Guangzhou Dreampharm Biotechnology Co.,Ltd

Clopidogrel Impurity Reference Standard

This product is a high-purity impurity reference standard related to Clopidogrel, intended strictly for pharmaceutical research, analytical testing, impurity profiling, method development, validation, and quality control. It is not for clinical, therapeutic, or human use.

Typical Impurity Types (examples include but are not limited to):

• Clopidogrel EP Impurity A

• Clopidogrel EP Impurity B

• Clopidogrel EP Impurity C

• Clopidogrel USP Related Compounds

• Clopidogrel Hydrolysis / Oxidation Impurities

• Other structurally related impurities of Clopidogrel

Key Features:

• High-purity impurity reference standard (typically ≥95–98% by HPLC)

• Supplied as solid powder in sealed, light-protective glass vials

• Suitable for impurity profiling using HPLC, LC-MS, and related analytical techniques

• Certificate of Analysis (COA) and characterization data available

Intended Use:

• Identification and quantification of Clopidogrel-related impurities

• Analytical method development and validation

• Stability studies and regulatory submission support

Storage:
Store at 2–8 °C, protected from light and moisture. Reseal immediately after use.