Description

Flutriafol Impurity A is a key chemical reference standard used for the analytical profiling and quality control of the fungicide Flutriafol. This compound is critical for ensuring the purity and safety of the active pharmaceutical ingredient (API) and agrochemical formulations. It is primarily utilized by analytical laboratories, regulatory bodies, and manufacturers in the pharmaceutical and agrochemical industries for method development, validation, and compliance testing.

Application

• Pharmaceutical Impurity Profiling: Serves as a certified reference material for the identification and quantification of impurities in Flutriafol API batches.
• Agrochemical Quality Control: Essential for ensuring the purity and efficacy of commercial Flutriafol-based fungicide products.
• Method Development & Validation: Used as a standard in HPLC, GC, and LC-MS methods to establish analytical procedures for regulatory submissions.
• Regulatory Compliance & Testing: Supports compliance with ICH guidelines (Q3A, Q3B) and other global regulatory standards for impurity control.
• Research & Development: Aids in the study of degradation pathways and stability testing of Flutriafol.
• Calibration Standard: Used to calibrate analytical instruments for accurate impurity detection in complex matrices.

Basic Information

Product Name	Flutriafol Impurity A
CAS No.	124774-27-2
Molecular Formula	C16H13F2N3O
Molecular Weight	301.29 g/mol
Synonyms	(2RS)-1-(2-Fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol; α-(2-Fluorophenyl)-α-(4-fluorophenyl)-1H-1,2,4-triazole-1-ethanol; Flutriafol Related Compound A; Flutriafol EP Impurity A; Flutriafol USP Impurity A; Flutriafol Metabolite; 1H-1,2,4-Triazole-1-ethanol, α-(2-fluorophenyl)-α-(4-fluorophenyl)-
EINECS	Contact for details

Quality Control

Our Flutriafol Impurity A is manufactured under strict quality control protocols to ensure high purity and batch-to-batch consistency suitable for analytical applications. Each batch is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We support compliance with ICH, USP, and EP guidelines, and specifications can be tailored to meet specific pharmacopeial or internal standards.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a desiccated environment to maintain stability and purity.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Individual impurity: ≤ 0.5% Total impurities: ≤ 2.0%
Water Content (KF)	≤ 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.