Description

Dasatinib Impurity 29 CAS NO 1417651-54-7 is a high-purity chemical reference standard used for analytical and research purposes. This compound is critical for pharmaceutical quality control, enabling the accurate identification and quantification of process-related impurities in Dasatinib drug substance and finished products. It is an essential tool for analytical chemists and quality assurance professionals in the pharmaceutical and biotechnology industries, supporting regulatory compliance and ensuring drug safety and efficacy.

Application

• Primary use as a certified reference standard for analytical method development and validation.
• Identification and quantification of impurities in Dasatinib Active Pharmaceutical Ingredient (API) during stability studies and release testing.
• Critical component in pharmaceutical quality control (QC) and quality assurance (QA) laboratories.
• Used in regulatory submissions (e.g., for FDA, EMA) to establish impurity profiles.
• Supporting research and development (R&D) for process chemistry optimization and impurity fate studies.
• Calibration standard for advanced analytical instrumentation such as HPLC, UPLC, and LC-MS.

Basic Information

Product Name	Dasatinib Impurity 29
CAS No.	1417651-54-7
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Dasatinib Related Compound 29; Dasatinib EP Impurity 29; Dasatinib USP Impurity 29; Dasatinib Process Impurity 29; BMS-354825 Impurity 29; Sprycel Impurity 29; N-(2-Chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1-piperazinyl]-2-methyl-4-pyrimidinyl]amino]-5-thiazolecarboxamide Impurity
EINECS	Contact for details

Quality Control

Every batch of Dasatinib Impurity 29 is manufactured and tested under strict quality management systems. Our products undergo rigorous analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and traceability. A comprehensive Certificate of Analysis (COA) is provided with each shipment, detailing batch-specific results. We support compliance with ICH Q3A/B guidelines and other relevant pharmacopeial standards (USP, EP).

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept in a desiccated environment to maintain stability and purity. Handle under an inert atmosphere if necessary for long-term storage.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (HPLC)	Conforms
Identification (MS)	Conforms
Purity (HPLC)	≥ 95.0%
Water Content (KF)	≤ 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.