Description

Prizidilol is a pharmaceutical intermediate and research chemical with significant importance in medicinal chemistry. This compound is primarily valued for its role in the synthesis and development of novel therapeutic agents, particularly in the cardiovascular domain. It is essential for pharmaceutical manufacturers and research institutions engaged in drug discovery and process development.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of active pharmaceutical ingredients (APIs) for cardiovascular research.
• Medicinal Chemistry Research: Used in structure-activity relationship (SAR) studies and the development of new drug candidates.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method validation in pharmaceutical laboratories.
• Process Development: Employed in the optimization and scale-up of synthetic routes within pilot plants and manufacturing facilities.
• Biochemical Research: Utilized in in-vitro studies to investigate biological pathways and mechanisms of action.

Basic Information

Product Name	Prizidilol
CAS No.	59010-44-5
Molecular Formula	C16H24N2O4
Molecular Weight	308.37 g/mol
Synonyms	Prizidilol Hydrochloride (common salt form); 1-(4-Hydroxy-3,5-diisopropylphenyl)-2-[(3-methylbutyl)amino]ethanol; SK&F 92657; (±)-Prizidilol; 4-[2-Hydroxy-3-[(3-methylbutyl)amino]propyl]-2,6-diisopropylphenol
EINECS	Contact for details

Quality Control

Our Prizidilol is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. We provide comprehensive quality documentation, including Certificates of Analysis (COA) with detailed chromatographic and spectroscopic data. The product is suitable for use under cGMP guidelines for pharmaceutical R&D.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). The material is hygroscopic (moisture-sensitive) and should be handled under an inert atmosphere to prevent degradation.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Water Content (KF)	≤ 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.