2,6-Lutidine

• Formula: C₇H₉N
• Molecular weight: 107.1531
• IUPAC Standard InChI: InChI=1S/C7H9N/c1-6-4-3-5-7(2)8-6/h3-5H,1-2H3 Copy

  
• IUPAC Standard InChIKey: OISVCGZHLKNMSJ-UHFFFAOYSA-N Copy
• CAS Registry Number: 108-48-5
• 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: Pyridine, 2,6-dimethyl-; α,α'-Dimethylpyridine; α,α'-Lutidine; 2,6-Dimethylpyridine; 2,6-Dimethypyridine; α,α'-Lutidin; NSC 2155
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• Information on this page:
  • Normal melting point
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
  • Phase change data
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  • Gas phase ion energetics data
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  • Gas Chromatography
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Normal melting 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 by: 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.

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]

Kyte, Jeffery, et al., 1960
Kyte, C.T.; Jeffery, G.H.; Vogel, A.I., Physical Properties and Chem. Constitution XXVII. Pyridine Derivatives, J. Chem. Soc., 1960, 1960, 4454. [all data]

Coulson, Cox, et al., 1959
Coulson, E.A.; Cox, J.D.; Herington, E.F.G.; Martin, J.F., The Preparation and Physical Properties of the Pure Lutidines, J. Chem. Soc., 1959, 1959, 1934. [all data]

Biddiscombe, Coulson, et al., 1954
Biddiscombe, D.P.; Coulson, E.A.; Handley, R.; Herington, E.F.G., The Preparation and Physical Properties of Pure Pyridine and Some Methyl Homologues, J. Chem. Soc., 1954, 1954, 1957. [all data]

Brown, Johnson, et al., 1954
Brown, H.C.; Johnson, S.; Podall, H., Purification and Physical Properties of 2,6-Lutidine and 2,4,6-Collidine, J. Am. Chem. Soc., 1954, 76, 5556. [all data]

Witschonke, 1954
Witschonke, C.R., Freezing point and purity data for some organic compounds, Anal. Chem., 1954, 26, 562-4. [all data]

Liplavk and Boliter, 1951
Liplavk, I.L.; Boliter, E.P., The Saturation Vapor Pressures of β-Picoline, γ-Picoline, and 2,6-Lutidine, J. Appl. Chem. USSR (Engl. Transl.), 1951, 24, 207. [all data]

Vanderwerf, Davidson, et al., 1948
Vanderwerf, C.A.; Davidson, A.W.; Michaelis, C.I., Compound Formation Betwee 2,6-Lutidine and Polyhalogenated Methanes, J. Am. Chem. Soc., 1948, 70, 908. [all data]

Coulson and Jones, 1946
Coulson, E.A.; Jones, J.I., Studies in coal tar bases. i. separation of beta-and gamma-picolines and 2:6-lutidine, J. Soc. Chem. Ind., London, Trans. Commun., 1946, 65, 169. [all data]

Notes

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• Symbols used in this document:
  

  Tfus	Fusion (melting) point

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