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.
2-Ethylhexanoic acid
2-Ethylhexanoic acid Potassium Salt
2-Ethylhexanoic acid Sodium Salt
3-cyclohexylpropionic acid
Ceftriaxone 3-ene isomer
Ceftriaxone Disodium Hemiheptahydrate
Ceftriaxone Disodium Hydrate
Ceftriaxone EP Impurity A
Ceftriaxone EP Impurity A Sodium Salt
Ceftriaxone EP Impurity B
Ceftriaxone EP Impurity C
Ceftriaxone EP Impurity C Sodium Salt
Ceftriaxone EP Impurity D
Ceftriaxone EP Impurity D Hydrochloride
Ceftriaxone EP Impurity E
Ceftriaxone EP Impurity E Hydrochloride
Ceftriaxone EP Impurity E Sodium Salt
Ceftriaxone Impurity 1
Ceftriaxone Impurity 2
Ceftriaxone Impurity 3
Ceftriaxone Impurity 4
Ceftriaxone Impurity Cefotaxime
Ceftriaxone Impurity MBT Potassium Salt
Ceftriaxone Impurity MBT Sodium Salt
Ceftriaxone Triazine Analog
