Terazosin Impurity-A

We will provide complete documentation support for every Standard Material. All analytical reports such as ¹H NMR, ¹³C NMR, Mass, FT-IR, HPLC Purity/GC Purity/QNMR Purity, Water content by KF/ Loss on Drying/TGA (Thermo-gravimetric Analysis). Certificate of Analysis with potency report. Each Standard Material SER (Structure Elucidation Report) with NMR, Mass, IR spectral interpretation. This whole analytical document can be included in eCTD, ANDA, DMF submissions to regulatory agencies.

Terazosin Impurity-A is primarily used as a reference standard for the analysis of the active ingredient of Terazosin and its formulations. It plays a crucial role in the development and validation of analytical methods, impurity profiling, and stability studies.

Terazosin Standard

Terazosin Hydrochloride Standard

Terazosin Hydrochloride Dihydrate Standard

Terazosin Impurity-B

Terazosin Impurity-C

Terazosin for system suitability A CRS

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