| Systematic IUPAC name
(S)-cyano (3-phenoxyphenyl) methyl-(S)-4-chloro-alpha-(1-methylethyl) benzeneacetate
| Other names
|Molar mass||419.91 g·mol−1|
|Vapor pressure||0 mmHg at 25 °C|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
In the United States, a limit of .05 ppm of the chemical's residue is permissible in food.
- Kelly, Kevin. "Environmental Fate of Esfenvalerate" (PDF). California Environmental Protection Agency. Retrieved January 10, 2013.
- Fishel, Frederick M. (2012). "Pesticide Toxicity Profile: Synthetic Pyrethroid Pesticides". University of Florida. Retrieved January 10, 2013.
- "Esfenvalerate". EXTONET (Extension Toxicology Network). Cooperative Extension Offices of Cornell University, Michigan State University, Oregon State University, and University of California at Davis. May 1994. Retrieved January 10, 2013.
- The Code of Federal Regulations of the United States of America. U.S. Government Printing Office. 2006. pp. 445–446.