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Everolimus EP Impurity C

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The product information provided on this website by ISPStandards is based on the best available understanding at the time of publication. Customers are responsible for verifying the accuracy of this information before making a purchase. ISPStandards may update product details as new information or specifications become available, without prior notice.

Description

Chemical Name: (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 
Synonym: 19-O-demethyl everolimus

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)/[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

Additional Information

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 .
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. ISP Standards products are for analytical purpose only and not for human use.

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