Therapeutic Uses
Anti-Cancer / Oncology
API Family
Clarithromycin
Storage Condition
Store at freezer (-20°C) for long term storage
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 K 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 K usage and description
Clarithromycin EP impurity K is a chemical compound that is used in the pharmaceutical industry as a reference standard or impurity. It is a derivative of clarithromycin, which is an antibiotic medication used to treat various bacterial infections.
The chemical name of Clarithromycin EP impurity K is (3R,4S,5S,6R)-4-Amino-3,5-dihydroxy-6-methyltetrahydro-2H-pyran-2-one. Its molecular formula is C6H11NO4, and its molecular weight is 161.16 g/mol.
When developing a clarithromycin drug product, it is important to monitor the level of Clarithromycin EP impurity K in the final product. The impurity may arise from the manufacturing process or storage conditions, and may affect the efficacy and safety of the drug product. Therefore, the use of Clarithromycin EP impurity K as a reference standard helps to ensure the quality of the final product.
In addition to its pharmaceutical uses, Clarithromycin EP impurity K has also been used in research studies to investigate the mechanism of action of clarithromycin and its derivatives. Its chemical structure and properties make it a useful tool for understanding the pharmacological properties of clarithromycin and related compounds.
Overall, Clarithromycin EP impurity K plays an important role in the pharmaceutical industry as a reference standard for quality control and in scientific research.
