Cefazolin EP Impurity F
| Product Name | Cefazolin EP Impurity F |
|---|---|
| Alternate Names | Cefazolin Impurities, Impurities of Cefazolin |
| CAT No. | CS-O-13459 |
| CAS No. | 21732-17-2 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 128.09 g/mol |
| Mol. For. | C₃H₄N₄O₂ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Cefazolin |
| Purity | >98% |
| Therapeutic | Antibiotics |
| Smileys | C1=NN=NN1CC(=O)O |
| Canonical Smiles | C1=NN=NN1CC(=O)O |
| InchIKey | GRWAIJBHBCCLGS-UHFFFAOYSA-N |
| Inchl | InChI=1S/C3H4N4O2/c8-3(9)1-7-2-4-5-6-7/h2H,1H2,(H,8,9) |
| IUPAC | 2-(tetrazol-1-yl)acetic acid |
| 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 |
Cefazolin EP Impurity F is a chemical compound that is commonly used as a reference standard in pharmaceutical research and development. It is a degradation product of Cefazolin, which is an antibiotic medication that is used to treat various bacterial infections. The impurity is formed when Cefazolin undergoes degradation in the presence of heat and light, and it is important to monitor its levels during the manufacturing process to ensure the purity and quality of the final product.
The chemical name of Cefazolin EP Impurity F is (6R,7R)-7-amino-3-[(1-methyltetrazol-5-yl)thio]methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid. Its molecular formula is C13H13N7O3S2, and its molecular weight is 391.4 g/mol. The compound is a white to off-white crystalline powder that is soluble in water and methanol.
In pharmaceutical research, Cefazolin EP Impurity F is used as a reference standard to identify and quantify impurities in Cefazolin formulations. It is also used in the development of analytical methods for the detection and quantification of impurities in other antibiotics. In addition, the compound is used to study the degradation pathways of Cefazolin and to develop strategies to prevent or minimize degradation during storage and handling.
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Related Compounds
Cefazolin EP Impurity A | Cefazolin EP Impurity L | Cefazolin EP Impurity D sodium salt | Cefazolin EP Impurity I | Cefazolin EP Impurity B | Cefazolin EP Impurity K | Cefazolin EP Impurity J | Cefazolin Related Compound D (Cefazolin open-ring lactone) | Cefazolin EP Impurity G (Triethylamine salt) | Cefazolin EP Impurity C | Cefazolin EP Impurity J disodium salt | Cefazolin EP Impurity C | Cefazolin EP Impurity G | Cefazolin EP Impurity E | Cefazolin EP Impurity H |