Ethane, nitro-

• Formula: C₂H₅NO₂
• Molecular weight: 75.0666
• IUPAC Standard InChI: InChI=1S/C2H5NO2/c1-2-3(4)5/h2H2,1H3 Copy

  
• IUPAC Standard InChIKey: MCSAJNNLRCFZED-UHFFFAOYSA-N Copy
• CAS Registry Number: 79-24-3
• 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: Nitroethane; C2H5NO2; Nitroetan; UN 2842; NE; Nitroparaffin
• Permanent link for this species. Use this link for bookmarking this species for future reference.
• Information on this page:
  • Condensed phase thermochemistry data
  • Phase change data
  • Reaction thermochemistry data
  • Ion clustering data
  • Gas Chromatography
  • References
  • Notes
• Other data available:
  • Henry's Law data
  • Gas phase ion energetics data
  • IR Spectrum
  • Mass spectrum (electron ionization)
• Data at other public NIST sites:
  • Gas Phase Kinetics Database
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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

Constant pressure heat capacity of liquid

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
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
AC - William E. Acree, Jr., James S. Chickos
DH - Eugene S. Domalski and Elizabeth D. Hearing

Enthalpy of vaporization

Antoine Equation Parameters

log₁₀(P) = A − (B / (T + C))
    P = vapor pressure (bar)
    T = temperature (K)

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Enthalpy of fusion

Entropy of fusion

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 as indicated in comments:
B - John E. Bartmess
M - Michael M. Meot-Ner (Mautner) and Sharon G. Lias

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

C₂H₄NO₂^- +  =

By formula: C₂H₄NO₂^- + H⁺ = C₂H₅NO₂

CAS Reg. No. 34533-65-8 + 2 = C₆H₁₅N₃O₆^-

By formula: CAS Reg. No. 34533-65-8 + 2C₂H₅NO₂ = C₆H₁₅N₃O₆^-

 +  = C₂H₅N₂O₄^-

By formula: NO₂^- + C₂H₅NO₂ = C₂H₅N₂O₄^-

C₂H₅N₂O₄^- + 2 = C₄H₁₀N₃O₆^-

By formula: C₂H₅N₂O₄^- + 2C₂H₅NO₂ = C₄H₁₀N₃O₆^-

C₄H₁₀N₃O₆^- + 3 = C₆H₁₅N₄O₈^-

By formula: C₄H₁₀N₃O₆^- + 3C₂H₅NO₂ = C₆H₁₅N₄O₈^-

C₆H₁₅N₄O₈^- + 4 = C₈H₂₀N₅O₁₀^-

By formula: C₆H₁₅N₄O₈^- + 4C₂H₅NO₂ = C₈H₂₀N₅O₁₀^-

C₆H₁₅N₃O₆^- + 3 = C₈H₂₀N₄O₈^-

By formula: C₆H₁₅N₃O₆^- + 3C₂H₅NO₂ = C₈H₂₀N₄O₈^-

C₈H₂₀N₄O₈^- + 4 = C₁₀H₂₅N₅O₁₀^-

By formula: C₈H₂₀N₄O₈^- + 4C₂H₅NO₂ = C₁₀H₂₅N₅O₁₀^-

C₄H₁₀N₂O₆^- + 2 = C₆H₁₅N₃O₈^-

By formula: C₄H₁₀N₂O₆^- + 2C₂H₅NO₂ = C₆H₁₅N₃O₈^-

C₆H₁₅N₃O₈^- + 3 = C₈H₂₀N₄O₁₀^-

By formula: C₆H₁₅N₃O₈^- + 3C₂H₅NO₂ = C₈H₂₀N₄O₁₀^-

C₈H₂₀N₄O₁₀^- + 4 = C₁₀H₂₅N₅O₁₂^-

By formula: C₈H₂₀N₄O₁₀^- + 4C₂H₅NO₂ = C₁₀H₂₅N₅O₁₂^-

C₄H₈N₂O₄^- + 2 = C₆H₁₃N₃O₆^-

By formula: C₄H₈N₂O₄^- + 2C₂H₅NO₂ = C₆H₁₃N₃O₆^-

C₄H₉N₂O₄^- + 2 = C₆H₁₄N₃O₆^-

By formula: C₄H₉N₂O₄^- + 2C₂H₅NO₂ = C₆H₁₄N₃O₆^-

C₂H₃NO₂^- +  = C₄H₈N₂O₄^-

By formula: C₂H₃NO₂^- + C₂H₅NO₂ = C₄H₈N₂O₄^-

C₂H₄NO₂^- +  = C₄H₉N₂O₄^-

By formula: C₂H₄NO₂^- + C₂H₅NO₂ = C₄H₉N₂O₄^-

C₂H₆NO₂⁺ +  = (C₂H₆NO₂⁺ • )

By formula: C₂H₆NO₂⁺ + C₂H₅NO₂ = (C₂H₆NO₂⁺ • C₂H₅NO₂)

Ion clustering 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:
B - John E. Bartmess
M - Michael M. Meot-Ner (Mautner) and Sharon G. Lias

Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. Searches may be limited to ion clustering reactions. A general reaction search form is also available.

Clustering reactions

C₂H₃NO₂^- +  = C₄H₈N₂O₄^-

By formula: C₂H₃NO₂^- + C₂H₅NO₂ = C₄H₈N₂O₄^-

C₂H₄NO₂^- +  = C₄H₉N₂O₄^-

By formula: C₂H₄NO₂^- + C₂H₅NO₂ = C₄H₉N₂O₄^-

C₂H₅N₂O₄^- + 2 = C₄H₁₀N₃O₆^-

By formula: C₂H₅N₂O₄^- + 2C₂H₅NO₂ = C₄H₁₀N₃O₆^-

C₂H₆NO₂⁺ +  = (C₂H₆NO₂⁺ • )

By formula: C₂H₆NO₂⁺ + C₂H₅NO₂ = (C₂H₆NO₂⁺ • C₂H₅NO₂)

C₄H₈N₂O₄^- + 2 = C₆H₁₃N₃O₆^-

By formula: C₄H₈N₂O₄^- + 2C₂H₅NO₂ = C₆H₁₃N₃O₆^-

C₄H₉N₂O₄^- + 2 = C₆H₁₄N₃O₆^-

By formula: C₄H₉N₂O₄^- + 2C₂H₅NO₂ = C₆H₁₄N₃O₆^-

C₄H₁₀N₂O₆^- + 2 = C₆H₁₅N₃O₈^-

By formula: C₄H₁₀N₂O₆^- + 2C₂H₅NO₂ = C₆H₁₅N₃O₈^-

C₄H₁₀N₃O₆^- + 3 = C₆H₁₅N₄O₈^-

By formula: C₄H₁₀N₃O₆^- + 3C₂H₅NO₂ = C₆H₁₅N₄O₈^-

C₆H₁₅N₃O₆^- + 3 = C₈H₂₀N₄O₈^-

By formula: C₆H₁₅N₃O₆^- + 3C₂H₅NO₂ = C₈H₂₀N₄O₈^-

C₆H₁₅N₃O₈^- + 3 = C₈H₂₀N₄O₁₀^-

By formula: C₆H₁₅N₃O₈^- + 3C₂H₅NO₂ = C₈H₂₀N₄O₁₀^-

C₆H₁₅N₄O₈^- + 4 = C₈H₂₀N₅O₁₀^-

By formula: C₆H₁₅N₄O₈^- + 4C₂H₅NO₂ = C₈H₂₀N₅O₁₀^-

C₈H₂₀N₄O₈^- + 4 = C₁₀H₂₅N₅O₁₀^-

By formula: C₈H₂₀N₄O₈^- + 4C₂H₅NO₂ = C₁₀H₂₅N₅O₁₀^-

C₈H₂₀N₄O₁₀^- + 4 = C₁₀H₂₅N₅O₁₂^-

By formula: C₈H₂₀N₄O₁₀^- + 4C₂H₅NO₂ = C₁₀H₂₅N₅O₁₂^-

 +  = C₂H₅N₂O₄^-

By formula: NO₂^- + C₂H₅NO₂ = C₂H₅N₂O₄^-

Gas Chromatography

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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

Kovats' RI, non-polar column, isothermal

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Kovats' RI, polar column, isothermal

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Van Den Dool and Kratz RI, non-polar column, temperature ramp

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Normal alkane RI, non-polar column, custom temperature program

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Normal alkane RI, polar column, custom temperature program

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References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Lebedeva and Ryadenko, 1973
Lebedeva, N.D.; Ryadenko, V.L.R., Enthalpies of formation of nitroalkanes, Russ. J. Phys. Chem. (Engl. Transl.), 1973, 47, 1382. [all data]

Cass, Fletcher, et al., 1958
Cass, R.C.; Fletcher, S.E.; Mortimer, C.T.; Quincey, P.G.; Springall, H.D., Heats of combustion and molecular structure. Part IV. Aliphatic nitroalkanes and nitric esters, J. Chem. Soc., 1958, 958-962. [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]

Holcomb and Dorsey, 1949
Holcomb, D.E.; Dorsey, C.L., Jr., Thermodynamic properties of nitroparaffins, Ind. Eng. Chem., 1949, 41, 2788-2792. [all data]

Liu and Ziegler, 1966
Liu, K.F.; Ziegler, W.T., Heat capacity from 80° to 300°K., melting point and heat of fusion of nitroethane, J. Chem. Eng. Data, 1966, 11, 187-189. [all data]

Toops, 1956
Toops, E.E., Physical Properties of High Purity Nitroparaffins, J. Phys. Chem., 1956, 60, 304-6. [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]

Toops, 1956, 2
Toops, Emory E., Physical Properties of Eight High-Purity Nitroparaffins, J. Phys. Chem., 1956, 60, 3, 304-306, https://doi.org/10.1021/j150537a012 . [all data]

Dykyj, 1970
Dykyj, J., Petrochemica, 1970, 10, 2, 51. [all data]

Stull, 1947
Stull, Daniel R., Vapor Pressure of Pure Substances. Organic and Inorganic Compounds, Ind. Eng. Chem., 1947, 39, 4, 517-540, https://doi.org/10.1021/ie50448a022 . [all data]

Tolstova, Kogan, et al., 1965
Tolstova, T.S.; Kogan, V.B.; Skorokhodova, V.L., Equilibrium Liquid-Steam in Systems Nitrobensol-Nitromethane, Nitrobensol-Nitroethane, Zh. Prikl. Khim. (Leningrad), 1965, 38, 11, 2617-2618. [all data]

Domalski and Hearing, 1996
Domalski, Eugene S.; Hearing, Elizabeth D., Heat Capacities and Entropies of Organic Compounds in the Condensed Phase. Volume III, J. Phys. Chem. Ref. Data, 1996, 25, 1, 1, https://doi.org/10.1063/1.555985 . [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, J. Am. Chem. Soc., 1979, 101, 6047. [all data]

Cumming and Kebarle, 1978
Cumming, J.B.; Kebarle, P., Summary of gas phase measurements involving acids AH. Entropy changes in proton transfer reactions involving negative ions. Bond dissociation energies D(A-H) and electron affinities EA(A), Can. J. Chem., 1978, 56, 1. [all data]

Wincel, 2004
Wincel, H., Gas-phase clustering reactions of NO2-, C2H3NO2-, C2H4NO2-C2H5NO2- and C2H5NO4- with C2H5NO2, Int. J. Mass Spectrom., 2004, 232, 2, 185-194, https://doi.org/10.1016/j.ijms.2004.01.003 . [all data]

Meot-Ner, Hunter, et al., 1979
Meot-Ner, (Mautner); Hunter, E.P.; Field, F.H., Ion Thermochemistry of Low Volatility Compounds in the Gas Phase. I. Intrinsic Basicities of Alpha - Amino Acids, J. Am. Chem. Soc., 1979, 101, 3, 686, https://doi.org/10.1021/ja00497a034 . [all data]

Görgényi and Héberger, 2003
Görgényi, M.; Héberger, K., Minimum in the temperature dependence of the Kováts retention indices of nitroalkanes and alkanenitriles on an apolar phase, J. Chromatogr. A, 2003, 985, 1-2, 11-19, https://doi.org/10.1016/S0021-9673(02)01842-3 . [all data]

Reddy, Dutoit, et al., 1992
Reddy, K.S.; Dutoit, J.-Cl.; Kovats, E. sz., Pair-wise interactions by gas chromatography. I. Interaction free enthalpies of solutes with non-associated primary alcohol groups, J. Chromatogr., 1992, 609, 1-2, 229-259, https://doi.org/10.1016/0021-9673(92)80167-S . [all data]

Dutoit, 1991
Dutoit, J., Gas chromatographic retention behaviour of some solutes on structurally similar polar and non-polar stationary phases, J. Chromatogr., 1991, 555, 1-2, 191-204, https://doi.org/10.1016/S0021-9673(01)87179-X . [all data]

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Boneva, S.; Dimov, N., Chromatographic retention indices of C₁-C₄ nitroparaffins, Zh. Anal. Khim., 1979, 34, 6, 902-905. [all data]

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Brown, I.; Chapman, I.L.; Nicholson, G.J., Gas chromatography of polar solutes in electron acceptor stationary phases, Aust. J. Chem., 1968, 21, 5, 1125-1141, https://doi.org/10.1071/CH9681125 . [all data]

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Rohrschneider, L., Eine methode zur charakterisierung von gaschromatographischen trennflüssigkeiten, J. Chromatogr., 1966, 22, 6-22, https://doi.org/10.1016/S0021-9673(01)97064-5 . [all data]

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Wehrli, A.; Kováts, E., Gas-chromatographische Charakterisierung ogranischer Verbindungen. Teil 3: Berechnung der Retentionsindices aliphatischer, alicyclischer und aromatischer Verbindungen, Helv. Chim. Acta, 1959, 7, 7, 2709-2736, https://doi.org/10.1002/hlca.19590420745 . [all data]

Hobbs and Conde, 1992
Hobbs, J.R.; Conde, E.P., Gas chromatographic retention indices of explosives and nitro-compounds in Advances in Analysis and Detection of Explosives: Proceedings of the 4th International Symposium on Analysis of Detection of Explosives, September 7-10, 1992, Jerusalem Israel, J. Yinon, ed(s)., Kluwer Academic Publishers, Netherlands, 1992, 153-164. [all data]

Flanagan, Streete, et al., 1997
Flanagan, R.J.; Streete, P.J.; Ramsey, J.D., Volatile Substance Abuse, UNODC Technical Series, No 5, United Nations, Office on Drugs and Crime, Vienna International Centre, PO Box 500, A-1400 Vienna, Austria, 1997, 56, retrieved from http://www.odccp.org/pdf/technical_series₁997-01-01₁.pdf. [all data]

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Zenkevich, I.G.; Chupalov, A.A., New Possibilities of Chromato Mass Pectrometric Identification of Organic Compounds Using Increments of Gas Chromatographic Retention Indices of Molecular Structural Fragments, Zh. Org. Khim. (Rus.), 1996, 32, 5, 656-666. [all data]

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Strete, P.J.; Ruprah, M.; Ramsey, J.D.; Flanagan, R.J., Detection and identification of volatile substances by headspace capillary gas chromatography to aid the diagnosis of acute poisoning, Analyst, 1992, 117, 7, 1111-1127, https://doi.org/10.1039/an9921701111 . [all data]

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Ramsey, J.D.; Flanagan, R.J., Detection and Identification of Volatile Organic Compounds in Blood by Headspace Gas Chromatography as an Aid to the Diagnosis of Solvent Abuse, J. Chromatogr., 1982, 240, 2, 423-444, https://doi.org/10.1016/S0021-9673(00)99622-5 . [all data]

Notes

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• Symbols used in this document:
  

  Cp,liquid	Constant pressure heat capacity of liquid
  Tboil	Boiling point
  Tfus	Fusion (melting) point
  Ttriple	Triple point temperature
  ΔcH°liquid	Enthalpy of combustion of liquid 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
  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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