Search Results for " Somatostatin "
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 |
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.
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