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Everolimus EP Impurity C

N° de SZ CAT:SZ-E024004
Número CASNA
Mol.F.C52H81NO14
Peso Molecular944.2
Status de FaturaCustom Synthesis

Nome Químico: (1R,9S,12S,15R,16E,18R,19R,21R,23S,24E,26E,28E,30S,32S,35R)-1,18,19-Trihydroxy-12-[(2R)-1-[(1S,3R,4R)-4-(2-hydroxyethoxy)-3-methoxycyclohexyl]propan-2-yl]-30-methoxy-15,17,21,23,29,35-hexamethyl-11,36-dioxa-4-azatricyclo[30.3.1.04,9]hexatriaconta-16,24,26,28-tetraene-2,3,10,14,20-pentone (as per EP)

Sinônimo: 19-O-demethyl everolimus

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: 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)/[C@@]([H])(O)[C@]2(O)[H])=O)[C@@]3([H])N(C(C([C@@]4(O)[C@@](C)([H])CC[C@](C[C@]([H])(OC)/C(C)=C/C=C/C=C/[C@@]([H])(C)C[C@@]([H])(C)C2=O)([H])O4)=O)=O)CCCC3

Everolimus EP Impurity C is chemically (1R,9S,12S,15R,16E,18R,19R,21R,23S,24E,26E,28E,30S,32S,35R)-1,18,19-Trihydroxy-12-[(2R)-1-[(1S,3R,4R)-4-(2-hydroxyethoxy)-3-methoxycyclohexyl]propan-2-yl]-30-methoxy-15,17,21,23,29,35-hexamethyl-11,36-dioxa-4-azatricyclo[30.3.1.04,9]hexatriaconta-16,24,26,28-tetraene-2,3,10,14,20-pentone (as per EP). It is also known as 19-O-demethyl everolimus. Everolimus EP Impurity C is supplied with detailed characterization data compliant with regulatory guideline. Everolimus EP Impurity C 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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