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Budesonide EP Impurity E | CAS 131918-64-4 - 请求报价

Budesonide EP Impurity E

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SZ目录编号:	SZ-B022006
CAS 号	131918-64-4
分子式	C25H32O6
分子量	428.5
投资状态	In Stock
运输条件	Room Temperature

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产品概览描述技术数据

化学名称 :16α,17-[(1RS)-Butylidenebis(oxy)]-11β,21-dihydroxypregna-1,4,14-triene-3,20-dione (as per EP); 16α,17-[Butylidenebis(oxy)]-11β,21-dihydroxypregna-1,4,14-triene-3,20-dione (as per USP)

异名 :Budesonide USP Related Compound E ; 14,15-Dehydrobudesonide (USP)

运输温度 : Room Temperature

HSN编码 :38229010

原产国 : India

微笑 :C[C@@]12[C@@]3(C(CO)=O)[C@@](OC(O3)CCC)([H])C=C1[C@]4([H])CCC5=CC(C=C[C@]5(C)[C@@]4([H])[C@@H](O)C2)=O

使用说明:所提供的化合物仅供实验室、研究、分析和科学用途，不可用于人体。

Budesonide EP Impurity E is chemically 16α,17-[(1RS)-Butylidenebis(oxy)]-11β,21-dihydroxypregna-1,4,14-triene-3,20-dione (as per EP); 16α,17-[Butylidenebis(oxy)]-11β,21-dihydroxypregna-1,4,14-triene-3,20-dione (as per USP). It is also known as Budesonide USP Related Compound E ; 14,15-Dehydrobudesonide (USP). Budesonide EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Budesonide 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 Budesonide.

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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