Telmisartan EP Impurity C

CAS No.: 144702-26-1 - Telmisartan EP Impurity C
CAS No. : 144702-26-1
Mol F. : C37H38N4O2
Mol W. : 570.72
Cat No. : SA33903
SKU: 72c6fb72da56 Categories: , Tags: ,
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Description

Product NameTelmisartan EP Impurity C
SynonymsTelmisartan t-Butyl Ester

2-(4-{[4-Methyl-6-(1-methyl-1H-1,3-benzodiazol-2-yl)-2-propyl-1H-1,3-benzodiazol-1-yl] methyl}phenyl)benzoic acid t-butyl ester

4’-[(1,4’-Dimethyl-2’-propyl[2,6’-bi-1H-benzimidazol]-1’-yl)methyl]-[1,1’-biphenyl]-2-carboxylic Acid 1,1-Dimethylethyl Ester

Related APITelmisartan
CategoryImpurities

Order Telmisartan EP Impurity C product with CAS: 144702-26-1 and speed up your project. This product is also known as Telmisartan t-Butyl Ester; 2-(4-{[4-Methyl-6-(1-methyl-1H-1,3-benzodiazol-2-yl)-2-propyl-1H-1,3-benzodiazol-1-yl] methyl}phenyl)benzoic acid t-butyl ester and can be used as a working standard or secondary reference standard. Additional internal validation as per respective FDA regulations/guidelines may require. Telmisartan EP Impurity C is used in Telmisartan impurity profiling as per limits and threshold values specified by respective drug legislations, FDA and pharmacopoeial guidelines during commercial production of Telmisartan and its related formulations. Moreover, Telmisartan t-Butyl Ester is also used in the process of Abbreviated New Drug Application (ANDA) filing to FDA and toxicity study of respective drug formulation.

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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.

Products provide by SynThink are for research and development (R&D) use only

If you need different pack size / quantity, please contact us or email us at enquiry@synthinkchemicals.com

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