4-叔丁基苯甲醛是合成医药、染料、香料和香料的重要中间体。据报告，它是在冰醋酸中用过氧化氢部分氧化 4- 叔 -丁基甲苯过程中形成的，由溴离子与乙酸钴 (II) 或乙酸铈 (III) 结合催化。在基体辅助激光解吸电离 (MALDI) 室中进行了 4- 叔 丁基苯胺和 4- 叔 丁基苯甲醛在乙醇中的 Schiff 碱反应，对生成的亚胺进行了实时检测。 4- 叔丁基苯甲醛适用于动力学研究，以评价 4-取代苯甲醛抑制蘑菇酪氨酸酶的动力学常数 (KI)。 4-tert-Butylbenzaldehyde is an important intermediate for the synthesis of medicines, dyes, flavor and fragrance compounds. It is reported to be formed during the partial oxidation of 4-tert-butyltoluene by hydrogen peroxide in glacial acetic acid, catalyzed by bromide ions in combination with cobalt(II) acetate or cerium(III) acetate. Schiff base reaction between 4-tert-butylaniline and 4-tert-butylbenzaldehyde in ethanol has been carried out on-chip in the matrix assisted laser desorption ionization (MALDI) chamber, the formed imine was detected in real time. 4-tert-Butylbenzaldehyde is suitable for use in a kinetic study to evaluate the kinetic constants (KI) for inhibition of mushroom tyrosinase by 4-substituted benzaldehydes.