Atomoxetine Impurity H is a specified degradation product and synthetic intermediate of the noradrenaline reuptake inhibitor Atomoxetine. It serves as a critical reference standard for quality control in pharmaceutical manufacturing, ensuring compliance with ICH guidelines regarding genotoxic impurities. The compound is characterized by its specific molecular structure C17H20N2O and is uniquely identified by CAS number 159644-89-8. Production typically involves controlled oxidation or hydrolysis pathways during the active pharmaceutical ingredient synthesis.
This substance is strictly for research and development purposes only and must not be used in clinical settings. Storage requires containment in sealed containers at temperatures between 2°C and 8°C within a well-ventilated area. Personnel handling this material must utilize appropriate personal protective equipment to prevent dermal contact or inhalation exposure.