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Hexaflumuron

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Catalog No. T5117Cas No. 86479-06-3

Hexaflumuron is a chitin synthesis inhibitor used to bait and eliminate termite colonies. Termites are unable to metabolize hexaflumuron and clearance is slow, resulting in up to 100% elimination. Hexaflumuron has also been tested for use with the raisin moth, cowpea weevil, and Asiatic rice borer with positive results.

Hexaflumuron

Hexaflumuron

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🥰Excellent
Purity: 99.76%
Catalog No. T5117Cas No. 86479-06-3
Hexaflumuron is a chitin synthesis inhibitor used to bait and eliminate termite colonies. Termites are unable to metabolize hexaflumuron and clearance is slow, resulting in up to 100% elimination. Hexaflumuron has also been tested for use with the raisin moth, cowpea weevil, and Asiatic rice borer with positive results.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
50 mg$40In StockIn Stock
100 mg$68In StockIn Stock
500 mg$156In StockIn Stock
1 g$198In StockIn Stock
1 mL x 10 mM (in DMSO)$29In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:99.76%
Color:White
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Product Introduction

Hexaflumuron AI Summary
Hexaflumuron exhibits a diverse bioactivity profile, functioning as both an antagonist and agonist in various signaling pathways. It acts as an antagonist of androgen receptor signaling (IC50: 35481.3 nM) and estrogen receptor alpha signaling (IC50: 8912.5 nM), while also serving as an agonist of the antioxidant response element (ARE) signaling pathway (IC50: 13685.4 nM) and an activator of the human pregnane X receptor (PXR) signaling pathway (IC50: 25118.9 nM). The compound further demonstrates significant larvicidal activity: 100.0% mortality against Culex pipiens pallens (mosquito) larvae at 0.25 mg/L after 8 days, and 80.0% mortality against Mythimna separata (Oriental armyworm) larvae at 10 mg/L on drug-pretreated corn leaves after 4 days. Additionally, it shows contact toxicity against Trichogramma nubilale (LC50: 9672.0 mgAi/L; LC95: 51197.0 mgAi/L), acute oral and contact toxicity against adult Anagrus nilaparvatae, and high toxicity in Daphnia magna (EC90: 0.5 ppb). The compound exhibits insecticidal effects against Plutella xylostella (diamondback moth) larvae, with an LC90 of 0.04 ppm and varying efficacy against fufenozide-resistant (LC50: 274.1 ug/mL) and susceptible (LC50: 9.56 ug/mL) strains, suggesting potential for insecticide applications with considerations for resistance management..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Hexaflumuron is a chitin synthesis inhibitor used to bait and eliminate termite colonies. Termites are unable to metabolize hexaflumuron and clearance is slow, resulting in up to 100% elimination. Hexaflumuron has also been tested for use with the raisin moth, cowpea weevil, and Asiatic rice borer with positive results.
Chemical Properties
Molecular Weight461.14
FormulaC16H8Cl2F6N2O3
Cas No.86479-06-3
SmilesFC(F)C(F)(F)Oc1c(Cl)cc(NC(=O)NC(=O)c2c(F)cccc2F)cc1Cl
Relative Density.1.4069 g/cm3 (Estimated)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 60 mg/mL (130.11 mM), Sonication is recommended.
H2O: Insoluble
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.1685 mL10.8427 mL21.6854 mL108.4269 mL
5 mM0.4337 mL2.1685 mL4.3371 mL21.6854 mL
10 mM0.2169 mL1.0843 mL2.1685 mL10.8427 mL
20 mM0.1084 mL0.5421 mL1.0843 mL5.4213 mL
50 mM0.0434 mL0.2169 mL0.4337 mL2.1685 mL
100 mM0.0217 mL0.1084 mL0.2169 mL1.0843 mL

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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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2 Enter the in vivo formulation:
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