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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Peso formulazione	310.86
Note sul grado di purezza	Research
Colore	White
Forma fisica	Solid
Molecular Weight (g/mol)	310.86
Conservazione consigliata	4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture)
SMILES	[H]Cl.O=C([C@H]1N(CCC)CCCC1)NC2=C(C)C=CC=C2C
Durata utile	4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture)
Formula molecolare	C₁₇H₂₇ClN₂O
Percent Purity	98.66%
Informazioni di solubilità	DMSO : 10 mg/mL (32.17 mM; Need ultrasonic) ∣H2O : 10 mg/mL (32.17 mM; Need ultrasonic)
CAS	98717-15-8
Da utilizzare con (applicazione)	Neuroscience-Neuromodulation
Materiale o nome chimico	Ropivacaine hydrochloride
Grado	Research

CAS RN 98717-15-8

CAS RN 98717-15-8

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