Description

Eugenol Impurity 25 is a high-purity chemical reference standard used for analytical and research purposes. This compound is critical for the quality control and regulatory compliance of products containing eugenol, a widely used flavor and fragrance agent. It is primarily required by analytical laboratories and quality assurance departments in the pharmaceutical, flavor & fragrance, and food ingredient industries to ensure product purity and safety.

Application

• Pharmaceutical Impurity Profiling: Used as a certified reference material (CRM) for the identification and quantification of impurities in eugenol-based active pharmaceutical ingredients (APIs) and finished drug products.
• Analytical Method Development & Validation: Serves as a critical standard for developing, calibrating, and validating HPLC, GC, and GC-MS methods in quality control laboratories.
• Flavor and Fragrance Quality Assurance: Essential for monitoring and controlling impurity levels in synthetic eugenol, a key component in perfumes, cosmetics, and food flavorings.
• Regulatory Compliance & Documentation: Supports compliance with stringent guidelines from pharmacopoeias (USP, EP) and regulatory bodies (FDA, ICH) by providing a traceable impurity standard.
• Research & Development: Utilized in stability studies and degradation pathway research for eugenol and related compounds.

Basic Information

Product Name	Eugenol Impurity 25
CAS No.	115234-25-8
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Eugenol Related Compound 25; Eugenol EP Impurity 25; Eugenol USP Impurity 25; 115234-25-8; Eugenol Specified Impurity 25; Eugenol Degradation Product; Eugenol Process Impurity
EINECS	Contact for details

Quality Control

Every batch of Eugenol Impurity 25 is manufactured and analyzed under strict quality management systems. Our products undergo rigorous identity, purity, and strength testing to ensure they meet the high standards required for reference materials. A comprehensive Certificate of Analysis (COA) is provided with each shipment, detailing the results of all analytical tests. We support compliance with USP, EP, and ICH guidelines.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Keep the container tightly sealed in a dry environment to maintain stability.

Specification

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

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