Description

Exaprolol is a selective β-adrenergic receptor antagonist (β-blocker) used in pharmaceutical research and development. This compound is valued for its high purity and consistent quality, which are critical for reliable pharmacological studies and the synthesis of advanced intermediates. It is primarily utilized by researchers and manufacturers in the pharmaceutical and biotechnology sectors focusing on cardiovascular therapeutics and receptor mechanism studies.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of advanced β-blocker APIs and related cardiovascular drugs.
• Biochemical Research: Used as a reference standard and active compound in studies of β-adrenergic receptor function and selectivity.
• Preclinical Development: Employed in pharmacological profiling, toxicity studies, and formulation development for new drug candidates.
• Academic Research: Serves as a tool compound in university and institutional labs for cardiovascular and autonomic nervous system research.
• Quality Control: Acts as a system suitability standard and impurity reference in analytical method development for β-blocker manufacturing.

Basic Information

Product Name	Exaprolol
CAS No.	55837-19-9
Molecular Formula	C15H24N2O3
Molecular Weight	280.36 g/mol
Synonyms	Exaprolol; 1-(Isopropylamino)-3-[4-(2-methoxyethyl)phenoxy]-2-propanol; (±)-Exaprolol; DL-Exaprolol; 55837-19-9; UNII-2JQ5608I3I; 2-Propanol, 1-(isopropylamino)-3-[4-(2-methoxyethyl)phenoxy]-; BRN 2933621
EINECS	Contact for details

Quality Control

Our Exaprolol is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling via HPLC and other validated methods, to ensure it meets the stringent requirements for pharmaceutical research. Certificates of Analysis (COA) detailing all specifications are provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 15-25°C). Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0%
Any single unknown impurity	≤0.5%
Residual Solvents (GC)	Complies with ICH guidelines
Loss on Drying	≤0.5%
Heavy Metals	≤20 ppm

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