Description

Capsaicin Impurity CAS NO 179617-58-4 is a high-purity reference standard used for analytical and research purposes. This compound is critical for ensuring the quality, safety, and regulatory compliance of capsaicin and related capsaicinoid products. It is primarily required by pharmaceutical R&D laboratories, analytical testing facilities, and manufacturers of active pharmaceutical ingredients (APIs) for method development, validation, and impurity profiling.

Application

• Pharmaceutical Impurity Profiling: Serves as a certified reference material for the identification and quantification of specific impurities in capsaicin API batches.
• Analytical Method Development & Validation: Used as a critical standard to develop, calibrate, and validate HPLC, UPLC, and GC analytical methods.
• Quality Control & Assurance (QC/QA): Essential for in-house quality control laboratories to monitor impurity levels and ensure batch-to-batch consistency.
• Regulatory Compliance & Documentation: Supports regulatory filings (e.g., for FDA, EMA) by providing characterized impurity data for drug master files (DMFs).
• Research & Development: Used in metabolic, stability, and degradation studies to understand the chemical behavior of capsaicin-based formulations.
• Contract Research Organizations (CROs): Employed as a key reagent in outsourced analytical testing and impurity isolation services.

Basic Information

Product Name	Capsaicin Impurity
CAS No.	179617-58-4
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Capsaicin Related Compound; Capsaicin Impurity Standard; Capsaicinoid Impurity; (E)-N-[(4-Hydroxy-3-methoxyphenyl)methyl]-8-methylnon-6-enamide (related compound); 179617-58-4; Capsaicin Analog; Capsaicin Process Impurity; Reference Standard for Capsaicin
EINECS	Contact for details

Quality Control

Our Capsaicin Impurity standard is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical characterization using advanced techniques such as HPLC, GC-MS, and NMR to confirm identity and purity. A detailed Certificate of Analysis (COA) is provided with each shipment, containing batch-specific data on purity, impurities, and analytical results. We support compliance with ICH guidelines for impurity qualification.

Storage

Preserve in a tightly closed container, protected from light. Store at controlled room temperature (15-25°C) in a dry environment. For long-term stability, consider storage at 2-8°C. Keep the container sealed to prevent moisture absorption and contamination.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (HPLC)	Conforms to reference standard
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 95.0%
Related Substances (HPLC)	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.