Description

Bopindolol is a potent, non-selective β-adrenergic receptor antagonist (β-blocker) with intrinsic sympathomimetic activity. This compound is a critical active pharmaceutical ingredient (API) used in the research and development of cardiovascular therapeutics. It is primarily utilized by pharmaceutical manufacturers and research institutions focused on creating treatments for hypertension, angina, and other cardiac conditions. The material is supplied as a high-purity chemical entity, Bopindolol CAS NO 62658-63-3, to support advanced pharmaceutical synthesis and analytical studies.

Application

• Pharmaceutical API Synthesis: Primary use as the active ingredient in the manufacture of β-blocker medications.
• Cardiovascular Research: A key reference standard and tool compound for studying β-adrenergic receptor pharmacology and cardiac function.
• Hypertension & Angina Drug Development: Used in R&D programs aimed at developing new or generic formulations for managing high blood pressure and chest pain.
• Metabolite Studies: Employed in pharmacokinetic and metabolic pathway research to understand drug behavior in biological systems.
• Analytical Standard: Serves as a high-purity certified reference material (CRM) for quality control testing in pharmaceutical laboratories.
• Preclinical Formulation: Used in the development and testing of various dosage forms, such as tablets or capsules, during early-stage trials.

Basic Information

Product Name	Bopindolol
CAS No.	62658-63-3
Molecular Formula	C23H30N2O3
Molecular Weight	382.50 g/mol
Synonyms	1-(tert-Butylamino)-3-[(2-methyl-1H-indol-4-yl)oxy]-2-propanol; 4-[2-(tert-Butylamino)-1-hydroxyethyl]-2-methyl-1H-indole; Bopindololum; LT 31-200; LT-31-200; LT31200; (+-)-1-(tert-Butylamino)-3-[(2-methylindol-4-yl)oxy]-2-propanol; 4-[2-(tert-Butylamino)-1-hydroxyethyl]-2-methylindole
EINECS	Contact for details

Quality Control

Our Bopindolol is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical research and development. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting critical parameters such as identity, purity, and impurity profiles. We adhere to cGMP principles where applicable to support our clients' regulatory requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (typically 15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed in a dry environment to prevent degradation. For long-term storage, consider using desiccants.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0%
Single Maximum Impurity	≤0.5%
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.