Therapeutic Uses
Anti-Cancer / Oncology
API Family
Clarithromycin
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Clarithromycin EP Impurity I, 118058-74-5
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 I 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 I usage and description
Clarithromycin EP Impurity I is a chemical substance that is used in the pharmaceutical industry as a reference standard and quality control agent for the analysis of Clarithromycin, a commonly prescribed antibiotic drug. The impurity is a byproduct of the manufacturing process of Clarithromycin and is present in small quantities in the final product.
The chemical name for Clarithromycin EP Impurity I is 6-O-Methylerythromycin A. It is a macrolide antibiotic that belongs to the group of erythromycin derivatives. The molecular formula of the impurity is C38H68N2O13, and its molecular weight is 760.95 g/mol. The impurity is a white to off-white powder that is soluble in water and methanol.
The usage of Clarithromycin EP Impurity I is essential in the evaluation of the quality and purity of Clarithromycin. The impurity is used as a reference standard for the identification and quantification of impurities in Clarithromycin samples. It is also used to validate the analytical methods used for the analysis of Clarithromycin.
In conclusion, Clarithromycin EP Impurity I is an essential chemical substance used in the pharmaceutical industry for the analysis and quality control of Clarithromycin. Its chemical properties and usage make it an essential reference standard for the identification and quantification of impurities in Clarithromycin samples.
