Alkyl cyanoacrylate instant adhesives are widely used because of their fast cure speed and versatility on a large number of substrates. Recent performance improvements, such as increased thermal resistance, resulted from the addition of latent acids and polymers, which do not copolymerize with the adhesive monomer, to the adhesive formulations. However, use of these additives can increase fixture time or reduce the anal adhesive strength. Two methods for possibly improving alkyl cyanoacrylate instant adhesives, without loss of cure speed or adhesive properties, could be either crosslinking the alkyl cyanoacrylate monomer with a dicyanoacrylate or copolymerizing it with a second 1,1 disubstituted electron-deficient olefin. A crosslinker, 1,4 butanediol dicyanoacrylate (BDDCA) and two monofunctional monomers, diethyl methylenemalonate (DEMM) and N,N diethyl-2-cyanoacrylamide (DECA), were prepared, in good purity, for adhesion studies with ethyl cyanoacrylate (ECA). Crosslinking ECA with BDDCA does improve solvent resistance, as determined by solvent swelling experiments. Glass fixture times are approximately the same for EGA, crosslinked EGA, the pure monomers, and monomer mixtures with EGA, while steel fixture times are generally slower. Crosslinking ECA with BDDCA does not improve lap-shear adhesion, either at room temperature or after thermal exposure at 121 degrees C. Lap-shear strength data, before and after heat exposure, revealed that the ECA/DEMM and the ECA/DECA monomer mixtures exhibit weaker lap-shear adhesive strength than ECA alone.