compared to 25:75 and 50:50 blends.
Animal Model: Euhyponomeutoides albithoracellus (male adults, 1-4 days post-emergence)[1]
Dosage: 1 ng (as part of synthetic candidate compound blend, 1 ng/μL per compound)
Administration: GC effluent delivery; single exposure
Result: Elicited strong, consistent electroantennographic responses in male moth antennae, with response amplitudes similar to those elicited by gland extracts from female moths.
Molecular Weight

254.41

Formula

C16H30O2

CAS No.
SMILES

C(CCCCCC/C=C/CC)CCCOC(C)=O

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
  • No file chosen (Maximum size is: 1024 Kb)
  • If you have published this work, please enter the PubMed ID.
  • Your name will appear on the site.
  • Molarity Calculator

  • Dilution Calculator

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass   Concentration   Volume   Molecular Weight *
= × ×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
× = ×
C1   V1   C2   V2
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Your Recently Viewed Products:

Inquiry Online

Your information is safe with us. * Required Fields.

Product Name

 

Requested Quantity *

Applicant Name *

 

Salutation

Email Address *

 

Phone Number *

Department

 

Organization Name *

City

State

Country or Region *

     

Remarks

Bulk Inquiry

Inquiry Information

Product Name:
(E)-11-Tetradecenyl acetate
Cat. No.:
HY-W106720
Quantity:
MCE Japan Authorized Agent: