Search Results for " Paclitaxel "
Paclitaxel EP Impurity H
| N° de SZ CAT: | SZ-P032132 |
| Número CAS | 78454-17-8 |
| Mol.F. | C45H49NO13 |
| Peso Molecular | 811.9 |
| Status de Fatura | In Stock |
| Shipping Condition | Ambient Temperature |
Nome Químico: 4-(acetyloxy)-13α-[[(2R,3S)-3-benzamido-2-hydroxy-3-phenylpropanoyl]oxy]-1,7α,10β-trihydroxy-9-oxo-5β,20-epoxytax-11-en-2α-yl benzoate
Sinônimo: 10-O-deacetyl-7-epi-paclitaxel (USP) ; 7-Epi 10-Desacetyl Paclitaxel ; Paclitaxel USP Related Compound B
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
Sorrisos: CC(O[C@@]1([C@](C[C@H]2O)([H])OC1)[C@@]([C@@]2(C3=O)C)([H])[C@@H]([C@@](C4(C)C)(C[C@H](OC([C@H](O)[C@H](C5=CC=CC=C5)NC(C6=CC=CC=C6)=O)=O)C(C)=C4[C@H]3O)O)OC(C7=CC=CC=C7)=O)=O
Paclitaxel EP Impurity H is chemically 4-(acetyloxy)-13α-[[(2R,3S)-3-benzamido-2-hydroxy-3-phenylpropanoyl]oxy]-1,7α,10β-trihydroxy-9-oxo-5β,20-epoxytax-11-en-2α-yl benzoate. It is also known as 10-O-deacetyl-7-epi-paclitaxel (USP) ; 7-Epi 10-Desacetyl Paclitaxel ; Paclitaxel USP Related Compound B. Paclitaxel EP Impurity H is supplied with detailed characterization data compliant with regulatory guideline. Paclitaxel EP Impurity H 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 Paclitaxel.
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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