9H-Pyrido[3,4-b]indole, 1-methyl-

• Formula: C₁₂H₁₀N₂
• Molecular weight: 182.2212
• IUPAC Standard InChI: InChI=1S/C12H10N2/c1-8-12-10(6-7-13-8)9-4-2-3-5-11(9)14-12/h2-7,14H,1H3 Copy

  
• IUPAC Standard InChIKey: PSFDQSOCUJVVGF-UHFFFAOYSA-N Copy
• CAS Registry Number: 486-84-0
• 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: Aribin; Aribine; Harman; Harmane; Locuturin; Locuturine; 1-Methyl-β-carboline; 1-Methyl-9H-pyrido[3,4-b]indole; Loturine; Passiflorin; Pyridobindole, L-methyl-; 1-Methyl-9H-pyrid(3,4-b)indole; 1-Methylnorharman; 1-Methyl-2-carboline; NSC 54439
• Permanent link for this species. Use this link for bookmarking this species for future reference.
• Information on this page:
  • Phase change data
  • Gas phase ion energetics data
  • References
  • Notes
• Other data available:
  • Mass spectrum (electron ionization)
  • Gas Chromatography
• Options:
  • Switch to SI units

Phase change data

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

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

Data compiled by: William E. Acree, Jr., James S. Chickos

Enthalpy of fusion

Gas phase ion energetics data

Go To: Top, Phase change data, References, Notes

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

Ionization energy determinations

References

Go To: Top, Phase change data, Gas phase ion energetics data, Notes

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

Burrows, Miguel, et al., 1996
Burrows, Hugh D.; Miguel, Maria da Graça M.; Varela, A. Paula; Becker, Ralph S., The aqueous solubility and thermal behaviour of some β-carbolines, Thermochimica Acta, 1996, 279, 77-82, https://doi.org/10.1016/S0040-6031(96)90063-5 . [all data]

Domelsmith and Houk, 1978
Domelsmith, L.N.; Houk, K.N., Photoelectron spectroscopic studies of hallucinogens: The use of ionization potentials in QSAR, NIDA Res. Monogr., 1978, 22, 423. [all data]

Notes

Go To: Top, Phase change data, Gas phase ion energetics data, References

• Symbols used in this document:
  

  ΔfusH

  Enthalpy of fusion

• 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.