Description

Monatepil is a high-purity pharmaceutical intermediate and research chemical with the CAS registry number 132019-54-6. This compound is of significant interest for its role in the synthesis and development of novel therapeutic agents targeting cardiovascular and neurological pathways. It is primarily utilized by research institutions, pharmaceutical development laboratories, and fine chemical manufacturers engaged in advanced drug discovery and process chemistry. Our supply ensures consistent quality and reliable availability for critical R&D and production workflows.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of active pharmaceutical ingredients (APIs) for cardiovascular research.
• Biochemical Research: Used in in vitro and in vivo studies to investigate receptor binding and pharmacological activity.
• Process Development: Serves as a critical raw material for scaling up and optimizing synthetic routes in pilot and commercial manufacturing.
• Reference Standard: Employed as an analytical standard in quality control laboratories for method development and validation.
• Academic Research: Utilized in university and institutional labs for medicinal chemistry and pharmacology projects.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for client-specific synthesis projects.

Basic Information

Product Name	Monatepil
CAS No.	132019-54-6
Molecular Formula	C24H28N2O3S
Molecular Weight	424.56 g/mol
Synonyms	Monatepil; 132019-54-6; 4-(3,4-Dimethoxyphenyl)-2-[2-[4-(2-methoxyphenyl)-1-piperazinyl]ethyl]-2H-1,2,4-triazine-3,5(2H,4H)-dione; FR 139317; FR-139317; 1,2,4-Triazine-3,5(2H,4H)-dione, 4-(3,4-dimethoxyphenyl)-2-[2-[4-(2-methoxyphenyl)-1-piperazinyl]ethyl]-
EINECS	Contact for details

Quality Control

Our Monatepil is manufactured under strict quality management systems to ensure it meets the high standards required for pharmaceutical research and development. Each batch undergoes comprehensive analytical testing, including HPLC for purity, identity confirmation by spectroscopic methods, and stringent control of residual solvents and impurities. A Certificate of Analysis (COA) is provided with every shipment, detailing all test results against established specifications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after each use to prevent degradation from atmospheric 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%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%

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