Cyclohexane
- Formula: C6H12
- Molecular weight: 84.1595
- IUPAC Standard InChIKey: XDTMQSROBMDMFD-UHFFFAOYSA-N
- CAS Registry Number: 110-82-7
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
The 3d structure may be viewed using Java or Javascript. - Isotopologues:
- Other names: Benzene, hexahydro-; Hexahydrobenzene; Hexamethylene; Hexanaphthene; Cicloesano; Cykloheksan; Rcra waste number U056; UN 1145; NSC 406835
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Gas phase thermochemistry data
Go To: Top, Condensed phase thermochemistry data, Phase change data, Reaction thermochemistry data, Henry's Law data, Gas phase ion energetics data, IR Spectrum, Mass spectrum (electron ionization), UV/Visible spectrum, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled as indicated in comments:
DRB - Donald R. Burgess, Jr.
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
GT - Glushko Thermocenter, Russian Academy of Sciences, Moscow
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔfH°gas | -124.6 | kJ/mol | N/A | Spitzer and Huffman, 1947 | Value computed using ΔfHliquid° value of -157.7±1.8 kj/mol from Spitzer and Huffman, 1947 and ΔvapH° value of 33.1 kj/mol from Prosen, Johnson, et al., 1946.; DRB |
ΔfH°gas | -123.1 ± 0.79 | kJ/mol | Ccb | Prosen, Johnson, et al., 1946 | ALS |
ΔfH°gas | -123.3 | kJ/mol | N/A | Moore, Renquist, et al., 1940 | Value computed using ΔfHliquid° value of -156.4±1.3 kj/mol from Moore, Renquist, et al., 1940 and ΔvapH° value of 33.1 kj/mol from Prosen, Johnson, et al., 1946.; DRB |
Quantity | Value | Units | Method | Reference | Comment |
S°gas | 298.19 | J/mol*K | N/A | Beckett C.W., 1947 | Close value of S(298.15 K)=298.78(0.75) J/mol*K was obtained by [43ASTSZA] from calorimetric data.; GT |
Constant pressure heat capacity of gas
Cp,gas (J/mol*K) | Temperature (K) | Reference | Comment |
---|---|---|---|
34.07 | 50. | Dorofeeva O.V., 1986 | There is an appreciable difference (up to 3.0-4.5 J/mol*K) between selected values of S(T) and Cp(T) and earlier statistically calculated values [ Brickwedde F.G., 1946, Beckett C.W., 1947, Kilpatrick J.E., 1947, Lippincott E.R., 1966] at high temperatures. It is due to using the most reliable molecular constants in [ Dorofeeva O.V., 1986].; GT |
42.59 | 100. | ||
54.80 | 150. | ||
69.05 | 200. | ||
95.20 | 273.15 | ||
105.3 ± 2.0 | 298.15 | ||
106.11 | 300. | ||
148.64 | 400. | ||
188.68 | 500. | ||
223.38 | 600. | ||
252.62 | 700. | ||
277.05 | 800. | ||
297.42 | 900. | ||
314.42 | 1000. | ||
328.66 | 1100. | ||
340.65 | 1200. | ||
350.79 | 1300. | ||
359.44 | 1400. | ||
366.85 | 1500. |
Constant pressure heat capacity of gas
Cp,gas (J/mol*K) | Temperature (K) | Reference | Comment |
---|---|---|---|
138.07 | 370. | Spitzer R., 1946 | Please also see Montgomery J.B., 1942.; GT |
143.1 ± 1.3 | 384. | ||
146.44 | 390. | ||
153.97 | 410. | ||
161.8 ± 1.7 | 428. | ||
174.5 ± 1.7 | 460. | ||
189.5 ± 2.1 | 495. | ||
196.7 ± 2.1 | 521. | ||
206.3 ± 2.1 | 544. |
Condensed phase thermochemistry data
Go To: Top, Gas phase thermochemistry data, Phase change data, Reaction thermochemistry data, Henry's Law data, Gas phase ion energetics data, IR Spectrum, Mass spectrum (electron ionization), UV/Visible spectrum, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled as indicated in comments:
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
DH - Eugene S. Domalski and Elizabeth D. Hearing
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔfH°liquid | -157.7 ± 1.8 | kJ/mol | Ccb | Spitzer and Huffman, 1947 | ALS |
ΔfH°liquid | -156.2 ± 0.79 | kJ/mol | Ccb | Prosen, Johnson, et al., 1946 | ALS |
ΔfH°liquid | -156.4 ± 1.3 | kJ/mol | Ccb | Moore, Renquist, et al., 1940 | Reanalyzed by Cox and Pilcher, 1970, Original value = -157.7 kJ/mol; ALS |
Quantity | Value | Units | Method | Reference | Comment |
ΔcH°liquid | -3930. ± 20. | kJ/mol | AVG | N/A | Average of 7 values; Individual data points |
Quantity | Value | Units | Method | Reference | Comment |
S°liquid | 203.89 | J/mol*K | N/A | Aston, Szasa, et al., 1943 | DH |
S°liquid | 204.35 | J/mol*K | N/A | Ruehrwein and Huffman, 1943 | DH |
S°liquid | 205.9 | J/mol*K | N/A | Parks, Huffman, et al., 1930 | Extrapolation below 90 K, 50.54 J/mol*K.; DH |
Constant pressure heat capacity of liquid
Cp,liquid (J/mol*K) | Temperature (K) | Reference | Comment |
---|---|---|---|
156.00 | 298.15 | Trejo, Costas, et al., 1991 | DH |
156.90 | 298.15 | Lainez, Rodrigo, et al., 1989 | DH |
143.9 | 326.5 | Voss and Sloan, 1989 | T = 326.5 to 450.0 K. Unsmoothed experimental datum.; DH |
155.96 | 298.15 | Saito and Tanaka, 1988 | DH |
154.32 | 298.15 | Shiohama, Ogawa, et al., 1988 | DH |
155.13 | 293.15 | Kalali, Kohler, et al., 1987 | T = 293.15, 313.15 K.; DH |
157.06 | 298.15 | Jimenez, Romani, et al., 1986 | DH |
155.85 | 298.15 | Ortega, 1986 | DH |
156.5 | 298.15 | Nkinamubanzi, Charlet, et al., 1985 | DH |
155.96 | 298.15 | Tanaka, Nakamichi, et al., 1985 | DH |
154.81 | 293.15 | Siddiqi, Svejda, et al., 1983 | DH |
156.4 | 298.15 | Grolier, Inglese, et al., 1982 | DH |
156.0 | 298.15 | Tanaka, 1982 | T = 293.15, 298.15, 303.15 K. Data at three temperatures.; DH |
156.149 | 298.15 | Fortier, D'Arcy, et al., 1979 | DH |
156.12 | 298.15 | Vesely, Zabransky, et al., 1979 | DH |
156.4 | 298.15 | Wilhelm, Grolier, et al., 1979 | DH |
156.35 | 298.15 | Grolier, Wilhelm, et al., 1978 | DH |
156.7 | 298. | Safir, 1978 | T = 298 to 313 K. Data calculated from equation Cp = 1.7493 + 0.00452 T kJ/kg*K.; DH |
156.12 | 298.15 | Vesely, Svoboda, et al., 1977 | T = 298 to 318 K.; DH |
156.07 | 298.15 | Fortier, Benson, et al., 1976 | DH |
156.070 | 298.15 | Fortier and Benson, 1976 | DH |
156.20 | 298.15 | Jolicoeur, Boileau, et al., 1975 | DH |
154.80 | 293.15 | Wilhelm, Zettler, et al., 1974 | T = 273 to 323 K.; DH |
159.6 | 298.15 | Subrahmanyam and Rajagopal, 1973 | T = 298 to 323 K.; DH |
155.2 | 298.15 | Wilhelm, Schano, et al., 1969 | Temperature 20, 30, and 40°C.; DH |
155.5 | 298. | Recko, 1968 | T = 24 to 40°C, equation only.; DH |
152.93 | 298. | Nikolaev, Rabinovich, et al., 1966 | T = 10 to 50°C.; DH |
155.31 | 298.00 | Moelwyn-Hughes and Thorpe, 1964 | T = 297 to 327 K.; DH |
155.2 | 311. | Swietoslawski and Zielenkiewicz, 1960 | Mean value 20 to 56°C.; DH |
154.2 | 300. | Auerbach, Sage, et al., 1950 | T = 300 to 366 K. Cp given as 0.4378 Btu/lb*R at 80°F.; DH |
155.85 | 295. | Aston, Szasa, et al., 1943 | T = 12 to 293 K.; DH |
156.31 | 298.15 | Ruehrwein and Huffman, 1943 | T = 13 to 302 K.; DH |
100.4 | 304.2 | Phillip, 1939 | DH |
143.9 | 298.9 | Parks, Huffman, et al., 1930 | T = 92 to 299 K. Value is unsmoothed experimental datum.; DH |
176.1 | 298. | Dejardin, 1919 | T = 22 to 50°C.; DH |
Phase change data
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Reaction thermochemistry data, Henry's Law data, Gas phase ion energetics data, IR Spectrum, Mass spectrum (electron ionization), UV/Visible spectrum, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled as indicated in comments:
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
BS - Robert L. Brown and Stephen E. Stein
AC - William E. Acree, Jr., James S. Chickos
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
DRB - Donald R. Burgess, Jr.
DH - Eugene S. Domalski and Elizabeth D. Hearing
CAL - James S. Chickos, William E. Acree, Jr., Joel F. Liebman, Students of Chem 202 (Introduction to the Literature of Chemistry), University of Missouri -- St. Louis
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
Tboil | 353.9 ± 0.2 | K | AVG | N/A | Average of 93 out of 116 values; Individual data points |
Quantity | Value | Units | Method | Reference | Comment |
Tfus | 279.6 ± 0.3 | K | AVG | N/A | Average of 38 out of 47 values; Individual data points |
Quantity | Value | Units | Method | Reference | Comment |
Ttriple | 279.7 ± 0.4 | K | AVG | N/A | Average of 8 values; Individual data points |
Quantity | Value | Units | Method | Reference | Comment |
Tc | 554. ± 1. | K | AVG | N/A | Average of 18 values; Individual data points |
Quantity | Value | Units | Method | Reference | Comment |
Pc | 40.7 ± 0.5 | bar | AVG | N/A | Average of 8 values; Individual data points |
Quantity | Value | Units | Method | Reference | Comment |
Vc | 0.308 | l/mol | N/A | Daubert, 1996 | |
Vc | 0.309 | l/mol | N/A | Young, 1972 | Uncertainty assigned by TRC = 0.003 l/mol; TRC |
Quantity | Value | Units | Method | Reference | Comment |
ρc | 3.24 ± 0.03 | mol/l | N/A | Daubert, 1996 | |
ρc | 3.26 | mol/l | N/A | Teja and Anselme, 1990 | Uncertainty assigned by TRC = 0.07 mol/l; TRC |
ρc | 3.230 | mol/l | N/A | Simon, 1957 | Uncertainty assigned by TRC = 0.04 mol/l; TRC |
ρc | 3.250 | mol/l | N/A | Young, 1910 | Uncertainty assigned by TRC = 0.02 mol/l; TRC |
ρc | 3.247 | mol/l | N/A | Young and Fortey, 1899 | Uncertainty assigned by TRC = 0.06 mol/l; TRC |
Quantity | Value | Units | Method | Reference | Comment |
ΔvapH° | 33.1 ± 0.4 | kJ/mol | AVG | N/A | Average of 19 out of 21 values; Individual data points |
Enthalpy of vaporization
ΔvapH (kJ/mol) | Temperature (K) | Method | Reference | Comment |
---|---|---|---|---|
29.97 | 353.9 | N/A | Majer and Svoboda, 1985 | |
33.334 | 298.15 | N/A | Aston, Szasa, et al., 1943 | P = 13.18 kPa; DH |
33.1 | 315. | EB | Gierycz, Kosowski, et al., 2009 | Based on data from 296. to 353. K.; AC |
32.7 | 315. | N/A | Lubomska, Banas, et al., 2002 | Based on data from 300. to 345. K.; AC |
31.9 | 324. | EB | Diogo, Santos, et al., 1995 | Based on data from 313. to 336. K.; AC |
32.2 | 375. | N/A | Lee and Holder, 1993 | Based on data from 360. to 470. K.; AC |
32.3 | 314. | C | Dong, Lin, et al., 1988 | AC |
31.1 | 332. | C | Dong, Lin, et al., 1988 | AC |
30.3 | 345. | C | Dong, Lin, et al., 1988 | AC |
30.0 | 355. | C | Dong, Lin, et al., 1988 | AC |
30.9 | 368. | A | Stephenson and Malanowski, 1987 | Based on data from 353. to 414. K.; AC |
29.6 | 427. | A | Stephenson and Malanowski, 1987 | Based on data from 412. to 491. K.; AC |
29.6 | 504. | A | Stephenson and Malanowski, 1987 | Based on data from 489. to 553. K.; AC |
32.9 | 308. | A,MM | Stephenson and Malanowski, 1987 | Based on data from 293. to 355. K. See also Willingham, Taylor, et al., 1945.; AC |
32.3 ± 0.1 | 313. | C | Majer, Svoboda, et al., 1979 | AC |
31.2 ± 0.1 | 333. | C | Majer, Svoboda, et al., 1979 | AC |
31.0 ± 0.1 | 338. | C | Majer, Svoboda, et al., 1979 | AC |
30.4 ± 0.1 | 348. | C | Majer, Svoboda, et al., 1979 | AC |
30.1 ± 0.1 | 353. | C | Majer, Svoboda, et al., 1979 | AC |
32.2 ± 0.1 | 313. | C | Svoboda, Veselý, et al., 1973 | AC |
31.9 ± 0.1 | 323. | C | Svoboda, Veselý, et al., 1973 | AC |
31.1 ± 0.1 | 333. | C | Svoboda, Veselý, et al., 1973 | AC |
30.6 ± 0.1 | 343. | C | Svoboda, Veselý, et al., 1973 | AC |
30.1 ± 0.1 | 354. | C | Svoboda, Veselý, et al., 1973 | AC |
32.5 | 318. | N/A | Gaw and Swinton, 1968 | Based on data from 303. to 343. K.; AC |
32.9 | 313. | N/A | Cruickshank and Cutler, 1967 | Based on data from 298. to 348. K.; AC |
32.8 | 331. | N/A | Marinichev and Susarev, 1965 | Based on data from 316. to 354. K.; AC |
31.4 ± 0.1 | 324. | C | McCullough, Person, et al., 1951 | AC |
30.4 ± 0.1 | 346. | C | McCullough, Person, et al., 1951 | AC |
30.1 | 354. | N/A | Spitzer and Pitzer, 1946 | AC |
Enthalpy of vaporization
ΔvapH = A exp(-αTr)
(1 − Tr)β
ΔvapH =
Enthalpy of vaporization (at saturation pressure)
(kJ/mol)
Tr = reduced temperature (T / Tc)
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Temperature (K) | 292. to 422. |
---|---|
A (kJ/mol) | 43.32 |
α | -0.1437 |
β | 0.4512 |
Tc (K) | 553.4 |
Reference | Majer and Svoboda, 1985 |
Entropy of vaporization
ΔvapS (J/mol*K) | Temperature (K) | Reference | Comment |
---|---|---|---|
111.80 | 298.15 | Aston, Szasa, et al., 1943 | P; DH |
Antoine Equation Parameters
log10(P) = A − (B / (T + C))
P = vapor pressure (bar)
T = temperature (K)
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Temperature (K) | A | B | C | Reference | Comment |
---|---|---|---|---|---|
323. to 523. | 4.13983 | 1316.554 | -35.581 | Kerns, Anthony, et al., 1974 | Coefficents calculated by NIST from author's data. |
303. to 343. | 3.9920 | 1216.93 | -48.621 | Gaw and Swinton, 1968, 2 | Coefficents calculated by NIST from author's data. |
315.70 to 353.90 | 3.17125 | 780.637 | -107.29 | Marinichev and Susarev, 1965, 2 | Coefficents calculated by NIST from author's data. |
293.06 to 354.73 | 3.96988 | 1203.526 | -50.287 | Williamham, Taylor, et al., 1945 |
Enthalpy of sublimation
ΔsubH (kJ/mol) | Temperature (K) | Method | Reference | Comment |
---|---|---|---|---|
27.6 | 265. | A | Stephenson and Malanowski, 1987 | Based on data from 223. to 280. K.; AC |
46.6 | 186. | B | Bondi, 1963 | AC |
37.2 | 273. | N/A | Jones, 1960 | Based on data from 268. to 278. K.; AC |
37.7 | 248. | A | Stull, 1947 | Based on data from 228. to 268. K.; AC |
36.5 | 274. | A | Rotinjanz and Nagornow, 1934 | Based on data from 269. to 279. K.; AC |
Enthalpy of fusion
ΔfusH (kJ/mol) | Temperature (K) | Reference | Comment |
---|---|---|---|
2.68 | 279.8 | Domalski and Hearing, 1996 | AC |
Entropy of fusion
ΔfusS (J/mol*K) | Temperature (K) | Reference | Comment |
---|---|---|---|
36.2 | 186.1 | Domalski and Hearing, 1996 | CAL |
9.57 | 279.8 |
Enthalpy of phase transition
ΔHtrs (kJ/mol) | Temperature (K) | Initial Phase | Final Phase | Reference | Comment |
---|---|---|---|---|---|
6.686 | 186.09 | crystaline, II | crystaline, I | Aston, Szasa, et al., 1943 | DH |
2.628 | 279.84 | crystaline, I | liquid | Aston, Szasa, et al., 1943 | DH |
6.7396 | 186.1 | crystaline, II | crystaline, I | Ruehrwein and Huffman, 1943 | DH |
2.6769 | 279.82 | crystaline, I | liquid | Ruehrwein and Huffman, 1943 | DH |
6.820 | 186.4 | crystaline, II | crystaline, I | Ziegler and Andrews, 1942 | DH |
2.728 | 279.4 | crystaline, I | liquid | Ziegler and Andrews, 1942 | DH |
6.234 | 185.9 | crystaline, II | crystaline, I | Parks, Huffman, et al., 1930 | DH |
2.423 | 279.3 | crystaline, I | liquid | Parks, Huffman, et al., 1930 | DH |
Entropy of phase transition
ΔStrs (J/mol*K) | Temperature (K) | Initial Phase | Final Phase | Reference | Comment |
---|---|---|---|---|---|
35.93 | 186.09 | crystaline, II | crystaline, I | Aston, Szasa, et al., 1943 | DH |
9.39 | 279.84 | crystaline, I | liquid | Aston, Szasa, et al., 1943 | DH |
36.21 | 186.1 | crystaline, II | crystaline, I | Ruehrwein and Huffman, 1943 | DH |
9.57 | 279.82 | crystaline, I | liquid | Ruehrwein and Huffman, 1943 | DH |
36.59 | 186.4 | crystaline, II | crystaline, I | Ziegler and Andrews, 1942 | DH |
9.76 | 279.4 | crystaline, I | liquid | Ziegler and Andrews, 1942 | DH |
33.53 | 185.9 | crystaline, II | crystaline, I | Parks, Huffman, et al., 1930 | DH |
8.68 | 279.3 | crystaline, I | liquid | Parks, Huffman, et al., 1930 | DH |
Reaction thermochemistry data
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Phase change data, Henry's Law data, Gas phase ion energetics data, IR Spectrum, Mass spectrum (electron ionization), UV/Visible spectrum, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled as indicated in comments:
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
M - Michael M. Meot-Ner (Mautner) and Sharon G. Lias
B - John E. Bartmess
Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. A general reaction search form is also available. Future versions of this site may rely on reaction search pages in place of the enumerated reaction displays seen below.
Individual Reactions
By formula: C6H10 + H2 = C6H12
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | -118. ± 6. | kJ/mol | AVG | N/A | Average of 8 values; Individual data points |
By formula: H4N+ + C6H12 = (H4N+ • C6H12)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 40. | kJ/mol | PHPMS | Deakyne and Meot-Ner (Mautner), 1985 | gas phase; Entropy change calculated or estimated, DG<, ΔrH<; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 84. | J/mol*K | N/A | Deakyne and Meot-Ner (Mautner), 1985 | gas phase; Entropy change calculated or estimated, DG<, ΔrH<; M |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
12. | 317. | PHPMS | Deakyne and Meot-Ner (Mautner), 1985 | gas phase; Entropy change calculated or estimated, DG<, ΔrH<; M |
By formula: C6H6+ + C6H12 = (C6H6+ • C6H12)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 46.9 | kJ/mol | PHPMS | Meot-Ner (Mautner), Hamlet, et al., 1978 | gas phase; Entropy change calculated or estimated; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 110. | J/mol*K | N/A | Meot-Ner (Mautner), Hamlet, et al., 1978 | gas phase; Entropy change calculated or estimated; M |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
13. | 295. | PHPMS | Meot-Ner (Mautner), Hamlet, et al., 1978 | gas phase; Entropy change calculated or estimated; M |
C6H11- + =
By formula: C6H11- + H+ = C6H12
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1750. ± 8.4 | kJ/mol | Bran | Peerboom, Rademaker, et al., 1992 | gas phase; B |
ΔrH° | 1702.1 ± 3.8 | kJ/mol | G+TS | Bohme, Lee-Ruff, et al., 1972 | gas phase; B |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | 1713. ± 9.2 | kJ/mol | H-TS | Peerboom, Rademaker, et al., 1992 | gas phase; B |
ΔrG° | >1665.2 | kJ/mol | IMRB | Bohme, Lee-Ruff, et al., 1972 | gas phase; B |
By formula: 2H2 + C6H8 = C6H12
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | -224.4 ± 1.2 | kJ/mol | Chyd | Turner, Mallon, et al., 1973 | liquid phase; solvent: Glacial acetic acid; ALS |
ΔrH° | -229.6 ± 0.42 | kJ/mol | Chyd | Kistiakowsky, Ruhoff, et al., 1936 | gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -231.7 ± 0.4 kJ/mol; At 355 °K; ALS |
By formula: 2H2 + C6H8 = C6H12
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | -233. | kJ/mol | Chyd | Roth, Adamczak, et al., 1991 | liquid phase; ALS |
ΔrH° | -225.5 ± 1.4 | kJ/mol | Chyd | Turner, Mallon, et al., 1973 | liquid phase; solvent: Glacial acetic acid; ALS |
By formula: C3H9Si+ + C6H12 = (C3H9Si+ • C6H12)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 159. | kJ/mol | PHPMS | Li and Stone, 1989 | gas phase; condensation; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 201. | J/mol*K | PHPMS | Li and Stone, 1989 | gas phase; condensation; M |
By formula: 3H2 + C6H6 = C6H12
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | -205.3 ± 0.63 | kJ/mol | Chyd | Kistiakowsky, Ruhoff, et al., 1936 | gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -208.4 ± 0.63 kJ/mol; At 355 °K; ALS |
By formula: HI + C6H11I = C6H12 + I2
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | -32.6 ± 8.4 | kJ/mol | Cm | Brennan and Ubbelohde, 1956 | gas phase; Reanalyzed by Cox and Pilcher, 1970, Original value = -28. ± 4.2 kJ/mol; ALS |
By formula: Li+ + C6H12 = (Li+ • C6H12)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 100. | kJ/mol | ICR | Staley and Beauchamp, 1975 | gas phase; switching reaction(Li+)H2O, from graph; Dzidic and Kebarle, 1970 extrapolated; M |
By formula: C6H12 = C6H12
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | -14.69 | kJ/mol | Eqk | Glasebrook and Lovell, 1939 | liquid phase; Heat of isomerization; ALS |
By formula: 2H2 + C6H8 = C6H12
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | -426.8 ± 7.9 | kJ/mol | Chyd | Roth, Adamczak, et al., 1991 | liquid phase; ALS |
By formula: C6H12O = C6H12 + H2
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 63.4 ± 2.3 | kJ/mol | Eqk | Fedoseenko, Yursha, et al., 1983 | gas phase; At 502 K; ALS |
By formula: C6H11Cl + HCl = C6H12 + Cl2
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | -143.1 | kJ/mol | Cm | Kirkbride, 1956 | liquid phase; ALS |
By formula: C6H12 = C6H12
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 18.1 ± 1.2 | kJ/mol | Eqk | Kabo and Andreevskii, 1973 | liquid phase; ALS |
Henry's Law data
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Phase change data, Reaction thermochemistry data, Gas phase ion energetics data, IR Spectrum, Mass spectrum (electron ionization), UV/Visible spectrum, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: Rolf Sander
Henry's Law constant (water solution)
kH(T) = k°H exp(d(ln(kH))/d(1/T) ((1/T) - 1/(298.15 K)))
k°H = Henry's law constant for solubility in water at 298.15 K (mol/(kg*bar))
d(ln(kH))/d(1/T) = Temperature dependence constant (K)
k°H (mol/(kg*bar)) | d(ln(kH))/d(1/T) (K) | Method | Reference | Comment |
---|---|---|---|---|
0.0051 | Q | N/A | missing citation give several references for the Henry's law constants but don't assign them to specific species. | |
0.0055 | 3200. | X | N/A | |
0.0062 | 710. | X | N/A | |
0.0056 | L | N/A | ||
0.0051 | V | N/A |
Gas phase ion energetics data
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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data evaluated as indicated in comments:
HL - Edward P. Hunter and Sharon G. Lias
L - Sharon G. Lias
Data compiled as indicated in comments:
B - John E. Bartmess
LL - Sharon G. Lias and Joel F. Liebman
LBLHLM - Sharon G. Lias, John E. Bartmess, Joel F. Liebman, John L. Holmes, Rhoda D. Levin, and W. Gary Mallard
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi
RDSH - Henry M. Rosenstock, Keith Draxl, Bruce W. Steiner, and John T. Herron
View reactions leading to C6H12+ (ion structure unspecified)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
IE (evaluated) | 9.88 ± 0.03 | eV | N/A | N/A | L |
Quantity | Value | Units | Method | Reference | Comment |
Proton affinity (review) | 686.9 | kJ/mol | N/A | Hunter and Lias, 1998 | HL |
Quantity | Value | Units | Method | Reference | Comment |
Gas basicity | 666.9 | kJ/mol | N/A | Hunter and Lias, 1998 | HL |
Ionization energy determinations
IE (eV) | Method | Reference | Comment |
---|---|---|---|
9.80 ± 0.05 | EI | Holmes and Lossing, 1991 | LL |
10.0 ± 0.03 | EI | Arimura and Yoshikawa, 1984 | LBLHLM |
9.82 | EQ | Sieck and Mautner(Meot-Ner), 1982 | LBLHLM |
9.88 ± 0.10 | EQ | Lias, 1982 | LBLHLM |
9.88 | PE | Kovac and Klasinc, 1978 | LLK |
9.88 ± 0.02 | PE | Bieri, Burger, et al., 1977 | LLK |
9.88 | EI | Lossing and Traeger, 1975 | LLK |
9.89 ± 0.01 | PE | Rang, Paldoia, et al., 1974 | LLK |
9.83 ± 0.05 | EI | Puttemans, 1974 | LLK |
9.84 | PE | Puttemans, 1974 | LLK |
9.88 ± 0.01 | PI | Sergeev, Akopyan, et al., 1973 | LLK |
9.87 | PE | Ikuta, Yoshihara, et al., 1973 | LLK |
9.88 ± 0.01 | S | Raymonda, 1972 | LLK |
9.89 | PE | Demeo and Yencha, 1970 | RDSH |
9.81 | PE | Dewar and Worley, 1969 | RDSH |
9.79 | PE | Al-Joboury and Turner, 1964 | RDSH |
9.88 ± 0.02 | PI | Watanabe, 1957 | RDSH |
11.0 ± 0.2 | EI | Hustrulid, Kusch, et al., 1938 | RDSH |
10.32 | PE | Kimura, Katsumata, et al., 1981 | Vertical value; LLK |
10.3 ± 0.1 | PE | Bieri, Burger, et al., 1977 | Vertical value; LLK |
10.3 | PE | Bruckmann and Klessinger, 1973 | Vertical value; LLK |
Appearance energy determinations
Ion | AE (eV) | Other Products | Method | Reference | Comment |
---|---|---|---|---|---|
C3H5+ | 13.20 ± 0.08 | C3H7 | EI | Rabbih, Selim, et al., 1981 | LLK |
C3H6+ | 12.00 ± 0.07 | C3H6 | EI | Rabbih, Selim, et al., 1981 | LLK |
C3H6+ | 11.23 ± 0.04 | C3H6 | PI | Sergeev, Akopyan, et al., 1973 | LLK |
C3H7+ | 13.50 ± 0.08 | C3H5 | EI | Rabbih, Selim, et al., 1981 | LLK |
C3H7+ | 11.49 ± 0.03 | C3H5 | PI | Sergeev, Akopyan, et al., 1973 | LLK |
C4H7+ | 11.21 ± 0.04 | C2H5 | PI | Sergeev, Akopyan, et al., 1973 | LLK |
C4H8+ | 11.15 ± 0.03 | C2H4 | EI | Rabbih, Selim, et al., 1981 | LLK |
C4H8+ | 11.45 | C2H4 | EI | Puttemans, 1974 | LLK |
C4H8+ | 11.08 ± 0.01 | C2H4 | PI | Sergeev, Akopyan, et al., 1973 | LLK |
C5H9+ | 9.88 | CH3 | EI | Lossing and Traeger, 1975, 2 | LLK |
C5H9+ | ≤11.06 | CH3 | EI | Lossing and Traeger, 1975 | LLK |
C5H9+ | 11.15 | CH3 | EI | Puttemans, 1974 | LLK |
C5H9+ | 11.07 ± 0.04 | CH3 | PI | Sergeev, Akopyan, et al., 1973 | LLK |
C6H11+ | 11.32 ± 0.05 | H | PI | Sergeev, Akopyan, et al., 1973 | LLK |
C6H11+ | 11.66 | H | EI | Pottie, Harrison, et al., 1961 | RDSH |
De-protonation reactions
C6H11- + =
By formula: C6H11- + H+ = C6H12
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1750. ± 8.4 | kJ/mol | Bran | Peerboom, Rademaker, et al., 1992 | gas phase; B |
ΔrH° | 1702.1 ± 3.8 | kJ/mol | G+TS | Bohme, Lee-Ruff, et al., 1972 | gas phase; B |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | 1713. ± 9.2 | kJ/mol | H-TS | Peerboom, Rademaker, et al., 1992 | gas phase; B |
ΔrG° | >1665.2 | kJ/mol | IMRB | Bohme, Lee-Ruff, et al., 1972 | gas phase; B |
IR Spectrum
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Data compiled by: Coblentz Society, Inc.
- GAS (25 mmHg, N2 ADDED, TOTAL PRESSURE 600 mmHg); PERKIN-ELMER 180; DIGITIZED BY NIST FROM HARD COPY (FROM TWO SEGMENTS); 2 cm-1 resolution
- LIQUID (NEAT); DOW KBr FOREPRISM-GRATING; DIGITIZED BY COBLENTZ SOCIETY (BATCH I) FROM HARD COPY; 2 cm-1 resolution
- SOLUTION (10% CCl4 FOR 3800-1350, AND 10% CS2 FOR 1350-400 CM-1); DOW KBr FOREPRISM-GRATING; DIGITIZED BY COBLENTZ SOCIETY (BATCH I) FROM HARD COPY; 2 cm-1 resolution
Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director
Mass spectrum (electron ionization)
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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director
Spectrum
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Additional Data
View image of digitized spectrum (can be printed in landscape orientation).
Due to licensing restrictions, this spectrum cannot be downloaded.
Owner | NIST Mass Spectrometry Data Center Collection (C) 2014 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. All rights reserved. |
---|---|
Origin | NIST Mass Spectrometry Data Center, 1998. |
NIST MS number | 291493 |
UV/Visible spectrum
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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: Victor Talrose, Eugeny B. Stern, Antonina A. Goncharova, Natalia A. Messineva, Natalia V. Trusova, Margarita V. Efimkina
Spectrum
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Additional Data
View image of digitized spectrum (can be printed in landscape orientation).
View spectrum image in SVG format.
Download spectrum in JCAMP-DX format.
Source | Pickett, Muntz, et al., 1951 |
---|---|
Owner | INEP CP RAS, NIST OSRD Collection (C) 2007 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. All rights reserved. |
Origin | INSTITUTE OF ENERGY PROBLEMS OF CHEMICAL PHYSICS, RAS |
Source reference | RAS UV No. 193 |
Instrument | Hilger prism spectrograph |
Melting point | 6.6 |
Boiling point | 80.7 |
References
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Phase change data, Reaction thermochemistry data, Henry's Law data, Gas phase ion energetics data, IR Spectrum, Mass spectrum (electron ionization), UV/Visible spectrum, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
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The Heat Capacity of Gaseous Cyclopentane, Cyclohexane and Methylcyclohexane,
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Study of a Liquid-Vapor Equilibrium in the Systems of Acetone/Methanol and Acetone/Cyclohexane at Temperatures 35, 45, 55 ºC and Pressure 760 Torr,
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Vapor Pressures and Boiling Points of Some Paraffin, Alkylcyclopentane, Alkylcyclohexane, and Alkylbenzene Hydrocarbons,
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Sublimation Pressure Data for Organic Compounds.,
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Stull, 1947
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Vapor Pressure of Pure Substances. Organic and Inorganic Compounds,
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The heat capacity of benzene-d6,
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Unconventional Ionic Hydrogen Bonds. 2. NH+ pi. Complexes of Onium Ions with Olefins and Benzene Derivatives,
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Meot-Ner (Mautner), Hamlet, et al., 1978
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Bonding Energies in Association Ions of Aromatic Molecules. Correlations with Ionization Energies,
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Acidity order of selected bronsted acids in the gas phase at 300K,
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Turner, Mallon, et al., 1973
Turner, R.B.; Mallon, B.J.; Tichy, M.; Doering, W.v.E.; Roth, W.R.; Schroder, G.,
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Kistiakowsky, Ruhoff, et al., 1936
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Intrinsic Acid - Base Properties of Molecules. Binding Energies of Li+ to pi - and n - Donor Bases,
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Kirkbride, 1956
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The heats of chlorination of some hydrocarbons and their chloro-derivatives,
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Ionization energies of homologous organic compounds and correlation with molecular size,
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Arimura and Yoshikawa, 1984
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Ionization efficiency and ionization energy of cyclic compounds by electron impact,
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Thermochemical information from ion-molecule rate constants,
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Photoelectron spectroscopy of adamantane and some adamantanones,
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Bieri, Burger, et al., 1977
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Stabilization in cyclopentadienyl, cyclopentenyl, and cyclopentyl cations,
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Rang, Paldoia, et al., 1974
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Puttemans, 1974
Puttemans, J.P.,
Ionisation de cycloalcanes (C5 a C12) en spectroscopie photoelectronique et par impact electronique,
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Sergeev, Akopyan, et al., 1973
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Photoionization processes in gaseous cyclohexane, and chloro- and bromocyclohexane,
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Photoelectron spectroscopy of cyclohexane, cyclopentane, and some related compounds,
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Raymonda, 1972
Raymonda, J.W.,
Rydberg states in cyclic alkanes,
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Dewar, M.J.S.; Worley, S.D.,
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Ionization potentials of some molecules,
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Hustrulid, A.; Kusch, P.; Tate, J.T.,
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Bruckmann, P.; Klessinger, M.,
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Lossing and Traeger, 1975, 2
Lossing, F.P.; Traeger, J.C.,
Free radicals by mass spectrometry XLVI. Heats of formation of C5H7 and C5H9 radicals and cations.,
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Pottie, Harrison, et al., 1961
Pottie, R.F.; Harrison, A.G.; Lossing, F.P.,
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Pickett, L.W.; Muntz, M.; McPherson, E.M.,
Vacuum ultraviolet absorption spectra of cyclic compounds. I. Cyclohexane, cyclohexene, cyclopentane, Cyclopentene and benzene,
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Notes
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- Symbols used in this document:
AE Appearance energy Cp,gas Constant pressure heat capacity of gas Cp,liquid Constant pressure heat capacity of liquid IE (evaluated) Recommended ionization energy Pc Critical pressure S°gas Entropy of gas at standard conditions S°liquid Entropy of liquid at standard conditions T Temperature Tboil Boiling point Tc Critical temperature Tfus Fusion (melting) point Ttriple Triple point temperature Vc Critical volume d(ln(kH))/d(1/T) Temperature dependence parameter for Henry's Law constant k°H Henry's Law constant at 298.15K ΔHtrs Enthalpy of phase transition ΔStrs Entropy of phase transition ΔcH°liquid Enthalpy of combustion of liquid at standard conditions ΔfH°gas Enthalpy of formation of gas at standard conditions ΔfH°liquid Enthalpy of formation of liquid at standard conditions ΔfusH Enthalpy of fusion ΔfusS Entropy of fusion ΔrG° Free energy of reaction at standard conditions ΔrH° Enthalpy of reaction at standard conditions ΔrS° Entropy of reaction at standard conditions ΔsubH Enthalpy of sublimation ΔvapH Enthalpy of vaporization ΔvapH° Enthalpy of vaporization at standard conditions ΔvapS Entropy of vaporization ρc Critical density - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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