Levetiracetam EP Impurity E | CAS 3886-69-9 - Request Quote
Levetiracetam EP Impurity E
| SZ CAT No: | SZ-L001012 |
| CAS No | 3886-69-9 |
| Mol.F. | C8H11N |
| Mol.Wt. | 121.2 |
| Inv. Status | In Stock |
| Rel. CAS No | 10277-86-8 (HCl salt) ; 48104-28-5 (HBr salt) |
| Shipping Condition | Room Temperature |
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Usage Note:
Levetiracetam EP Impurity E is chemically (1R)-1-Phenylethan-1-amine (as per EP). Levetiracetam EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Levetiracetam 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 Levetiracetam.
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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Levetiracetam EP Impurity E for Method Validation
Levetiracetam Reference Standard
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Levetiracetam EP Impurity E for Forced Degradation Studies
Levetiracetam EP Impurity E Identification Standards
Levetiracetam 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.