Propranolol HCl impurity A is a synthetic byproduct arising from the incomplete oxidation of the propanol side chain during Propranolol synthesis. It retains the 1-isopropyl-3-(1-naphthyloxy) core but lacks the terminal hydroxyl group, featuring a secondary amine at the propyl carbon instead. This structural deviation creates a distinct naphthoxy-alkylamine motif with reduced polarity compared to the parent compound. The absence of the hydroxyl group eliminates hydrogen bonding capacity, altering chromatographic behavior. This impurity serves as an HPLC reference standard for quantifying process-related deviations in Propranolol HCl API batches.
On Request| Std | Catalog # | Quantity | Price |
|---|---|---|---|
| USP | 1576016 โ | 25 mg | USD 903.00 |
C1=CC=C2C(=C1)C=CC=C2OCC(CO)O
InChI=1S/C13H14O3/c14-8-11(15)9-16-13-7-3-5-10-4-1-2-6-12(10)13/h1-7,11,14-15H,8-9H2
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