Sertraline EP Impurity A; rac-trans-Sertraline

CAS No. : 79836-45-6(base);79617-99-5(HCl)
Mol F. : C17H17Cl2N
Mol W. : 306.23
Cat No. : SA36501
Clear
*DISCOUNT MAY BE APPLICABLE

Description

Product Name Sertraline EP Impurity A; rac-trans-Sertraline
Synonyms Sertraline BP Impurity A

Sertraline USP Related Compound A

trans-4-(3,4-Dichlorophenyl)-1,2,3,4-tetrahydro-N-methyl-1-naphthalen amine

Related API Sertraline
Category Impurities

Sertraline EP Impurity A; rac-trans-Sertraline product with CAS: 79836-45-6(base);79617-99-5(HCl) is also known as Sertraline BP Impurity A; Sertraline USP Related Compound A. This product can be used as a working standard or secondary reference standard (additional internal validation as per respective FDA regulations/guidelines may require). Sertraline EP Impurity A; rac-trans-Sertraline is used in Sertraline impurity profiling as per limits and threshold values specified by respective drug legislation, FDA, and pharmacopoeial guidelines during commercial production of Sertraline and its related formulations. Moreover, Sertraline BP Impurity A 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 Sertraline developed in our R&D.

Product quantity / packs as per your requirement, just let us know!

Please contact us or email us at [email protected]

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 [email protected]

Terms and Conditions

In-Stock products will be shipped in 24 Hrs. For others please enquire.

Shipping Free for purchase above $5000
Delivery In-Stock, products will be delivered in 8-15 days via FedEx in the USA, Europe, and other countries.
Return Policy Returns/replacement accepted if you are not satisfied with the quality of the product, (please send us an email with the reason/issues which are facing, within 15 days, after receipt of the product).
Order Place your order online or by email [email protected] (YOU DON'T NEED TO PAY WHILE PLACING THE ORDER. Click here for more info)
After Sales Support  Please write to us. Our R&D team will provide all possible support.

For more info please check FAQs. 

Please check the detailed terms and conditions.

RFQ / Enquire about Sertraline EP Impurity A; rac-trans-Sertraline