Levomilnacipran

Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Levomilnacipran reference materials. Our portfolio includes both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope-labeled compounds, and nitrosamine derivatives (N-NO products). These reference standards play a crucial role in pharmaceutical R&D, aiding in formulation development, ANDA/DMF submissions, quality control, method validation, stability studies, and impurity profiling—including the identification and assessment of potentially genotoxic impurities.

Each Levomilnacipran-related product is rigorously characterized and delivered with a detailed Certificate of Analysis (COA) and comprehensive analytical data to ensure regulatory compliance. Upon request, we also offer EP/USP traceable standards. To maintain the highest quality standards, all materials are subject to periodic re-testing and continuous quality monitoring.

Levomilnacipran

Picture of Levomilnacipran
CAT No: VS-L076000
CAS No: 96847-55-1
Mol.F.: C15H22N2O
Mol.Wt.: 246.35
Status: Custom Synthesis

Levomilnacipran Impurity 1

Picture of Levomilnacipran Impurity 1
CAT No: VS-L076001
CAS No: 1237261-65-2
Mol.F.: C23H24N2O3
Mol.Wt.: 376.44
Status: Custom Synthesis

Contact

040-23076623, 040-4852 9278

E-Mail

info@venkatasailifesciences.com