Pyridine, 2,4,6-trimethyl-

• Formula: C₈H₁₁N
• Molecular weight: 121.1796
• IUPAC Standard InChI: InChI=1S/C8H11N/c1-6-4-7(2)9-8(3)5-6/h4-5H,1-3H3 Copy

  
• IUPAC Standard InChIKey: BWZVCCNYKMEVEX-UHFFFAOYSA-N Copy
• CAS Registry Number: 108-75-8
• Chemical structure:
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• Other names: α,γ,α'-Collidine; γ-Collidine; s-Collidine; 2,4,6-Collidine; 2,4,6-Trimethylpyridine; sym-Collidine; 2,4,6-Kollidin; gamma-Collidine; NSC 460
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • Phase change data
  • Gas phase ion energetics 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]

Assal, 1966
Assal, F.A., Vapour-liquid equilibria in phenol-pyridine base systems, Bull. Acad. Pol. Sci., Ser. Sci. Chim., 1966, 14, 603. [all data]

Jankun-Pinska, 1965
Jankun-Pinska, J., Liquid-liquid equilibrium in series of ternary systems formed by pyridine bases benzene and water. III. 3,5-lutidine-benzene-water and 2,4,6-collidine-benzene-water, Bull. Acad. Pol. Sci., Ser. Sci. Chim., 1965, 13, 121. [all data]

Razniewska, 1964
Razniewska, T., Poliazeotropic ethylene glycol systems. I. a series of saddle azeotropes formed by ethylene glycol, phenol and pyridine bases, Rocz. Chem., 1964, 38, 851. [all data]

Runge and Hummel, 1951
Runge, F.; Hummel, H., Catalytic conversion of actylene with ammonia, Chem. Tech. (Leipzig), 1951, 3, 163. [all data]

Hackmann, Wibaut, et al., 1943
Hackmann, J.Th.; Wibaut, J.P.; Gitsels, H.P.L., Basic N compounds from cracked distillates of California petroleum, Recl. Trav. Chim. Pays-Bas, 1943, 62, 229. [all data]

Herz, Kahovec, et al., 1943
Herz, E.; Kahovec, L.; Kohlraush, K.W.F., The Raman Effect CXLII. Nitrogen Compounds 26-Pyridine and its Homolog, Z. Phys. Chem., Abt. B, 1943, 53, 124. [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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