Somatostatin EP Impurity E

N° de SZ CAT:	SZ-S092005
Número CAS	NA
Mol.F.	C78H106N18O20S2
Peso Molecular	1679.9
Status de Fatura	Custom Synthesis

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Nome Químico: N6.9-acetylsomatostatin

Sinônimo: [Lys(Ac)9]somatostatin

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: O=C([C@@H](NC([C@H](CO)NC([C@H]([C@H](O)C)NC([C@H](CC1=CC=CC=C1)NC([C@H]([C@H](O)C)NC([C@H](CCCCNC(C)=O)NC([C@H](CC2=CNC3=C2C=CC=C3)NC([C@H](CC4=CC=CC=C4)NC([C@H](CC5=CC=CC=C5)NC([C@H](CC(N)=O)NC([C@H](CCCCN)N6)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)CSSC[C@H](NC(CNC([C@@H](N)C)=O)=O)C6=O)O

Somatostatin EP Impurity E is chemically N6.9-acetylsomatostatin. It is also known as [Lys(Ac)9]somatostatin. Somatostatin EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Somatostatin 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 Somatostatin.

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.

Somatostatin EP Impurity E

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