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Paclitaxel EP Impurity F

N° de SZ CAT:SZ-P032120
Número CAS153083-53-5
Mol.F.C47H59NO14
Peso Molecular862.0
Status de FaturaUnder QC Approval

Nome Químico: (αR,​βS)​-α-Hydroxy-​β-​[methyl(1-​oxohexyl)​amino]​-​benzenepropanoic Acid (2aR,​4S,​4aS,​6R,​9S,​11S,​12S,​12aR,​12bS)​-​6,​12b-​bis(acetyloxy)​-​12-​(benzoyloxy)​-​2a,​3,​4,​4a,​5,​6,​9,​10,​11,​12,​12a,​12b-​dodecahydro-​4,​11-​dihydroxy-​4a,​8,​13,​13-​tetramethyl-​5-​oxo-​7,​11-​methano-​1H-​cyclodeca[3,​4]​benz[1,​2-​b]​oxet-​9-​yl Ester; [2aR-[2aα,4β,4aβ,6β,9α(αR*,βS*),11α,12α,12aα,12bα]]-α-Hydroxy-β-[methyl(1-oxohexyl)amino]-benzenepropanoic acid 6,12b-bis(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-yl Ester; 7,11-Methano-1H-cyclo;

Sinônimo: N-Methyl Paclitaxel C ; N-Debenzoyl-N-hexanoyl-N-methylpaclitaxel

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: CC(O[C@@]1([C@@H](C[C@@H]2O)OC1)[C@@]([C@@]2(C3=O)C)([H])[C@@H]([C@@](C4(C)C)(C[C@H](OC([C@H](O)[C@@H](N(C(CCCCC)=O)C)C5=CC=CC=C5)=O)C(C)=C4[C@H]3OC(C)=O)O)OC(C6=CC=CC=C6)=O)=O

Paclitaxel EP Impurity F is chemically (αR,​βS)​-α-Hydroxy-​β-​[methyl(1-​oxohexyl)​amino]​-​benzenepropanoic Acid (2aR,​4S,​4aS,​6R,​9S,​11S,​12S,​12aR,​12bS)​-​6,​12b-​bis(acetyloxy)​-​12-​(benzoyloxy)​-​2a,​3,​4,​4a,​5,​6,​9,​10,​11,​12,​12a,​12b-​dodecahydro-​4,​11-​dihydroxy-​4a,​8,​13,​13-​tetramethyl-​5-​oxo-​7,​11-​methano-​1H-​cyclodeca[3,​4]​benz[1,​2-​b]​oxet-​9-​yl Ester; [2aR-[2aα,4β,4aβ,6β,9α(αR*,βS*),11α,12α,12aα,12bα]]-α-Hydroxy-β-[methyl(1-oxohexyl)amino]-benzenepropanoic acid 6,12b-bis(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-yl Ester; 7,11-Methano-1H-cyclo;. It is also known as N-Methyl Paclitaxel C ; N-Debenzoyl-N-hexanoyl-N-methylpaclitaxel. Paclitaxel EP Impurity F is supplied with detailed characterization data compliant with regulatory guideline. Paclitaxel 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 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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