Sertraline
Sertraline Impurities & Reference Standards
Sertraline is recognized as an active pharmaceutical ingredient (API) that supports formulation development, process validation, and quality assurance in drug manufacturing. The compound carries the molecular formula C17H17Cl2N, corresponding to a molecular weight of 306.23 g/mol. High-purity Sertraline and its related substances / process impurities are essential for analytical method development, method validation, quality control, and regulatory submissions under ICH, USP, BP, and EP guidelines. Our Sertraline reference standards are provided with full documentation — Certificate of Analysis (CoA), HPLC chromatographic data, and spectral characterization — to support pharmaceutical R&D and GMP manufacturing.
Associated Impurities
Sertraline Impurity – C(3-Deschloro)Racemic
- CAS No: 871838-58-3
- Mol. F.: C17H17Cl2N
Sertraline Impurity – D (4-Deschloro)Racemic
- CAS No: 55056-87-6
- Mol. F.: C17H17Cl2N
Sertraline Impurity – D (Pure Chirality)
- CAS No: 871838-58-3
- Mol. F.: C17H17Cl2N
Sertraline Impurity – G (Cis-isomer ML-05)
- CAS No: 79617-95-1
- Mol. F.: C17H17Cl2N
Setralone Impurity (Impurity – F) Racemic
- CAS No: 79560-19-3
- Mol. F.: C17H17Cl2N
Setralone Impurity (Impurity – F) Racemic
- CAS No: 155748-61-1
- Mol. F.: C17H17Cl2N