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Tigecycline
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Tigecycline 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 Tigecycline-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.
Tigecycline
Tigecycline USP Related Compound A
Tigecycline USP Related Compound B
Tigecycline EP Impurity B
Tigecycline EP Impurity A
Tigecycline USP Related Compound F
Tigecycline Tricyclic Analog
Tigecycline 12-Oxo-11-Hydroxy Impurity
Tigecycline Metabolite M4
Tigecycline Open Ring Impurity
Tigecycline EP System Suitability CRS
Tigecycline Impurity 1
Tigecycline Impurity 2
Tigecycline Impurity 3
Tigecycline Impurity 4
Tigecycline Impurity 5
Tigecycline Impurity 6
Tigecycline Impurity 7
Tigecycline Impurity 8
Desmethyl Tigecycline nitroso Impurity 1
Desmethyl Tigecycline nitroso Impurity 2
Tigecycline quinone analog
Tigecycline EP Impurity C
N-Nitroso Tigecycline
