Cefazolin EP Impurity E
| Product Name | Cefazolin EP Impurity E |
|---|---|
| Alternate Names | Cefazolin Impurities, Impurities of Cefazolin |
| CAT No. | CS-T-35187 |
| CAS No. | 29490-19-5 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 132.21 g/mol |
| Mol. For. | C3H4N2S2 |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Cefazolin |
| Therapeutic | Antibiotics |
| Smileys | CC(S1)=NNC1=S |
| Canonical Smiles | C1COCCOCCOCCO1 |
| InchIKey | XQQZRZQVBFHBHL-UHFFFAOYSA-N |
| Inchl | InChI=1S/C8H16O4/c1-2-10-5-6-12-8-7-11-4-3-9-1/h1-8H2 |
| IUPAC | 1,4,7,10-tetraoxacyclododecane |
| 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 E is a chemical compound that is used as a reference standard for the detection and quantification of impurities in pharmaceutical products. Cefazolin is a broad-spectrum antibiotic that is commonly used to treat bacterial infections, and Impurity E is a byproduct that can be formed during the manufacturing process.
Chemically, Cefazolin EP Impurity E is known as N-formylglycine, and its molecular formula is C3H5NO3. It is a white crystalline powder that is soluble in water and has a melting point of 181-183°C.
In pharmaceutical analysis, Cefazolin EP Impurity E is typically used as a reference standard in chromatography methods, such as high-performance liquid chromatography (HPLC). By comparing the retention time and peak area of Impurity E in a sample to those of the reference standard, analysts can determine the level of impurities in the sample.
It is important to note that the presence of Impurity E in pharmaceutical products can indicate potential quality issues, as it may affect the efficacy and safety of the medication. Therefore, accurate and reliable detection and quantification of Impurity E is critical in ensuring the quality of pharmaceutical products.
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Related Compounds
Cefazolin EP Impurity C | Cefazolin EP Impurity H | Cefazolin EP Impurity C | Cefazolin EP Impurity B | Cefazolin EP Impurity G (Triethylamine salt) | Cefazolin Related Compound D (Cefazolin open-ring lactone) | Cefazolin EP Impurity D sodium salt | Cefazolin EP Impurity J disodium salt | Cefazolin EP Impurity F | Cefazolin EP Impurity K | Cefazolin EP Impurity I | Cefazolin EP Impurity J | Cefazolin EP Impurity A | Cefazolin EP Impurity L | Cefazolin EP Impurity G |