Description

Bometolol CAS NO 65008-93-7 is a high-purity pharmaceutical intermediate and active ingredient. This compound is critical for ensuring the efficacy and consistency of final drug formulations, particularly in cardiovascular and ophthalmic applications. It is primarily required by pharmaceutical manufacturers, advanced research institutions, and fine chemical suppliers engaged in the synthesis of β-adrenergic blocking agents.

Application

• Pharmaceutical Active Ingredient (API): Core component in the synthesis of β-blocker medications.
• Cardiovascular Drug Research: Key intermediate for developing new therapeutic agents targeting hypertension and arrhythmias.
• Ophthalmic Solution Formulation: Used in the production of eye drops for managing glaucoma.
• Chemical Reference Standard: Serves as a high-purity standard for analytical testing and quality control in laboratories.
• Process Development & Scale-up: Essential for process chemistry research and pilot-scale manufacturing in fine chemical synthesis.
• Academic & Institutional Research: Utilized in pharmacological studies and biochemical pathway investigations.

Basic Information

Product Name	Bometolol
CAS No.	65008-93-7
Molecular Formula	C17H28N2O5
Molecular Weight	340.42 g/mol
Synonyms	Bometolol; 1-(tert-Butylamino)-3-[(5-methyl-2-benzoxazolyl)oxy]-2-propanol; Bometololum; Bometolol Hydrochloride (salt form); BOM; (RS)-1-(tert-Butylamino)-3-[(5-methyl-1,3-benzoxazol-2-yl)oxy]propan-2-ol
EINECS	Contact for details

Quality Control

Our Bometolol is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, residual solvent analysis, and identification by IR and NMR spectroscopy, to ensure it meets stringent pharmaceutical-grade specifications. Certificates of Analysis (COA) detailing all test results are available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed after each use to prevent moisture absorption.

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 ≤ 1.0%
Any single unknown impurity	≤ 0.5%
Loss on Drying	≤ 1.0%
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.