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Hydrolysis 14-37 Liraglutide Impurity - Solicitar cotización

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Hydrolysis 14-37 Liraglutide Impurity

N° de SZ CAT:SZ-L098004
Número CAS
NA
Mol.F.
C139H220N34O40
Peso Molecular
3007.5
Status de Fatura
Synthesis on demand
Condición de envío Cold Shipment -20°C

Nome Químico :

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Nota de Uso:

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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A SynZeal atualizará estes detalhes conforme novos desenvolvimentos ou descobertas nas especificações do produto, sem aviso prévio.

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