Description

Flutriafol Impurity D is a high-purity chemical reference standard critical for analytical and regulatory purposes. This compound is essential for the quality control and method validation processes in the development and manufacturing of the triazole fungicide Flutriafol. It is primarily required by pharmaceutical and agrochemical research laboratories, as well as quality assurance departments, to ensure product purity, safety, and compliance with stringent international regulations.

Application

• Pharmaceutical Impurity Profiling: Used as a certified reference material for the identification and quantification of impurities in Flutriafol active pharmaceutical ingredients (APIs).
• Agrochemical Quality Control: Serves as a critical standard in HPLC and GC methods to monitor and control the purity of Flutriafol technical material and formulated products.
• Method Development and Validation: Essential for developing, calibrating, and validating analytical methods in compliance with ICH Q2(R1) and other regulatory guidelines.
• Regulatory Submissions: Provides necessary data for impurity identification in regulatory filings to agencies such as the EPA, FDA, and ECHA.
• Stability Studies: Employed as a marker to track degradation products in stability testing of Flutriafol under various storage conditions.
• Academic and Industrial Research: Used in studies investigating the metabolism, environmental fate, and toxicological profile of Flutriafol and related compounds.

Basic Information

Product Name	Flutriafol Impurity D
CAS No.	110933-21-6
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 D; Flutriafol EP Impurity D; Flutriafol USP Impurity D; Flutriafol Metabolite; UNII-8V5Q8F66QN
EINECS	Contact for details

Quality Control

Every batch of Flutriafol Impurity D is manufactured and analyzed under strict quality management systems. Our products undergo rigorous quality testing, including advanced chromatographic techniques, to ensure compliance with pharmacopeial standards such as USP and EP. A comprehensive Certificate of Analysis (COA) is provided with each shipment, detailing purity, identity, and impurity profiles.

Storage

Preserve in a tightly closed container, protected from light. Store at controlled room temperature (15-25°C) in a dry environment. The material is light-sensitive (store away from light).

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%
Residual Solvents (GC)	Complies with ICH Q3C
Water Content (KF)	≤ 0.5% w/w

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