Description

n-(4-Trifluoromethoxyphenyl)Anthranilic Acid is a specialized organic compound featuring a trifluoromethoxy-substituted biphenyl core with an anthranilic acid moiety. This structure is significant for its role as a key pharmaceutical intermediate, particularly in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. It is primarily needed by manufacturers in the pharmaceutical, agrochemical, and advanced material research sectors seeking high-purity building blocks for complex synthesis.

Application

• Pharmaceutical Intermediate: A critical precursor in the synthesis of novel NSAIDs (Non-Steroidal Anti-Inflammatory Drugs) and other therapeutic agents.
• Agrochemical Synthesis: Used in the research and development of advanced pesticides and herbicides, leveraging the stability of the trifluoromethoxy group.
• Chemical Research & Development: Serves as a versatile building block in organic synthesis for creating complex fluorinated compounds.
• Material Science: Investigated for incorporation into specialty polymers and advanced organic materials requiring specific thermal and chemical resistance.
• Analytical Reference Standard: Employed as a high-purity standard in quality control laboratories for HPLC, LC-MS, and NMR analysis.

Basic Information

Product Name	n-(4-Trifluoromethoxyphenyl)Anthranilic Acid
CAS No.	51679-41-5
Molecular Formula	C14H10F3NO3
Molecular Weight	297.23 g/mol
Synonyms	2-[[(4-Trifluoromethoxy)phenyl]amino]benzoic acid; N-(4-(Trifluoromethoxy)phenyl)anthranilic acid; 2-Amino-N-[4-(trifluoromethoxy)phenyl]benzoic acid; 4-Trifluoromethoxydiphenylamine-2-carboxylic acid; Flufenamic Acid Impurity; Flufenamic Acid Related Compound; NFLX; Benzoic acid, 2-[[[4-(trifluoromethoxy)phenyl]amino]]-
EINECS	Contact for details

Quality Control

Our n-(4-Trifluoromethoxyphenyl)Anthranilic Acid is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC for purity and identity confirmation via IR and NMR spectroscopy, to ensure it meets the high standards required for pharmaceutical intermediate applications. A comprehensive 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, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept sealed to minimize exposure to atmospheric humidity.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
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.