Venkatasai is a leading innovator in the field of pharmaceutical reference standards, offering high-quality Reference Standards of Abacavir, including both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope-labeled compounds, and nitrosamines (N-NO products). Our Abacavir impurity reference standards play a vital role in pharmaceutical research, supporting product development, ANDA and DMF filings, quality control (QC), method validation, and stability studies. They are also instrumental in identifying unknown impurities and evaluating genotoxic potential. All Abacavir-related products are thoroughly characterized and supplied with comprehensive Certificates of Analysis (COA) and analytical data that comply with regulatory standards. EP/USP traceable standards can also be provided upon request. Furthermore, all supplied products undergo periodic re-testing to ensure continued quality and reliability.
(S,S)-3-Hydroxy Lovastatin
4-O-tert-Butyldimethylsilyl Epi Lovastatin
6’-Exomethylene Lovastatin
6’-Hydroxymethyl Lovastatin Sodium Salt
Acetyllovastatin
Cis-2,3-Dehydro Lovastatin Acid Sodium Salt
Des(2-methylbutyryl) Lovastatin Hydroxy Acid Sodium Salt
Epi Lovastatin Hydroxy Acid Sodium Salt
Lovastatin
Lovastatin 3,5-Acetonide Lovastatin Ester
Lovastatin Diol Lactone 4-tert-Butyldimethylsilyl Ether
Lovastatin EP Impurity A
Lovastatin EP Impurity B
Lovastatin EP Impurity B Sodium Salt
Lovastatin EP Impurity C
Lovastatin EP Impurity D
Lovastatin EP Impurity E
Lovastatin EP Impurity F
Lovastatin Hydroxy Acid 3,5-Acetonide
Lovastatin Hydroxy Acid 3,5-Acetonide Allyl Ester
Lovastatin Hydroxy Acid Allyl Ester
Lovastatin Hydroxy Impurity
Lovastatin Impurity 1
Lovastatin Impurity 2
Lovastatin Keto Impurity
Lovastatin Lactone Diol
