Description

Chloroxylenol Related Compound A (25 Mg) (2-Chloro-3,5-Dimethylphenol) is a high-purity analytical reference standard, essential for quality control and research. This compound is critical for ensuring the purity, safety, and efficacy of pharmaceutical and disinfectant products where chloroxylenol is a key active ingredient. It is primarily needed by analytical laboratories, pharmaceutical manufacturers, and regulatory bodies for precise identification and quantification in method development and validation.

Application

• Pharmaceutical Impurity Profiling: Serves as a certified reference material for the identification and quantification of related substances in Chloroxylenol API and finished drug products.
• Analytical Method Development: Used as a primary standard in HPLC, GC, and other chromatographic techniques to develop and validate quality control assays.
• Disinfectant & Antiseptic Formulation Analysis: Critical for testing the purity and stability of active ingredients in commercial disinfectants, antiseptic soaps, and wound care solutions.
• Regulatory Compliance & Pharmacopoeial Testing: Essential for meeting the testing requirements of USP, EP, BP, and other international pharmacopoeias for chloroxylenol-based products.
• Research & Development: Used in stability studies, degradation pathway elucidation, and metabolic research involving phenolic antiseptics.
• Quality Assurance/Quality Control (QA/QC): Provides a benchmark for in-house quality control laboratories to ensure batch-to-batch consistency and product safety.

Basic Information

Product Name	Chloroxylenol Related Compound A (2-Chloro-3,5-Dimethylphenol)
CAS No.	5538-41-0
Molecular Formula	C8H9ClO
Molecular Weight	156.61 g/mol
Synonyms	2-Chloro-3,5-dimethylphenol; 3,5-Dimethyl-2-chlorophenol; 2-Chloro-3,5-xylenol; Chloroxylenol Impurity A; PCMX Related Compound A; 2-Chloro-3,5-dimethylhydroxybenzene
EINECS	226-885-4

Quality Control

This high-purity reference standard is manufactured under strict quality control conditions. Each batch is characterized using advanced analytical techniques including NMR, Mass Spectrometry, and HPLC to confirm identity and purity. Certificates of Analysis (COA) are provided, detailing batch-specific results for all critical parameters. Our quality system is designed to support compliance with GMP/GLP principles for use in regulated laboratories.

Storage

Preserve in a tightly closed container, protected from light. Store at controlled room temperature (15-25°C) in a dry, well-ventilated area. Keep away from strong oxidizing agents.

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 individual impurity ≤ 1.0%
Residual Solvents (GC)	Complies with ICH guidelines
Loss on Drying	≤ 0.5%

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