Ethane, nitro-

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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

Quantity Value Units Method Reference Comment
Tboil387.6 ± 0.8KAVGN/AAverage of 6 values; Individual data points
Quantity Value Units Method Reference Comment
Tfus183.63KN/AToops, 1956Uncertainty assigned by TRC = 0.05 K; TRC
Quantity Value Units Method Reference Comment
Ttriple183.69KN/ALiu and Ziegler, 1966Uncertainty assigned by TRC = 0.04 K; based on analysis of melting curve; TRC
Quantity Value Units Method Reference Comment
Δvap41.6 ± 0.42kJ/molVHolcomb and Dorsey, 1949ALS

Enthalpy of vaporization

ΔvapH (kJ/mol) Temperature (K) Method Reference Comment
38.6339.EBStephenson and Malanowski, 1987Based on data from 324. to 388. K. See also Toops, 1956, 2 and Dykyj, 1970.; AC
41.3267.N/AStull, 1947Based on data from 252. to 387. K.; AC

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
390.0 to 459.1.74671207.774-269.20Tolstova, Kogan, et al., 1965Coefficents calculated by NIST from author's data.
252. to 387.4.712671671.266-31.963Stull, 1947Coefficents calculated by NIST from author's data.

Enthalpy of fusion

ΔfusH (kJ/mol) Temperature (K) Reference Comment
9.853183.69Liu and Ziegler, 1966DH
9.85183.7Domalski and Hearing, 1996AC

Entropy of fusion

ΔfusS (J/mol*K) Temperature (K) Reference Comment
53.64183.69Liu and Ziegler, 1966DH

In addition to the Thermodynamics Research Center (TRC) data available from this site, much more physical and chemical property data is available from the following TRC products:


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- + Hydrogen cation = Ethane, nitro-

By formula: C2H4NO2- + H+ = C2H5NO2

Quantity Value Units Method Reference Comment
Δr1489. ± 9.2kJ/molG+TSBartmess, Scott, et al., 1979gas phase; value altered from reference due to change in acidity scale; B
Δr1496. ± 12.kJ/molG+TSCumming and Kebarle, 1978gas phase; B
Quantity Value Units Method Reference Comment
Δr1462. ± 8.4kJ/molIMREBartmess, Scott, et al., 1979gas phase; value altered from reference due to change in acidity scale; B
Δr1469. ± 8.4kJ/molIMRECumming and Kebarle, 1978gas phase; B

CAS Reg. No. 34533-65-8 + 2Ethane, nitro- = C6H15N3O6-

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

Quantity Value Units Method Reference Comment
Δr61.09 ± 0.84kJ/molTDAsWincel, 2004gas phase; B
Quantity Value Units Method Reference Comment
Δr26.4kJ/molTDAsWincel, 2004gas phase; B

Nitrogen oxide anion + Ethane, nitro- = C2H5N2O4-

By formula: NO2- + C2H5NO2 = C2H5N2O4-

Quantity Value Units Method Reference Comment
Δr66.1 ± 2.1kJ/molTDAsWincel, 2004gas phase; B
Quantity Value Units Method Reference Comment
Δr37.2kJ/molTDAsWincel, 2004gas phase; B

C2H5N2O4- + 2Ethane, nitro- = C4H10N3O6-

By formula: C2H5N2O4- + 2C2H5NO2 = C4H10N3O6-

Quantity Value Units Method Reference Comment
Δr62.3 ± 2.1kJ/molTDAsWincel, 2004gas phase; B
Quantity Value Units Method Reference Comment
Δr28.5kJ/molTDAsWincel, 2004gas phase; B

C4H10N3O6- + 3Ethane, nitro- = C6H15N4O8-

By formula: C4H10N3O6- + 3C2H5NO2 = C6H15N4O8-

Quantity Value Units Method Reference Comment
Δr49.4 ± 2.1kJ/molTDAsWincel, 2004gas phase; B
Quantity Value Units Method Reference Comment
Δr16.7kJ/molTDAsWincel, 2004gas phase; B

C6H15N4O8- + 4Ethane, nitro- = C8H20N5O10-

By formula: C6H15N4O8- + 4C2H5NO2 = C8H20N5O10-

Quantity Value Units Method Reference Comment
Δr46.0 ± 2.1kJ/molTDAsWincel, 2004gas phase; B
Quantity Value Units Method Reference Comment
Δr11.3kJ/molTDAsWincel, 2004gas phase; B

C6H15N3O6- + 3Ethane, nitro- = C8H20N4O8-

By formula: C6H15N3O6- + 3C2H5NO2 = C8H20N4O8-

Quantity Value Units Method Reference Comment
Δr56.9 ± 1.3kJ/molTDAsWincel, 2004gas phase; B
Quantity Value Units Method Reference Comment
Δr19.7kJ/molTDAsWincel, 2004gas phase; B

C8H20N4O8- + 4Ethane, nitro- = C10H25N5O10-

By formula: C8H20N4O8- + 4C2H5NO2 = C10H25N5O10-

Quantity Value Units Method Reference Comment
Δr49.8 ± 2.1kJ/molTDAsWincel, 2004gas phase; B
Quantity Value Units Method Reference Comment
Δr8.79kJ/molTDAsWincel, 2004gas phase; B

C4H10N2O6- + 2Ethane, nitro- = C6H15N3O8-

By formula: C4H10N2O6- + 2C2H5NO2 = C6H15N3O8-

Quantity Value Units Method Reference Comment
Δr53.1 ± 2.1kJ/molTDAsWincel, 2004gas phase; B
Quantity Value Units Method Reference Comment
Δr18.4kJ/molTDAsWincel, 2004gas phase; B

C6H15N3O8- + 3Ethane, nitro- = C8H20N4O10-

By formula: C6H15N3O8- + 3C2H5NO2 = C8H20N4O10-

Quantity Value Units Method Reference Comment
Δr47.3 ± 2.1kJ/molTDAsWincel, 2004gas phase; B
Quantity Value Units Method Reference Comment
Δr10.0kJ/molTDAsWincel, 2004gas phase; B

C8H20N4O10- + 4Ethane, nitro- = C10H25N5O12-

By formula: C8H20N4O10- + 4C2H5NO2 = C10H25N5O12-

Quantity Value Units Method Reference Comment
Δr43.9 ± 2.1kJ/molTDAsWincel, 2004gas phase; B
Quantity Value Units Method Reference Comment
Δr2.9kJ/molTDAsWincel, 2004gas phase; B

C4H8N2O4- + 2Ethane, nitro- = C6H13N3O6-

By formula: C4H8N2O4- + 2C2H5NO2 = C6H13N3O6-

Quantity Value Units Method Reference Comment
Δr63.6 ± 3.3kJ/molTDAsWincel, 2004gas phase; B
Quantity Value Units Method Reference Comment
Δr23.8kJ/molTDAsWincel, 2004gas phase; B

C4H9N2O4- + 2Ethane, nitro- = C6H14N3O6-

By formula: C4H9N2O4- + 2C2H5NO2 = C6H14N3O6-

Quantity Value Units Method Reference Comment
Δr64.4 ± 3.3kJ/molTDAsWincel, 2004gas phase; B
Quantity Value Units Method Reference Comment
Δr25.9kJ/molTDAsWincel, 2004gas phase; B

C2H3NO2- + Ethane, nitro- = C4H8N2O4-

By formula: C2H3NO2- + C2H5NO2 = C4H8N2O4-

Quantity Value Units Method Reference Comment
Δr65.7 ± 3.3kJ/molTDAsWincel, 2004gas phase; B
Quantity Value Units Method Reference Comment
Δr35.6kJ/molTDAsWincel, 2004gas phase; B

C2H4NO2- + Ethane, nitro- = C4H9N2O4-

By formula: C2H4NO2- + C2H5NO2 = C4H9N2O4-

Quantity Value Units Method Reference Comment
Δr67.8 ± 3.3kJ/molTDAsWincel, 2004gas phase; B
Quantity Value Units Method Reference Comment
Δr37.7kJ/molTDAsWincel, 2004gas phase; B

C2H6NO2+ + Ethane, nitro- = (C2H6NO2+ • Ethane, nitro-)

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

Quantity Value Units Method Reference Comment
Δr130.kJ/molPHPMSMeot-Ner, Hunter, et al., 1979gas phase; M
Quantity Value Units Method Reference Comment
Δr140.J/mol*KPHPMSMeot-Ner, Hunter, et al., 1979gas phase; M

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 Japan AIST/NIMC Database- Spectrum MS-NW- 669
NIST MS number 227638

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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

View large format table.

Column type Active phase Temperature (C) I Reference Comment
CapillaryHP-1100.618.58Görgényi and Héberger, 2003N2; Column length: 30. m; Phase thickness: 3. μm
CapillaryHP-1110.619.51Görgényi and Héberger, 2003N2; Column length: 30. m; Phase thickness: 3. μm
CapillaryHP-1120.620.51Görgényi and Héberger, 2003N2; Column length: 30. m; Phase thickness: 3. μm
CapillaryHP-120.616.27Görgényi and Héberger, 2003N2; Column length: 30. m; Phase thickness: 3. μm
CapillaryHP-130.615.97Görgényi and Héberger, 2003N2; Column length: 30. m; Phase thickness: 3. μm
CapillaryHP-140.615.90Görgényi and Héberger, 2003N2; Column length: 30. m; Phase thickness: 3. μm
CapillaryHP-150.616.07Görgényi and Héberger, 2003N2; Column length: 30. m; Phase thickness: 3. μm
CapillaryHP-160.616.25Görgényi and Héberger, 2003N2; Column length: 30. m; Phase thickness: 3. μm
CapillaryHP-170.616.67Görgényi and Héberger, 2003N2; Column length: 30. m; Phase thickness: 3. μm
CapillaryHP-180.617.22Görgényi and Héberger, 2003N2; Column length: 30. m; Phase thickness: 3. μm
CapillaryHP-190.617.81Görgényi and Héberger, 2003N2; Column length: 30. m; Phase thickness: 3. μm
PackedC78, Branched paraffin130.567.8Reddy, Dutoit, et al., 1992Chromosorb G HP; Column length: 3.3 m
PackedApolane130.572.Dutoit, 1991Column length: 3.7 m
PackedSF-96100.638.Boneva and Dimov, 1979N2; Column length: 2. m
PackedSF-96110.638.Boneva and Dimov, 1979N2; Column length: 2. m
PackedSF-9690.634.Boneva and Dimov, 1979N2; Column length: 2. m
PackedApiezon L100.592.Brown, Chapman, et al., 1968N2, DCMS-treated Chromosorb W; Column length: 2.3 m
PackedApiezon L150.609.Brown, Chapman, et al., 1968N2, DCMS-treated Chromosorb W; Column length: 2.3 m
PackedDC-200100.623.Rohrschneider, 1966Column length: 4. m
PackedApiezon L100.598.Rohrschneider, 1966Column length: 5. m
PackedApiezon L130.590.Wehrli and Kováts, 1959Celite; Column length: 2.25 m
PackedApiezon L70.583.Wehrli and Kováts, 1959Celite; Column length: 2.25 m

Kovats' RI, polar column, isothermal

View large format table.

Column type Active phase Temperature (C) I Reference Comment
CapillaryHP-Innowax100.1194.2Görgényi and Héberger, 2003Column length: 30. m; Phase thickness: 0.5 μm
CapillaryHP-Innowax110.1196.2Görgényi and Héberger, 2003Column length: 30. m; Phase thickness: 0.5 μm
CapillaryHP-Innowax120.1199.2Görgényi and Héberger, 2003Column length: 30. m; Phase thickness: 0.5 μm
CapillaryHP-Innowax50.1179.4Görgényi and Héberger, 2003Column length: 30. m; Phase thickness: 0.5 μm
CapillaryHP-Innowax60.1181.3Görgényi and Héberger, 2003Column length: 30. m; Phase thickness: 0.5 μm
CapillaryHP-Innowax70.1183.9Görgényi and Héberger, 2003Column length: 30. m; Phase thickness: 0.5 μm
CapillaryHP-Innowax80.1187.3Görgényi and Héberger, 2003Column length: 30. m; Phase thickness: 0.5 μm
CapillaryHP-Innowax90.1190.2Görgényi and Héberger, 2003Column length: 30. m; Phase thickness: 0.5 μm
PackedCarbowax 20M100.1168.Rohrschneider, 1966Column length: 2. m

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

View large format table.

Column type Active phase I Reference Comment
CapillaryDB-5636.89Hobbs and Conde, 199230. m/0.25 mm/0.25 μm, 5. K/min; Tstart: 40. C; Tend: 300. C

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

View large format table.

Column type Active phase I Reference Comment
CapillaryMethyl Silicone590.N/AProgram: not specified
CapillarySPB-1618.Flanagan, Streete, et al., 199760. m/0.53 mm/5. μm, He; Program: 40C(6min) => 5C/min => 80C => 10C/min => 200C
CapillaryPolydimethyl siloxanes623.Zenkevich and Chupalov, 1996Program: not specified
CapillarySPB-1618.Strete, Ruprah, et al., 199260. m/0.53 mm/5.0 μm, Helium; Program: 40 0C (6 min) 5 0C/min -> 80 0C 10 0C/min -> 200 0C
CapillarySPB-1655.Strete, Ruprah, et al., 199260. m/0.53 mm/5.0 μm, Helium; Program: not specified

Normal alkane RI, polar column, custom temperature program

View large format table.

Column type Active phase I Reference Comment
CapillaryCarbowax 20M1161.Ramsey and Flanagan, 1982Program: not specified

References

Go To: Top, Phase change data, Reaction thermochemistry data, Mass spectrum (electron ionization), Gas Chromatography, Notes

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

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

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

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

Brown, Chapman, et al., 1968
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]

Rohrschneider, 1966
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]

Wehrli and Kováts, 1959
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/technicalseries1997-01-011.pdf. [all data]

Zenkevich and Chupalov, 1996
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]

Strete, Ruprah, et al., 1992
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]

Ramsey and Flanagan, 1982
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

Go To: Top, Phase change data, Reaction thermochemistry data, Mass spectrum (electron ionization), Gas Chromatography, References