Input interpretation
![organic solvents | melting point](../image_source/32f10aa7d0b0b5f22efa1e448006bb8f.png)
organic solvents | melting point
Summary
![median | -43.5 °C highest | 17.5 °C (dimethyl sulfoxide) lowest | -129.67 °C (N-pentane) distribution |](../image_source/fbfec5be2df9b514b19d717a75e1bb49.png)
median | -43.5 °C highest | 17.5 °C (dimethyl sulfoxide) lowest | -129.67 °C (N-pentane) distribution |
Distribution plots
![(melting point in degrees Celsius)](../image_source/cf7b6a96be77f5eec1a31af1aaeeafb1.png)
(melting point in degrees Celsius)
Melting point rankings
![1 | N-pentane | -129.67 °C 2 | ethanol | -114 °C 3 | tetrahydrofuran | -108 °C 4 | methanol | -98 °C 5 | N-hexane | -95.35 °C 6 | acetone | -94 °C 7 | N-heptane | -91 °C 8 | chloroform | -63 °C 9 | acetonitrile | -48 °C 10 | chlorobenzene | -45 °C 11 | pyridine | -42 °C 12 | ethylene dichloride | -35 °C 13 | nitromethane | -29 °C 14 | carbon tetrachloride | -23 °C 15 | ethylene glycol | -13 °C 16 | cyclohexane | 5.5 °C 17 | benzene | 5.5 °C 18 | hexamethylphosphoric triamide | 7 °C 19 | acetic acid | 16.2 °C 20 | dimethyl sulfoxide | 17.5 °C](../image_source/d88b3e1010b7d29e684b7d82fa910c88.png)
1 | N-pentane | -129.67 °C 2 | ethanol | -114 °C 3 | tetrahydrofuran | -108 °C 4 | methanol | -98 °C 5 | N-hexane | -95.35 °C 6 | acetone | -94 °C 7 | N-heptane | -91 °C 8 | chloroform | -63 °C 9 | acetonitrile | -48 °C 10 | chlorobenzene | -45 °C 11 | pyridine | -42 °C 12 | ethylene dichloride | -35 °C 13 | nitromethane | -29 °C 14 | carbon tetrachloride | -23 °C 15 | ethylene glycol | -13 °C 16 | cyclohexane | 5.5 °C 17 | benzene | 5.5 °C 18 | hexamethylphosphoric triamide | 7 °C 19 | acetic acid | 16.2 °C 20 | dimethyl sulfoxide | 17.5 °C
Unit conversions for median melting point -43.5 °C
![229.7 K (kelvins)](../image_source/15771188ef83a34b2b54d6fed1501ebd.png)
229.7 K (kelvins)
![-46.3 °F (degrees Fahrenheit)](../image_source/cb1c4daea49922bdb6a6a73722edfa0d.png)
-46.3 °F (degrees Fahrenheit)
![413.4 °R (degrees Rankine)](../image_source/07dd05e8564332d072d37d1917c1ceb8.png)
413.4 °R (degrees Rankine)
![-34.8 °Ré (degrees Réaumur)](../image_source/ae27760ee2f0535314678491d794828c.png)
-34.8 °Ré (degrees Réaumur)
![-15.34 °Rø (degrees Rømer)](../image_source/83055a62e4e86a16d1f2a4891626b04b.png)
-15.34 °Rø (degrees Rømer)
Comparison for median melting point -43.5 °C
![25.72 °C below temperature of the ice/salt mixture defining the zero point of the Fahrenheit temperature scale (0 °F)](../image_source/53070407912bc4a20c224b68678d6694.png)
25.72 °C below temperature of the ice/salt mixture defining the zero point of the Fahrenheit temperature scale (0 °F)
![3.5 °C below Celsius/Fahrenheit crossover temperature (-40 °C)](../image_source/68dab56994268ae6d535ea1b698d30f4.png)
3.5 °C below Celsius/Fahrenheit crossover temperature (-40 °C)
![34.5 °C above boiling point of dry ice-acetone slurry (-78 °C)](../image_source/b0ad9ddfb0ec779d1ad2aa83ddd7c2e7.png)
34.5 °C above boiling point of dry ice-acetone slurry (-78 °C)
Corresponding quantities
![Thermodynamic energy E from E = kT: | 20 meV (millielectronvolts)](../image_source/894f2954c34edf6e08612d8647725ffb.png)
Thermodynamic energy E from E = kT: | 20 meV (millielectronvolts)
![Blackbody energy flux Φ from Φ = σT^4: | 158 W/m^2 (watts per square meter)](../image_source/941f6845f1008a2089ec2931113954e5.png)
Blackbody energy flux Φ from Φ = σT^4: | 158 W/m^2 (watts per square meter)
![Approximate luminous exitance from a planar blackbody radiator perpendicular to its surface: | 4.8×10^-30 lx (lux)](../image_source/fdbf8d47ba3d602f07b34669e2d5bc1b.png)
Approximate luminous exitance from a planar blackbody radiator perpendicular to its surface: | 4.8×10^-30 lx (lux)