Reactive carbonyl species (RCS), such as acrolein (ACR), glyoxal (GO), and methylglyoxal (MGO), have received extensive attention recently as a result of their high activity and toxicity in vitro and in vivo. In the present study, propyl gallate (PG), a common food antioxidant, was found to effectively trap more ACR than butylated hydroxytoluene and butylated hydroxyanisole through the formation of mono-ACR adducts (PG−ACR) and di-ACR adducts (PG−2ACR). The two adducts were successfully purified, and their structures were elucidated on the basis of their high-resolution mass spectrometry and 1 H, 13 C, and two-dimensional nuclear magnetic resonance data. We further identified that PG−ACR had the ability to continue to trap GO and MGO to form PG−ACR−GO and PG−ACR−MGO, respectively, by liquid chromatography−tandem mass spectrometry (LC−MS/MS). Furthermore, we verified that PG could inhibit the production of ACR, GO, and MGO via trapping these RCS simultaneously to form the corresponding adducts in pound cakes using LC−MS/MS.