Cefazolin EP Impurity A
| Product Name | Cefazolin EP Impurity A |
|---|---|
| Alternate Names | Cefazolin Impurities, Impurities of Cefazolin |
| CAT No. | CS-T-03085 |
| CAS No. | 30246-33-4 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 344.43 g/mol |
| Mol. For. | C₁₁H₁₂N₄O₃S₃ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Cefazolin |
| Purity | 95% |
| Therapeutic | Antibiotics |
| Smileys | OC(C(N1[C@@]2([H])[C@H](N)C1=O)=C(CS2)CSC3=NN=C(C)S3)=O |
| Canonical Smiles | CC1=NN=C(S1)SCC2=C(N3C(C(C3=O)N)SC2)C(=O)O |
| InchIKey | HJSGHKMSDOLGJJ-HZGVNTEJSA-N |
| Inchl | InChI=1S/C11H12N4O3S3/c1-4-13-14-11(21-4)20-3-5-2-19-9-6(12)8(16)15(9)7(5)10(17)18/h6,9H,2-3,12H2,1H3,(H,17,18)/t6-,9-/m1/s1 |
| IUPAC | (6R,7R)-7-amino-3-[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanylmethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic 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 A is a chemical substance that is commonly used in the pharmaceutical industry as a reference standard during the development and testing of Cefazolin EP, an antibiotic medication used to treat a wide range of bacterial infections. This impurity is a necessary component to ensure the purity and consistency of the final product, as it is used to identify and quantify any potential impurities or contaminants that may be present.
Chemically, Cefazolin EP Impurity A is known as 7-(D-α-Aminophenylacetamido)-3-methyl-3-cephem-4-carboxylic acid, and it is a derivative of the cephalosporin family of antibiotics. It is a white to off-white powder that is soluble in water and has a molecular weight of 397.44 g/mol.
In terms of usage, Cefazolin EP Impurity A is typically used as a reference material during the development and testing of Cefazolin EP. This impurity is used to verify the identity, purity, and potency of the final product, as well as to ensure that it meets the necessary quality standards for use in the treatment of bacterial infections.
Overall, Cefazolin EP Impurity A is an important component in the development and testing of Cefazolin EP, and it plays a critical role in ensuring the safety and efficacy of this important antibiotic medication.
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Related Compounds
Cefazolin EP Impurity L | Cefazolin EP Impurity F | Cefazolin EP Impurity H | Cefazolin EP Impurity C | Cefazolin EP Impurity G | Cefazolin EP Impurity D sodium salt | Cefazolin Related Compound D (Cefazolin open-ring lactone) | Cefazolin EP Impurity J | Cefazolin EP Impurity I | Cefazolin EP Impurity E | Cefazolin EP Impurity G (Triethylamine salt) | Cefazolin EP Impurity K | Cefazolin EP Impurity B | Cefazolin EP Impurity C | Cefazolin EP Impurity J disodium salt |