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Synonyms:
Bupivacaine N-oxide hydrochloride
| 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 | BupivacaineN-oxide hydrochloride is a metabolite of Bupivacaine. Bupivacaine acts as an NMDA receptor inhibitor and can block sodium, L-type calcium, and potassium channels. It effectively blocks SCN5A channels, with an IC50 of 69.5 μM. Bupivacaine is used in research related to chronic pain. |
| Molecular Weight | 340.89 |
| Formula | C18H29ClN2O2 |
| Cas No. | 1796927-05-3 |
| Smiles | Cl.O=C(NC=1C(=CC=CC1C)C)C2CCCCN2(=O)CCCC |
| 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.
| Size | Quantity | Unit Price | Amount | Operation |
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