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Tocainide hydrochloride, a sodium channel blocker, inhibits the sodium channels in the pain-producing foci in nerve membranes. It is an orally effective antiarrhythmic agent, structurally and pharmacologically similar to lidocaine [1][2].

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 2 mg | $52 | 5 days | 5 days | |
| 1 mL x 10 mM (in DMSO) | $98 | - | In Stock |
| Description | Tocainide hydrochloride, a sodium channel blocker, inhibits the sodium channels in the pain-producing foci in nerve membranes. It is an orally effective antiarrhythmic agent, structurally and pharmacologically similar to lidocaine [1][2]. |
| Targets&IC50 | Na+ channel: |
| In vivo | Tocainide (100 mg/kg) effectively reduces ventricular ectopic activity in unanesthetized dogs with coronary occlusion. Cessation of tocainide in models of digitalis toxicity and coronary occlusion rapidly causes a resurgence of ventricular ectopic activity [1]. |
| Molecular Weight | 228.718 |
| Formula | C11H17ClN2O |
| Cas No. | 71395-14-7 |
| Smiles | Cl.CC(N)C(=O)Nc1c(C)cccc1C |
| Relative Density. | 1.31g/cm3 |
| 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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