Description

Azoxystrobin Impurity 2 is a high-purity chemical reference standard used for analytical and research purposes. This compound is critical for ensuring the quality, safety, and regulatory compliance of the active pharmaceutical ingredient (API) Azoxystrobin. It is primarily required by pharmaceutical manufacturers and agrochemical research laboratories for method development, validation, and impurity profiling studies.

Application

• Pharmaceutical Impurity Profiling: Serves as a certified reference material for the identification and quantification of impurities in Azoxystrobin API batches.
• Analytical Method Development: Used as a standard to develop and validate HPLC, GC, or LC-MS methods for quality control laboratories.
• Regulatory Compliance & Documentation: Essential for preparing regulatory submission documents (e.g., for FDA, EMA) that require detailed impurity characterization.
• Stability Studies: Employed in forced degradation and shelf-life studies to monitor impurity formation over time.
• Chemical Research: Used as a building block or intermediate in synthetic chemistry research related to strobilurin fungicides.
• Quality Assurance/Quality Control (QA/QC): Provides a benchmark for in-house testing to ensure batch-to-batch consistency and purity of commercial Azoxystrobin.

Basic Information

Item	Details
Product Name	Azoxystrobin Impurity 2
CAS No.	2184107-36-4
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Azoxystrobin Related Compound 2; Azoxystrobin Specified Impurity 2; Azoxystrobin Process Impurity; Methyl (2E)-2-{2-[6-(2-cyanophenoxy)pyrimidin-4-yloxy]phenyl}-3-methoxyacrylate (Impurity of Azoxystrobin); Strobilurin Impurity; (E)-Methyl 2-(2-((6-(2-cyanophenoxy)pyrimidin-4-yl)oxy)phenyl)-3-methoxyacrylate
EINECS	Contact for details

Quality Control

Every batch of Azoxystrobin Impurity 2 is manufactured and analyzed under strict quality management systems. We provide comprehensive analytical data including HPLC purity, residual solvent analysis, and identity confirmation (IR, NMR, MS). A detailed Certificate of Analysis (COA) is supplied with each product, ensuring traceability and compliance with relevant pharmacopeial guidelines for reference standards.

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 and should be handled under appropriate conditions to maintain stability.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 95.0%
Related Substances (HPLC)	Individual unknown impurity ≤ 1.0% Total impurities ≤ 5.0%
Residual Solvents (GC)	Complies with ICH guidelines

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