Description

Pirogliride Tartrate is a high-purity pharmaceutical intermediate and active pharmaceutical ingredient (API). This compound is of significant commercial interest for its role in the research and development of novel therapeutic agents. It is primarily utilized by pharmaceutical manufacturers, research institutions, and fine chemical suppliers engaged in advanced drug synthesis.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of advanced drug candidates and active pharmaceutical ingredients (APIs).
• Research & Development: Used in preclinical and clinical research for investigating new therapeutic pathways and formulations.
• Reference Standard: Serves as a certified reference material (CRM) for analytical method development, validation, and quality control in laboratories.
• Fine Chemical Synthesis: Employed in multi-step organic synthesis for creating complex, high-value specialty chemicals.

Basic Information

Product Name	Pirogliride Tartrate
CAS No.	62625-19-8
Molecular Formula	C17H20N2O3 • C4H6O6
Molecular Weight	486.46 g/mol
Synonyms	Pirogliride Tartrate Salt; Pirogliride L-Tartrate; 1-(3,4-Dichlorobenzyl)-3-(methylamino)-2-pyrrolidinone Tartrate; 1-[(3,4-Dichlorophenyl)methyl]-3-(methylamino)-2-pyrrolidinone (2R,3R)-2,3-Dihydroxybutanedioate; Pirogliride Acid Tartrate; Pirogliride Hydrogen Tartrate
EINECS	Contact for details

Quality Control

Our Pirogliride Tartrate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation, to ensure it meets stringent specifications for pharmaceutical use. A Certificate of Analysis (COA) detailing all test results is 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 minimize exposure to atmospheric moisture.

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)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0%
Water Content (KF)	≤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.