Description

n-(4-Fluorophenyl)Anthranilic Acid is a specialized organic compound featuring a fluorinated biphenyl structure linked to an anthranilic acid moiety. This unique molecular architecture makes it a valuable pharmacophore and key synthetic intermediate in advanced organic synthesis. It is primarily required by pharmaceutical R&D and fine chemical manufacturers for developing novel active ingredients and high-value specialty chemicals.

Application

• Pharmaceutical Intermediate: A crucial building block in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules.
• Agrochemical Synthesis: Used in the research and production of advanced herbicides and pesticides, leveraging the fluorine atom for enhanced biological activity.
• Material Science Research: Serves as a precursor for developing specialty polymers, liquid crystals, and organic electronic materials.
• Dye and Pigment Manufacturing: Acts as an intermediate in the synthesis of complex organic dyes and colorants.
• Academic & Industrial R&D: Employed in medicinal chemistry and organic synthesis research for structure-activity relationship (SAR) studies.
• Chemical Reference Standard: Used as a high-purity analytical standard for quality control and regulatory testing in related industries.

Basic Information

Product Name	n-(4-Fluorophenyl)Anthranilic Acid
CAS No.	54-60-4
Molecular Formula	C13H10FNO2
Molecular Weight	231.22 g/mol
Synonyms	2-[(4-Fluorophenyl)amino]benzoic acid; N-(p-Fluorophenyl)anthranilic acid; 4'-Fluoro-2-aminodiphenyl-2'-carboxylic acid; Flufenamic Acid Impurity; 2-Carboxy-4'-fluorodiphenylamine; 4-Fluorodiphenylamine-2-carboxylic acid; N-(4-Fluorophenyl)-2-aminobenzoic acid; Benzoic acid, 2-[(4-fluorophenyl)amino]-
EINECS	200-207-7

Quality Control

Our n-(4-Fluorophenyl)Anthranilic Acid is manufactured under strict quality management systems. Every batch undergoes comprehensive analytical testing, including HPLC, NMR, and IR spectroscopy, to ensure high purity and consistent identity. A detailed Certificate of Analysis (COA) is provided with each shipment, confirming compliance with agreed specifications. We support cGMP and ISO 9001 standards for pharmaceutical and industrial applications.

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 strong oxidizing agents and bases. The container should be kept tightly sealed to minimize exposure to moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥98.0%
Loss on Drying	≤0.5%
Residue on Ignition	≤0.1%
Heavy Metals	≤20 ppm
Related Substances (HPLC)	Total impurities ≤2.0%
Single Unknown Impurity	≤0.5%

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