Description

Pidolacetamol CAS NO 114485-92-6 is a high-purity pharmaceutical intermediate, also known as 4-Acetamidophenyl 2-pyrrolidin-5-one, with significant importance in modern drug synthesis. Its primary value lies in its role as a key precursor for developing advanced analgesic and antipyretic pharmaceutical compounds, ensuring high yield and purity in critical manufacturing processes. This product is essential for research institutions, pharmaceutical manufacturers, and fine chemical companies engaged in the development and production of next-generation active pharmaceutical ingredients (APIs).

Application

• Pharmaceutical Intermediate: Serves as a critical building block in the synthesis of novel analgesic and antipyretic drug candidates.
• API Development: Used in research and development for creating new Active Pharmaceutical Ingredients with improved efficacy and safety profiles.
• Fine Chemical Synthesis: Employed in multi-step organic synthesis for producing complex molecules in medicinal chemistry.
• Biochemical Research: Utilized in academic and industrial laboratories for studying metabolic pathways and drug-receptor interactions.
• Process Chemistry: Applied in scale-up and optimization of manufacturing routes for pharmaceutical production.
• Reference Standard: Can be supplied as a high-purity standard for analytical method development and quality control in pharmaceutical analysis.

Basic Information

Product Name	Pidolacetamol
CAS No.	114485-92-6
Molecular Formula	C12H14N2O2
Molecular Weight	218.25 g/mol
Synonyms	4-Acetamidophenyl 2-pyrrolidin-5-one; N-(4-(2-Oxo-1-pyrrolidinyl)phenyl)acetamide; 1-[4-(Acetylamino)phenyl]-2-pyrrolidinone; Pidolacetam; Pidolacetamum; UNII-2Q4Q2N32QY
EINECS	Contact for details

Quality Control

Our Pidolacetamol is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity suitable for pharmaceutical applications. Each lot undergoes comprehensive analytical testing, including identification, assay, and impurity profiling via advanced techniques like HPLC and GC. We provide full traceability and Certificates of Analysis (COA) are available for every shipment, confirming compliance with agreed specifications. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Keep away from heat, open flames, and incompatible materials. The container must be kept tightly sealed to protect the product from 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)	≥ 98.5%
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.