Hydrolysis 14-37 Liraglutide Impurity - Request Quote
Hydrolysis 14-37 Liraglutide Impurity
| SZ CAT No: | SZ-L098004 |
| CAS No | NA |
| Mol.F. | C139H220N34O40 |
| Mol.Wt. | 3007.5 |
| Inv. Status | Synthesis on demand |
| Shipping Condition | Cold Shipment -20°C |
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Hydrolysis 14-37 Liraglutide Impurity is chemically N5-((2S,5S,8S,11S,14S,17S)-17-((S)-2-((S)-2-((S)-5-amino-2-(2-((S)-2-((S)-2-((S)-2-((S)-2-((S)-2-((S)-2-((S)-2-((S)-2-amino-3-hydroxypropanamido)-3-carboxypropanamido)-3-methylbutanamido)-3-hydroxypropanamido)-3-hydroxypropanamido)-3-(4-hydroxyphenyl)propanamido)-4-methylpentanamido)-4-carboxybutanamido)acetamido)-5-oxopentanamido)propanamido)propanamido)-11-benzyl-8-((S)-sec-butyl)-14-(2-carboxyethyl)-2-(((S)-1-(((S)-1-(((S)-1-((2-(((S)-1-((carboxymethyl)amino)-5-guanidino-1-oxopentan-2-yl)amino)-2-oxoethyl)amino)-5-guanidino-1-oxopentan-2-yl)amino)-3-methyl-1-oxobutan-2-yl)amino)-4-methyl-1-oxopentan-2-yl)carbamoyl)-1-(1H-indol-3-yl)-5-methyl-4,7,10,13,16-pentaoxo-3,6,9,12,15-pentaazahenicosan-21-yl)-N2-palmitoyl-L-glutamine. Hydrolysis 14-37 Liraglutide Impurity is supplied with detailed characterization data compliant with regulatory guideline. Hydrolysis 14-37 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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