Description

Pirmenol Hydrochloride is a high-purity pharmaceutical intermediate and active pharmaceutical ingredient (API) with significant therapeutic relevance. This compound is valued for its role in the research and development of cardiac antiarrhythmic agents. It is primarily utilized by pharmaceutical manufacturers, research institutions, and chemical synthesis facilities engaged in cardiovascular drug development and advanced organic synthesis.

Application

• Pharmaceutical API Synthesis: Serves as a key intermediate or the final active ingredient in the production of antiarrhythmic medications.
• Cardiovascular Research: Used as a reference standard or experimental compound in pharmacological studies targeting heart rhythm disorders.
• Biochemical Research: Employed in in-vitro and in-vivo studies to investigate ion channel modulation and cardiac electrophysiology.
• Reference Standard: Provides a certified material for quality control and analytical method development in pharmaceutical laboratories.
• Chemical Intermediate: Acts as a building block for the synthesis of novel analogs and derivatives in medicinal chemistry programs.

Basic Information

Product Name	Pirmenol Hydrochloride
CAS No.	61477-94-9
Molecular Formula	C22H30N2O•HCl
Molecular Weight	374.95 g/mol
Synonyms	Pirmenol HCl; CI-845; (±)-α-[(2-Methyl-1-pyrrolidinyl)methyl]-α-phenyl-2-pyridinemethanol Hydrochloride; (RS)-Pirmenol Hydrochloride; Pirmenol Monohydrochloride; 2-Pyridinemethanol, α-[(2-methyl-1-pyrrolidinyl)methyl]-α-phenyl-, hydrochloride (1:1), (±)-; 4-(2-Methylpyrrolidin-1-yl)-1,2-diphenylbutan-1-ol Hydrochloride
EINECS	Contact for details

Quality Control

Our Pirmenol Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling via HPLC, to ensure it meets stringent specifications for pharmaceutical use. Certificates of Analysis (COA) detailing all test results are provided with every shipment to guarantee traceability and compliance with cGMP guidelines where applicable.

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). Due to its hygroscopic nature, the container must be kept tightly sealed after opening to prevent moisture absorption.

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)	≥98.5%
Water Content (KF)	≤1.0%
Residue on Ignition	≤0.1%
Heavy Metals	≤20 ppm
Related Substances (HPLC)	Total impurities ≤1.5%; Any single impurity ≤0.5%

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