Description

Oxprenolol is a non-selective β-adrenergic receptor blocking agent, commonly referred to as a β-blocker. This compound is of significant commercial and research interest for its role as a key pharmaceutical intermediate in the synthesis of active pharmaceutical ingredients (APIs). It is primarily utilized by manufacturers in the pharmaceutical and life science research sectors for the development and production of cardiovascular medications.

Application

• Pharmaceutical Intermediate: Primary use as a building block in the synthesis of β-blocker APIs.
• Cardiovascular Research: Used in preclinical and clinical research studies investigating hypertension and angina.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method validation in laboratories.
• Active Pharmaceutical Ingredient (API) Manufacturing: A critical raw material in the production of finished dosage forms.
• Biochemical Research: Employed in studies of adrenergic receptor mechanisms and signal transduction pathways.

Basic Information

Product Name	Oxprenolol
CAS No.	6452-71-7
Molecular Formula	C15H23NO3
Molecular Weight	265.35 g/mol
Synonyms	1-(2-Allylphenoxy)-3-(isopropylamino)-2-propanol; Oxprenololum; Trasicor; Coretal; Apsolox; Captol; Slow-Trasicor; (RS)-Oxprenolol
EINECS	229-256-3

Quality Control

Our Oxprenolol is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency, meeting the stringent requirements for pharmaceutical intermediates. Certificates of Analysis (COA) detailing specifications such as assay, related substances, and residual solvents are provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and should be kept in a dry environment to prevent degradation.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.