Yohimbine EP Impurity E | CAS 50439-68-4 - Request Quote
Yohimbine EP Impurity E
| SZ CAT No: | SZ-Y001006 |
| CAS No | 50439-68-4 |
| Mol.F. | C22H28N2O3 |
| Mol.Wt. | 368.5 |
| Inv. Status | Synthesis on demand |
| Rel. CAS No | 7149-57-7 (HCl salt) |
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Usage Note:
Yohimbine EP Impurity E is chemically Methyl (2Z)-2-[(2S,3R,12bS)-3-ethyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-3-methoxyprop-2-enoate (as per EP). Yohimbine EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Yohimbine EP Impurity E 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 Yohimbine.
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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Yohimbine EP Impurity E for Method Validation
Yohimbine Reference Standard
Yohimbine EP Impurity E for ANDA Filing
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Yohimbine EP Impurity E Identification Standards
Yohimbine EP Impurity E for DMF Filing
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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 developments or findings in product specifications without further notice.


