The effects of electrochemically pre-dissolved hydrogen on room-temperature fracture initiation in Beta-C titanium (Ti-3Al-8V-6Cr-4Mo-4Zr wt pct) have been investigated using circumferentially notched tensile specimens. Finite element-based analysis of notch stress fields was used to define relationships between the local threshold stress for crack initiation vs total internal hydrogen concentration. The as-received, solution heat treated (ST, σy.2 pct=865 MPa) and the ST + peak-aged conditions (STA, σy.2% pct=1260 MPa) were compared after defining the relationships between the fracture process zone hydrogen concentration, hydrogen-metal interactions (i.e., hydrostatic stress field occlusion, trapping, hydriding), and the resulting fracture initiation behavior of each. Solutionized + peak-aged (β+α) Beta-C fractured intergranularly above total hydrogen concentrations of ∼1000 wt ppm. (5.1 at. pct). A fracture mode consistent with cleavage occurred at ∼2100 wt ppm. (10.7 at. pct). Solutionized Beta-C resisted hydrogen-assisted cracking (e.g., did not crack intergranularly) but was not immune; cleavage cracking was provoked at ∼4000 wt ppm. (20.4 at. pct). Coldworked ST Beta-C (CW, σy.2 pct=1107 MPa) did not crack intergranularly; fracture initiation behavior was similar to the ST condition regardless of specimen orientation. This suggests that high yield strength alone does not account for the susceptibility to intergranular cracking observed in the STA β+α condition. Stroke-rate studies and X-ray diffraction investigation of H partitioning suggests that equilibrium hydriding and/or irreversible trapping does not singularly control intergranular fracture initiation of the STA condition. Fractographic evidence and finite element results show that a finite plastic zone exists prior to intergranular fracture of the STA condition. This suggests that a criterion for fracture that incorporates plastic strain and stress should be considered.