Biological Activity
Bupivacaine is a more potent inhibitor of cAMP production than are chemically related local anesthetics that are less prone to produce cardiovascular toxicity.
Targets
Sodium channel | ||||
In vitro | DMSO | 65 mg/mL (200.06 mM) | |
Water | 23 mg/mL (70.79 mM) | ||
Ethanol | 65 mg/mL (200.06 mM) | ||
* <1 mg/ml means slightly soluble or insoluble. * Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
0.1 mM | 30.78 mL | 153.89 mL | 307.79 mL |
0.5 mM | 6.16 mL | 30.78 mL | 61.56 mL |
1 mM | 3.08 mL | 15.39 mL | 30.78 mL |
5 mM | 0.62 mL | 3.08 mL | 6.16 mL |
*The above data is based on the productmolecular weight 324.9 . Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Catalog Num | A10168 |
---|---|
M. Wt | 324.9 |
Formula | C18H28N2O.HCl |
Solubility | DMSO |
Purity | >98% |
Storage | at -20°C 3 years Powder |
CAS No. | 18010-40-7 |
Synonyms | Marcain, Marcaine, Sensorcaine, Vivacaine |
SMILES | CCCCN1CCCCC1C(=O)NC2=C(C=CC=C2C)C.Cl |
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