Clarithromycin EP impurity D
| Product Name | Clarithromycin EP impurity D |
|---|---|
| Alternate Names | Clarithromycin Impurities, Impurities of Clarithromycin |
| CAT No. | CS-T-52214 |
| CAS No. | 101666-68-6 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 733.93 g/mol |
| Mol. For. | C₃₇H₆₇NO₁₃ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Clarithromycin |
| Purity | Not less than 98 % |
| Therapeutic | Anti-Cancer / Oncology |
| Smileys | CCC1C(C(C(C(=O)C(CC(C(C(C(C(C(=O)O1)C)OC2CC(C(C(O2)C)O)(C)OC)C)OC3C(C(CC(O3)C)NC)O)(C)OC)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 |
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.
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Related Compounds
Clarithromycin EP impurity H | Clarithromycin_EDO | Clarithromycin_MEDO | Clarithromycin EP impurity I | Clarithromycin EP impurity G | Clarithromycin EP impurity N | Clarithromycin EP impurity A | Clarithromycin EP impurity P | N-Nitroso-N-Desmethyl-Clarithromycin | Clarithromycin EP impurity L | Clarithromycin EP impurity O | Clarithromycin EP impurity E | Clarithromycin EP impurity M | Clarithromycin-N-methyl-13C-D3 | Clarithromycin_EO | Clarithromycin 9-Oxime | Clarithromycin 2’-O-Acetate | Clarithromycin EP impurity F | Clarithromycin Impurity 4 | Clarithromycin Corresponding impurity of erythromycin E | Clarithromycin EP impurity K | Clarithromycin EP impurity J | Clarithromycin EP impurity C | Clarithromycin EP impurity B |