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Synonyms:
(Z)-7-Tetradecen-2-one
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| 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. |
| Molecular Weight | 210.36 |
| Formula | C14H26O |
| Cas No. | 146955-45-5 |
| Smiles | C(C/C=C\CCCCCC)CCC(C)=O |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
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.
1) Add 100 μL of the DMSO
stock solution to 400 µL PEG300
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 ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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