Propylamine

• Formula: C₃H₉N
• Molecular weight: 59.1103
• IUPAC Standard InChI: InChI=1S/C3H9N/c1-2-3-4/h2-4H2,1H3 Copy

  
• IUPAC Standard InChIKey: WGYKZJWCGVVSQN-UHFFFAOYSA-N Copy
• CAS Registry Number: 107-10-8
• 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: 1-Propanamine; n-Propylamine; Mono-n-propylamine; Monopropylamine; Propanamine; 1-Aminopropane; 1-Propylamine; n-C3H7NH2; Rcra waste number U194; UN 1277; NSC 7490
• Permanent link for this species. Use this link for bookmarking this species for future reference.
• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
  • Phase change data
  • Reaction thermochemistry data
  • Henry's Law data
  • Gas phase ion energetics data
  • Ion clustering data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
• Data at other public NIST sites:
  • Computational Chemistry Comparison and Benchmark Database
• Options:
  • Switch to calorie-based units

Data at NIST subscription sites:

• NIST / TRC Web Thermo Tables, "lite" edition (thermophysical and thermochemical data)
• NIST / TRC Web Thermo Tables, professional edition (thermophysical and thermochemical data)

NIST subscription sites provide data under the NIST Standard Reference Data Program, but require an annual fee to access. The purpose of the fee is to recover costs associated with the development of data collections included in such sites. Your institution may already be a subscriber. Follow the links above to find out more about the data in these sites and their terms of usage.

Normal boiling point

Go To: Top, 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:
BS - Robert L. Brown and Stephen E. Stein
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

References

Go To: Top, Normal boiling point, Notes

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

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]

Majer and Svoboda, 1985
Majer, V.; Svoboda, V., Enthalpies of Vaporization of Organic Compounds: A Critical Review and Data Compilation, Blackwell Scientific Publications, Oxford, 1985, 300. [all data]

Krichevtsov and Komarov, 1970
Krichevtsov, B.K.; Komarov, V.M., Liquid-Vapor Equilibria in Systems Formed by n-Propylamines, n-Propyl Alcohol, and Water, Zh. Prikl. Khim. (Leningrad), 1970, 43, 112-5. [all data]

Sudaricov, Phrolov, et al., 1963
Sudaricov, B.N.; Phrolov, U.G.; Ilichev, V.A.I.; Pushcov, A.A.; Zaharov-Narcissov, O.I.; Ochkin, A.B., Physicochemical Properties of Certain n-Aliphatic Amines, Tr. Inst. - Mosk. Khim. -Tekhnol. Inst. im. D. I. Mendele- eva, 1963, 43, 21. [all data]

Holmberg, 1962
Holmberg, K.E., Isotopic Effects in Systems Containing an Amine and Carbon Dioxide, Acta Chem. Scand., 1962, 16, 2117. [all data]

James, 1952
James, A.T., Biochem. J., 1952, 52, 242. [all data]

Barcelo, Le Fevre, et al., 1951
Barcelo, J.R.; Le Fevre, R.J.W.; Smythe, B.M., Variations of dipole moment with state for n-propyl and n-butylamines with notes on the apparent moments of in solutions of certain other amines., Trans. Faraday Soc., 1951, 47, 357. [all data]

Schuerch and Huntress, 1949
Schuerch, C.; Huntress, E.H., The Schmidt Reaction II. A New Rearangement Obseved during Degradation of Triethylacetic Acid, J. Am. Chem. Soc., 1949, 71, 2238. [all data]

Lecat, 1946
Lecat, M., Azeotropes of Amines, Ann. Soc. Sci. Bruxelles, Ser. 1, 1946, 60, 169. [all data]

Butler and Ramchandani, 1935
Butler, J.A.V.; Ramchandani, C.N., The Solubility of Non-electrolytes. Part II. The Influence of the Polar Group on the Free Energy of Hydration of Aliphatic Compounds., J. Chem. Soc., 1935, 1935, 952. [all data]

Wohlisch, 1924
Wohlisch, E., Biochem. Z., 1924, 153, 128. [all data]

Timmermans and Mattaar, 1921
Timmermans, J.; Mattaar, J.F., Freezing points of orgainic substances VI. New experimental determinations., Bull. Soc. Chim. Belg., 1921, 30, 213. [all data]

Bewad, 1900
Bewad, I., Zh. Russ. Fiz.-Khim. O-va., 1900, 32, 506. [all data]

Linebarger, 1896
Linebarger, C.E., Am. Chem. J., 1896, 18, 429. [all data]

Perkin, 1889
Perkin, W.H., The Magneto Rotatory Power of Nitrogne Compounds. also of Hydrochloric Hydrobromic and Hydroioidic Acids and of some of the Salts of Ammonia and the Compound Ammonias, J. Chem. Soc., 1889, 55, 680. [all data]

Schiff, 1886
Schiff, R., Chem. Ber., 1886, 19, 560. [all data]

Hofmann, 1882
Hofmann, A.W., Chem. Ber., 1882, 15, 762. [all data]

Linnemann, 1872
Linnemann, E., Justus Liebigs Ann. Chem., 1872, 161, 46. [all data]

Silva, 1869
Silva, R.D., Z. Chem., 1869, 3, 638. [all data]

Mendias, 1862
Mendias, O., Justus Liebigs Ann. Chem., 1862, 121, 136. [all data]

Notes

Go To: Top, Normal boiling point, References

• Symbols used in this document:
  

  Tboil

  Boiling point

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
• The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. However, NIST makes no warranties to that effect, and NIST shall not be liable for any damage that may result from errors or omissions in the Database.
• Customer support for NIST Standard Reference Data products.