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Linaclotide Dimer Impurity

SZ CAT No:SZ-L076014
CAS No
NA
Mol.F.
C118H160N30O42S12
Mol.Wt.
3055.5
Inv. Status
Synthesis on demand
Shipping Condition Room Temperature

Chemical Name :

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Usage Note:

Linaclotide Dimer Impurity is chemically (2S,2'S)-2,2'-(((3S,3'S,6R,6'R,9S,9'S,15R,15'R,20R,20'R,23S,23'S,26S,26'S,29R,29'R,32R,32'R,37R,37'R,40S,40'S,45aS,45a'S)-6,6'-(disulfanediylbis(methylene))bis(32-amino-40-(2-amino-2-oxoethyl)-26-(2-carboxyethyl)-23-(4-hydroxybenzyl)-9-((R)-1-hydroxyethyl)-29-(mercaptomethyl)-3-methyl-1,4,7,10,13,22,25,28,31,38,41,47-dodecaoxotetracontahydro-19H-37,20-(epiminomethano)pyrrolo[2,1-s][1,2,27,28]tetrathia[5,8,11,14,17,20,23,32,35,38,41]undecaazacyclotritetracontine-6,15-diyl-15-carbonyl))bis(azanediyl))bis(3-(4-hydroxyphenyl)propanoic acid). Linaclotide Dimer Impurity is supplied with detailed characterization data compliant with regulatory guideline. Linaclotide Dimer 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 Linaclotide.

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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Linaclotide Reference Standard

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Linaclotide Dimer Impurity for DMF Filing

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