Input interpretation
weak acids | melting point
Summary
median | 123 °C highest | 300 °C (L-leucine and L-tyrosine) lowest | -115 °C (triethylamine) distribution | | (based on 49 values; 5 unavailable)
Entities with missing values
fulminic acid | hypochlorous acid | ethanethiol | sulfurous acid | L-alanine (total: 5)
Distribution plots
(melting point in degrees Celsius)
Melting point rankings
1 | triethylamine | -115 °C 2 | hydrogen sulfide | -85 °C 3 | hydrogen fluoride | -83.36 °C 4 | ethyl acetoacetate | -43 °C 5 | nitromethane | -29 °C 6 | phenyl mercaptan | -15 °C 7 | dinitromethane | -15 °C 8 | hydrogen cyanide | -13.4 °C 9 | hydrogen peroxide | -0.43 °C 10 | peroxyacetic acid | 0.1 °C ⋮ | | 40 | L-proline | 228 °C 41 | L-asparagine | 235 °C 42 | glycine | 240 °C 43 | L-aspartic acid | 251 °C 44 | L-phenylalanine | 272.5 °C 45 | L-isoleucine | 280 °C 46 | L-histidine | 282 °C 47 | L-tryptophan | 290 °C 48 | L-tyrosine | 300 °C 49 | L-leucine | 300 °C (based on 49 values; 5 unavailable)
Unit conversions for median melting point 123 °C
396.2 K (kelvins)
253.4 °F (degrees Fahrenheit)
713.1 °R (degrees Rankine)
98.4 °Ré (degrees Réaumur)
72.07 °Rø (degrees Rømer)
Comparison for median melting point 123 °C
4 °C below hottest temperature of a Concorde nose tip (127 °C)
23.02 °C above water boiling point (at standard pressure) (99.9839 °C)
103 °C above conventional US room temperature (68 °F)
Corresponding quantities
Thermodynamic energy E from E = kT: | 34 meV (millielectronvolts)
Blackbody energy flux Φ from Φ = σT^4: | 1397 W/m^2 (watts per square meter)
Approximate luminous exitance from a planar blackbody radiator perpendicular to its surface: | 2.2×10^-14 lx (lux)
Nearest corresponding gas marks for median melting point 123 °C (degrees Celsius)
| temperature | usage gas mark 1/2 | 120 °C | United Kingdom thermostat 4 | 120 °C | France (actual measurements may vary)