Molybdenum traded flat at 525.05 CNY/Kg on September 10, 2025. Over the past month, Molybdenum's price has risen 7.15%, and is up 8.82% compared to the same time last year, according to trading on a contract for difference (CFD) that tracks the benchmark market for this commodity. Molybdenum - values, historical data, forecasts and news - updated on September of 2025.

View monthly updates and historical trends for Molybdenum Spot Price. Source: International Monetary Fund. Track economic data with YCharts analytics.

In 2024, the Indian ferro-molybdenum market decreased by -38.4% to $65M, falling for the second consecutive year after three years of growth. In general, consumption continues to indicate a perceptible contraction. Over the period under review, the market hit record highs at $109M in 2022; however, from 2023 to 2024, consumption remained at a lower figure.

Chilean Copper Commission (Cochilco) database on Copper providing data on (spot and future) 'prices' for copper, Gold, Silver, Molybdenum/Palladium, Selenium from LME (London Metal Exchange) and COMEX (Commodity Exchange), on 'copper's exchange inventories' from LME, COMEX and SHFE (Shanghai Futures Exchange), on 'exchange-traded copper contracts' from LME and COMEX, on 'copper futures and options: LME volume and open interests' from LME and on 'global copper, molybdenum, gold and silver production'.

Website: http://www.cochilco.cl:4040/boletin-web/

Substitution of a methyl by a trifluoromethyl moiety in well-known β-ketimines afforded the ligands (Ar)NC(Me)CH2CO(CF3) (HLH, Ar = C6H5; HLMe, A r= 2,6-Me2C6H3; HLiPr, Ar = 2,6-iPr2C6H3). Subsequent complexation to the [MoO2]2+ core leads to the formation of novel complexes of general formula MoO2(LR)2. For reasons of comparison the oxo-imido complex MoO(NtBu)(LMe)2 has also been synthesized. Complexes 1–4 were investigated in oxygen atom transfer (OAT) reactions using the substrate trimethylphosphine. The respective products after OAT, the reduced MoIV complexes MoO(PMe3)(LR)2 and Mo(NtBu)(PMe3)(LMe)2, were isolated. All complexes have been characterized by NMR spectroscopy, and 1–4 also by cyclic voltammetry. A positive shift of the MoVI–MoV reduction wave upon fluorination was observed. Furthermore, molecular structures of complexes 2, 4, 5, and 8 have been determined via single crystal X-ray diffraction analysis. Complex 8 represents a rare example of a MoIV phosphino-imido complex. Kinetic measurements by UV–vis spectroscopy of the OAT reactions from complexes 1–4 to PMe3 showed them to be more efficient than previously reported nonfluorinated ones, with ligand L′ = (Ar)NC(Me)CH2CO(CH3) MoO2(L′)2 and MoO(NtBu)(L′)2, respectively. Thermodynamic activation parameters ΔH‡ and ΔS‡ of the OAT reactions for complexes 2 and 4 have been determined. The activation enthalpy for the reaction employing 2 is significantly smaller (12.3 kJ/mol) compared to the reaction with the nonfluorinated complex 9 (60.8 kJ/mol). The change of the entropic term ΔS‡ is small. The reaction of the oxo-imido complex 4 to 8 revealed a significant electron-donating contribution of the imido substituent.