Description

Mazapertine Succinate CAS NO 134208-18-7 is a high-purity pharmaceutical intermediate and active pharmaceutical ingredient (API). This compound is of significant interest for research and development within the pharmaceutical industry due to its specific pharmacological profile. It is primarily required by pharmaceutical manufacturers and advanced research institutions engaged in the development of new therapeutic agents.

Application

• Pharmaceutical Intermediate: Serves as a critical building block in the synthesis of advanced drug candidates.
• Active Pharmaceutical Ingredient (API) Research: Used in preclinical and clinical research for the development of new medications.
• Reference Standard: Employed as a certified reference material (CRM) for analytical method development and quality control in laboratories.
• Biochemical Research: Utilized in studies investigating specific biological pathways and receptor interactions.
• Process Development & Scale-up: Essential for optimizing synthetic routes and manufacturing processes in pilot plants.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects.

Basic Information

Product Name	Mazapertine Succinate
CAS No.	134208-18-7
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Mazapertine succinate; Succinic acid compound with Mazapertine; Mazapertine hydrogen succinate; 1-(4-Fluorophenyl)-4-((4-(2-methoxyphenyl)-1-piperazinyl)methyl)-2(1H)-pyridinone succinate; UNII-0Q3VKZ3V9F; Mazapertine (succinate); 2(1H)-Pyridinone, 1-(4-fluorophenyl)-4-[[4-(2-methoxyphenyl)-1-piperazinyl]methyl]-, butanedioate (1:1)
EINECS	Contact for details

Quality Control

Our Mazapertine Succinate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide full traceability and Certificates of Analysis (COA) are available for every shipment, detailing key parameters such as assay and impurity profiles. Our quality commitment aligns with cGMP principles where applicable for pharmaceutical intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (typically 15-25°C). Keep the container tightly sealed in a dry environment to maintain product integrity.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0%
Residual Solvents (GC)	Complies with ICH guidelines
Loss on Drying	≤1.0%

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