Therapeutic Uses
Anti-Cancer / Oncology
API Family
Clarithromycin
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
N-Desmethyl Clarithromycin ; Clarithromycin Impurity D
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
Not less than 98 %
Hazard Compound
No -Refer MSDS for accurate information
Clarithromycin EP Impurity D 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 D usage and description
Clarithromycin is a type of antibiotic that is commonly used in the treatment of bacterial infections. It belongs to the macrolide class of antibiotics and works by inhibiting the growth of bacteria. However, during the manufacturing process of Clarithromycin, impurities may be formed. One such impurity is Clarithromycin EP impurity D.
Clarithromycin EP impurity D is a degradation product of Clarithromycin that may form during the storage or transportation of the drug. It is important to monitor the levels of this impurity in Clarithromycin formulations, as it may affect the potency and safety of the drug.
From a chemical standpoint, Clarithromycin EP impurity D is a compound with the molecular formula C43H71NO14. It is a derivative of Clarithromycin and contains a lactone ring structure. The impurity can be identified and quantified using analytical techniques such as high-performance liquid chromatography (HPLC).
In terms of usage, Clarithromycin EP impurity D is not intended for use in humans. Instead, it is used as a reference standard for analytical purposes. Pharmaceutical companies may use this impurity as a benchmark to ensure the quality and purity of their Clarithromycin formulations.
In conclusion, Clarithromycin EP impurity D is an impurity that can form during the manufacturing, storage or transportation of Clarithromycin. Although it is not intended for human use, it is important to monitor its levels in Clarithromycin formulations to ensure the safety and efficacy of the drug.
