The occurrence of carbonate-rich mantle rocks and diamonds in kimberlite rocks provide evidence for the presence of CO2 in the mantle. Carbon is recycled into the mantle via subduction and released through volcanic outgassing. An important fraction is retained at depth where partial melting of subducted lithologies produce alkali-rich carbonates along the CaCO3-MgCO3-K2CO3 join that infiltrate the mantle wedge [1]. Although volumetrically minor, these melts act as effective metasomatic agents that are related to source regions for diamond-bearing kimberlites [2]. The mobility of carbon at depth is controlled by the physical properties of carbonate liquids that remain largely unknown [3,4]. Here we report in-situ density measurements of alkaline carbonates at crustal and upper mantle conditions using synchrotron X-ray absorption in a Paris-Edinburgh press at beamline Psiché (Synchrotron Soleil). Experiments were conducted in several compositions along the CaCO3-K2CO3 and MgCO3-K2CO3 join up to 1400 K and 3 GPa. The starting materials included a mixture of synthetic K2CO3 and natural calcite and K2Mg(CO3)2 glasses synthesized at 0.15 GPa and 1098 K in an internally heated pressure vessel. The samples were cold pressurized and heated until the molten stage was confirmed by X-ray diffraction. The results were fitted to derive the first robust model for the density of alkali carbonates that mimic liquids from the incipient melting of subducted lithologies at crustal and upper mantle conditions. We combine the results of the present study with available data on the viscosity of carbonate liquids and molecular dynamic predictions to discuss the mobility and migration rates of carbonate liquids in the upper mantle.[1] Litasov et al. 2012 Geology 41, 79-82. [2] Grassi and Schmidt 2011, Contrib Min Petr 162, 169-191. [3] Dobson et al. 1996, EPSL 143, 207-215. [4] Kono et al. 2014 Nature Communications 5:5091.