Description

Dexindoprofen CAS NO 53086-13-8 is a high-purity, non-steroidal anti-inflammatory drug (NSAID) compound belonging to the arylpropionic acid derivative class. It serves as a critical active pharmaceutical ingredient (API) and a key intermediate in the synthesis of advanced therapeutic agents. This compound is essential for pharmaceutical manufacturers and research institutions focused on developing and producing analgesic and anti-inflammatory medications. Its consistent quality and reliable supply are paramount for ensuring the efficacy and safety of the final pharmaceutical products.

Application

• Pharmaceutical API Synthesis: Primary use as the active pharmaceutical ingredient in the formulation of prescription and over-the-counter (OTC) analgesic and anti-inflammatory drugs.
• Research & Development: A vital reference standard and building block in medicinal chemistry for developing new NSAID derivatives with improved efficacy and safety profiles.
• Preclinical Studies: Used in pharmacological and toxicological research to investigate mechanisms of action, pharmacokinetics, and therapeutic potential.
• Analytical Standard: Serves as a high-purity certified reference material (CRM) for quality control testing, method validation, and regulatory compliance in pharmaceutical analysis.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for the production of generic and proprietary pharmaceutical formulations.

Basic Information

Item	Details
Product Name	Dexindoprofen
CAS No.	53086-13-8
Molecular Formula	C18H17FO2
Molecular Weight	284.33 g/mol
Synonyms	Dexindoprofen; Dexindoprofenum; (+)-2-(4-Isobutylphenyl)propionic acid derivative; (S)-2-(3-Fluoro-4-phenylphenyl)propanoic acid; (2S)-2-[3-Fluoro-4-(phenyl)phenyl]propanoic acid; Dexindoprofen (API); S-Dexindoprofen
EINECS	Contact for details

Quality Control

Our Dexindoprofen is manufactured under strict quality management systems to ensure it meets the stringent requirements of the pharmaceutical industry. Every batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling via advanced techniques like HPLC and GC. A Certificate of Analysis (COA) is provided with each shipment, detailing all test results against predefined specifications. We support compliance with major pharmacopoeial standards (USP, EP) and regulatory frameworks such as GMP, ICH Q7, and REACH.

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. Store away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference standard
Identification (HPLC)	Retention time matches reference
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.0% Any single impurity ≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C
Heavy Metals	≤ 20 ppm
Loss on Drying	≤ 0.5%
Specific Rotation	Contact for details

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