Paclitaxel EP Impurity J | CAS 2757197-26-3 - Request Quote
Paclitaxel EP Impurity J
| SZ CAT No: | SZ-P032043 |
| CAS No | 2757197-26-3 |
| Mol.F. | C49H53NO15 |
| Mol.Wt. | 896.0 |
| Inv. Status | In Stock |
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Paclitaxel EP Impurity J is chemically 4-(acetyloxy)-13α-[[(2R,3S)-3-benzamido-2-hydroxy-3-phenylpropanoyl]oxy]-1,7β-dihydroxy-9-oxo-10β-[(3-oxobutanoyl)oxy]-5β,20-epoxytax-11-en-2α-yl benzoate (as per EP) ; (2aR,4S,4aS,6R,9S,11S,12S,12aR,12bS)-6-Acetoxy-9-{[(2R,3S)-3-benzamido-2-hydroxy-3-phenylpropanoyl]oxy}-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-12b-[(3-oxobutanoyl)oxy]-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-1H-7,11-methanocyclodeca[3,4]benzo[1,2-b]oxet-12-yl benzoate (as per USP). It is also known as 10-O-deacetyl-10-O-(3-oxobutanoyl)paclitaxel (EP) ; 10-Acetoacetylpaclitaxel (USP). Paclitaxel EP Impurity J is supplied with detailed characterization data compliant with regulatory guideline. Paclitaxel EP Impurity J 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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Paclitaxel EP Impurity J for Method Validation
Paclitaxel Reference Standard
Paclitaxel EP Impurity J for ANDA Filing
Paclitaxel EP Impurity J for Forced Degradation Studies
Paclitaxel EP Impurity J Identification Standards
Paclitaxel EP Impurity J for DMF Filing
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