Physical and chemical properties of pyrethroids

Rev Environ Contam Toxicol. 2002:174:49-170. doi: 10.1007/978-1-4757-4260-2_3.

Abstract

The physical and chemical properties of the pyrethroids bifenthrin, cyfluthrin, cypermethrin (also zetacypermethrin), deltamethrin, esfenvalerate (also fenvalerate), fenpropathrin, lambda-cyhalothrin (also cyhalothrin), permethrin, and tralomethrin have been reviewed and summarized in this paper. Physical properties included molecular weight, octanol-water partition coefficient, vapor pressure, water solubility, Henry's law constant, fish biocencentration factor, and soil sorption, desorption, and Freundlich coefficients. Chemical properties included rates of degradation in water as a result of hydrolysis, photodecomposition, aerobic or anaerobic degradation by microorganisms in the absence of light, and also rates of degradation in soil incubated under aerobic or anaerobic conditions. Collectively, the pyrethroids display a highly nonpolar nature of low water solubility, low volatility, high octanol-water partition coefficients, and have high affinity for soil and sediment particulate matter. Pyrethroids have low mobility in soil and are sorbed strongly to the sediments of natural water systems. Although attracted to living organisms because of their nonpolar nature, their capability to bioconcentrate is mitigated by their metabolism and subsequent elimination by the organisms. In fish, bioconcentration factors (BCF) ranged from 360 and 6000. Pyrethroids in water solution tend to be stable at acid and neutral pH but [table: see text] become increasingly susceptible to hydrolysis at pH values beyond neutral. Exceptions at higher pH are bifenthrin (stable), esfenvalerate (stable), and permethrin (half-life, 240 d). Pyrethroids vary in susceptibility to sunlight. Cyfluthrin and tralomethrin in water had half-lives of 0.67 and 2.5 d; lambda-cyhalothrin, esfenvalerate, deltamethrin, permethrin, and cypermethrin were intermediate with a range of 17-110 d; and bifenthrin and fenpropathrin showed the least susceptibility with half-lives of 400 and 600 d, respectively. Pyrethroids on soil can also undergo photolysis, often at rates similar to that in water. Half-lives ranged from 5 to 170 d. [table: see text] Pyrethroids are degradable in soils with half-lives ranging from 3 to 96 d aerobically, and 5 to 430 d anaerobically. For those pyrethroids studied in water (cypermethrin, deltamethrin, esfenvalerate, fenpropathrin, and lambda-cyhalothrin), aerobic and anaerobic degradation often continued at rates similar to that displayed in soil.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adsorption
  • Animals
  • Biodegradation, Environmental
  • Biological Availability
  • Fishes
  • Hydrolysis
  • Insecticides / chemistry*
  • Insecticides / metabolism
  • Insecticides / pharmacokinetics
  • Molecular Weight
  • Photochemistry
  • Pyrethrins / chemistry*
  • Pyrethrins / metabolism
  • Pyrethrins / pharmacokinetics
  • Soil Pollutants / metabolism
  • Soil Pollutants / pharmacokinetics*
  • Solubility
  • Tissue Distribution
  • Volatilization
  • Water Pollutants / metabolism
  • Water Pollutants / pharmacokinetics*

Substances

  • Insecticides
  • Pyrethrins
  • Soil Pollutants
  • Water Pollutants