Capecitabine EP Impurity C | CAS 161599-46-8 - Request Quote
Capecitabine EP Impurity C
| SZ CAT No: | SZ-C003004 |
| CAS No | 161599-46-8 |
| Mol.F. | C13H16FN3O6 |
| Mol.Wt. | 329.3 |
| Inv. Status | In Stock |
| Rel. CAS No | 880633-96-5 (HCl salt) |
| Shipping Condition | Room Temperature |
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Usage Note:
Capecitabine EP Impurity C is chemically 1-(2,3-di-O-acetyl-5-deoxy-β-D-ribofuranosyl)-4-amino-5-fluoropyrimidin-2(1H)-one (as per EP). It is also known as Capecitabine Diacetyl Amino Impurity. Capecitabine EP Impurity C is supplied with detailed characterization data compliant with regulatory guideline. Capecitabine EP Impurity C 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 Capecitabine.
The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.
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Capecitabine EP Impurity C for Method Validation
Capecitabine Reference Standard
Capecitabine EP Impurity C for ANDA Filing
Capecitabine EP Impurity C for Forced Degradation Studies
Capecitabine EP Impurity C Identification Standards
Capecitabine EP Impurity C for DMF Filing
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