Cefuroxime EP Impurity E
| Catalog No. | KMC124026 |
|---|---|
| CAS No. | 97232-97-8 |
| Alt. name | trans-Cefuroxime |
| Formula | C16H16N4O8S |
| FW | 424.4 |
| Unit | Price | Stock |
|---|---|---|
| 100 mg | Enquire | Enquire |
| Chemical Name: | (6R,7R)-3-[(Carbamoyloxy)methyl]-7-[[(E)-(furan-2-yl)(methoxyimino)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (as per EP) |
|---|---|
| Purity: | >95% |
| Storage: | Store at 2-8 deg. C for long term storage |
| Shipping: | Product is stable to be Shipped at Room Temperature |
Cefuroxime EP Impurity E is chemically (6R,7R)-3-[(Carbamoyloxy)methyl]-7-[[(E)-(furan-2-yl)(methoxyimino)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (as per EP) .
Cefuroxime EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline.
Cefuroxime EP Impurity E can be used for the analytical method development, method validation (AMV), Quality Controlled (QC)
application for Abbreviated New Drug Application (ANDA) or during commercial production of Cefuroxime EP Impurity E.
The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. K.M.Pharma products are for analytical purpose only and not for human use.
The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. K.M.Pharma products are for analytical purpose only and not for human use.
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