Lansoprazole Sulfide 4-Hydroxy Impurity

CAS No.: 131926-97-1 - Lansoprazole Sulfide 4-Hydroxy Impurity

CAS No. : 131926-97-1
Mol F. : C14H13N3OS
Mol W. : 271.34
Cat No. : SA35912
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Description

Product NameLansoprazole Sulfide 4-Hydroxy Impurity
SynonymsLansoprazole Sulfide Des(trifluoroethyl) Impurity

2-[(1H-Benzimidazol-2-ylthio)methyl]-3-methyl-4-pyridinol

Related APILansoprazole
CategoryImpurities

Lansoprazole Sulfide 4-Hydroxy Impurity product with CAS: 131926-97-1 is also known as Lansoprazole Sulfide Des(trifluoroethyl) Impurity; 2-[(1H-Benzimidazol-2-ylthio)methyl]-3-methyl-4-pyridinol. This product can be used as a working standard or secondary reference standard (additional internal validation as per respective FDA regulations/guidelines may require). Lansoprazole Sulfide 4-Hydroxy Impurity is used in Lansoprazole impurity profiling as per limits and threshold values specified by respective drug legislation, FDA, and pharmacopoeial guidelines during commercial production of Lansoprazole and its related formulations. Moreover, Lansoprazole Sulfide Des(trifluoroethyl) Impurity is also used in the process of Abbreviated New Drug Application (ANDA) filing to FDA and toxicity study of respective drug formulation. Please also find out other impurities of Lansoprazole developed in our R&D.

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Certificate of Analysis (CoA) and Characterization Data:

All products are provided with a certificate of analysis (CoA) along with the characterization data like 1H-NMR, MASS, HPLC Purity, MSDS, etc. (whatever relevant and possible). Moreover, additional data like 13C-NMR, 13C-DEPT NMR, GC, GC-MS, IC, Potency, TGA, etc. will be provided on request (extra charges may apply). 

This product can be used as a working standard or secondary reference standard. Additional internal validation as per respective FDA regulations/guidelines may require. This product provided by SynThink is generally used for Abbreviated New Drug Application (ANDA) filing to FDA, toxicity study of respective drug formulation, Quality Control (QC) and analytical studies during commercial production of the API]. Please also find out process impurities, degradation impurities, potential impurities of related api/drug developed by our R&D.

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