MedChemExpress Ropivacaine hydrochloride is a potent sodium channel blocker and blocks impulse conduction via reversible inhibition of sodium ion influx in nerve fibrese. Ropivacaine is also an inhibitor of K2P (two-pore domain potassium channel) TREK-1 with an IC50 of 402.7 μM in COS-7 cell's membrane. Ropivacaine is widely used for neuropathic pain management in vivo.

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Información de solubilidad	DMSO : 10 mg/mL (32.17 mM; Need ultrasonic) ∣H2O : 10 mg/mL (32.17 mM; Need ultrasonic)
Forma física	Solid
Almacenamiento recomendado	4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture)
Color	Blanco
SMILES	[H]Cl.O=C([C@H]1N(CCC)CCCC1)NC2=C(C)C=CC=C2C
Notas de grado de pureza	Research
Duración de almacenamiento	4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture)
Formula Weight (peso de la fórmula)	310.86
Fórmula molecular	C₁₇H₂₇ClN₂O
CAS	98717-15-8
Nombre del producto químico o material	Ropivacaine hydrochloride
Porcentaje de pureza	98.66%
Peso molecular (g/mol)	310.86
Grado	Research
Para utilizar con (aplicación)	Neuroscience-Neuromodulation

CAS RN 98717-15-8

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