Ethane, 1,1,1-trichloro-

• Formula: C₂H₃Cl₃
• Molecular weight: 133.404
• IUPAC Standard InChI: InChI=1S/C2H3Cl3/c1-2(3,4)5/h1H3 Copy

  
• IUPAC Standard InChIKey: UOCLXMDMGBRAIB-UHFFFAOYSA-N Copy
• CAS Registry Number: 71-55-6
• 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.
• Species with the same structure:
  • trichloroethane
• Other names: α-Trichloroethane; Aerothene TT; Chlorotene; Chlorothane NU; Chlorothene; Chlorothene NU; Chlorothene VG; Chlorten; Inhibisol; Methylchloroform; Methyltrichloromethane; Trichloroethane; 1,1,1-Trichloroethane; CH3CCl3; α-T; Chloroethene NU; Chloroform, methyl-; NCI-C04626; Solvent 111; Trichloro-1,1,1-ethane; 1,1,1-Trichloraethan; 1,1,1-Tricloroetano; CF 2; Chloroetene; Chloroethene; Chlorothene SM; Ethana NU; ICI-CF 2; Rcra waste number U226; Tafclean; 1,1,1-TCE; Trichloromethylmethane; Tri-ethane; UN 2831; 1,1,1-Trichlorethane; Distillex DS1; Ethana; Solvethane; Cleanite; F 140a; Genklene LB; HCC 140a; Three One A; Three One S
• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
  • Phase change data
  • Reaction thermochemistry data
  • Henry's Law data
  • Gas phase ion energetics data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
• Data at other public NIST sites:
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  • Gas Phase Kinetics Database
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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:
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
BS - Robert L. Brown and Stephen E. Stein

References

Go To: Top, Normal boiling point, Notes

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

Krishnaiah and Surendranath, 1996
Krishnaiah, A.; Surendranath, K.N., Densities, Speeds of Sound, and Viscosities of Mixtures of Oxolane with Chloroethanes and Chloroethenes, J. Chem. Eng. Data, 1996, 41, 1012-1014. [all data]

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]

Surendranath, Ramanjaneyulu, et al., 1988
Surendranath, K.N.; Ramanjaneyulu, K.; Krishnaiah, A., Viscosities of binary liquid mixtures of acetonitrile with chlorinated ethanes and ethylenes at 303.15 K, Indian J. Technol., 1988, 26, 379-82. [all data]

Paul, Krug, et al., 1986
Paul, H.-I.; Krug, J.; Gutsche, B.; Knapp, H., Measurements of VLE, hE, and vE for Binary Mixtures of Dibutyl Ether with 1-Chloropentane, 1,2-Dichloroethane, and 1,1,1-Trichloroethane trichloroethane, J. Chem. Eng. Data, 1986, 31, 448. [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]

Reddy and Rao, 1985
Reddy, K.D.; Rao, M.V.P., Excess volumes of nitrobenzene with the alkyl-substituted chloroethanes at 303.15 and 313.15 K., J. Chem. Eng. Data, 1985, 30, 36. [all data]

Viswanath and Rao, 1982
Viswanath, D.S.; Rao, M.V., Isobaric vapor-liquid equilibria of the p-xylene + 1,1,1- trichloroethane system., J. Chem. eng. Data, 1982, 27, 414-6. [all data]

Hanson and Van Winkle, 1967
Hanson, D.O.; Van Winkle, M., Alteration of the Relative Volatility of n-Hexane-1-Hexene by Oxygenated and Chlorinated Solvents, J. Chem. Eng. Data, 1967, 12, 319. [all data]

Holland, Roberts, et al., 1956
Holland, R.S.; Roberts, G.N.; Smyth, C.P., Microwave Absorption and Molecular Structure in Liquids XI. The Relaxation Times of Three Nearly Spherical Molecules in the Pure Liquid & in Solution, J. Am. Chem. Soc., 1956, 78, 20. [all data]

Timmermans and Hennaut-Roland, 1955
Timmermans, J.; Hennaut-Roland, M., Work of the International Bureau of Physical-Chemical Standards. IX. The Physical Constants of Twenty Organic Compounds, J. Chim. Phys. Phys.-Chim. Biol., 1955, 52, 223. [all data]

Crowe and Smyth, 1950
Crowe, R.W.; Smyth, C.P., Heat capacities, dielectric constants and molecular rotational freedom in solid trichloroethanes and disubstituted propanes, J. Am. Chem. Soc., 1950, 72, 4009. [all data]

Maryott, Hobbs, et al., 1941
Maryott, A.A.; Hobbs, M.E.; Gross, P.M., Bond Moment Additivity and the Electric Moments of Some Halogenated Hydrocarbons, J. Am. Chem. Soc., 1941, 63, 659. [all data]

Turkevich and Smyth, 1940
Turkevich, A.; Smyth, C.P., Molecular Rotation and Polymorphism in the Methyl Chloromethanes, J. Am. Chem. Soc., 1940, 62, 2468-74. [all data]

Earp and Glasstone, 1935
Earp, D.P.; Glasstone, S., Dielectric polarisation and molecular-compound formation in solution, J. Chem. Soc., 1935, 1935, 1709. [all data]

Lecat, 1927
Lecat, M., New binary azeotropes: 7th list, Ann. Soc. Sci. Bruxelles, Ser. B, 1927, 47, 108-14. [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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