Description

Nefiracetam CAS NO 77191-36-7 is a synthetic nootropic compound belonging to the racetam family, recognized for its cognitive-enhancing properties. It is a high-purity active pharmaceutical ingredient (API) of significant interest for advanced neurological research and development. This compound is primarily utilized by pharmaceutical manufacturers and research institutions focused on cognitive health and neuropharmacology.

Application

• Pharmaceutical Intermediates: Serves as a key active ingredient in the formulation of nootropic and neuroprotective drug candidates.
• Neurological Research: Used in preclinical and clinical studies investigating mechanisms of learning, memory, and cognitive function.
• Reference Standards: Employed as a certified reference material (CRM) for analytical method development and quality control in laboratories.
• Biochemical Studies: Applied in studies exploring synaptic plasticity, neurotransmitter systems, and neuronal signal transduction pathways.
• Dietary Supplement R&D: Investigated for potential use in advanced cognitive support formulations under strict regulatory frameworks.

Basic Information

Product Name	Nefiracetam
CAS No.	77191-36-7
Molecular Formula	C14H18N2O2
Molecular Weight	246.31 g/mol
Synonyms	Nefiracetam; DM-9384; N-(2,6-Dimethylphenyl)-2-(2-oxo-1-pyrrolidinyl)acetamide; Translon
EINECS	Contact for details

Quality Control

Our Nefiracetam is manufactured under a strict quality management system to ensure batch-to-batch consistency and high purity. All material is accompanied by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles, typically determined by HPLC, IR, and NMR. We support compliance with cGMP guidelines for pharmaceutical intermediates, and specifications can be aligned with client-specific pharmacopeial requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept under dry, inert conditions to maintain stability and purity.

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)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 0.5%
Heavy Metals	≤ 20 ppm

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