In fluids of sufficient temperature
and residence time, certain
organic species are observed to equilibrate, and their abundances
become diagnostic of reaction conditions, including temperature, redox
state, and pH. Organic species released from remote geologic and planetary
settings can therefore serve as geochemical tracers for environments
that are difficult to observe directly. Here, we provide a framework
for selecting organic compounds as geochemical tracers based on kinetic
modeling. We characterized temperature-dependent rates of deamination
substitution reactions for aqueous protonated benzylamines, i.e.,
benzylaminiums, to form benzyl alcohols and ammonium. Hydrothermal
experiments were conducted at 200–300 °C at liquid–vapor
water saturation pressures with ring-substituted benzylaminiums expected
to have comparable deamination rates to environmentally abundant aminiums,
e.g., amino acids. We compared rates extrapolated from experiments
to idealized natural systems, taking into account fluid temperatures
and residence times. Our results indicate that reversible deamination/hydration
reactions may equilibrate over geologic time scales across diverse
environments, including those approaching freezing temperatures for
the most reactive benzylaminium. Therefore, similar reaction constituents
may be useful targets for the exploration of potentially habitable
subsurface environments, such as icy ocean worlds of the solar system.
Our investigation supports previous findings that aqueous deamination
of benzylaminiums operates via two simultaneous substitution mechanisms,
SN1 and SN2. We find that for certain benzylaminiums,
rates of each mechanism should be modeled individually to improve
extrapolation across temperatures. Extrapolations of observed (i.e.,
bulk) deamination kinetics to near-ambient temperatures (∼50
°C) without mechanistic considerations can produce discrepancies
in reaction half-lives on the order of a billion years.