1-Propanamine, N,N-dipropyl-

• Formula: C₉H₂₁N
• Molecular weight: 143.2697
• IUPAC Standard InChI: InChI=1S/C9H21N/c1-4-7-10(8-5-2)9-6-3/h4-9H2,1-3H3 Copy

  
• IUPAC Standard InChIKey: YFTHZRPMJXBUME-UHFFFAOYSA-N Copy
• CAS Registry Number: 102-69-2
• Chemical structure:
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• Other names: Tri-n-propylamine; Tripropylamine; N,N-Dipropyl-1-propylamine; (n-C3H7)3N; UN 2260; Propyldi-n-propylamine; N,N-Dipropyl-1-propanamine
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• 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
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Normal boiling point

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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

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.

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]

Christie and Crisp, 1967
Christie, A.O.; Crisp, D.J., Activity coefficients of the n-primary, secondary and tertiary aliphatic amines in aqueous solution, J. Appl. Chem., 1967, 17, 11. [all data]

James and Martin, 1952
James, A.T.; Martin, A.J.P., Gas-Liquid Partition Chromatography, Analyst (London), 1952, 77, 915. [all data]

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

Vogel, 1948
Vogel, A.I., Physical Properties and Chemical Constitution Part XXII. Some Primary Secondary and Tertiary Amines, J. Chem. Soc., 1948, 1948, 1825. [all data]

Borrows, Hargreaves, et al., 1947
Borrows, E.T.; Hargreaves, B.M.C.; Page, J.E.; Resuggan, J.C.L.; Robinson, F.A., Preparation and Properties of Some Long Chain Aliphatic Amines, J. Chem. Soc., 1947, 1947, 197. [all data]

Olin and Schwoegler, 1945
Olin, J.F.; Schwoegler, E.J., , 1945. [all data]

Skita and Keil, 1929
Skita, A.; Keil, F., Monatsh. Chem., 1929, 53-54, 753. [all data]

Timmermans, 1921
Timmermans, J., The Freezing Points of Organic Substances IV. New Exp. Determinations, Bull. Soc. Chim. Belg., 1921, 30, 62. [all data]

Mailhe, 1918
Mailhe, A., Direct Transformation of secondary and tertiary amines to nitriles, C. R. Hebd. Seances Acad. Sci., 1918, 166, 996. [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]

Zander, 1882
Zander, A., The Specific Volume of Some Allyl-, Propyl-, and OTher COmpounds, Justus Liebigs Ann. Chem., 1882, 214, 138-93. [all data]

Notes

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• Symbols used in this document:
  

  Tboil

  Boiling point

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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