Description

Nicogrelate is a synthetic organic compound with significant pharmacological activity. This compound is valued for its role as a key intermediate in the research and development of novel therapeutic agents, particularly in the cardiovascular and metabolic disease sectors. It is primarily sought by pharmaceutical R&D laboratories, fine chemical manufacturers, and academic research institutions engaged in drug discovery and process chemistry.

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of advanced active pharmaceutical ingredients (APIs) targeting platelet aggregation.
• Biochemical Research: Used as a reference standard and a tool compound in pharmacological studies to investigate anti-thrombotic mechanisms.
• Fine Chemical Synthesis: Serves as a versatile precursor for creating more complex molecular structures in medicinal chemistry programs.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for scale-up and cGMP production of developmental drugs.

Basic Information

Product Name	Nicogrelate
CAS No.	80614-21-7
Molecular Formula	C14H15N3O4
Molecular Weight	289.29 g/mol
Synonyms	2-[(3-Pyridinylcarbonyl)amino]-N-(2,2,2-trifluoroethyl)benzeneacetamide; 2-[[(3-Pyridinyl)carbonyl]amino]-N-(2,2,2-trifluoroethyl)benzeneacetamide; Nicogrelate; AG-1; AG 1; AG1
EINECS	Contact for details

Quality Control

Our Nicogrelate is manufactured under a strict quality management system. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation (IR, NMR), to ensure it meets the high standards required for research and development applications. 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 place at controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed in a low-humidity environment to prevent degradation.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Single Unknown Impurity	≤ 0.5%
Loss on Drying	≤ 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.