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This work studied the oxidative degradation performance of manganese gluconate as a liquid redox sulfur recovery (LRSR) agent. The degradation of gluconate in an aerated sulfide containing 0.1 M manganese/0.8 M gluconate/pH 13 solution was 11% in 47 h and 20% in 100 h of reaction time. With the total price of chelates being more or less comparable, these were superior to the degradation resistance of EDTA chelate in a solution of 0.1 M iron/0.2 M EDTA/pH 8 which degraded by about 30% in 47 h, and NTA in Fe-NTA (0.1 M metal/0.2 M chelate/pH 6.5), which was degraded by 40% in 100 h of reaction time. At pH of 13, 0.1 M Metal, and 0.8 M gluconate, manganese degraded gluconate more severely than iron and copper. At a lower chelate to metal molar ratio (RCM) of 2 and as well as at a lower pH of 10, the manganese gluconate degradation, expressed as relative concentration to its initial concentration, was faster than at RCM of 8 and pH of 13. All of these observations can be explained among others by the well-known Fenton reaction hydroxyl radicals mechanism as the main cause of the degradation process.