Description

A-796260 Degradant is a high-purity chemical reference standard used for analytical and research purposes. This compound is critical for pharmaceutical development, specifically in the study of drug stability, impurity profiling, and method validation. It is primarily utilized by research scientists and quality control laboratories in the pharmaceutical, biotechnology, and contract research organization (CRO) sectors.

Application

• Pharmaceutical Impurity Profiling: Serves as a certified reference material for the identification and quantification of degradation products in active pharmaceutical ingredients (APIs).
• Analytical Method Development: Used as a standard to develop and validate stability-indicating HPLC, UPLC, or LC-MS methods.
• Forced Degradation Studies: Employed in stress testing to understand the degradation pathways of parent drug compounds under various conditions.
• Quality Control & Assurance: Acts as a system suitability standard and for routine quality control testing to ensure batch-to-batch consistency and regulatory compliance.
• Regulatory Submissions: Provides essential data for drug master files (DMFs), investigational new drug (IND) applications, and new drug applications (NDAs).
• Academic & Industrial Research: Supports fundamental research in medicinal chemistry, pharmacokinetics, and metabolic studies.

Basic Information

Product Name	A-796260 Degradant
CAS No.	1616469-10-3
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	A-796260 Related Compound; A-796260 Impurity; Degradant of A-796260; A796260 Degradant; CAS 1616469-10-3; (Chemical name to be confirmed); (IUPAC name to be confirmed)
EINECS	Contact for details

Quality Control

Every batch of A-796260 Degradant is manufactured and controlled under a strict quality management system. Our products undergo rigorous analytical testing, including chromatographic purity and identity confirmation, to ensure compliance with industry standards for reference materials. A comprehensive Certificate of Analysis (COA) detailing purity, assay, and impurity levels is provided with each shipment and is available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store at controlled room temperature (15-25°C) or as specified on the certificate of analysis. Keep the container in a dry, well-ventilated place. Handle and store in accordance with good laboratory practices.

Specification

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

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