Sno particles were synthesized by an alkali-assisted hydrothermal and microwave methods. the aqueous-based reactions were carried out at pH ~ 8, under inert atmosphere (Ar). The reactions were taken under different times, and a full XRD structural analysis was made to evaluate the conversion from the Sn 6 o 4 (OH) 4 intermediate to Sno particles. Williamson-Hall analysis showed that the size and strain of the Sno particles were time and route treatment dependent. Microwave heating yielded a single tetragonal SnO phase after 1 h of thermal treatment, and TEM images revealed sphericalshaped SnO nanoparticles with an average size of 9(1) nm. While by the hydrothermal treatment single SnO phase was obtained only after 4 hours, yielding non-uniform and elongated particles with submicrometric size. A dissolution-recrystallization process was taken into account as the mechanism for Sno particles formation, in which hydroxylated complexes, Sn 2 (OH) 6 −2 , then condense to form the oxide. the time-shorting reaction provided by the microwave-assisted synthesis may be attributed to better heat distribution. Tin monoxide (SnO-Sn +2) and tin dioxide (SnO 2-Sn +4) are well-known semiconductors with p-type and n-type electronic properties, respectively 1-4. Their applications have encompassed technological areas such as optoelectronics, energy storage and sensing 5-8. SnO 2 is a pale-yellow solid with rutile-type structure and wide-bandgap (Eg = 3.6 eV) and very used for transparent conductive electrodes 7 , gas sensors 1,8 , electrochromic devices 3 and photoelectrodes 3,4. While SnO is a dark solid with tetragonal structure and variable optical bandgap (Eg = 2.7-3.4 eV) 9-11 , and used for gas sensor devices 12 , electrodes for rechargeable Li-ion batteries 13-15 , supercapacitors 16 , native p-type conducting material 17 , as well as catalyst and photocatalyst 18,19. The preparation of the SnO phase is harder than SnO 2 one, due to the favorable oxidation of the Sn +2 to the thermodynamically more stable Sn +4. Therefore, the synthetic challenge is to avoid this favorable oxidation, aside from the implementation of procedures that lead to well-controlled size and morphology. In this context, microand nano-crystalline SnO particles have been made by chemical/physical procedures, such as hydrothermal and solvothermal preparations, electrochemistry, ultrasound-and microwave-assisted routes, ionic liquids 19-26 , and thermal vapor deposition, thermal evaporation 3 , thermal chemical vapor deposition (CVD) 4 , and mechanical ball milling 8. Moreover, organic additives, surfactants, inert atmosphere (Ar or N 2) and reductive (H 2) gases are applied with purposes of improving the yield forward the lower valence phase 15,25,27,28. Thermal vapor deposition and a long time of a hydrothermal treatment have been pointed out as the better conditions to obtain single-crystalline SnO particles 26,29. Furthermore, in aqueous based-synthesis, the intermediate tin (II) oxyhydroxide, Sn 6 O 4 (OH) 4 , is often prepared from the hydroxylation ...