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Article
Comparison of the QSAR models for toxicity and biodegradability of anilines and phenols
Chemosphere (1997)
  • J Damborsky
  • Terry W Schultz, University of Tennessee - Knoxville
Abstract

Structure-activity models for toxicity and biodegradability of groups of m-anilines and p-phenols were developed and compared. Hydrophobicity was the most important property in determining toxicity. Whereas, electronic and steric properties were the more important in modeling biodegradation.

Publication Date
February, 1997
Citation Information
J Damborsky and Terry W Schultz. "Comparison of the QSAR models for toxicity and biodegradability of anilines and phenols" Chemosphere Vol. 34 Iss. 2 (1997)
Available at: http://works.bepress.com/terry_schultz/91/