Nuclear magnetic resonance (NMR) and magnetic resonance imaging (MRI) are two extremely important techniques with applications ranging from molecular structure determination to human imaging.However,inmany cases the applicability of NMR and MRI are limited by inherently poor sensitivity and insufficient nuclear spin lifetime.H ere we demonstrate acost-efficient and fast techniquethat tackles both issues simultaneously.W eu se the signal amplification by reversible exchange (SABRE) technique to hyperpolarizet he target 1 Hnuclei and store this polarization in long-lived singlet (LLS) form after suitable radiofrequency (rf) pulses.C ompared to the normal scenario,weachieve three orders of signal enhancement and one order of lifetime extension, leading to 1 HNMR signal detection 15 minutes after the creation of the detected states.The creation of such hyperpolarized long-lived polarization reflects an important step forward in the pipeline to see such agents used as clinical probes of disease.Nuclear spin hyperpolarization has evolved as one of most important developments in NMR and MRI in recent years as it starts finding applications in human metabolomics, [1][2][3][4] where their detection holds great potential to create tools for the diagnose of diseases.A mong the various hyperpolarization techniques, [5] dynamic nuclear polarization (DNP) [6] and para-hydrogen-induced hyperpolarization (PHIP) [7] are two of the most popular techniques.I n2 009, an important variant to the PHIP technique [8,9] termed SABRE [10] was described that no longer required am olecular change to use para-hydrogen (p-H 2 )d erived hyperpolarization. Instead, in SABRE am etal catalyst reversibly binds p-H 2 and the hyperpolarization target. Thed ormant magnetism of p-H 2 transfers into the target through the scalar-coupling framework of these catalysts as illustrated in Scheme 1. Since its inception, this method has stimulated many developments which include the hyperpolarization of al arge class of molecules comprising of 1 H, 13 C, 15 N, and 31 Pn uclei. [11][12][13][14] When compared to dissolution DNP,S ABRE provides alow cost alternative that takes just seconds to hyperpolarize the agent in acontinuous process that, while being inherently simple in concept, can be augmented by rf excitation. [15] In order to advance the future integration of SABRE with molecular imaging,i ti sh ighly desirable to create hyperpolarized targets,t he magnetism of which survives transfer into ad iagnostically relevant region of the body.T his requirement is based on observations with DNP and PHIP, techniques that have been used to successfully prepare and detect 13 C-based magnetization in vivo [3,4] and also show potential for 15 N-based agents. [16] These reported low-gamma nuclei-based in vivo studies employ relatively slowly relaxing Zeeman-derived magnetization in order to overcome the rate of signal loss,b ut these approaches inherently measure aw eaker response than would be provided by 1 Hd etection, whilst requiring al arger gradient ...