kJ/mol ΔG° f @25°C kJ/mol S° @25°C J/(mol K) C p @25°C J/(mol K) Bromoform (g) CHBr 3 25 16 331 71 Chloroform (l) CHCl 3 -134.1 -73.7 201.7 114.2 Chloroform (g) CHCl 3 -102.7 6.0 295.7 65.7 Formic acid (l) CH 2 O 2 -425 -361.4 129 99 Formic acid (g) CH 2 O 2 -378.7 Methyl (g) CH 3 145.7 47.9 194.2 38.7 Bromomethane (l) CH 3 Br -59.8 Bromomethane (g) CH 3 Br -35.4 -26.3 246.4 42.4 Chloromethane (g) CH 3 Cl -81.9 -63 234.6 40.8 Fluormethane (g) CH 3 F -234 -210 222.9 37.5 Iodomethane (l) CH 3 I -13.6 136.2 126 Iodomethane (g) CH 3 I 14.4 16 254.1 44.1 Nitromethane (l) CH 3 NO 2 -112.6 -14.4 171.8 106.6 Nitromethane (g) CH 3 NO2 -80.8 -7 282.9 55.5 Methane (g) CH 4 -74.6 -50.5 186.3 35.7 Methanol (l) CH 4 O -239.2 -166.6 126.8 81.1 Methanol (g) CH 4 O -201 -162.3 239.9 44.1 Methylamine (l) CH 5 N -47.3 35.7 150.2 102.1 Methylamine (g) CH 5 N -22.5 32.7 242.9 50.1 Ethyne (acetylene) (g) C 2 H 2 226.9 209 201 44 Ethene (g) C 2 H 4 52.5 68.4 219.3 42.9 Acetic acid (l) C 2 H4O 2 -484.3 -389.9 159.8 123.3 Acetic acid (g) C 2 H4O 2 -432.2 -374.2 283.5 63.4 Bromoethane (l) C 2 H 5 Br -90.5 -25.8 198.7 100.8 Bromoethane (g) C 2 H 5 Br -61.9 -23.9 286.7 64.5 Chloroethane (l) C 2 H 5 Cl -136.8 -59.3 190.8 104.3 Chloroethane (g) C 2 H 5 Cl -112.1 -60.4 276 62.8 Nitroethane (l) C2H 5 NO 2 -143.9 134.4 Nitroethane (g) C2H 5 NO 2 -103.8 -5 320.5 79 Ethane (g) C 2 H 6 -84 -32 229.2 52.5 Ethanol (l) C 2 H 6 O -277.6 -174.8 160.7 112.3 Ethanol (g) C 2 H 6 O -234.8 -167.9 281.6 65.6 Methoxymethane (l) C 2 H 6 O -203,3 Methoxymethane (g) C 2 H 6 O -184.1 -112.6 266.4 Ethylamine (l) C 2 H 7 N -74.1 130 Ethylamine (g) C 2 H 7 N -47.5 36.3 283.8 71.5 Cyclopropene (g) C 3 H 4 277.1 286 244 53 Propyne (g) C 3 H 4 185 194 248 61 Cyclopropane (l) C 3 H 6 35.2 Cyclopropane (g) C 3 H 6 53.3 104.5 237.5 55.6 Propene (g) C 3 H 6 20 62 267 64 Acetone (l) C 3 H 6 O -248.4 199.8 126.3 Acetone (g) C 3 H 6 O -217.1 -152.7 295.3 74.5 Propanoic acid (l) C 3 H 6 O 2 -510.7 191 152.8 Propanoic acid (g) C 3 H 6 O 2 -455.7 Propane (l) C 3 H 8 -120.9 Propane (g) C 3 H 8 -103.8 -23.4 270.3 73.6 1-Propanol (l) C 3 H 8 O -302.6 193.6 143.9 1-Propanol (g) C 3 H 8 O -255.1 322.6 85.6 2-Propanol (l) C 3 H 8 O -318.1 181.1 156.5 2-Propanol (g) C 3 H 8 O -272.6 309.2 89.3 1-Propanamine (g) C 3 H 9 N -72 40 324 1-Butyne (l) C 4 H 6 141.4 1-Butyne (g) C 4 H 6 165.2 202 291 81 2-Butyne (l) C 4 H 6 119.1 2-Butyne (g) C 4 H 6 145.7 185 283 78 Cyclobutene (g) C 4 H 6 156.7 175 64 64 2-Methyl-1-propene (g) C 4 H 8 -17 58 294 89 1-Butene (l) C 4 H 8 -20.8 227 118 1-Butene (g) C 4 H 8 0.1 71 306 86 Cyclobutane (l) C 4 H 8 3.7 Cyclobutane (g) C 4 H 8 27.7 110 265 nd Butanoic acid (l) C 4 H 8 O 2 -533.8 222.2 178.6 Butanoic acid (g) C 4 H 8 O 2 -475.9 2-Methylpropane (g) C 4 H 10 -135 -21 295 97 Butane (l) C 4 H 10 -147.3 140.9 Butane (g) C 4 H 10 -125.7 -17 310 98 1-Butanol (l) C 4 H 10 O -327.3 225.8 177.2 1-Butanol (g) C 4 H 10 O -274.9 2-Butanol (l) C 4 H 10 O -342.6 214.9 196.9 2-Butanol (g) C 4 H 10 O -292.8 359.5 112.7 1-Pentyne (g) C 5 H 8 144 210 330 105 2-Pentyne (g) C 5 H 8 129 194 332 99 Cyclopentene (l) C 5 H 8 4.3 201.2 122.4 Cyclopentene (g) C 5 H 8 34 111 290 75 1-Pentene (l) C 5 H 10 -46.9 262.6 154 1-Pentene (g) C 5 H 10 -21.1 79 346 110 2-Methyl-1-butene (g) C 5 H 10 -35.2 66 340 112 2-Methyl-1-butene (l) C 5 H 10 -61.1 254 157.2 Cyclopentane (l) C 5 H 10 -105.1 204.5 128.8 Cyclopentane (g) C 5 H 10 -76.4 39 293 83 Pentanoic acid (l) C 5 H 10 O 2 -559.4 259.8 210.3 Pentanoic acid (g) C 5 H 10 O 2 -491.9 2,2-Dimethylpropane (g) C 5 H 12 -166 -15 306 122 2-Methylbutane (g) C 5 H 12 -155 -15 344 119 Pentane (l) C 5 H 12 -173.5 167.2 Pentane (g) C 5 H 12 -146.9 -8 349 120 1-Pentanol (l) C 5 H 12 O -351.6 208.1 1-Pentanol (g) C 5 H 12 O -294.6 2-Pentanol (l) C 5 H 12 O -365.2 2-Pentanol (g) C 5 H 12 O -311 3-Pentanol (l) C 5 H 12 O -368.9 239.7 3-Pentanol (g) C 5 H 12 O -314.9 Methyl tert-butyl ether(l) C 5 H 12 O -313.6 265.3 187.5 Methyl tert-butyl ether(g) C 5 H 12 O -283.7 Benzene (l) C6H6 49.1 124.5 173.4 136 Benzene (g) C6H6 82.9 129.7 269.2 82.4 Aniline (l) C6H7N 191.9 Aniline (g) C6H7N 87.5 -7 317.9 107.9 1-Hexyne (g) C6H10 124 219 369 128 Cyclohexene (l) C6H10 -28.5 214.6 148.3 Cyclohexene (g) C6H10 -5 107 311 105 1-Hexene (l) C6H12 -74.2 295.2 183.3 1-Hexene (g) C6H12 -43.5 87 385 132 2-Methyl-1-pentene (g) C6H12 -59.4 2-Methyl-1-pentene (l) C6H12 -90 Cyclohexane (l) C6H12 -156.4 154.9 Cyclohexane (g) C6H12 -123.4 32 298 106 Methylcyclopentane(g) C6H12 -106.2 Methylcyclopentane(l) C6H12 -137.9 Hexanoic acid (l) C6H12O2 -583.8 Hexanoic acid (g) C6H12O2 -511.9 2,2-Dimethylbutane(g) C6H14 -185.9 -10 358 142 2,2-Dimethylbutane(l) C6H14 -213.8 272.5 191.9 2-Methylpentane (g) C6H14 -174.6 -5 381 144 2-Methylpentane (l) C6H14 -204.6 290.6 193.7 3-Methylpentane (g) C6H14 -171.9 -2 380 143 3-Methylpentane (l) C6H14 -202.4 292.5 190.7 Hexane (l) C6H14 -198.7 195.6 Hexane (g) C6H14 -166.9 -0.3 388 143 1-Hexanol (l) C6H14O -377.5 287.4 240.4 1-Hexanol (g) C6H14O 315.9 2-Hexanol (l) C6H14O -392 2-Hexanol (g) C6H14O -333.5 Phenol (s) C7H6O -165.1 144 127.4 Phenol (g) C7H6O -96.4 -33 316 104 Methylbenzene(l) C7H8 12.0 220 156 Methylbenzene(g) C7H8 50.0 122 321 104 1-Heptene (l) C7H14 -97.9 327.6 211.8 1-Heptene (g) C7H14 -62.3 96 424 15 Cycloheptane (l) C7H14 -156.6 Cycloheptane (g) C7H14 -118.1 Ethylcyclopentane (l) C7H14 -163.4 279.9 Ethylcyclopentane (g) C7H14 -126.9 Methylcyclohexane(g) C7H14 -154.7 Methylcyclohexane(l) C7H14 -190.1 184.8 Heptanoic acid (l) C7H14O2 -610.2 265.4 Heptanoic acid (g) C7H14O2 -536.2 2,2-Dimethylpentane (g) C7H16 -205.7 2,2-Dimethylpentane (l) C7H16 -238.3 300.3 221.1 2-Methylhexane (g) C7H16 -194.5 2-Methylhexane (l) C7H16 -229.5 323.3 222.9 3-Methylhexane (g) C7H16 -191.3 3-Methylhexane (l) C7H16 -226.4 Heptane (l) C7H16 -224.2 224.7 Heptane (g) C7H16 -187.6 8 428 166 1-Heptanol (l) C7H16O -403.3 272.1 1-Heptanol (g) C7H16O -336.5 Ethylbenzene (l) C8H10 -12.3 183.2 Ethylbenzene (g) C8H10 29.9 131 361 128 1-Octene (l) C8H16 -124.5 241 1-Octene (g) C8H16 -81.3 104 463 178 Cyclooctane (l) C8H16 -167.7 Cyclooctane (g) C8H16 -124.4 Ethylcyclohexane (l) C8H16 -212.1 280.9 211.8 Ethylcyclohexane (g) C8H16 -171.5 Octanoic acid (l) C8H16O2 -636 297.9 Octanoic acid (g) C8H16O2 -554.3 2-Methylheptane (g) C8H18 -215.3 2-Methylheptane (l) C8H18 -255 356.4 252 3-Methylheptane (g) C8H18 -212.5 3-Methylheptane(l) C8H18 -252.3 362.6 250.2 Octane (l) C8H18 -250.1 254.6 Octane (g) C8H18 -208.5 16 467 189 1-Octanol (l) C8H18O -426.5 305.2 1-Octanol (g) C8H18O -355.6 2,2-Dimethylhexane (g) C8H19 -224.5 2,2-Dimethylhexane (l) C8H19 -261.9 Propylcyclohexane (g) C9H1 -192 420 242 Propylbenzene (g) C9H12 8 137 401 154 1-Nonyne (l) C9H16 16.3 1-Nonyne (g) C9H16 62.3 Nonanoic acid (l) C9H18O2 -659.7 362.4 Nonanoic acid (g) C9H18O2 -577.3 2,2-Dimethylheptane(g) C 9 H 20 -246 2,2-Dimethylheptane(l) C 9 H 20 -288.1 Nonane (l) C 9 H 20 -274.7 284.4 Nonane (g) C 9 H 20 -228.2 25 506 212 1-Nonanol (l) C 9 H 20 O -453.4 1-Nonanol (g) C 9 H 20 O -376.5 Naphthalene (g) C 10 H 8 151 224 336 Butylbenzene (l) C 10 H 14 -63.2 321.2 243.4 Butylbenzene (g) C 10 H 14 -11.8 1-Decene (l) C 10 H 20 -173.8 425 300.8 1-Decene (g) C 10 H 20 -123.3 301 Butylcyclohexane (l) C 10 H 20 -263.1 345 271 Butylcyclohexane (g) C 10 H 20 -213.7 Decanoic acid (s) C 10 H 20 O 2 -713.7 Decanoic acid (l) C 10 H 20 O 2 -684.3 Decanoic acid (g) C 10 H 20 O 2 -594.9 2-Methylnonane (g) C 10 H 22 -260.2 2-Methylnonane (l) C 10 H 22 -309.8 420.1 313.3 Decane (l) C 10 H 22 -300.9 314.4 Decane (g) C 10 H 22 -249.5 33 545 235 1-Decanol (l) C 10 H 22 O -478.1 370.6 1-Decanol (g) C 10 H 22 O -396.6 1-Methylnaphthalene (l) C 11 H 10 56.3 254.8 224.4 2-Methylnaphthalene (s) C 11 H 10 44.9 220 196 2-Methylnaphthalene (g) C 11 H 10 106.7 1-Undecene (g) C 11 H 22 344.9 Undecane (l) C 11 H 24 -327.2 344.9 Undecane (g) C 11 H 24 -270.8 42 584 257 1-Undecanol (l) C 11 H 24 O -504.8 1-Dodecene (l) C 12 H 24 -226.2 484.8 360.7 1-Dodecene (g) C 12 H 24 -165.4 Dodecanoic acid (s) C 12 H 24 O 2 -774.6 404.3 Dodecanoic acid (l) C 12 H 24 O 2 -737.9 Dodecanoic acid (g) C 12 H 24 O 2 642 Dodecane (l) C 12 H 26 -350.9 375.8 Dodecane (g) C 12 H 26 -289.4 50 623 280 1-Dodecanol (l) C 12 H 26 O -528.5 438.1 1-Dodecanol (g) C 12 H 26 O -436.6 Anthracene (g) C 14 H 10 231 Phenantrene (g) C 14 H 10 207 Decylcyclopentane (l) C 15 H 30 -367.3 Decylbenzene (l) C 16 H 26 -218.3 Decylbenzene (g) C 16 H 26 -138.6 1-Hexadecene (l) C 16 H 32 -328.7 587.9 488.9 1-Hexadecene (g) C 16 H 32 -248.4 Hexadecanoic acid (s) C 16 H 32 O 2 -891.5 452.4 460.7 Hexadecanoic acid (l) C 16 H 32 O 2 -838.1 Hexadecanoic acid (g) C 16 H 32 O 2 -737.1 N-hexadecane (l) C 16 H 34 -456.1 501.6 N-hexadecane (g) C 16 H 34 -374.8 Chrysene (s) C 18 H 12 145.3 Chrysene (g) C 18 H 12 269.8 See also Standard state and enthalpy of formation, Gibbs free energy of formation, entropy and heat capacity for ΔH° f , ΔG° f , S° and C p for more than 370 inorganic substances and gases , common liquids and fluids , food and foodstuff , metals and semimetals , common solids and other common substances for tabulated values of specific heat capacity, c p .
For conversion of units, use the Specific heat online unit converter.
The specific heat capacity can be calculated from the molar heat capacity, and vise versa:
c p = C p / M and
C p = c p . M
where
c p = specific heat capacity
C p = molar heat capacity
M = molar weight of the actual substance (g/mol).
Sponsored Links
Related Topics Heating systems - capacity and design of boilers, pipelines, heat exchangers, expansion systems and more.
Material properties of gases, fluids and solids - densities, specific heats, viscosities and more.
Work, heat and energy systems.
Related Documents Properties of alternative fuels like biodiesel, E85, CNG and more.
Heat of combustion (energy content) for som common substances - with examples how to calculate heat of combustion.
The amount of heat required to change the temperature of a substance by one degree.
Physical constants for more than 280 common inorganic compounds. Density is given for the actual state at 25°C and for liquid phase at melting point temperature.
Specific heat of commonly used metals like aluminum, iron, mercury and many more - imperial and SI units.
Online calculator, figures and tables showing dynamic and kinematic viscosity of methane, CH4 , at varying temperature and pressure - Imperial and SI Units.
Figures and tables with Prandtl Number of liquid and gaseous propane at varying temperarure and pressure, SI and Imperial units.
Definition and explanation of the terms standard state and standard enthalpy of formation, with listing of values for standard enthalpy and Gibbs free energy of formation, as well as standard entropy and molar heat capacity, of 370 inorganic compounds.
Internationally agreed, internally consistent, values for the thermodynamic properties (standard enthalpy of formation, entropy and [H°(298)-H°(0)]) of key chemical substances.
Definition and examples of calculation of weighted average bed temperature in adiabatic reactors.
Sponsored Links
Search Engineering ToolBox
the most efficient way to navigate the Engineering ToolBox! About Engineering ToolBox! We don't collect information from our users. Only emails and answers are saved in our archive. Cookies are only used in the browser to improve user experience.
Some of our calculators and applications let you save application data to your local computer. These applications will - due to browser restrictions - send data between your browser and our server. We don't save this data.
Google use cookies for serving our ads and handling visitor statistics. Please read Google Privacy & Terms for more information about how you can control adserving and the information collected.
AddThis use cookies for handling links to social media. Please read AddThis Privacy for more information.
≡