Search Thermo Fisher Scientific
Element Search
Structure Search
Thermo Scientific Chemicals
Felodipine
A dihydropyridine calcium channel blocker | CAS: 72509-76-3 | C18H19Cl2NO4 | 384.253 g/mol
| Catalog Number | Quantity |
|---|---|
| ALFJ61195.MC | 100 mg |
Catalog number ALFJ61195.MC
View Price:Sign InSign in to see your account pricing. Need an account? Register with us today.
Quantity:
100 mg
Specifications
Chemical Name or MaterialFelodipine
CAS72509-76-3
Health Hazard 1H302
Health Hazard 2GHS H Statement
H302
Harmful if swallowed.
H302
Harmful if swallowed.
Health Hazard 3P264b-P270-P301+P312-P330-P501c
View more
Felodipine is used as a dihydropyridine calcium channel blocker. It displays high vascular selectivity; lowers arterial blood pressure without altering cardiac contractility. Antihypertensive.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Felodipine is used as a dihydropyridine calcium channel blocker. It displays high vascular selectivity; lowers arterial blood pressure without altering cardiac contractility. Antihypertensive.
Solubility
Soluble in DMSO. Insoluble in water
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from strong oxidizing agents.
Felodipine is used as a dihydropyridine calcium channel blocker. It displays high vascular selectivity; lowers arterial blood pressure without altering cardiac contractility. Antihypertensive.
Solubility
Soluble in DMSO. Insoluble in water
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from strong oxidizing agents.
RUO – Research Use Only
General References:
- Ljung. Vascular selectivity of felodipine: experimental pharmacology. J.Cardiovasc.Pharmacol. 1990, 15,(4), S11-6.
- Furukawa et al. Selectivities of dihydropyridine derivatives in blocking Ca2+ channel subtypes expressed inXenopus oocytes. J.Pharmacol.Exp.Ther. 1999, 291,(2), 464-73.