Description

Eltenac CAS NO 72895-88-6 is a non-steroidal anti-inflammatory drug (NSAID) compound belonging to the fenamate class. This active pharmaceutical ingredient (API) is valued for its potent anti-inflammatory, analgesic, and antipyretic properties, making it a critical intermediate in pharmaceutical synthesis. It is primarily required by manufacturers in the pharmaceutical industry for the development and production of prescription and veterinary medications targeting pain and inflammation.

Application

• Pharmaceutical API Synthesis: Primary use as an active ingredient in the manufacture of finished dosage forms such as tablets, capsules, and topical formulations.
• Anti-inflammatory Medications: Core component in drugs designed to treat conditions like arthritis, musculoskeletal pain, and post-operative inflammation.
• Analgesic Drug Production: Used in the development of prescription pain relief medications.
• Veterinary Pharmaceutical Applications: Incorporated into anti-inflammatory treatments for animals.
• Research & Development: Serves as a key reference standard and building block in medicinal chemistry research for new NSAID derivatives.
• Specialty Chemical Intermediate: Utilized in fine chemical synthesis for creating more complex pharmaceutical molecules.

Basic Information

Product Name	Eltenac
CAS No.	72895-88-6
Molecular Formula	C17H14ClNO2
Molecular Weight	299.75 g/mol
Synonyms	Eltenac; 2-[(2,6-Dichlorophenyl)amino]benzeneacetic acid; 2-[(2,6-Dichlorophenyl)amino]benzenacetic acid; Eltenac (USAN); UNII-7Q2K5R5N5B; 7Q2K5R5N5B; CCG-39161; Benzeneacetic acid, 2-[(2,6-dichlorophenyl)amino]-; NSC-758452
EINECS	Contact for details

Quality Control

Our Eltenac is manufactured under strict quality management systems to ensure it meets the high-purity standards required for pharmaceutical use. Each batch undergoes comprehensive analytical testing, including identification, assay, and impurity profile analysis via HPLC and other pharmacopeial methods. A Certificate of Analysis (COA) documenting all test results is provided to guarantee traceability and compliance with cGMP guidelines.

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 to protect from moisture.

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% - 102.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Heavy Metals	≤ 20 ppm
Loss on Drying	≤ 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.