Therapeutic Uses
Anti-Cancer / Oncology
API Family
Clarithromycin
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Clarithromycin (9E)-O-Methyloxime
Application Notes
Useful research chemical for a range of applications
Hazard Compound
No -Refer MSDS for accurate information
Clarithromycin EP impurity G 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 G usage and description
Clarithromycin EP impurity G, also known as 14-hydroxy-6-O-methylerythromycin A, is a chemical compound that is commonly used as a reference standard in the pharmaceutical industry. It is an impurity that is found in Clarithromycin, which is a macrolide antibiotic that is used to treat a wide range of bacterial infections.
Clarithromycin EP impurity G is used to identify and quantify the impurity in Clarithromycin drugs during quality control testing. It is important to monitor the levels of impurities in pharmaceuticals because they can affect the safety and efficacy of the drug.
The chemical formula of Clarithromycin EP impurity G is C40H68N2O14, and it has a molecular weight of 812.98 g/mol. It is a white to off-white powder that is soluble in water and has a melting point of 173-175°C.
Clarithromycin EP impurity G is synthesized by the methylation of 14-hydroxyerythromycin A using diazomethane. It is a semi-synthetic compound that is structurally related to erythromycin A.
In conclusion, Clarithromycin EP impurity G is an important reference standard that is used to ensure the quality and safety of Clarithromycin drugs. Its usage and chemical information are critical for the pharmaceutical industry to produce safe and effective drugs for patients.
