As a white to off – white crystalline powder, it has good solubility in organic solvents, suitable for formulating oral tablets and suspensions with once – daily dosing convenience. It strictly complies with GMP standards and meets the needs of pulmonary hypertension drug manufacturers, cardiovascular drug developers and clinical supply chains. It is mainly indicated for WHO Group I pulmonary arterial hypertension (PAH) to improve exercise capacity, delay clinical deterioration and reduce hospitalization risksNational Center for Biotechnology Information. Compared with similar drugs, it has fewer drug interactions and lower liver injury risks, which is a reliable raw material for long – term PAH treatment.