In contrast to previously reported electron-super-rich trihydroxy-, triamino- and diaminohydroxymethyl radicals, the title aminodihydroxymethyl radical (1) generates a fraction of metastable species in, the form of their deuterium isotopologues. The lifetimes of metastable radicals produced by femtosecond collisional electron transfer to aminodihydroxymethyl cations exceed 4 us. The main fraction of 1 dissociates by fast loss of a hydroxyl hydrogen atom to form carbamic acid. Loss of an amino hydrogen atom is less facile and becomes <10% competitive at high internal energies or if the main dissociation is slowed down by deuterium isotope effects. RRKM calculations of unimolecular rate constants on a CCSD(T)/aug-cc-pVTZ potential energy surface gave a reasonably good fit for the competitive dissociations of I but not for the fraction of nondissociating radicals. The metastable species are attributed to excited electronic states which are predicted to have favorable Franck-Condon factors for being formed by collisional electron transfer.