Physico-chemical characterization of high energetic nitropyrazoles has been conducted, including studies on the thermal decomposition under non-isothermal and isothermal conditions, burning behavior, and flame structure. The thermal stability of dinitropyrazoles, such as 3,4-dinitro-IH-pyrazole (3,4-DNP), N-(3,5-dinitro-1H-pyrazol-4-y1)-[1,2,4]triazolo[4,3-b][1,2,4,51tetrazin-6-amine (ADNPTrTz), and 3,3',4,4'-tetranitro-1,1'H-bipyrazole-5,5' (TNBP) in the liquid phase lies between stability of nitramines RDX and HMX. The decomposition of dinitropyrazole moiety in 3,4-DNP and TNBP starts from a nitro group loss. If the nitropyrazole molecule contains the amino group, the thermal decomposition may begin with NO2 group isomerization followed by decomposition of either the pyrazole ring or formed furazan cycle. The pyrazole moiety is resistant to oxidation by NO2, leading to low heat effect at the initial decomposition stages and bringing about difficulties in determining real kinetics from DCS experiments. The activation energy of decomposition of 4-amino-3,5-dinitro-1H-pyrazole (ADNP) appeared to be rather low (108.8 kJ mol(-1)) that might be indicative of possible hazard in handling this compound, even though its decomposition temperature is high enough. Combustion studies have shown that the burning rate of the nitropyrazoles depends on the surface temperature as well as on the condensed-phase heat release rate which, in turn, is subject to the decomposition kinetics. Thermocouple-aided measurements have revealed the surface temperatures of 3,4-DNP and ADNP both to be high enough and close to that of RDX. A shortage of heat to warm up the compound to the surface temperature is supposed to be a reason for (a) the observed combustion instability of ADNP and ADNPTrTz at low pressures, (b) occurrence of high pressure limit of 3,4-DNP combustion, and (c) inability of TNBP to burn at pressures up to 15 MPa. (C) 2017 Elsevier B.V. All rights reserved.