Search Results for " Raloxifene "
Raloxifene EP Impurity C
| N° de SZ CAT: | SZ-R007004 |
| Número CAS | 195454-31-0 |
| Mol.F. | C28H27NO5S |
| Peso Molecular | 489.6 |
| Status de Fatura | In Stock |
| Shipping Condition | Ambient Temperature |
Nome Químico: [6-hydroxy-2-(4-hydroxyphenyl)-1-benzothiophen-3-yl][4-[2-(piperidin-1-yl)ethoxy]phenyl]methanone N-oxide.(as per EP) ; 1-(2-{4-[6-Hydroxy-2-(4-hydroxyphenyl)benzothiophene-3-carbonyl]phenoxy}ethyl)piperidine 1-oxide (as per USP)
Sinônimo: Raloxifene USP Related Compound C ; Raloxifene N-Oxide
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
Sorrisos: O=C(C1=C(C2=CC=C(O)C=C2)SC3=CC(O)=CC=C31)C4=CC=C(OCC[N+]5([O-])CCCCC5)C=C4
Raloxifene EP Impurity C is chemically [6-hydroxy-2-(4-hydroxyphenyl)-1-benzothiophen-3-yl][4-[2-(piperidin-1-yl)ethoxy]phenyl]methanone N-oxide.(as per EP) ; 1-(2-{4-[6-Hydroxy-2-(4-hydroxyphenyl)benzothiophene-3-carbonyl]phenoxy}ethyl)piperidine 1-oxide (as per USP). It is also known as Raloxifene USP Related Compound C ; Raloxifene N-Oxide . Raloxifene EP Impurity C is supplied with detailed characterization data compliant with regulatory guideline. Raloxifene 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 Raloxifene.
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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