Search Results for " Ivermectin "
Ivermectin EP Impurity E
| N° de SZ CAT: | SZ-I020006 |
| Número CAS | NA |
| Mol.F. | C49H76O14 |
| Peso Molecular | 889.1 |
| Status de Fatura | Custom Synthesis |
Nome Químico: 5-O,12-Didemethyl-12-ethyl-22,23-dihydroavermectin A1a (as per EP)
Sinônimo: 12-demethyl-12-ethyl-H2B1a
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
Sorrisos: O[C@]1([C@H](C(O[C@H](C2)C[C@@H](C/C=C3\C)O[C@]42CC[C@H](C)[C@]([C@@H](C)CC)([H])O4)=O)C=C(C)[C@H]5O)[C@]5([H])OC/C1=C\C=C\[C@@H]([C@@H]3O[C@H](O[C@@H](C)[C@@H]6O[C@@H](C[C@H](OC)[C@H]7O)O[C@H]7C)C[C@@H]6OC)CC
Ivermectin EP Impurity E is chemically 5-O,12-Didemethyl-12-ethyl-22,23-dihydroavermectin A1a (as per EP) . It is also known as 12-demethyl-12-ethyl-H2B1a. Ivermectin EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Ivermectin 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 Ivermectin.
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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