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Abstract The degassing of CO₂and S from arc volcanoes is fundamentally important to global climate, eruption forecasting, ore deposits, and the cycling of volatiles through subduction zones. However, all existing thermodynamic/empirical models have difficulties reproducing CO₂‐H₂O‐S trends observed in melt inclusions and provide widely conflicting results regarding the relationships between pressure and CO₂/SO₂in the vapor. In this study, we develop an open‐source degassing model, Sulfur_X, to track the evolution of S, CO₂, H₂O, and redox states in melt and vapor in ascending mafic‐intermediate magma. Sulfur_X describes sulfur degassing by parameterizing experimentally derived sulfur partition coefficients for two equilibria: RxnI. FeS (m) + H₂O (v)  H₂S (v) + FeO (m), and RxnII. CaSO₄(m)  SO₂(v) + O₂(v) + CaO (m), based on the sulfur speciation in the melt (m) and co‐existing vapor (v). Sulfur_X is also the first to track the evolution offO₂and sulfur and iron redox states accurately in the system using electron balance and equilibrium calculations. Our results show that a typical H₂O‐rich (4.5 wt.%) arc magma with high initial S⁶⁺/ΣS ratio (>0.5) will degas much more (∼2/3) of its initial sulfur at high pressures (>200 MPa) than H₂O‐poor ocean island basalts with low initial S⁶⁺/ΣS ratio (<0.1), which will degas very little sulfur until shallow pressures (<50 MPa). The pressure‐S relationship in the melt predicted by Sulfur_X provides new insights into interpreting the CO₂/S_Tratio measured in high‐T volcanic gases in the run‐up to the eruption.