Product Name |
Azithromycin N-Oxide |
Alternate Names |
Azithromycin Impurities, Impurities of Azithromycin |
CAT No. |
CS-O-07326
|
CAS No. |
90503-06-3 |
Category |
Impurities |
Stock |
IN-Stock
|
Mol. Wt. |
764.98 g/mol |
Mol. For. |
C₃₈H₇₂N₂O₁₃
|
Hazardous |
This is a Hazardous Compound
|
COA |
View Sample COA
|
MSDS |
View Sample MSDS
|
Parent API |
Azithromycin |
Purity |
Not less than 95 % |
Therapeutic |
Antibiotics |
Smileys |
CCC1C(C(C(N(CC(CC(C(C(C(C(C(=O)O1)C)OC2CC(C(C(O2)C)O)(C)OC)C)OC3C(C(CC(O3)C)[N+](C)(C)[O-])O)(C)O)C)C)C)O)(C)O |
Controlled |
No |
Shipping |
Free for purchase above 1000$ |
Delivery |
In-Stock, products will be dispatched within 24 hours via FedEx for USA, Europe, and other countries. |
Return |
Returns/replacement accepted if you are not satisfied with the quality of the product, (please send us an email with the reason/issues which are facing, within 15 days, after receipt of the product). |
Ordering |
Place your order online or by email sales@clearsynth.com |
If you find a better price anywhere else we guarantee Price match.
What is the usage and chemical information of Azithromycin N-Oxide ?
Azithromycin EP Impurity L is a chemical compound that is commonly used as a reference standard for the analysis of azithromycin. Azithromycin is a macrolide antibiotic that is used to treat a variety of bacterial infections. This impurity is often used in the quality control and testing of azithromycin pharmaceuticals to ensure that they meet the necessary purity requirements.
The chemical formula of Azithromycin EP Impurity L is C38H72N2O12. It is a white crystalline powder with a molecular weight of 760.98 g/mol. This impurity is a by-product of the azithromycin synthesis process, and it is typically present in small quantities in azithromycin products.
Azithromycin EP Impurity L is classified as a macrolide antibiotic, which means that it works by inhibiting bacterial protein synthesis. It does this by binding to the 50S ribosomal subunit of the bacterial cell, which prevents the translation of mRNA into protein. This ultimately leads to the death of the bacterial cell.
In conclusion, Azithromycin EP Impurity L is an important reference standard used in the testing and quality control of azithromycin pharmaceuticals. It is a by-product of the azithromycin synthesis process and is classified as a macrolide antibiotic. Its chemical formula is C38H72N2O12, and it works by inhibiting bacterial protein synthesis.