Hydrolysis 16-37 Liraglutide Impurity - Request Quote
Hydrolysis 16-37 Liraglutide Impurity
| SZ CAT No: | SZ-L098031 |
| CAS No | NA |
| Mol.F. | C132H210N32O35 |
| Mol.Wt. | 2805.3 |
| Inv. Status | Synthesis on demand |
| Shipping Condition | Cold Shipment -20°C |
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Usage Note:
Hydrolysis 16-37 Liraglutide Impurity is chemically . It is also known as Fragment-[10-31]-Liraglutide. Hydrolysis 16-37 Liraglutide Impurity is supplied with detailed characterization data compliant with regulatory guideline. Hydrolysis 16-37 Liraglutide Impurity 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 Liraglutide.
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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Liraglutide Reference Standard
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Hydrolysis 16-37 Liraglutide Impurity Identification Standards
Hydrolysis 16-37 Liraglutide Impurity for DMF Filing
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