Therapeutic Uses
Anti-Cancer / Oncology
API Family
Clarithromycin
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
(10E)-10,11-Didehydro-11-deoxy-6-O-methylerythromycinA;Oxacyclotetradecane,Erythromycin Derivative
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
Not less than 95%
Hazard Compound
Yes -Refer MSDS for accurate information
Clarithromycin EP Impurity N 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 N usage and description
Clarithromycin EP impurity N is a chemical compound that is commonly used in the pharmaceutical industry as a reference standard for the identification and quantification of impurities in Clarithromycin, which is a semi-synthetic macrolide antibiotic used to treat various bacterial infections. It is also known as 6-O-Methylerythromycin A and has a molecular formula of C41H68N2O14.
Clarithromycin EP impurity N is a white to off-white crystalline powder that is sparingly soluble in water but soluble in most organic solvents. It is a derivative of erythromycin and differs from Clarithromycin by the presence of a methyl group attached to the 6-position of the erythronolide ring.
The usage of Clarithromycin EP impurity N is mainly in the development and validation of analytical methods for the quantification of impurities in Clarithromycin. It is also used for the characterization of Clarithromycin and its related substances in quality control during the manufacturing process.
Chemically, Clarithromycin EP impurity N is classified as a macrolide antibiotic and its structure contains a large lactone ring with several functional groups attached. Its purity is typically measured using high-performance liquid chromatography (HPLC) and is required to be above 98% for use as a reference standard.
Overall, Clarithromycin EP impurity N is an important reference standard that plays a vital role in ensuring the quality and safety of Clarithromycin-based medications.
