Benzoic acid, 4-methyl-
- Formula: C8H8O2
- Molecular weight: 136.1479
- IUPAC Standard InChIKey: LPNBBFKOUUSUDB-UHFFFAOYSA-N
- CAS Registry Number: 99-94-5
- 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. - Other names: p-Toluic acid; p-Methylbenzoic acid; p-Toluylic acid; Crithminic acid; 4-Methylbenzoic acid; 4-Toluic acid; para-Toluic acid; NSC 2215; p-Carboxytoluene; p-Tolylcarboxylic acid
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Gas phase thermochemistry data
Go To: Top, Condensed phase thermochemistry data, Phase change data, Reaction thermochemistry data, Gas phase ion energetics data, IR Spectrum, Mass spectrum (electron ionization), UV/Visible spectrum, Gas Chromatography, 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.
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔfH°gas | -78.97 ± 0.36 | kcal/mol | Ccb | Colomina, Jimenez, et al., 1986 | see Colomina, Boned, et al., 1961; ALS |
ΔfH°gas | -78.97 | kcal/mol | N/A | Corral, 1960 | Value computed using ΔfHsolid° value of -429.2±1.1 kj/mol from Corral, 1960 and ΔsubH° value of 98.8 kj/mol from Colomina, Jimenez, et al., 1986.; DRB |
ΔfH°gas | -77.56 | kcal/mol | N/A | Breitenbach and Derkosch, 1951 | Value computed using ΔfHsolid° value of -423.3±3.8 kj/mol from Breitenbach and Derkosch, 1951 and ΔsubH° value of 98.8 kj/mol from Colomina, Jimenez, et al., 1986.; DRB |
Condensed phase thermochemistry 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 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°solid | -102.6 ± 0.36 | kcal/mol | Ccb | Colomina, Jimenez, et al., 1986 | see Colomina, Boned, et al., 1961; ALS |
ΔfH°solid | -102.58 ± 0.26 | kcal/mol | Ccb | Corral, 1960 | Different experiments; ALS |
ΔfH°solid | -101.17 ± 0.90 | kcal/mol | Ccb | Breitenbach and Derkosch, 1951 | Reanalyzed by Cox and Pilcher, 1970, Original value = -101.0 kcal/mol; ALS |
Quantity | Value | Units | Method | Reference | Comment |
ΔcH°solid | -923.1 ± 0.2 | kcal/mol | Ccb | Colomina, Jimenez, et al., 1986 | see Colomina, Boned, et al., 1961; Corresponding ΔfHºsolid = -102.6 kcal/mol (simple calculation by NIST; no Washburn corrections); ALS |
ΔcH°solid | -923.10 ± 0.22 | kcal/mol | Ccb | Corral, 1960 | Different experiments; Corresponding ΔfHºsolid = -102.57 kcal/mol (simple calculation by NIST; no Washburn corrections); ALS |
ΔcH°solid | -924.5 | kcal/mol | Ccb | Breitenbach and Derkosch, 1951 | Corresponding ΔfHºsolid = -101.2 kcal/mol (simple calculation by NIST; no Washburn corrections); ALS |
Constant pressure heat capacity of solid
Cp,solid (cal/mol*K) | Temperature (K) | Reference | Comment |
---|---|---|---|
40.39 | 298. | Andrews, Lynn, et al., 1926 | T = 22 to 225 C.; DH |
Phase change 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 compiled as indicated in comments:
BS - Robert L. Brown and Stephen E. Stein
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
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
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
Tboil | 547.7 | K | N/A | Aldrich Chemical Company Inc., 1990 | BS |
Quantity | Value | Units | Method | Reference | Comment |
Tfus | 455. | K | N/A | Sugunan and Thomas, 1993 | Uncertainty assigned by TRC = 2. K; TRC |
Tfus | 450.15 | K | N/A | Ipatieff, Corson, et al., 1936 | Uncertainty assigned by TRC = 2.5 K; TRC |
Tfus | 452.8 | K | N/A | Andrews, Lynn, et al., 1926, 2 | Uncertainty assigned by TRC = 0.3 K; TRC |
Quantity | Value | Units | Method | Reference | Comment |
ΔsubH° | 23.6 ± 0.1 | kcal/mol | ME | Monte, Almeida, et al., 2004 | Based on data from 320. to 337. K.; AC |
ΔsubH° | 23.6 ± 0.07 | kcal/mol | ME | Colomina, Jimenez, et al., 1986, 2 | Based on data from 318. to 337. K.; AC |
ΔsubH° | 23.6 ± 0.07 | kcal/mol | V | Colomina, Jimenez, et al., 1986 | see Colomina, Boned, et al., 1961; ALS |
ΔsubH° | 23.6 | kcal/mol | N/A | Colomina, Jimenez, et al., 1986 | DRB |
Enthalpy of fusion
ΔfusH (kcal/mol) | Temperature (K) | Reference | Comment |
---|---|---|---|
5.430 | 452.8 | Acree, 1991 | AC |
5.4302 | 452.8 | Andrews, Lynn, et al., 1926 | DH |
Entropy of fusion
ΔfusS (cal/mol*K) | Temperature (K) | Reference | Comment |
---|---|---|---|
12.0 | 452.8 | Andrews, Lynn, et al., 1926 | DH |
Reaction thermochemistry 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 compiled by: 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
C8H7O2- + =
By formula: C8H7O2- + H+ = C8H8O2
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 341.0 ± 2.1 | kcal/mol | G+TS | Kebarle and McMahon, 1977 | gas phase |
ΔrH° | 340.7 ± 2.1 | kcal/mol | G+TS | Decouzon, Exner, et al., 1996 | gas phase; relative to benzoate at 333.0 kcal/mol |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | 334.0 ± 2.0 | kcal/mol | IMRE | Kebarle and McMahon, 1977 | gas phase |
ΔrG° | 333.7 ± 2.0 | kcal/mol | IMRE | Decouzon, Exner, et al., 1996 | gas phase; relative to benzoate at 333.0 kcal/mol |
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
Data compiled as indicated in comments:
B - John E. Bartmess
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi
View reactions leading to C8H8O2+ (ion structure unspecified)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
Proton affinity (review) | 200.0 | kcal/mol | N/A | Hunter and Lias, 1998 | HL |
Quantity | Value | Units | Method | Reference | Comment |
Gas basicity | 192.6 | kcal/mol | N/A | Hunter and Lias, 1998 | HL |
Ionization energy determinations
IE (eV) | Method | Reference | Comment |
---|---|---|---|
9.2 ± 0.2 | EI | Benoit, 1973 | LLK |
9.4 | PE | Meeks, Wahlborg, et al., 1981 | Vertical value; LLK |
Appearance energy determinations
Ion | AE (eV) | Other Products | Method | Reference | Comment |
---|---|---|---|---|---|
C7H7+ | 12.6 ± 0.2 | COOH | EI | Benoit, 1973 | LLK |
C8H7O+ | 12.1 ± 0.2 | OH | EI | Benoit, 1973 | LLK |
De-protonation reactions
C8H7O2- + =
By formula: C8H7O2- + H+ = C8H8O2
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 341.0 ± 2.1 | kcal/mol | G+TS | Kebarle and McMahon, 1977 | gas phase; B |
ΔrH° | 340.7 ± 2.1 | kcal/mol | G+TS | Decouzon, Exner, et al., 1996 | gas phase; relative to benzoate at 333.0 kcal/mol; B |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | 334.0 ± 2.0 | kcal/mol | IMRE | Kebarle and McMahon, 1977 | gas phase; B |
ΔrG° | 333.7 ± 2.0 | kcal/mol | IMRE | Decouzon, Exner, et al., 1996 | gas phase; relative to benzoate at 333.0 kcal/mol; B |
IR Spectrum
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Data compiled by: Coblentz Society, Inc.
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
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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 | Chemical Concepts |
NIST MS number | 153859 |
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.
Spectrum
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Additional Data
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Download spectrum in JCAMP-DX format.
Source | Lang (editor), 1969 |
---|---|
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. 19057 |
Instrument | Unicam SP 700 |
Melting point | 176-178 |
Gas Chromatography
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: NIST Mass Spectrometry Data Center, William E. Wallace, director
Normal alkane RI, non-polar column, temperature ramp
Column type | Active phase | I | Reference | Comment |
---|---|---|---|---|
Capillary | DB-5 | 1213. | Ali, Wurster, et al., 2008 | 30. m/0.25 mm/0.25 μm, Helium, 70. C @ 1. min, 3. K/min; Tend: 220. C |
Capillary | DB-5 | 1213. | Awadi Ali, Wurster, et al., 2008 | 70. C @ 1. min, 3. K/min; Column length: 30. m; Column diameter: 0.25 mm; Tend: 220. C |
References
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, Gas Chromatography, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Colomina, Jimenez, et al., 1986
Colomina, M.; Jimenez, P.; Roux, M.V.; Turrion, C.,
Propiedades termoquimicas de derivados del acido benzoico. XIII. Presiones de vapor y entalpias de sublimacion y formacion de los acidos toluicos,
An. Quim., 1986, 82, 126-130. [all data]
Colomina, Boned, et al., 1961
Colomina, M.; Boned, M.L.; Turrion, C.,
Investigaciones termoquimicas sobre los acidos alquilbenzoicos. I. Acidos toluicos,
An. Fis. Quim., 1961, 57, 655-664. [all data]
Corral, 1960
Corral, L.B.,
Investigaciones termoquimicas sobre los acidos toluicos y dimetilbenzoicos,
Rev. R. Acad. Cienc., 1960, 54, 365-403. [all data]
Breitenbach and Derkosch, 1951
Breitenbach, J.W.; Derkosch, J.,
Verbrennungswarmen von peroxyden und verwandten verbindungen sowie von polystrolen,
Monatsh. Chem., 1951, 82, 177-179. [all data]
Cox and Pilcher, 1970
Cox, J.D.; Pilcher, G.,
Thermochemistry of Organic and Organometallic Compounds, Academic Press, New York, 1970, 1-636. [all data]
Andrews, Lynn, et al., 1926
Andrews, D.H.; Lynn, G.; Johnston, J.,
The heat capacities and heat of crystallization of some isomeric aromatic compounds,
J. Am. Chem. Soc., 1926, 48, 1274-1287. [all data]
Aldrich Chemical Company Inc., 1990
Aldrich Chemical Company Inc.,
Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 1. [all data]
Sugunan and Thomas, 1993
Sugunan, S.; Thomas, B.,
Salting Coefficients of 2-, 3-, and 4-Methylbenzoic Acids,
J. Chem. Eng. Data, 1993, 38, 520-1. [all data]
Ipatieff, Corson, et al., 1936
Ipatieff, V.N.; Corson, B.B.; Pines, H.,
Influence of Sulfuric Acid Concentration upon Reaction between Olefins and Benzene,
J. Am. Chem. Soc., 1936, 58, 919-22. [all data]
Andrews, Lynn, et al., 1926, 2
Andrews, D.H.; Lynn, G.; Johnston, J.,
The Heat Capacities and Heat of Crystallization of Some Isomeric Aromatic Compounds,
J. Am. Chem. Soc., 1926, 48, 1274. [all data]
Monte, Almeida, et al., 2004
Monte, Manuel J.S.; Almeida, Ana R.R.P.; Ribeiro da Silva, Manuel A.V.,
Thermodynamic study of the sublimation of eight 4-n-alkylbenzoic acids,
The Journal of Chemical Thermodynamics, 2004, 36, 5, 385-392, https://doi.org/10.1016/j.jct.2004.02.001
. [all data]
Colomina, Jimenez, et al., 1986, 2
Colomina, M.; Jimenez, P.; Roux, M.V.; Turrion, C.,
Propiedades termoquimicas de derivados del acido benzoico. XIII. Presiones de vapor y entalpias de sublimacion y formacion de los acidos toluicos,
An. Quim., 1986, 82, 126. [all data]
Acree, 1991
Acree, William E.,
Thermodynamic properties of organic compounds: enthalpy of fusion and melting point temperature compilation,
Thermochimica Acta, 1991, 189, 1, 37-56, https://doi.org/10.1016/0040-6031(91)87098-H
. [all data]
Kebarle and McMahon, 1977
Kebarle, P.; McMahon, T.B.,
Intrinsic Acidities of Substituted Phenols and Benzoic Acids Determined by Gas Phase Proton Transfer Equilibria,
J. Am. Chem. Soc., 1977, 99, 7, 2222, https://doi.org/10.1021/ja00449a032
. [all data]
Decouzon, Exner, et al., 1996
Decouzon, M.; Exner, O.; Gal, J.-F.; Maria, P.-C.,
Non-classical Buttressing Effect: Gas-phase Ionization of Some Methyl Substituted Benzoic Acids,
J. Chem. Soc. Perkin Trans., 1996, 2, 4, 475, https://doi.org/10.1039/p29960000475
. [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]
Benoit, 1973
Benoit, F.,
Substituent effects in mass spectrometry. III. Substituent effects in the dissociation of the molecular ions of para and meta subtituted benzoic acids,
Org. Mass Spectrom., 1973, 7, 295. [all data]
Meeks, Wahlborg, et al., 1981
Meeks, J.; Wahlborg, A.; McGlynn, S.P.,
Photoelectron spectroscopy of carbonyls: Benzoic acid and its derivatives,
J. Electron Spectrosc. Relat. Phenom., 1981, 22, 43. [all data]
Lang (editor), 1969
Lang (editor), L.,
Absorption Spectra in the Ultraviolet and Visible Region, 1969, 12, 33. [all data]
Ali, Wurster, et al., 2008
Ali, N.A.A.; Wurster, M.; Arnold, N.; Teichert, A.; Schmidt, J.; Lindequist, U.; Wessjohann, L.,
Chemical composition and biological activities of essential oils from the oleogum resins of three endemic soqotraen Boswellia species,
Rec. Nat. Prod., 2008, 2, 1, 6-12. [all data]
Awadi Ali, Wurster, et al., 2008
Awadi Ali, N.A.; Wurster, M.; Arnold, N.; Teicher, A.; Schmidt, J.; Lindequist, U.; Wessjohann, L.,
Chemical composition and biological activity of essential oils from the Oleogum resins of three endemic soqotraen Boswellia species,
Rec. Nat. Prod., 2008, 2, 1, 6-12. [all data]
Notes
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, Gas Chromatography, References
- Symbols used in this document:
AE Appearance energy Cp,solid Constant pressure heat capacity of solid Tboil Boiling point Tfus Fusion (melting) point ΔcH°solid Enthalpy of combustion of solid at standard conditions ΔfH°gas Enthalpy of formation of gas at standard conditions ΔfH°solid Enthalpy of formation of solid 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 ΔsubH° Enthalpy of sublimation at standard conditions - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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