Abacavir Pharmaceutical Reference Standards

Aligns Pharma science supply high-quality impurities reference standards of Abacavir, pharmacopeial and non-pharmacopeial Abacavir impurities, metabolites, stable isotope products, and nitrosamines (N-NO products). Abacavir impurities reference standards are useful in pharmaceutical research. They are useful in product development, ANDA and DMF filing, quality control (QC), method validation, and stability studies. It is also useful in the identification of unknown impurities and the assessment of genotoxic potential.

Abacavir is an antiviral nucleoside reverse transcriptase inhibitor used in combination with other antiretrovirals for the treatment of HIV. Abacavir (ABC) is a powerful nucleoside analog reverse transcriptase inhibitor (NRTI) used to treat HIV and AIDS. Chemically, it is a synthetic carbocyclic nucleoside and is the enantiomer with 1S, 4R absolute configuration on the cyclopentene ring. In vivo, Abacavir sulfate dissociates to its free base, Abacavir.

Our Abacavir impurities reference standard offering includes:

• Abacavir related products are thoroughly characterized with NMR, MASS, IR and HPLC/ GC purity.
• Abacavir products are supplied with detailed COA & analytical data meeting regulatory compliance.
• We can also provide Abacavir EP/USP traceable standards based on your requirements.
• The supplied Abacavir related products are re-tested at regular intervals.