Description

[4-(3-Fluoro-4-Methylphenyl)Phenyl]Acetic Acid is a high-purity, non-steroidal anti-inflammatory drug (NSAID) intermediate and a versatile building block in advanced organic synthesis. Its value lies in its precise molecular structure, which is critical for the development of novel pharmaceutical compounds targeting inflammation and pain. This compound is essential for research and development chemists, process scale-up scientists, and manufacturers in the pharmaceutical and fine chemical industries who require reliable, high-quality intermediates for API production.

Application

• Pharmaceutical Intermediate: A key precursor in the synthesis of next-generation non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules.
• Active Pharmaceutical Ingredient (API) Development: Serves as a core building block for constructing complex molecular architectures in medicinal chemistry research.
• Biochemical Research: Used in proteomics and enzyme inhibition studies to investigate inflammatory pathways.
• Material Science: Potential monomer or additive for creating specialized polymers with unique properties.
• Agrochemical Synthesis: Intermediate for developing advanced crop protection agents with enhanced efficacy.
• Reference Standard: Serves as an analytical standard for quality control and regulatory compliance in pharmaceutical manufacturing.

Basic Information

Product Name	[4-(3-Fluoro-4-Methylphenyl)Phenyl]Acetic Acid
CAS No.	1365272-72-5
Molecular Formula	C15H13FO2
Molecular Weight	244.26 g/mol
Synonyms	2-[4-(3-Fluoro-4-methylphenyl)phenyl]acetic acid; (4'-{3-Fluoro-4-methylphenyl}phenyl)acetic acid; 4-(3-Fluoro-4-methylphenyl)benzeneacetic acid; 2-(4-(3-Fluoro-4-methylphenyl)phenyl)acetic acid; FMPPA; Fluoro-methyl-biphenyl acetic acid; CAS 1365272-72-5
EINECS	Contact for details

Quality Control

Our [4-(3-Fluoro-4-Methylphenyl)Phenyl]Acetic Acid is manufactured under strict quality management systems. Every batch undergoes rigorous analytical testing, including HPLC, NMR, and mass spectrometry, to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing all critical specifications. Our quality commitment supports compliance with cGMP and ICH guidelines 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, sparks, and open flame. For long-term storage, consider an inert atmosphere to maintain optimal stability.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Any single impurity	≤ 0.5%
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.