(R)-Amlodipine is the enantiomerically pure stereoisomer of the calcium channel blocker amlodipine, characterized by the (R)-configuration at the chiral center of the 1,4-dihydropyridine core. Its structure features a 2-methyl-5-(2-aminoethoxy)-4-(2-chlorophenyl) substituent system, with the dihydropyridine ring adopting a cis-diaxial orientation. The compound exhibits distinct chiral discrimination in pharmacokinetic profiles compared to its S-enantiomer. This impurity arises during enantioselective synthesis or racemic resolution processes and serves as a critical chiral HPLC reference standard for enantiomeric purity determination in amlodipine active pharmaceutical ingredient (API) batches.
On Request| Std | Catalog # | Quantity | Price |
|---|---|---|---|
| USP | 1A01970 โ | 25 mg | USD 702.00 |
CCOC(=O)C1=C(NC(=C([C@H]1C2=CC=CC=C2Cl)C(=O)OC)C)COCCN
InChI=1S/C20H25ClN2O5/c1-4-28-20(25)18-15(11-27-10-9-22)23-12(2)16(19(24)26-3)17(18)13-7-5-6-8-14(13)21/h5-8,17,23H,4,9-11,22H2,1-3H3/t17-/m1/s1
HTIQEAQVCYTUBX-QGZVFWFLSA-N