Abstract
THE properties of phthiocerane, the hydrocarbon derived from the wax alcohol phthiocerol1,2 of the tubercle bacillus, for a pure specimen of which we are indebted to Prof. R. J. Anderson, Yale University, indicate a branched-chain structure3, probably a long chain with a methyl side-chain near one end4. For comparison with phthiocerane, a series of hydrocarbons having a total of 34, 35 and 36 carbon atoms*, with a methyl side-chain in position 2-, 3-, 4-, or 5- from one end, have been synthesized at Uppsala, partly by the use of new synthetic methods5. The melting points of the synthetic hydrocarbons are plotted in Fig. 1 (the data for the n-hydrocarbons (1-methyl) are from Piper et al.6). The 2-methyl compounds melt at much higher temperatures than phthiocerane, and also differ in thermal behaviour and crystal structure (crystallize when pure only in tilted forms). The 3-, 4-, and 5-methyl substituted hydrocarbons, on the other hand, crystallize from acetone like phthiocerane with vertical chains, and also behave similarly on melting and solidification.
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Sutherland, G. B. B. M., and Thompson, H. W. (to be published shortly).
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STÄLLBERG-STENHAGEN, S., STENHAGEN, E., SHEPPARD, N. et al. Infra-Red Spectrum and Molecular Structure of Phthiocerane. Nature 160, 580–582 (1947). https://doi.org/10.1038/160580a0
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DOI: https://doi.org/10.1038/160580a0
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