Methylparaben
- Formula: C8H8O3
- Molecular weight: 152.1473
- IUPAC Standard InChIKey: LXCFILQKKLGQFO-UHFFFAOYSA-N
- CAS Registry Number: 99-76-3
- 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: Benzoic acid, 4-hydroxy-, methyl ester; Benzoic acid, p-hydroxy-, methyl ester; p-Carbomethoxyphenol; p-Hydroxybenzoic acid, methyl ester; p-Methoxycarbonylphenol; Abiol; Maseptol; Methaben; Methyl chemosept; Methyl p-hydroxybenzoate; Methyl Butex; Methyl Parasept; Methyl 4-hydroxybenzoate; Methylben; Metoxyde; Moldex; Nipagin; Nipagin M; Paridol; Preserval; Preserval M; Septos; Solbrol; Solbrol M; Tegosept M; 4-(Methoxycarbonyl)phenol; 4-Hydroxybenzoic acid, methyl ester; Aseptoform; Metaben; Methyl ester of p-hydroxybenzoic acid; Methylester kyseliny p-hydroxybenzoove; Methyl parahydroxybenzoate; p-Oxybenzoesauremethylester; Lexgard M; NSC 3827; Paraben M; Metagin; p-Hydroxybenzoic methyl ester; component of Heb-Cort MC; Paraben; Parasept; Methyl p-oxybenzoate; Methyl //p//-Hydroxybenzoate; Methylparaben USP; Nigagin; Solparol; Preserval MS; Solparol (Salt/Mix); Preserval MS (Salt/Mix)
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Phase change data
Go To: Top, Gas phase ion energetics data, Mass spectrum (electron ionization), 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
AC - William E. Acree, Jr., James S. Chickos
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
Tfus | 398.4 | K | N/A | Manzo and Ahumanda, 1990 | Uncertainty assigned by TRC = 0.5 K; TRC |
Quantity | Value | Units | Method | Reference | Comment |
ΔvapH° | 83.1 | kJ/mol | CGC | Temprado, Roux, et al., 2005 | AC |
Quantity | Value | Units | Method | Reference | Comment |
ΔsubH° | 98.8 ± 0.8 | kJ/mol | GS | Perlovich, Rodionov, et al., 2005 | Based on data from 303. to 327. K.; AC |
Enthalpy of vaporization
ΔvapH (kJ/mol) | Temperature (K) | Method | Reference | Comment |
---|---|---|---|---|
81.5 | 461. | A | Stephenson and Malanowski, 1987 | Based on data from 446. to 517. K.; AC |
Enthalpy of fusion
ΔfusH (kJ/mol) | Temperature (K) | Reference | Comment |
---|---|---|---|
25.3 | 399.2 | Giordano, Bettini, et al., 1999 | AC |
24.31 | 398.5 | Manzo and Ahumada, 1990 | AC |
Gas phase ion energetics data
Go To: Top, Phase change data, Mass spectrum (electron ionization), 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
Data compiled as indicated in comments:
B - John E. Bartmess
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
Proton affinity (review) | 863.4 | kJ/mol | N/A | Hunter and Lias, 1998 | HL |
Quantity | Value | Units | Method | Reference | Comment |
Gas basicity | 832.5 | kJ/mol | N/A | Hunter and Lias, 1998 | HL |
De-protonation reactions
C8H7O3- + =
By formula: C8H7O3- + H+ = C8H8O3
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1410. ± 8.8 | kJ/mol | G+TS | Fujio, McIver, et al., 1981 | gas phase; value altered from reference due to change in acidity scale; B |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | 1382. ± 8.4 | kJ/mol | IMRE | Fujio, McIver, et al., 1981 | gas phase; value altered from reference due to change in acidity scale; B |
Mass spectrum (electron ionization)
Go To: Top, Phase change 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 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, 1990. |
NIST MS number | 118948 |
References
Go To: Top, Phase change data, Gas phase ion energetics data, Mass spectrum (electron ionization), Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Manzo and Ahumanda, 1990
Manzo, R.H.; Ahumanda, A.A.,
Effects of solvent medium on solubility. V: Enthalpic and entropic contributions to the free energy changes of Di-substituted benzene derivatives in ethanol: Water and ethanol: Cyclohexane mixtures,
J. Pharm. Sci., 1990, 79, 12, 1109, https://doi.org/10.1002/jps.2600791214
. [all data]
Temprado, Roux, et al., 2005
Temprado, Manuel; Roux, Maria Victoria; Umnahanant, Patamaporn; Zhao, Hui; Chickos, James S.,
The Thermochemistry of 2,4-Pentanedione Revisited: Observance of a Nonzero Enthalpy of Mixing between Tautomers and Its Effects on Enthalpies of Formation,
J. Phys. Chem. B, 2005, 109, 25, 12590-12595, https://doi.org/10.1021/jp0515131
. [all data]
Perlovich, Rodionov, et al., 2005
Perlovich, German L.; Rodionov, Sergey V.; Bauer-Brandl, Annette,
Thermodynamics of solubility, sublimation and solvation processes of parabens,
European Journal of Pharmaceutical Sciences, 2005, 24, 1, 25-33, https://doi.org/10.1016/j.ejps.2004.09.007
. [all data]
Stephenson and Malanowski, 1987
Stephenson, Richard M.; Malanowski, Stanislaw,
Handbook of the Thermodynamics of Organic Compounds, 1987, https://doi.org/10.1007/978-94-009-3173-2
. [all data]
Giordano, Bettini, et al., 1999
Giordano, Ferdinando; Bettini, Ruggero; Donini, Cristina; Gazzaniga, Andrea; Caira, Mino R.; Zhang, Geoffrey G.Z.; Grant, David J.W.,
Physical properties of parabens and their mixtures: Solubility in water, thermal behavior, and crystal structures,
J. Pharm. Sci., 1999, 88, 11, 1210-1216, https://doi.org/10.1021/js9900452
. [all data]
Manzo and Ahumada, 1990
Manzo, Ruben H.; Ahumada, Amelia A.,
Effects of solvent medium on solubility. V: Enthalpic and entropic contributions to the free energy changes of Di-substituted benzene derivatives in ethanol: Water and ethanol: Cyclohexane mixtures,
J. Pharm. Sci., 1990, 79, 12, 1109-1115, https://doi.org/10.1002/jps.2600791214
. [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]
Fujio, McIver, et al., 1981
Fujio, M.; McIver, R.T., Jr.; Taft, R.W.,
Effects on the acidities of phenols from specific substituent-solvent interactions. Inherent substituent parameters from gas phase acidities,
J. Am. Chem. Soc., 1981, 103, 4017. [all data]
Notes
Go To: Top, Phase change data, Gas phase ion energetics data, Mass spectrum (electron ionization), References
- Symbols used in this document:
Tfus Fusion (melting) point ΔfusH Enthalpy of fusion ΔrG° Free energy of reaction at standard conditions ΔrH° Enthalpy of reaction at standard conditions ΔsubH° Enthalpy of sublimation at standard conditions ΔvapH Enthalpy of vaporization ΔvapH° Enthalpy of vaporization at standard conditions - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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