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Hydrolysis 14-37 Liraglutide Impurity - Request Quote

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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

Chemical Name :

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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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