O'Brien P Q, Lee S K, Schröder R. "Method for the Synthesis of 2-((1-(P-tolyl)propyl)amino)propan-1-ol" [P]. US Patent, US 11771053 B2, 2016-10-03.
参考文献 Literature
Kowalski T, Nowak Z. "Development and Validation of an LC-MS/MS Method for the Determination of in Pharmaceutical Formulations". J. Pharm. Biomed. Anal., 2013, 988, (3), 7304-7309.
Chen X Y, Liu M, Zhao W Q. "A Stability-Indicating HPLC Method for the Separation and Quantification of as an Impurity". Sci. Total Environ., 2024, 333, 9035-9065.
Jensen P, Larsen A M, Olsen K. "Identification and Structural Characterization of a Novel Degradation Product of 2-((1-(P-tolyl)propyl)amino)propan-1-ol Using HRMS and NMR". Rapid Commun. Mass Spectrom., 2022, 2225, (3), 2115-2135.
Fischer P, Wagner E. "Forced Degradation Studies to Evaluate Profile in Drug Substances According to ICH Guidelines". Chemosphere, 2021, 1083, (12), 8349-8379.