Category:
Preclinical Research Services
CAS NO:
34523-34-7
Standard:
USP, EP,
Paracetamol EP Impurity G (CAS 610-97-5) is a critical reference standard defined in the European Pharmacopoeia for the identification and quantification of degradation products in paracetamol. It is primarily synthesized via nitration pathways or oxidative side-reactions during active pharmaceutical ingredient manufacturing.
Strictly store in sealed containers at controlled temperatures below 25°C. Handle using appropriate PPE to avoid skin contact; this substance is not intended for clinical administration but serves solely as an analytical reference material.