1-Pentanamine

• Formula: C₅H₁₃N
• Molecular weight: 87.1634
• IUPAC Standard InChI: InChI=1S/C5H13N/c1-2-3-4-5-6/h2-6H2,1H3 Copy

  
• IUPAC Standard InChIKey: DPBLXKKOBLCELK-UHFFFAOYSA-N Copy
• CAS Registry Number: 110-58-7
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Other names: Pentylamine; n--Amylamine; n-Pentylamine; Amylamine; Monoamylamine; Norleucamine; 1-Aminopentane; 1-Pentylamine; n-C5H11NH2
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • Phase change data
  • Henry's Law data
  • Gas phase ion energetics data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
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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

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]

American Tokyo Kasei, 1988
American Tokyo Kasei, TCI American Organic Chemical 88/89 Catalog, American Tokyo Kasei, Portland, OR, 1988, 1610. [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]

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]

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]

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

Arnett, Miller, et al., 1950
Arnett, E.M.; Miller, J.G.; Day, A.R., J. Am. Chem. Soc., 1950, 72, 5635. [all data]

Brown and Jones, 1942
Brown, R.; Jones, W.E., J. Chem. Soc., 1942, 1942, 782. [all data]

Winans and Adkins, 1932
Winans, C.F.; Adkins, H., The Alkylation of Amines as Catalyzed by Nickel, J. Am. Chem. Soc., 1932, 54, 306. [all data]

Adams and Marvel, 1919
Adams, R.; Marvel, C.S., Organic Chemical Reagents VI. Reagents from n-Butyl Alcohol, J. Am. Chem. Soc., 1919, 42, 311. [all data]

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

Wurtz, 1867
Wurtz, A., Z. Chem., 1867, 3, 38. [all data]

Brazrier and Gossleth, 1850
Brazrier, J.S.; Gossleth, G., Contributions Towards the History of Caproic and Oenanthylic Acids, J. Chem. Soc., 1850, 3, 210. [all data]

Wurtz, 1850
Wurtz, A., Ann. Chim. Phys., 1850, 30, 491. [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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