Description

Falintolol is a potent and selective β-adrenergic receptor antagonist (β-blocker) of significant interest in pharmaceutical research and development. Its primary value lies in its potential as a key intermediate or active pharmaceutical ingredient (API) for the synthesis of novel cardiovascular therapeutics. This compound is essential for research organizations, pharmaceutical manufacturers, and fine chemical suppliers operating in the global life sciences sector, particularly those focused on cardiology and metabolic disorders.

Application

• Pharmaceutical Intermediate: Serves as a critical building block in the multi-step synthesis of advanced β-blocker drug candidates.
• Active Pharmaceutical Ingredient (API) Research: Used in preclinical and clinical research for developing new treatments for hypertension, angina, and arrhythmias.
• Biochemical Research: Employed as a tool compound in pharmacological studies to investigate β-adrenergic receptor function and signaling pathways.
• Reference Standard: Utilized as a high-purity analytical standard for quality control and method development in pharmaceutical analysis (HPLC, LC-MS).
• Process Chemistry Development: Acts as a model compound for optimizing synthetic routes, scaling up production, and developing robust manufacturing processes.

Basic Information

Product Name	Falintolol
CAS No.	90581-63-8
Molecular Formula	C17H28N2O4
Molecular Weight	324.42 g/mol
Synonyms	Falintolol; 1-(4-Fluorophenyl)-4-[2-hydroxy-3-(isopropylamino)propoxy]indole; 4-[2-Hydroxy-3-(isopropylamino)propoxy]-1-(4-fluorophenyl)-1H-indole; 1-(p-Fluorophenyl)-4-[2-hydroxy-3-(isopropylamino)propoxy]indole; BRN 2937388; CHEMBL2103876; SCHEMBL15450419; DTXSID201310051
EINECS	Contact for details

Quality Control

Our Falintolol is manufactured under strict quality management systems. Every batch undergoes comprehensive analytical testing, including identification by spectroscopic methods (IR, NMR), purity assessment by HPLC, and control of specified impurities. We provide a detailed Certificate of Analysis (COA) with each shipment, ensuring traceability and compliance with your research or cGMP-grade requirements. Our quality commitment supports your need for reliable and consistent material in critical development workflows.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive); the container must be kept tightly sealed in a dry environment to prevent degradation. Keep away from incompatible materials.

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)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

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