Therapeutic Uses
Anti-Asthma / COPD
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
4-(1-hydroxy-2-((2-hydroxy-4-(1-hydroxy-2-((6-(4-phenylbutoxy)hexyl) amino)ethyl)benzyl)(6-(4-phenylbutoxy)hexyl)amino)ethyl)-2-(hydroxymethyl)phenol
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
Not less than 90%
Hazard Compound
No -Refer MSDS for accurate information
Salmeterol Dimer Impurity is a drug product that is used as an analytical standard for HPLC, as well as in research and development of drugs.
Refund Policy
We are committed to offering products of the highest quality in order to meet the needs of our customers, and have elaborate systems in
place to ensure that material specifications, their certification and all handling and storage conditions are communicated at the time of
material handover.
We have invested in the highest quality packaging materials and use international logistics partners to service our customers. While all
possible precautions have been taken to deliver the required product(s), there may be some rare situations when our product does not
meet your requirements. Should that arise, please contact us with your concerns and we will endeavour to address them on a priority
basis. If there is no other option, we will either replace your product(s) or issue a refund or account credit, whichever you prefer.
If there is an issue with one or more of our products, our policy is that it must be reported to us within 45 days of your receiving shipment.
While we will always address product issues after the 45 day return window has passed, we cannot issue a refund or account credit. As
always, we appreciate your support.
Salmeterol Dimer Impurity usage and description
Salmeterol EP Impurity G is a chemical compound that is primarily used in the pharmaceutical industry as a reference standard or impurity marker for the analysis of Salmeterol, which is a long-acting beta-agonist medication used in the treatment of asthma and chronic obstructive pulmonary disease (COPD).
Chemically, Salmeterol EP Impurity G is a derivative of Salmeterol and has a molecular formula of C26H32N2O4. It is a white to off-white powder that is sparingly soluble in water but soluble in organic solvents such as methanol and dichloromethane.
In terms of usage, Salmeterol EP Impurity G is commonly used as a reference standard or impurity marker in the development and validation of analytical methods for the determination of Salmeterol in pharmaceutical formulations. It is also used in quality control and batch release testing for Salmeterol-containing products such as inhalers and nebulizers.
Overall, Salmeterol EP Impurity G plays an important role in ensuring the safety, efficacy, and quality of Salmeterol-containing medications. Its availability as a reference standard or impurity marker allows for accurate and reliable analysis of Salmeterol, which is crucial in the development and manufacturing of pharmaceutical products.
