Description

Pirmenol is a pharmaceutical active ingredient and a class Ia antiarrhythmic agent with sodium channel blocking properties. This compound is critical for the research and development of new cardiovascular therapeutics, offering a specific mechanism of action for managing cardiac arrhythmias. It is primarily utilized by pharmaceutical R&D laboratories, academic research institutions, and manufacturers of fine chemicals and reference standards.

Application

• Pharmaceutical Research & Development: Serves as a key intermediate or active pharmaceutical ingredient (API) in the development of novel antiarrhythmic drugs.
• Biochemical Research: Used as a pharmacological tool to study sodium channel function and cardiac electrophysiology in vitro.
• Reference Standard: Employed as a high-purity analytical standard for quality control and method validation in pharmaceutical analysis.
• Fine Chemical Synthesis: Acts as a building block for the synthesis of more complex molecules or derivatives with potential therapeutic value.

Basic Information

Product Name	Pirmenol
CAS No.	68252-19-7
Molecular Formula	C22H30N2O
Molecular Weight	338.49 g/mol
Synonyms	Pirmenol Hydrochloride (common salt form); CI-845; (±)-α-[(2-Methyl-1-pyrrolidinyl)methyl]-α-phenyl-2-pyridinemethanol; 2-Pyridinemethanol, α-[(2-methyl-1-pyrrolidinyl)methyl]-α-phenyl-; α-(2-Methyl-1-pyrrolidinylmethyl)-α-phenyl-2-pyridinemethanol
EINECS	Contact for details

Quality Control

Our Pirmenol is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification (IR, HPLC), assay (HPLC), and impurity profiling to ensure high chemical purity and consistency. Certificates of Analysis (COA) detailing all specifications are provided with every shipment to support your quality assurance and regulatory needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (15-25°C). Keep the container tightly sealed to protect from moisture.

Specification

Item	Specification
Appearance	White to off-white 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% Any single impurity ≤ 1.0%
Residual Solvents (GC)	Complies with ICH guidelines
Loss on Drying	≤ 0.5%

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