Detection of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), which is responsible for numerous damages when overproduced, is crucial for a better understanding of H<sub>2</sub>O<sub>2</sub>-mediated signalling in physiological and pathological processes. For this purpose, various“<i>off-on</i>” small fluorescent probes relying on a boronate trigger have been developed. However, they suffer from low kinetics and do not allow forH<sub>2</sub>O<sub>2</sub>-detection<sub></sub>with a short response time. Therefore, more reactive sensors are still awaited. To address this issue, we have successfully developed the first generation of borinic-based fluorescent probes containing a coumarin-scaffold. We determined the <i>in vitro</i>kinetic constants of the probe toward H<sub>2</sub>O<sub>2</sub>-promotedoxidation. We measured 1.9x10<sup>4</sup>m<sup>-1</sup>.s<sup>-1</sup>as a second order rate constant, which is 10 000 faster than its boronic counterpart (1.8 m<sup>-1</sup>.s<sup>-1</sup>). This remarkable reactivity was also effective in a cellular context, rendering the borinic trigger an advantageous new tool for H<sub>2</sub>O<sub>2</sub>detection.