Inkjet printing enables the production of higher-resolution objects compared to other layer-by-layer additive manufacturing techniques, thanks to the exceptionally small droplets generated during the process 1. However, designing recyclable materials for inkjet printing remains a significant challenge. The polymeric resins must meet low-viscosity requirements while ensuring that deposited droplets solidify rapidly, to prevent inaccurate placement or material flow. This study presents a proof of concept utilizing reversible Diels-Alder chemistry for inkjet printing, achieving a balance between recyclability and material strength. The formulation consists of multi-armed furan monomers and an aliphatic bismaleimide, BMI–689. The kinetics of the Diels-Alder reaction between furan and maleimide groups were analyzed using variable-temperature attenuated total reflectance infrared (ATR-FTIR) spectroscopy, complemented by nuclear magnetic resonance (NMR) spectroscopy 2. This approach combined with rheological studies, provides insights into gelation behavior and reaction conversion under various conditions and formulations during the printing process. We highlight the range of material stiffness and elasticity and the tunability of the mechanical properties, being supported by tensile tests. The overall robustness of printed objects can be further improved by introducing a post-curing step where double Diels-Alder reactions are introduced 3. Overall, this work presents an alternative to the conventional inkjet formulations (irreversible acrylate cross-linking) and offers a promising avenue for developing recyclable inkjet-printed materials with other dissociative reversible reactions as well.