Loratadine 8-Dechloro-7-Chloro Impurity

CAS No.: 1346602-19-4 - Loratadine 8-Dechloro-7-Chloro Impurity
CAS No. : 1346602-19-4
Mol F. : C22H23ClN2O2
Mol W. : 382.88
Cat No. : SA34020
SKU: 5d4ae55feb41 Categories: , Tags: ,
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Description

Product NameLoratadine 8-Dechloro-7-Chloro Impurity
Synonyms4-(7-Chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)-1-piperidine carboxylic acid ethyl ester

Ethyl 4-(7-Chloro-5,6-dihydro-11H-benzo[5,6] cyclohepta[1,2-b]pyridin-11-ylidene)-1-piperidinecarboxyate

Related APILoratadine
CategoryImpurities

Order Loratadine 8-Dechloro-7-Chloro Impurity product with CAS: 1346602-19-4 and speed up your project. This product is also known as 4-(7-Chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)-1-piperidine carboxylic acid ethyl ester; Ethyl 4-(7-Chloro-5,6-dihydro-11H-benzo[5,6] cyclohepta[1,2-b]pyridin-11-ylidene)-1-piperidinecarboxyate and can be used as a working standard or secondary reference standard. Additional internal validation as per respective FDA regulations/guidelines may require. Loratadine 8-Dechloro-7-Chloro Impurity is used in Loratadine impurity profiling as per limits and threshold values specified by respective drug legislations, FDA and pharmacopoeial guidelines during commercial production of Loratadine and its related formulations. Moreover, 4-(7-Chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)-1-piperidine carboxylic acid ethyl 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.

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