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Paracetamol
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Paracetamol 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 Paracetamol-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.
Paracetamol EP Impurity A
Paracetamol EP Impurity B
Paracetamol EP Impurity C
Paracetamol EP Impurity D
Paracetamol EP Impurity E
Paracetamol EP Impurity F
Paracetamol EP Impurity G
Paracetamol EP Impurity H
Paracetamol EP Impurity I
Paracetamol EP Impurity J
Paracetamol EP Impurity K
Paracetamol EP Impurity L
Paracetamol EP Impurity M
Paracetamol EP Impurity M HCl
Paracetamol EP Impurity N
Paracetamol EP Impurity O
4-Hydroxyphenylacetamide
Paracetamol Dimer
Acetaminophen Impurity A (DMF)
2-Chloro-N-phenylacetamide
Paracetamol Impurity 1
N-Nitroso Paracetamol
Acetaminophen-d4
N-Nitroso Paracetamol EP Impurity M
