La impureza de abiraterona 12 | identificada bajo CAS 165334-72-5 | es un subproducto clave a considerar en el control de calidad y desarrollo farmacéutico | ya que afecta la pureza del lote y la seguridad del producto final. Esta impureza suele originarse en etapas de síntesis y puede presentar retos analíticos por similitud estructural con el compuesto principal | requiriendo técnicas como HPLC | LC-MS y RMN para su identificación y cuantificación precisas. Su evaluación incluye estudios de estabilidad | límites de aceptación y estrategias de purificación específicas para minimizar su presencia en procesos de fabricación y cumplir normativas regulatorias.
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