Description

Monatepil is a high-purity pharmaceutical intermediate and research chemical with significant therapeutic potential. This compound is primarily valued for its role in the development and synthesis of novel cardiovascular and neurological agents. It is essential for pharmaceutical R&D laboratories, contract manufacturing organizations (CMOs), and academic institutions engaged in medicinal chemistry and pharmacology. The material is supplied under stringent quality control to ensure consistency for critical research and development applications.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of active pharmaceutical ingredients (APIs) targeting calcium channel and α-adrenergic receptor modulation.
• Research & Development: Used in preclinical and clinical research studies investigating treatments for hypertension and related cardiovascular conditions.
• Reference Standard: Serves as an analytical standard for quality control and method validation in pharmaceutical manufacturing.
• Medicinal Chemistry: A crucial scaffold for structure-activity relationship (SAR) studies and the development of new chemical entities.
• Contract Manufacturing: Supplied to CMOs for scale-up synthesis under current Good Manufacturing Practice (cGMP) conditions.
• Academic Research: Utilized in university and institutional labs for pharmacological studies and educational purposes.

Basic Information

Product Name	Monatepil
CAS No.	103377-41-9
Molecular Formula	C27H29N3O3S
Molecular Weight	475.60 g/mol
Synonyms	Monatepil; 4-(Diphenylmethyl)-1-piperazinecarbothioic Acid (4-Methoxy-1-naphthalenyl)methyl Ester; FR-34235; FR34235; TCV-3B; 1-[[(4-Methoxy-1-naphthyl)methyl]thio]carbonyl-4-(benzhydryl)piperazine
EINECS	Contact for details

Quality Control

Our Monatepil is manufactured and tested to meet the exacting standards required for pharmaceutical research and development. Quality is assured through a comprehensive battery of analytical tests, including HPLC for purity, residual solvent analysis, and identification by spectroscopic methods. We operate under a robust Quality Management System and can provide supporting documentation, including detailed Certificates of Analysis (COA), upon request to ensure full traceability and compliance with your project requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed in a dry environment to prevent degradation. For long-term storage, consider using desiccants.

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%
Related Substances (HPLC)	Total impurities ≤1.5%
Any single unknown 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.