Therapeutic Uses
Anti-Cancer / Oncology
API Family
Clarithromycin
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Clarithromycin F (EP) ; 2-Demethyl-2-(hydroxymethyl)-6-O-methylerythromycin A
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
Clarithromycin EP impurity A 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.
Clarithromycin EP impurity A usage and description
Clarithromycin EP Impurity A is a chemical compound that is commonly used in pharmaceutical research and development. It is a synthetic impurity that is structurally related to Clarithromycin, which is an antibiotic medication used to treat a variety of bacterial infections. Clarithromycin EP Impurity A is used as a reference standard in analytical testing methods to ensure the purity and quality of Clarithromycin drug products.
The chemical formula of Clarithromycin EP Impurity A is C44H72N2O14, and it has a molecular weight of 853.04 g/mol. It is a white to off-white powder that is soluble in water and organic solvents. The compound is stable under normal conditions, and it does not pose any significant health hazards or environmental risks.
Clarithromycin EP Impurity A is typically synthesized by chemical reactions that involve the use of various reagents and catalysts. The purity of the compound is determined by high-performance liquid chromatography (HPLC) or other analytical techniques.
In summary, Clarithromycin EP Impurity A is a synthetic impurity that is used as a reference standard in pharmaceutical research and development. It is a stable and non-hazardous compound that plays a critical role in ensuring the quality and safety of Clarithromycin drug products.
