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(Z)-7-Tetradecen-2-one

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(Z)-7-Tetradecen-2-one is a species-specific nematicide that can induce terminal embryonic development, morphological abnormalities, and irreversible developmental arrest in Pristionchus pacificus, while also increasing eggshell permeability. Additionally, (Z)-7-Tetradecen-2-one exhibits olfactory attraction effects on Pristionchus pacificus and can be utilized for studying host-nematode symbiotic relationships.


(Z)-7-Tetradecen-2-one

Cas No. 146955-45-5
Pack SizePriceUSA StockGlobal StockQuantity
10 mgInquiry10-14 weeks10-14 weeks
50 mgInquiry10-14 weeks10-14 weeks
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction

Bioactivity
Description
(Z)-7-Tetradecen-2-one is a species-specific nematicide that can induce terminal embryonic development, morphological abnormalities, and irreversible developmental arrest in Pristionchus pacificus, while also increasing eggshell permeability. Additionally, (Z)-7-Tetradecen-2-one exhibits olfactory attraction effects on Pristionchus pacificus and can be utilized for studying host-nematode symbiotic relationships.
In vitro
(Z)-7-Tetradecen-2-one, with a volatility of 0.5% and applied at 10 μL for 2-4 hours, induces irreversible terminal embryogenesis in 100% of Pristionchus pacificus PS312 early embryos. For embryos aged 0-4 hours, the minimum lethal exposure duration outside the uterus is 4 hours, while for those aged 4-8 hours, it is 3 hours, leading to abnormal embryonic morphology, partial tissue differentiation, and complete developmental arrest. Additionally, a 4-hour exposure to (Z)-7-Tetradecen-2-one (0.5% volatility) enhances eggshell permeability in Pristionchus pacificus PS312, PS1843, RS5186 embryos, with 65%-90% of embryos in sensitive strains showing FM4-64 staining of embryonic tissues after exposure, associating with irreversible developmental arrest. In Pristionchus pacificus strains from the Pacific region, this compound causes 100% irreversible developmental arrest, but in RS5278 and RS5419 strains, it results in 40%-60% arrest, while leaving Caenorhabditis elegans N2 embryos unaffected. Furthermore, (Z)-7-Tetradecen-2-one at a dilution of 0.1-10% for 9-15 hours exhibits strong attraction towards Pristionchus pacificus, yet acts as a repellent or has no effect on other tested nematode species.
Chemical Properties
Molecular Weight210.36
FormulaC14H26O
Cas No.146955-45-5
SmilesC(C/C=C\CCCCCC)CCC(C)=O
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.

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Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 µL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 µL Tween 80 and mix well until fully clarified.

3) Add 450 µL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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Related Tags: (Z)-7-Tetradecen-2-one in vitro | (Z)-7-Tetradecen-2-one formula | (Z)-7-Tetradecen-2-one molecular weight