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Propranolol HCl impurity A

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
Molecular Formula C13H14O3
Molecular Weight 218.2500
CAS Number 36112-95-5 โœ“ Verified
PubChem CID 37369 โ†—
Purity N/A
Product Type API Impurity
Parent Drug Propranolol
Lead Time On Request
IUPAC Name 3-naphthalen-1-yloxypropane-1,2-diol
Official Reference Standards
Std Catalog # Quantity Price
USP 1576016 โ†— 25 mg USD 903.00

๐Ÿ“ Synonyms

Propranolol glycol 36112-95-5 FU45BO16RF 3-(alpha-Naphthoxy)-1,2-propanediol RefChem:869701 3-(1-Naphthalenyloxy)-1,2-propanediol Propanolol glycol Propranolol EP Impurity A 3-naphthalen-1-yloxypropane-1,2-diol 1,2-Propanediol, 3-(1-naphthalenyloxy)-

๐Ÿ”ฌ Chemical Identifiers

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
BYNNMWGWFIGTIC-UHFFFAOYSA-N

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