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Semaglutide Impurity 12

SZ CAT No:SZ-S072020
CAS No
NA
Mol.F.
C185H286N46O58
Mol.Wt.
4082.6
Inv. Status
Synthesis on demand
Shipping Condition Cold Shipment -20°C

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Semaglutide Impurity 12 is chemically (3S,9S,12S,15S,18S,21S,24S,27S,30S,33S,36S,39S,48S,51S,54R,57S,79R)-57-(((6S,12S,15S,18S,21S,24S,30S,33S)-21-((1H-indol-3-yl)methyl)-1-amino-30-benzyl-27-((S)-sec-butyl)-35-carboxy-6-((carboxymethyl)carbamoyl)-12-(3-guanidinopropyl)-1-imino-18-isobutyl-15-isopropyl-24-methyl-8,11,14,17,20,23,26,29,32-nonaoxo-2,7,10,13,16,19,22,25,28,31-decaazapentatriacontan-33-yl)carbamoyl)-3-(2-((S)-2-amino-3-(1H-imidazol-4-yl)propanamido)-2-methylpropanamido)-48-(3-amino-3-oxopropyl)-12-benzyl-39-(2-carboxyethyl)-33-(4-hydroxybenzyl)-9,15-bis((R)-1-hydroxyethyl)-18,27,30-tris(hydroxymethyl)-36-isobutyl-24-isopropyl-51,54-dimethyl-4,7,10,13,16,19,22,25,28,31,34,37,40,43,46,49,52,55,63,72,76,81-docosaoxo-65,68-dioxa-5,8,11,14,17,20,23,26,29,32,35,38,41,44,47,50,53,56,62,71,75,80-docosaazaheptanonacontane-1,21,79,97-tetracarboxylic acid. Semaglutide Impurity 12 is supplied with detailed characterization data compliant with regulatory guideline. Semaglutide Impurity 12 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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