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Semaglutide Impurity 70

SZ CAT No:SZ-S072251
CAS No
NA
Mol.F.
C176H252N42O49
Mol.Wt.
3740.2
Inv. Status
Synthesis on demand

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Semaglutide Impurity 70 is chemically (4S,10S,13S,16S,19S,22S,25S,28S,31S,34S,37S,40S,43S,49S,52S,55S,58S,61S,64S,68S,71S,74S,77S,80S,86S)-19-((1H-indol-3-yl)methyl)-43-(3-amino-3-oxopropyl)-34-(4-aminobutyl)-28,77-dibenzyl-86-(2-((S)-2-((tert-butoxycarbonyl)amino)-3-(1-trityl-1H-imidazol-4-yl)propanamido)-2-methylpropanamido)-25-((S)-sec-butyl)-31,49-bis(2-carboxyethyl)-4,10-bis(3-guanidinopropyl)-55-(4-hydroxybenzyl)-74,80-bis((R)-1-hydroxyethyl)-58,61,71-tris(hydroxymethyl)-16,52-diisobutyl-13,64-diisopropyl-22,37,40-trimethyl-3,6,9,12,15,18,21,24,27,30,33,36,39,42,45,48,51,54,57,60,63,66,70,73,76,79,82,85-octacosaoxo-2,5,8,11,14,17,20,23,26,29,32,35,38,41,44,47,50,53,56,59,62,65,69,72,75,78,81,84-octacosaazaoctaoctacontane-1,68,88-tricarboxylic acid. Semaglutide Impurity 70 is supplied with detailed characterization data compliant with regulatory guideline. Semaglutide Impurity 70 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 Semaglutide.

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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