Advanced experiments in gene technology demonstrate that even small amounts of free DNA molecules are sufficient to cause infections, re-combinations or biological transformations and new methods with extremely low detection limits for the presence of DNA molecules have been developed. Therefore, detection of DNA contaminations or prevention of amplification artifacts in PCR experiments are essential in all applications. Accordingly, the complete decontamination of equipment and laboratory surfaces from any DNA molecules is important for biological containment and safety. These new developments motivated us to investigate the molecular mechanism of action of our product DNA-Exitus™ in comparison to other commercially available DNA decontamination reagents. Two major problems were apparent: First, none of the conventional reagents destroyed DNA molecules efficiently and second, all reagents contained components with corrosive or even toxic properties. Consequently, we saw the necessity to develop new solutions for effective DNA decontamination. For the first time we present the completely new DNA decontamination reagent DNA-ExitusPlus™. In comparison with conventional products, DNA-ExitusPlus™ guarantees fast and efficient destruction of nucleic acids without corrosive or toxic properties.