Search Results for " Entecavir "
Entecavir EP Impurity F
| SZ CAT No: | SZ-E014007 |
| CAS No | 649761-24-0 |
| Mol.F. | C27H31N5O2Si |
| Mol.Wt. | 485.7 |
| Inv. Status | Under QC Approval |
| Rel. CAS No | 701278-11-7 (HCl salt) |
Chemical Name: 2-Amino-9-[(1S,3R,4S)-3-[(benzyloxy)methyl]-4-[dimethyl(phenyl)silyl]-2-methylidenecyclopentyl]-1,9-dihydro-6H-purin-6-one (as per EP) ; 9-[(1S,3R,4S)-4-Dimethylphenylsilyl-3-(benzyloxymethyl)-2-methylenecyclopentyl]guanine (as per USP)
Synonym: Entecavir USP Related Compound A ;
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
Smiles: O=C1C2=C(N([C@]3(C[C@@]([Si](C)(C4=CC=CC=C4)C)([H])[C@@]([H])(COCC5=CC=CC=C5)C3=C)[H])C=N2)N=C(N)N1
Entecavir EP Impurity F is chemically 2-Amino-9-[(1S,3R,4S)-3-[(benzyloxy)methyl]-4-[dimethyl(phenyl)silyl]-2-methylidenecyclopentyl]-1,9-dihydro-6H-purin-6-one (as per EP) ; 9-[(1S,3R,4S)-4-Dimethylphenylsilyl-3-(benzyloxymethyl)-2-methylenecyclopentyl]guanine (as per USP). It is also known as Entecavir USP Related Compound A ; . Entecavir EP Impurity F is supplied with detailed characterization data compliant with regulatory guideline. Entecavir 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 Entecavir.
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.
Related products
Disclaimer
SynZeal product information given on this website is as per the existing understanding while publishing the details on website. The customer is responsible for assessing the accuracy of the information at the time of actual purchase.
SynZeal will update these details as per new development or finding in product specification without further noticed.