Description

Niaprazine is a high-purity pharmaceutical intermediate and active ingredient with significant therapeutic potential. Its value lies in its specific chemical structure, which is critical for the synthesis of advanced pharmaceutical compounds. This product is essential for research institutions and pharmaceutical manufacturers engaged in the development and production of specialized medications, particularly in the central nervous system therapeutic area.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of complex active pharmaceutical ingredients (APIs).
• Neuropharmacological Research: Used in preclinical and clinical research studies investigating new therapeutic agents.
• Reference Standard: Serves as a certified reference material (CRM) for analytical method development and quality control in laboratories.
• Process Development: Employed in scaling up and optimizing synthetic routes within process chemistry departments.
• Formulation Studies: Utilized in the development of final dosage forms, such as tablets or capsules, during pharmaceutical R&D.

Basic Information

Product Name	Niaprazine
CAS No.	27367-90-4
Molecular Formula	C20H27FN2O2
Molecular Weight	346.44 g/mol
Synonyms	1-(3-(4-Fluorophenyl)-1-piperazinyl)-1-(2-methoxyphenyl)-2-propanone; Niaprazine; Niaprazinum; Niaprazine [INN]; Niaprazine [USAN]; Niaprazine [BAN]; Niaprizine; F-82; EINECS 248-423-1
EINECS	248-423-1

Quality Control

Our Niaprazine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency, meeting the stringent requirements for pharmaceutical intermediates. Certificates of Analysis (COA) detailing results for assay, related substances, residual solvents, and other critical parameters are provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.0% Any single impurity ≤ 0.5%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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