1-Propanethiol, 2-methyl-

• Formula: C₄H₁₀S
• Molecular weight: 90.187
• IUPAC Standard InChI: InChI=1S/C4H10S/c1-4(2)3-5/h4-5H,3H2,1-2H3 Copy

  
• IUPAC Standard InChIKey: BDFAOUQQXJIZDG-UHFFFAOYSA-N Copy
• CAS Registry Number: 513-44-0
• 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: Isobutyl mercaptan; 1-Isobutanethiol; 2-Methyl-1-propanethiol; iso-C4H9SH; Isobutanethiol; 2-Methyl-1-propylthiol; 2-Methyl propanethiol; 2-methylpropane-1-thiol
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
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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]

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]

Morris, Lanum, et al., 1960
Morris, J.C.; Lanum, W.J.; Helm, R.V.; Haines, W.E.; Cook, G.L.; Ball, J.S., Purification and Properties of Ten Organic Sulfur Compounds, J. Chem. Eng. Data, 1960, 5, 112-6. [all data]

Birch, 1953
Birch, S.F., Sulphur Compounds in Petroleum, J. Inst. Pet., 1953, 39, 185. [all data]

Zinner, 1953
Zinner, H., Perparation of Mercaptans, Chem. Ber., 1953, 86, 825. [all data]

Denyer, Fidler, et al., 1949
Denyer, R.L.; Fidler, F.A.; Lowry, R.A., Azeotrope Formation Between Thiols and Hydrocarbons, Ind. Eng. Chem., 1949, 41, 2727-37. [all data]

Trotter and Thompson, 1946
Trotter, I.F.; Thompson, H.W., Infrared SPectra of Thiols, Sulfides, and Disulfides, J. Chem. Soc., 1946, 1946, 481. [all data]

Ingold, Jessop, et al., 1933
Ingold; Jessop; Kuriyam; Mandour, Influence of Poles and Polar Linkages on the Course Pursued by Elimination Reactions XVIII. Thermal Decompostion of Sulphoniumm Hydroxides, J. Chem. Soc., 1933, 1933, 3455. [all data]

Backer and Dijkstra, 1932
Backer, H.J.; Dijkstra, N.D., The Thioethers of Pentaerythritol, Recl. Trav. Chim. Pays-Bas, 1932, 51, 289. [all data]

Birch and Norris, 1925
Birch, S.F.; Norris, W.S.G.P., The Chemistry of Petroleum Part I. The Occurence of Compounds of Sulphur in the Liqht Distillate from the Crude Oil of Maindan-i-Naftun, J. Chem. Soc., 1925, 127, 898. [all data]

Sabatier and Mailhe, 1910
Sabatier, P.; Mailhe, A., General Methods for Direct Preparation of Thiols by Catalysic Splitting of Alcohols, C. R. Hebd. Seances Acad. Sci., 1910, 150, 1217. [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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