Guangzhou Dreampharm Biotechnology Co.,Ltd

Salmeterol Impurity Reference Standard

This product is a high-purity impurity reference standard related to Salmeterol, 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):

• Salmeterol EP Impurity A

• Salmeterol EP Impurity B

• Salmeterol EP Impurity C

• Salmeterol USP Related Compounds

• Other structurally related impurities of Salmeterol

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 Salmeterol-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.