Allopurinol USP Impurity - 请求报价
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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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Allopurinol USP Impurity 用于方法验证
Allopurinol 对照标准
Allopurinol USP Impurity 用于ANDA申报
Allopurinol USP Impurity 用于强制降解研究
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Allopurinol USP Impurity 用于DMF申报
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