1-Piperidinamine

• Formula: C₅H₁₂N₂
• Molecular weight: 100.1622
• IUPAC Standard InChI: InChI=1S/C5H12N2/c6-7-4-2-1-3-5-7/h1-6H2 Copy

  
• IUPAC Standard InChIKey: LWMPFIOTEAXAGV-UHFFFAOYSA-N Copy
• CAS Registry Number: 2213-43-6
• 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: Piperidine, 1-amino-; N-Aminopiperidine; 1-Aminopiperidine; 1,1-Pentamethylenehydrazine; N-piperidylamine
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• Information on this page:
  • Gas phase ion energetics data
  • Gas Chromatography
  • References
  • Notes
• Other data available:
  • Phase change data
  • Mass spectrum (electron ionization)
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Gas phase ion energetics 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: Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi

View reactions leading to C₅H₁₂N₂⁺ (ion structure unspecified)

Ionization energy determinations

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

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

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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.

Nelsen and Buschek, 1974
Nelsen, S.F.; Buschek, J.M., Photoelectron spectra of hydrazines. IV. Empirical estimation of lone pair-lone pair dihedral angles and prediction of lone pair ionization potentials for some cyclic and bicyclic hydrazines, J. Am. Chem. Soc., 1974, 96, 6982. [all data]

Zenkevich, 2001
Zenkevich, I.G., Encyclopedia of Chromatography. Derivatization of Carbonyls for GC Analysis, MArcel Dekker, Inc., New York - Basel, 2001, 233. [all data]

Notes

Go To: Top, Gas phase ion energetics data, Gas Chromatography, References

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