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Lovastatin
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Lovastatin 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 Lovastatin-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.
Lovastatin
Lovastatin EP Impurity A
Lovastatin EP Impurity B
Lovastatin EP Impurity C
Lovastatin EP Impurity D
Lovastatin EP Impurity E
Lovastatin EP Impurity F
Lovastatin Hydroxy Acid Allyl Ester
Lovastatin Hydroxy Acid 3,5-Acetonide Allyl Ester
Lovastatin Hydroxy Acid 3,5-Acetonide
Lovastatin 3,5-Acetonide Lovastatin Ester
Lovastatin Diol Lactone 4-tert-Butyldimethylsilyl Ether
4-O-tert-Butyldimethylsilyl Epi Lovastatin
Cis-2,3-Dehydro Lovastatin Acid Sodium Salt
Des(2-methylbutyryl) Lovastatin Hydroxy Acid Sodium Salt
Epi Lovastatin
Epi Lovastatin Hydroxy Acid Sodium Salt
6’-Exomethylene Lovastatin
Lovastatin Lactone Diol
(S,S)-3-Hydroxy Lovastatin
6’-Hydroxymethyl Lovastatin Sodium Salt
Keto Lovastatin
Lovastatin Hydroxy Impurity
Lovastatin Keto Impurity
Lovastatin Impurity 1
Lovastatin Impurity 2
Lovastatin EP Impurity B Sodium Salt
Acetyllovastatin
