Search Results for " Everolimus "
Everolimus EP Impurity F
| SZ CAT No: | SZ-E024007 |
| CAS No | NA |
| Mol.F. | C55H89NO16 |
| Mol.Wt. | 1020.3 |
| Inv. Status | Custom Synthesis |
Chemical Name: (1R,9S,12S,15R,16E,18R,19S,20R,21R,23S,24S,25E,27Ξ,28E,30S,32S,35R)-27-ethoxy-1,18,20-trihydroxy-12-[(2R)-1-[(1S,3R,4R)-4-(2-hydroxyethoxy)-3-methoxycyclohexyl]propan-2-yl]-19,30-dimethoxy-15,17,21,23,29,35-hexamethyl-11,36,37-trioxa-4-azatetracyclo[30.3.1.120,24.04,9]heptatriaconta-16,25,28-triene-2,3,10,14-tetrone
Synonym: Everolimus Cyclic Hemiacetal (USP)
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
Smiles: O=C(O[C@@]([C@@](C)([H])C[C@]1([H])CC[C@](OCCO)([H])[C@@](OC)([H])C1)([H])CC([C@@](C)([H])/C=C([C@@]([H])(O)[C@]([H])(OC)[C@@](O2)(O)[C@]([H])(C)C[C@]([H])(C)[C@@]2([H])/C=C/C(OCC)/C=C(C)/[C@](OC)([H])C[C@](O3)([H])CC[C@](C)([H])[C@]3(O)C4=O)\C)=O)[C@@]5([H])N(C4=O)CCCC5
Everolimus EP Impurity F is chemically (1R,9S,12S,15R,16E,18R,19S,20R,21R,23S,24S,25E,27Ξ,28E,30S,32S,35R)-27-ethoxy-1,18,20-trihydroxy-12-[(2R)-1-[(1S,3R,4R)-4-(2-hydroxyethoxy)-3-methoxycyclohexyl]propan-2-yl]-19,30-dimethoxy-15,17,21,23,29,35-hexamethyl-11,36,37-trioxa-4-azatetracyclo[30.3.1.120,24.04,9]heptatriaconta-16,25,28-triene-2,3,10,14-tetrone. It is also known as Everolimus Cyclic Hemiacetal (USP). Everolimus EP Impurity F is supplied with detailed characterization data compliant with regulatory guideline. Everolimus EP Impurity F 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 Everolimus .
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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