2-Propanol, 2-methyl-
- Formula: C4H10O
- Molecular weight: 74.1216
- IUPAC Standard InChIKey: DKGAVHZHDRPRBM-UHFFFAOYSA-N
- CAS Registry Number: 75-65-0
- 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: tert-Butyl alcohol; tert-Butanol; Ethanol, 1,1-Dimethyl-; Trimethylcarbinol; Trimethylmethanol; 1,1-Dimethylethanol; 2-Methyl-2-propanol; tert-C4H9OH; t-Butanol; tert-Butyl hydroxide; 2-Methylpropanol-2; 2-Methylpropan-2-ol; Alcool butylique tertiaire; Butanol tertiaire; t-Butyl hydroxide; Methanol, trimethyl-; NCI-C55367; 2-Methyl n-propan-2-ol; Methyl-2 propanol-2; Tert.-butyl alcohol
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Gas phase thermochemistry data
Go To: Top, Condensed phase thermochemistry data, Gas phase ion energetics data, 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
DRB - Donald R. Burgess, Jr.
GT - Glushko Thermocenter, Russian Academy of Sciences, Moscow
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔfH°gas | -74.72 ± 0.21 | kcal/mol | Eqk | Wiberg and Hao, 1991 | Heat of hydration; ALS |
ΔfH°gas | -74.9 ± 0.35 | kcal/mol | Ccb | Skinner and Snelson, 1960 | ALS |
ΔfH°gas | -74.02 | kcal/mol | N/A | Taft and Riesz, 1955 | Value computed using ΔfHliquid° value of -356.0 kj/mol from Taft and Riesz, 1955 and ΔvapH° value of 46.3 kj/mol from Skinner and Snelson, 1960.; DRB |
Constant pressure heat capacity of gas
Cp,gas (cal/mol*K) | Temperature (K) | Reference | Comment |
---|---|---|---|
8.568 | 50. | Thermodynamics Research Center, 1997 | p=1 bar. Selected values of S(T) and Cp(T) are in good agreement with those of [ Beynon E.T., 1963] because of using practically the same molecular constants in two calculations. Please also see Chao J., 1986.; GT |
12.60 | 100. | ||
16.83 | 150. | ||
20.38 | 200. | ||
25.404 | 273.15 | ||
27.158 ± 0.050 | 298.15 | ||
27.290 | 300. | ||
34.175 | 400. | ||
40.246 | 500. | ||
45.327 | 600. | ||
49.591 | 700. | ||
53.229 | 800. | ||
56.370 | 900. | ||
59.097 | 1000. | ||
61.472 | 1100. | ||
63.540 | 1200. | ||
65.337 | 1300. | ||
66.902 | 1400. | ||
68.265 | 1500. | ||
70.96 | 1750. | ||
72.87 | 2000. | ||
74.26 | 2250. | ||
75.26 | 2500. | ||
76.00 | 2750. | ||
76.55 | 3000. |
Constant pressure heat capacity of gas
Cp,gas (cal/mol*K) | Temperature (K) | Reference | Comment |
---|---|---|---|
31.87 ± 0.27 | 360.55 | Stromsoe E., 1970 | Ideal gas heat capacities are given by [ Stromsoe E., 1970] as a linear function Cp=f1*(a+bT). This expression approximates the experimental values with the average deviation of 1.13 J/mol*K. The accuracy of the experimental heat capacities [ Stromsoe E., 1970] is estimated as less than 0.3%. Please also see Beynon E.T., 1963.; GT |
31.699 | 365.15 | ||
32.56 ± 0.27 | 372.85 | ||
32.971 | 383.15 | ||
33.27 ± 0.27 | 385.65 | ||
34.149 | 401.15 | ||
34.68 ± 0.27 | 410.85 | ||
35.390 | 419.15 | ||
36.699 | 437.15 | ||
36.30 ± 0.27 | 439.85 | ||
36.39 ± 0.27 | 441.45 | ||
38.02 ± 0.27 | 470.75 | ||
39.61 ± 0.27 | 499.25 | ||
41.25 ± 0.27 | 528.75 | ||
43.84 ± 0.27 | 575.05 | ||
44.76 ± 0.27 | 591.55 |
Condensed phase thermochemistry data
Go To: Top, Gas phase thermochemistry data, Gas phase ion energetics data, 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 | -85.86 ± 0.20 | kcal/mol | Eqk | Wiberg and Hao, 1991 | Heat of hydration; ALS |
ΔfH°liquid | -85.87 ± 0.19 | kcal/mol | Ccb | Skinner and Snelson, 1960 | ALS |
ΔfH°liquid | -85.0 | kcal/mol | Eqk | Taft and Riesz, 1955 | ALS |
Quantity | Value | Units | Method | Reference | Comment |
ΔcH°liquid | -631.92 ± 0.19 | kcal/mol | Ccb | Skinner and Snelson, 1960 | Corresponding ΔfHºliquid = -85.86 kcal/mol (simple calculation by NIST; no Washburn corrections); ALS |
Quantity | Value | Units | Method | Reference | Comment |
S°liquid | 45.29 | cal/mol*K | N/A | Parks, Kelley, et al., 1929 | Extrapolation bloew 90 K, 45.19 J/mol*K. Revision of previous data.; DH |
S°liquid | 47.20 | cal/mol*K | N/A | Parks and Anderson, 1926 | Extrapolation below 90 K, 53.35 J/mol*K.; DH |
Quantity | Value | Units | Method | Reference | Comment |
ΔcH°solid | -629.4 | kcal/mol | Ccb | Raley, Rust, et al., 1948 | Corresponding ΔfHºsolid = -88.4 kcal/mol (simple calculation by NIST; no Washburn corrections); ALS |
Quantity | Value | Units | Method | Reference | Comment |
S°solid,1 bar | 40.839 | cal/mol*K | N/A | Oetting F.L., 1963 | crystaline, I phase; DH |
Constant pressure heat capacity of liquid
Cp,liquid (cal/mol*K) | Temperature (K) | Reference | Comment |
---|---|---|---|
51.475 | 298.15 | Caceres-Alonso, Costas, et al., 1988 | DH |
53.031 | 299.15 | Okano, Ogawa, et al., 1988 | DH |
50.2 | 298. | De Visser, Perron, et al., 1977 | DH |
50.2 | 298.15 | De Visser, Perron, et al., 1977, 2 | T = 298.15, 313.15, 328.15 K.; DH |
53.75 | 298.15 | Murthy and Subrahmanyam, 1977 | DH |
52.25 | 298.15 | Skold, Suurkuusk, et al., 1976 | DH |
53.70 | 300. | Parks and Anderson, 1926 | T = 87 to 300 K. Value is unsmoothed experimental datum.; DH |
Constant pressure heat capacity of solid
Cp,solid (cal/mol*K) | Temperature (K) | Reference | Comment |
---|---|---|---|
34.921 | 298.15 | Oetting F.L., 1963 | crystaline, I phase; T = 15 to 330 K.; DH |
Gas phase ion energetics data
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, References, Notes
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
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi
RDSH - Henry M. Rosenstock, Keith Draxl, Bruce W. Steiner, and John T. Herron
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
IE (evaluated) | 9.90 ± 0.03 | eV | N/A | N/A | L |
Quantity | Value | Units | Method | Reference | Comment |
Proton affinity (review) | 191.8 | kcal/mol | N/A | Hunter and Lias, 1998 | HL |
Quantity | Value | Units | Method | Reference | Comment |
Gas basicity | 184.6 | kcal/mol | N/A | Hunter and Lias, 1998 | HL |
Ionization energy determinations
IE (eV) | Method | Reference | Comment |
---|---|---|---|
9.90 ± 0.03 | PIPECO | Shao, Baer, et al., 1988 | LL |
9.97 ± 0.02 | PE | Cocksey, Eland, et al., 1971 | LLK |
10.23 | PE | Baker, Betteridge, et al., 1971 | LLK |
10.23 | PE | Baker, Betteridge, et al., 1971 | LLK |
10.26 | PE | Benoit and Harrison, 1977 | Vertical value; LLK |
10.25 ± 0.03 | PE | Peel and Willett, 1975 | Vertical value; LLK |
10.25 | PE | Robin and Kuebler, 1973 | Vertical value; LLK |
Appearance energy determinations
Ion | AE (eV) | Other Products | Method | Reference | Comment |
---|---|---|---|---|---|
C3H7O+ | 9.86 | CH3 | EI | Lossing, 1977 | LLK |
C3H7O+ | 10.1 ± 0.2 | CH3 | EI | Beauchamp, Caserio, et al., 1974 | LLK |
C3H7O+ | 9.87 ± 0.03 | CH3 | PI | Potapov and Sorokin, 1972 | LLK |
C3H7O+ | 9.87 | CH3 | EI | Potapov and Sorokin, 1970 | RDSH |
C3H7O+ | 10.2 | CH3 | EI | Harrison, Ivko, et al., 1966 | RDSH |
De-protonation reactions
C4H9O- + =
By formula: C4H9O- + H+ = C4H10O
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 374.7 ± 1.0 | kcal/mol | D-EA | Ramond, Davico, et al., 2000 | gas phase; B |
ΔrH° | 374.6 ± 2.1 | kcal/mol | G+TS | Bartmess, Scott, et al., 1979 | gas phase; value altered from reference due to change in acidity scale; B |
ΔrH° | 376.00 ± 0.70 | kcal/mol | CIDT | DeTuri and Ervin, 1999 | gas phase; B |
ΔrH° | 374.3 ± 2.0 | kcal/mol | CIDC | Haas and Harrison, 1993 | gas phase; Both metastable and 50 eV collision energy.; B |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | 368.1 ± 1.1 | kcal/mol | H-TS | Ramond, Davico, et al., 2000 | gas phase; B |
ΔrG° | 368.0 ± 2.0 | kcal/mol | IMRE | Bartmess, Scott, et al., 1979 | gas phase; value altered from reference due to change in acidity scale; B |
ΔrG° | 367.7 ± 2.1 | kcal/mol | H-TS | Haas and Harrison, 1993 | gas phase; Both metastable and 50 eV collision energy.; B |
References
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Gas phase ion energetics data, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Wiberg and Hao, 1991
Wiberg, K.B.; Hao, S.,
Enthalpies of hydration of alkenes. 4. Formation of acyclic tert-alcohols,
J. Org. Chem., 1991, 56, 5108-5110. [all data]
Skinner and Snelson, 1960
Skinner, H.A.; Snelson, A.,
The heats of combustion of the four isomeric butyl alcohols,
Trans. Faraday Soc., 1960, 56, 1776-1783. [all data]
Taft and Riesz, 1955
Taft, R.W., Jr.; Riesz, P.,
Thermodynamic properties for the system isobutene-t-butyl alcohol,
J. Am. Chem. Soc., 1955, 77, 902-904. [all data]
Thermodynamics Research Center, 1997
Thermodynamics Research Center,
Selected Values of Properties of Chemical Compounds., Thermodynamics Research Center, Texas A&M University, College Station, Texas, 1997. [all data]
Beynon E.T., 1963
Beynon E.T., Jr.,
The thermodynamic properties of 2-methyl-2-propanol,
J. Phys. Chem., 1963, 67, 2761-2765. [all data]
Chao J., 1986
Chao J.,
Thermodynamic properties of key organic oxygen compounds in the carbon range C1 to C4. Part 2. Ideal gas properties,
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Stromsoe E., 1970
Stromsoe E.,
Heat capacity of alcohol vapors at atmospheric pressure,
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Parks, Kelley, et al., 1929
Parks, G.S.; Kelley, K.K.; Huffman, H.M.,
Thermal data on organic compounds. V. A revision of the entropies and free energies of nineteen organic compounds,
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Parks and Anderson, 1926
Parks, G.S.; Anderson, C.T.,
Thermal data on organic compounds. III. The heat capacities, entropies and free energies of tertiary butyl alcohol, mannitol, erythritol and normal butyric acid,
J. Am. Chem. Soc., 1926, 48, 1506-1512. [all data]
Raley, Rust, et al., 1948
Raley, J.H.; Rust, F.F.; Vaughan, W.E.,
Decompositions of Di-t-alkyl peroxides. I. Kinetics,
J. Am. Chem. Soc., 1948, 70, 88-94. [all data]
Oetting F.L., 1963
Oetting F.L.,
The heat capacity and entropy of 2-methyl-2-propanol from 15 to 330 K,
J. Phys. Chem., 1963, 67, 2757-2761. [all data]
Caceres-Alonso, Costas, et al., 1988
Caceres-Alonso, M.; Costas, M.; Andreoli-Ball, L.; Patterson, D.,
Steric effects on the self-association of branched and cyclic alcohols in inert solvents. Apparent heat capacities of secondary and tertiary alcohols in hydrocarbons,
Can. J. Chem., 1988, 66, 989-998. [all data]
Okano, Ogawa, et al., 1988
Okano, T.; Ogawa, H.; Murakami, S.,
Molar excess volumes, isentropic compressions, and isobaric heat capacities of methanol-isomeric butanol systems at 298.15 K,
Can. J. Chem., 1988, 66, 713-717. [all data]
De Visser, Perron, et al., 1977
De Visser, C.; Perron, G.; Desnoyers, J.E.,
Volumes and heat capacities of ternary aqueous systems at 25°C. Mixtures of urea, tert-butyl alcohol, N,N-dimethylformamide, and water,
J. Amer. Chem. Soc., 1977, 99, 5894-5900. [all data]
De Visser, Perron, et al., 1977, 2
De Visser, C.; Perron, G.; Desnoyers, J.E.,
The heat capacities, volumes and expansibilities of tert-butyl alcohol - water mixtures form 6 to 65°C,
Can. J. Chem., 1977, 55, 856-762. [all data]
Murthy and Subrahmanyam, 1977
Murthy, N.M.; Subrahmanyam, S.V.,
Behaviour of excess heat capacity of aqueous non-electrolytes,
Indian J. Pure Appl. Phys., 1977, 15, 485-489. [all data]
Skold, Suurkuusk, et al., 1976
Skold, R.; Suurkuusk, J.; Wadso, I.,
Thermochemistry of solutions of biochemical model compounds. 7. Aqueous solutions of some amides, t-butanol, and pentanol,
J. Chem. Thermodynam., 1976, 8, 1075-1080. [all data]
Hunter and Lias, 1998
Hunter, E.P.; Lias, S.G.,
Evaluated Gas Phase Basicities and Proton Affinities of Molecules: An Update,
J. Phys. Chem. Ref. Data, 1998, 27, 3, 413-656, https://doi.org/10.1063/1.556018
. [all data]
Shao, Baer, et al., 1988
Shao, J.D.; Baer, T.; Lewis, D.K.,
Dissociation dynamics of energy-selected ion-dipole complexes. 2. Butyl alcohol ions,
J. Phys. Chem., 1988, 92, 5123. [all data]
Cocksey, Eland, et al., 1971
Cocksey, B.J.; Eland, J.H.D.; Danby, C.J.,
The effect of alkyl substitution on ionisation potential,
J. Chem. Soc., 1971, (B), 790. [all data]
Baker, Betteridge, et al., 1971
Baker, A.D.; Betteridge, D.; Kemp, N.R.; Kirby, R.E.,
Application of photoelectron spectrometry to pesticide analysis. II.Photoelectron spectra of hydroxy-, and halo-alkanes and halohydrins,
Anal. Chem., 1971, 43, 375. [all data]
Benoit and Harrison, 1977
Benoit, F.M.; Harrison, A.G.,
Predictive value of proton affinity. Ionization energy correlations involving oxygenated molecules,
J. Am. Chem. Soc., 1977, 99, 3980. [all data]
Peel and Willett, 1975
Peel, J.B.; Willett, G.D.,
Photoelectron spectroscopic studies of the higher alcohols,
Aust. J. Chem., 1975, 28, 2357. [all data]
Robin and Kuebler, 1973
Robin, M.B.; Kuebler, N.A.,
Excited electronic states of the simple alcohols,
J. Electron Spectrosc. Relat. Phenom., 1973, 1, 13. [all data]
Lossing, 1977
Lossing, F.P.,
Heats of formation of some isomeric [CnH2n+1]+ ions. Substitutional effects on ion stability,
J. Am. Chem. Soc., 1977, 99, 7526. [all data]
Beauchamp, Caserio, et al., 1974
Beauchamp, J.L.; Caserio, M.C.; McMahon, T.B.,
Ion-molecule reactions of tert-butyl alcohol by ion cyclotron resonance spectroscopy,
J. Am. Chem. Soc., 1974, 96, 6243. [all data]
Potapov and Sorokin, 1972
Potapov, V.K.; Sorokin, V.V.,
Kinetic energies of products of dissociative photoionization of molecules. I. Aliphatic ketones and alcohols,
Khim. Vys. Energ., 1972, 6, 387. [all data]
Potapov and Sorokin, 1970
Potapov, V.K.; Sorokin, V.V.,
Investigation of ionic molecular reactions proceeding during photoionization of aromatic compounds and alcohols,
Dokl. Akad. Nauk SSSR, 1970, 195, 616, In original 848. [all data]
Harrison, Ivko, et al., 1966
Harrison, A.G.; Ivko, A.; Van Raalte, D.,
Energetics of formation of some oxygenated ions and the proton affinities of carbonyl compounds,
Can. J. Chem., 1966, 44, 1625. [all data]
Ramond, Davico, et al., 2000
Ramond, T.M.; Davico, G.E.; Schwartz, R.L.; Lineberger, W.C.,
Vibronic structure of alkoxy radicals via photoelectron spectroscopy,
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. [all data]
Bartmess, Scott, et al., 1979
Bartmess, J.E.; Scott, J.A.; McIver, R.T., Jr.,
The gas phase acidity scale from methanol to phenol,
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DeTuri and Ervin, 1999
DeTuri, V.F.; Ervin, K.M.,
Competitive threshold collision-induced dissociation: Gas-phase acidities and bond dissociation energies for a series of alcohols,
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Haas and Harrison, 1993
Haas, M.J.; Harrison, A.G.,
The Fragmentation of Proton-Bound Cluster Ions and the Gas-Phase Acidities of Alcohols,
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. [all data]
Notes
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Gas phase ion energetics data, References
- Symbols used in this document:
AE Appearance energy Cp,gas Constant pressure heat capacity of gas Cp,liquid Constant pressure heat capacity of liquid Cp,solid Constant pressure heat capacity of solid IE (evaluated) Recommended ionization energy S°liquid Entropy of liquid at standard conditions S°solid,1 bar Entropy of solid at standard conditions (1 bar) ΔcH°liquid Enthalpy of combustion of liquid at standard conditions ΔcH°solid Enthalpy of combustion of solid at standard conditions ΔfH°gas Enthalpy of formation of gas at standard conditions ΔfH°liquid Enthalpy of formation of liquid at standard conditions ΔrG° Free energy of reaction at standard conditions ΔrH° Enthalpy of reaction at standard conditions - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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