Description

Amtolmetin Guacil is a non-steroidal anti-inflammatory drug (NSAID) prodrug, specifically designed to improve gastrointestinal tolerability. This compound is of significant commercial interest for its targeted therapeutic action, offering a favorable safety profile for long-term pain and inflammation management. It is primarily required by pharmaceutical manufacturers and research institutions engaged in the development of advanced analgesic and anti-inflammatory formulations.

Application

• Pharmaceutical Active Ingredient (API): Core component in the manufacture of prescription medications for treating osteoarthritis, rheumatoid arthritis, and other inflammatory conditions.
• Analgesic Formulations: Used in the development of drugs aimed at managing mild to moderate pain with reduced gastric side effects.
• Research & Development: Serves as a key reference standard and intermediate in pharmacological studies and the development of new NSAID prodrugs.
• Veterinary Medicine: Potential application in anti-inflammatory treatments for animals, subject to regional regulatory approvals.

Basic Information

Product Name	Amtolmetin Guacil
CAS No.	87344-06-7
Molecular Formula	C23H23N3O6
Molecular Weight	437.45 g/mol
Synonyms	Amtolmetin Guacyl; Eufans; Amtolmetine Guacil; [4-Methoxy-2-methyl-1H-indol-3-yl]acetic acid 2-methoxycarbonylphenyl ester; 2-[(4-Methoxy-2-methyl-1H-indol-3-yl)acetoxy]benzoic acid methyl ester; GUA-101; McN-4668; McN4668
EINECS	Contact for details

Quality Control

Our Amtolmetin Guacil is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling via HPLC and other pharmacopeial methods, to ensure it meets high-grade pharmaceutical standards. 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 a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.5%
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.