Semaglutide Iso Asp Impurity - 请求报价
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Semaglutide Iso Asp Impurity is chemically (3S,9S,12S,15S,18S,21S,25S,28S,31S,34S,37S,40S,46S,49S,52S,55S,82S)-55-(((6S,12S,15S,18S,21S,24S,27S,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)-46-(3-amino-3-oxopropyl)-12-benzyl-40-(2-carboxyethyl)-34-(4-hydroxybenzyl)-9,15-bis((R)-1-hydroxyethyl)-18,28,31-tris(hydroxymethyl)-37-isobutyl-25-isopropyl-49,52-dimethyl-4,7,10,13,16,19,23,26,29,32,35,38,41,44,47,50,53,61,70,79,84-henicosaoxo-63,66,72,75-tetraoxa-5,8,11,14,17,20,24,27,30,33,36,39,42,45,48,51,54,60,69,78,83-henicosaazahectane-1,21,82,100-tetracarboxylic acid. Semaglutide Iso Asp Impurity is supplied with detailed characterization data compliant with regulatory guideline. Semaglutide Iso Asp 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 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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Semaglutide Iso Asp Impurity 成本
Semaglutide Iso Asp Impurity 供应商
Semaglutide Iso Asp Impurity 分销商
Semaglutide Iso Asp Impurity 用于方法验证
Semaglutide 对照标准
Semaglutide Iso Asp Impurity 用于ANDA申报
Semaglutide Iso Asp Impurity 用于强制降解研究
Semaglutide Iso Asp Impurity 鉴别标准
Semaglutide Iso Asp Impurity 用于DMF申报
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