Somatostatin EP Impurity B

Chemical Name: (4R,7S,10S,13S,16S,19S,22S,25S,28S,31S,34R)-19-((1H-indol-3-yl)methyl)-28-(2-amino-2-oxoethyl)-16,31-bis(4-aminobutyl)-34-(2-((S)-2-aminopropanamido)acetamido)-13,22,25-tribenzyl-10-((R)-1-hydroxyethyl)-7-(hydroxymethyl)-6,9,12,15,18,21,24,27,30,33-decaoxo-1,2-dithia-5,8,11,14,17,20,23,26,29,32-decaazacyclopentatriacontane-4-carboxylic acid.

Country of Origin: India

Product Category: Somatostatin Impurities

Somatostatin EP Impurity B is identified by CAS No. 85734-83-4 and is chemically known as (4R,7S,10S,13S,16S,19S,22S,25S,28S,31S,34R)-19-((1H-indol-3-yl)methyl)-28-(2-amino-2-oxoethyl)-16,31-bis(4-aminobutyl)-34-(2-((S)-2-aminopropanamido)acetamido)-13,22,25-tribenzyl-10-((R)-1-hydroxyethyl)-7-(hydroxymethyl)-6,9,12,15,18,21,24,27,30,33-decaoxo-1,2-dithia-5,8,11,14,17,20,23,26,29,32-decaazacyclopentatriacontane-4-carboxylic acid.

Somatostatin EP Impurity B is provided with comprehensive characterization data in accordance with regulatory guidelines. It is suitable for use in analytical method development, method validation (AMV), Quality Control (QC) applications for Abbreviated New Drug Applications (ANDA) and commercial production of Somatostatin.

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