Description

6-Methyl-3-Pyridoyl-2-Pyrrolidinone is a high-purity, advanced pharmaceutical intermediate with a distinct pyrrolidinone-pyridine hybrid structure. This compound is valued for its role as a critical building block in the synthesis of novel active pharmaceutical ingredients (APIs), particularly in central nervous system (CNS) and oncology research. It is essential for R&D chemists and process development scientists in the pharmaceutical, agrochemical, and fine chemical industries seeking to develop new therapeutic agents and specialty molecules.

Application

• Pharmaceutical Intermediate: A key synthon for the research and development of new drug candidates, especially in neurological and oncological therapeutic areas.
• Active Pharmaceutical Ingredient (API) Synthesis: Serves as a core structural motif in the multi-step synthesis of complex target molecules.
• Agrochemical Research: Used in the discovery and development of new pesticides and herbicides due to its bioactive heterocyclic framework.
• Fine Chemical Production: Employed in custom synthesis and contract manufacturing for specialized chemical products.
• Academic & Institutional R&D: A valuable reagent for medicinal chemistry and organic synthesis research in university and institutional laboratories.
• Ligand and Catalyst Development: Potential use in creating novel ligands for metal catalysis or as a scaffold for functional materials.

Basic Information

Item	Detail
Product Name	6-Methyl-3-Pyridoyl-2-Pyrrolidinone
CAS No.	1076198-57-6
Molecular Formula	C11H12N2O2
Molecular Weight	204.23 g/mol
Synonyms	6-Methyl-3-pyridinoyl-2-pyrrolidinone; 2-Pyrrolidinone, 6-methyl-3-pyridoyl-; 3-(6-Methylpyridin-3-yl)carbonyl-2-pyrrolidinone; 1-(6-Methylpyridin-3-yl)-2-oxopyrrolidine-3-carboxaldehyde (tautomer); 6-Methylnicotinoyl-2-pyrrolidinone; 3-(6-Methyl-3-pyridyl)carbonyl-2-pyrrolidinone; 6-Methyl-3-pyridoyl-pyrrolidin-2-one
EINECS	Contact for details

Quality Control

Our 6-Methyl-3-Pyridoyl-2-Pyrrolidinone is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via NMR and IR spectroscopy, to ensure it meets the high standards required for pharmaceutical R&D. A Certificate of Analysis (COA) detailing all specifications 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). Keep the container tightly sealed in a dry environment to maintain product integrity.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Water Content (KF)	≤ 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.