Description

Milenperone is a high-purity chemical compound of significant interest in advanced pharmaceutical research and development. Its primary value lies in its utility as a key intermediate or reference standard for the synthesis and analytical characterization of complex active pharmaceutical ingredients (APIs). This product is essential for research organizations, pharmaceutical manufacturers, and analytical laboratories engaged in the development of novel therapeutic agents, particularly within the neuropharmacology domain. We supply Milenperone CAS NO 59831-64-0 to the global market with a commitment to consistent quality and reliable supply chain integrity.

Application

• Pharmaceutical Intermediate: Serves as a critical building block in the multi-step synthesis of target drug molecules.
• Reference Standard: Used for analytical method development, validation, and quality control (QC) testing in pharmaceutical laboratories.
• Biochemical Research: Employed in preclinical studies to investigate pharmacological activity and structure-activity relationships (SAR).
• Active Pharmaceutical Ingredient (API) Development: Functions as a core structural component in the R&D of new chemical entities (NCEs).
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects.
• Academic Research: Utilized by universities and research institutes for scientific studies in medicinal chemistry.

Basic Information

Item	Details
Product Name	Milenperone
CAS No.	59831-64-0
Molecular Formula	C₂₃H₂₆FN₃O₂
Molecular Weight	395.47 g/mol
Synonyms	4'-Fluoro-4-[4-(2-pyrimidinyl)-1-piperazinyl]butyrophenone; FG-5606; R-34,400; 1-[4-(4-Fluorophenyl)-4-oxobutyl]-4-(pyrimidin-2-yl)piperazine; Milenperon; Milenperonum
EINECS	Contact for details

Quality Control

Our Milenperone is manufactured under a strict quality management system. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for research and development applications. Certificates of Analysis (COA) detailing purity, identity, and impurity profiles are provided with every shipment. We adhere to cGMP (current Good Manufacturing Practice) principles where applicable to ensure traceability and consistency.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (typically 15-25°C). Keep away from incompatible materials. For long-term storage, consider conditions under an inert atmosphere to ensure stability.

Specification

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