Guangzhou Dreampharm Biotechnology Co.,Ltd

Edoxaban Impurity Reference Standard

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

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

• Edoxaban EP Impurity A

• Edoxaban EP Impurity B

• Edoxaban EP Impurity C

• Edoxaban USP Related Compounds

• Process-related impurities

• Degradation impurities (hydrolysis, oxidation)

Key Features:

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

• Supplied as solid powder in sealed, light-protective containers

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

• Certificate of Analysis (COA) and characterization data available

Intended Use:

• Identification and quantification of Edoxaban-related impurities

• Analytical method development and validation

• Stability testing and regulatory submission support

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