Description

Fenclorac is a synthetic organic compound belonging to the arylacetic acid class, known for its specific biological activity. This compound is valued in advanced chemical synthesis and research for its role as a key intermediate or active pharmaceutical ingredient (API) precursor. It is primarily required by the pharmaceutical industry for the development of novel therapeutic agents, as well as by research institutions and fine chemical manufacturers engaged in specialized organic synthesis.

Application

• Pharmaceutical intermediate for the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs) and other active pharmaceutical ingredients (APIs).
• Key building block in advanced organic chemistry research and process development.
• Reference standard for analytical method development and quality control in pharmaceutical laboratories.
• Precursor in the development of agrochemicals and other specialty fine chemicals.

Basic Information

Product Name	Fenclorac
CAS No.	36616-54-3
Molecular Formula	C14H10Cl2O2
Molecular Weight	281.14 g/mol
Synonyms	2-[(2,4-Dichlorophenyl)amino]benzoic acid; Fentiazac; Fentiazac (USAN); Fentiazacum; Fentiazac [INN]; Fentiazac [USAN]; Fentiazac (INN); 2-[(2,4-Dichlorophenyl)amino]benzenecarboxylic acid
EINECS	253-124-4

Quality Control

Our Fenclorac is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide Certificates of Analysis (COA) with detailed results for parameters including assay, related substances, and residual solvents, meeting the stringent requirements for pharmaceutical intermediates. Specifications can be aligned with customer-specific pharmacopeial standards (e.g., USP, EP) upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed to prevent moisture absorption, which may affect product stability.

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%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%

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