Therapeutic Uses
Anti-Cancer / Oncology
API Family
Clarithromycin
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
Not less than 90%
Hazard Compound
Yes -Refer MSDS for accurate information
Clarithromycin EP impurity H 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 H usage and description
Clarithromycin EP impurity H is a chemical compound that is used in the pharmaceutical industry as a reference standard for the quality control of clarithromycin, a commonly used antibiotic medication. The impurity is used to ensure that the clarithromycin being produced is of high quality and purity, as impurities can affect the safety and efficacy of the medication.
Chemically, Clarithromycin EP impurity H is known as 6-O-Methylclarithromycin, and it is a derivative of clarithromycin. It is a white to off-white powder with a molecular formula of C38H69NO13 and a molecular weight of 747.95 g/mol.
During the production process of clarithromycin, impurities can be introduced through various means, including synthesis, storage, and handling. Impurities can affect the stability and efficacy of the medication, and may even pose a risk to patient safety. Therefore, strict quality control measures are necessary to ensure the purity and quality of the final product.
In summary, Clarithromycin EP impurity H is a reference standard used in the pharmaceutical industry to ensure the purity and quality of clarithromycin. Its chemical properties and usage play a critical role in maintaining the safety and efficacy of this commonly used antibiotic medication.
