Allopurinol USP Impurity

Allopurinol USP Impurity

VS CAT No VS-A074009
CAS No NA
Mol.F. C12H14N4O4
Mol.Wt. 278.3
Inv. Status Custom Synthesis

Chemical Name: Ethyl-(E/Z)-3-(2-carbethoxy-2-cyanoethenyl)amino-1H-pyrazole-4-carboxylate (as per USP)

Shipping Temperature: Ambient

Country of Origin: India

Smiles: CCOC(C1=C(N/C=C(C#N)\C(OCC)=O)NN=C1)=O.CCOC(C2=C(N/C=C(C(OCC)=O)\C#N)NN=C2)=O

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. Vsquare products are for analytical purpose only and not for human use.