[1,1'-Biphenyl]-4-amine

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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 by: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Quantity Value Units Method Reference Comment
Δcsolid-1523.78kcal/molCcbBrull, 1935 

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

Quantity Value Units Method Reference Comment
Tboil575.2KN/AWeast and Grasselli, 1989BS
Tboil575.KN/ABuckingham and Donaghy, 1982BS
Quantity Value Units Method Reference Comment
Tfus326.0 - 326.7KN/ABuckingham and Donaghy, 1982BS
Tfus324.15KN/AKumler and Halverstadt, 1941Uncertainty assigned by TRC = 0.6 K; TRC

Reduced pressure boiling point

Tboil (K) Pressure (atm) Reference Comment
464.20.020Weast and Grasselli, 1989BS
464.0.020Buckingham and Donaghy, 1982BS
439.0.007Buckingham and Donaghy, 1982BS

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 by: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

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

4-(N-Methylamino)biphenyl = 0.5[1,1'-Biphenyl]-4-amine, N,N-dimethyl- + 0.5[1,1'-Biphenyl]-4-amine

By formula: C13H13N = 0.5C14H15N + 0.5C12H11N

Quantity Value Units Method Reference Comment
Δr0.3kcal/molEqkMatvienko, Kachurin, et al., 1982liquid phase; Methanesulfonic acid

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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Mass 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 G. VANDER VELDE
NIST MS number 27135

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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.

Brull, 1935
Brull, L., Sui calori di combustione di alcuni derivati del bifenil, Gazz. Chim. Ital., 1935, 65, 19-28. [all data]

Weast and Grasselli, 1989
CRC Handbook of Data on Organic Compounds, 2nd Editon, Weast,R.C and Grasselli, J.G., ed(s)., CRC Press, Inc., Boca Raton, FL, 1989, 1. [all data]

Buckingham and Donaghy, 1982
Buckingham, J.; Donaghy, S.M., Dictionary of Organic Compounds: Fifth Edition, Chapman and Hall, New York, 1982, 1. [all data]

Kumler and Halverstadt, 1941
Kumler, W.D.; Halverstadt, I.F., The Dipole Moment of Sulfanilamide and Related Compounds, J. Am. Chem. Soc., 1941, 63, 2182. [all data]

Matvienko, Kachurin, et al., 1982
Matvienko, N.M.; Kachurin, O.I.; Chekhuta, V.G., Kinetics and equilibrium of the transalkylation reaction of N-methylarylamines, Russ. Chem. Rev., 1982, 48, 42-45. [all data]


Notes

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