Volume 64, Issue 5 pp. 883-885
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Synthesis and cmc determination of a series of aliphatic diamines

Larry J. Powers

Larry J. Powers

Department of Molecular Biology, College of Pharmacy, Center for the Health Sciences, University of Tennessee, Memphis, TN 38163

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E. O. Dillingham

E. O. Dillingham

Department of Molecular Biology, College of Pharmacy, Center for the Health Sciences, University of Tennessee, Memphis, TN 38163

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George E. Bass

Corresponding Author

George E. Bass

Department of Molecular Biology, College of Pharmacy, Center for the Health Sciences, University of Tennessee, Memphis, TN 38163

Department of Molecular Biology, College of Pharmacy, Center for the Health Sciences, University of Tennessee, Memphis, TN 38163Search for more papers by this author
First published: May 1975
Citations: 3

Abstract

Fifteen aliphatic diamines substituted with one long alkyl chain (C10-C18), a varying number of methylene groups separating the nitrogens (two to six), and various aliphatic substituents were synthesized and their CMC's were determined. While the length of the long alkyl chain plays a dominant role in influencing the CMC, the other N-alkyl substituents as well as the length of the methylene chain separating the two nitrogens of the diamine are significant factors.

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