Allopurinol USP Impurity - Request Quote
Allopurinol USP Impurity
| SZ CAT No: | SZ-A074009 |
| CAS No | NA |
| Mol.F. | C12H14N4O4 |
| Mol.Wt. | 278.3 |
| Inv. Status | Synthesis on demand |
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Usage Note:
Allopurinol USP Impurity is chemically Ethyl-(E/Z)-3-(2-carbethoxy-2-cyanoethenyl)amino-1H-pyrazole-4-carboxylate (as per USP). Allopurinol USP Impurity is supplied with detailed characterization data compliant with regulatory guideline. Allopurinol USP Impurity 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 Allopurinol.
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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