Description

Bevantolol CAS NO 59170-23-9 is a selective β-1 adrenergic receptor antagonist (β-blocker) of pharmaceutical significance. This compound is a key intermediate in the synthesis of active pharmaceutical ingredients (APIs) for cardiovascular medications. It is essential for pharmaceutical R&D laboratories, chemical synthesis units, and manufacturers specializing in cardiovascular and related therapeutic agents.

Application

• Pharmaceutical Intermediate: Primary use as a critical building block in the synthesis of final β-blocker drug substances.
• Cardiovascular Research: Used in preclinical and clinical research studies targeting hypertension, angina, and arrhythmias.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method development in pharmaceutical analysis.
• Chemical Synthesis: Employed in organic synthesis for the development of novel β-adrenergic ligands and related chemical entities.
• API Manufacturing: Integral component in the scaled-up production processes for finished dosage forms.

Basic Information

Product Name	Bevantolol
CAS No.	59170-23-9
Molecular Formula	C20H25NO4
Molecular Weight	343.42 g/mol
Synonyms	Bevantolol; (±)-Bevantolol; 1-[[2-(3,4-Dimethoxyphenyl)ethyl]amino]-3-(3-methylphenoxy)-2-propanol; 1-(3,4-Dimethoxyphenethylamino)-3-(m-tolyloxy)-2-propanol; DL-Bevantolol; Bevantololum; Bevantolol Hydrochloride (salt form); N-[(3,4-Dimethoxyphenethyl)amino]-3-(3-methylphenoxy)-2-propanol
EINECS	Contact for details

Quality Control

Our Bevantolol is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, identity confirmation by IR and NMR, and residual solvent analysis, to ensure it meets stringent pharmaceutical-grade specifications. Certificates of Analysis (COA) with full traceability are provided.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive); ensure the container is sealed tightly after each use to prevent degradation from atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥98.5%
Related Substances (HPLC)	Total impurities ≤1.5% Any single unknown impurity ≤0.5%
Loss on Drying	≤0.5%
Residue on Ignition	≤0.1%
Heavy Metals	≤20 ppm

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