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Title: Dichlorodiphenyldichloroethylene  
Author: World Heritage Encyclopedia
Language: English
Subject: DDT, Environmental impact of pesticides, Dichlorodiphenyldichloroethane, Xenoestrogen, Lindane
Collection: Aromatic Compounds, Chloroarenes, Organochloride Insecticides
Publisher: World Heritage Encyclopedia


IUPAC name
Other names
Abbreviations p,p'-DDE
ChemSpider  Y
Jmol-3D images Image
Molar mass 318.02 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
 Y  (: Y/N?)

Dichlorodiphenyldichloroethylene (DDE) is a

  1. ^ ATSDR - Public Health Statement: DDT, DDE, and DDD
  2. ^ Pesticide Residues in Foods, Dichlorodiphenyltrichloroethane and Dichlorodiphenyldichloroethylene Content in Prepared Foods
  3. ^ Breast milk excretion Kinetic of b-HCH, pp'DDE and pp'DDT. Bulletin of Environmental Contamination and Toxicology, 2009 Dec;83(6):869-73
  5. ^ Stokstad, E (2007). "Species conservation. Can the bald eagle still soar after it is delisted?". Science 316 (5832): 1689–90.  
  6. ^ "Endangered and Threatened Wildlife and Plants; 12-Month Petition Finding and Proposed Rule To Remove the Brown Pelican (Pelecanus occidentalis) From the Federal List of Endangered and Threatened Wildlife; Proposed Rule," Fish and Wildlife Service, U.S. Department of the Interior, February 20, 2008. 73 FR 9407
  7. ^ a b c d ATSDR - Toxicological Profile: DDT, DDE, DDD
  8. ^ California Wild Spring 1994 - Peregrine Falcons
  9. ^ Recovery Plan for the California Condor, U.S. Fish and Wildlife Service, April 1996, page 23
  10. ^ DDE concentration and percent eggshell thinning in Double-crested Conmorant eggs(North Channel, Lake Huron, Ont.)
  11. ^ Guillette, Louis J., Jr. (2006). "Endocrine Disrupting Contaminants" (PDF). Retrieved 2007-02-02. 
  12. ^ Lundholm, C.E. (1997). "DDE-Induced eggshell thinning in birds". Comp Biochem Physiol C Pharmacol Toxicol Endocrinol 118 (2): 113–28.  
  13. ^ Division of Environmental Quality
  14. ^ Chemical fact sheet: Organochlorine - The Breast Cancer Fund
  15. ^ Questions about Endocrine Disruptors
  16. ^ Longnecker, M. P.; Gladen, B. C.; Cupul-Uicab, L. A.; Romano-Riquer, S. P.; Weber, J.-P.; Chapin, R. E.; Hernandez-Avila, M. (2007). "In utero exposure to the antiandrogen 1,1-dichloro-2,2-bis(p-chlorophenyl)ethylene (DDE) in relation to anogenital distance in male newborns from Chiapas, México". American Journal of Epidemiology 165 (9): 1015–22.  
  17. ^ Pesticide Exposure Linked to Parkinson's, Alzheimer's Disease


DDT, pesticide, bioaccumulation, birds of prey, endocrine disruptor, endocrine system, neurotoxicity, oxidative stress, dopamine

See Also

Animal studies show that organochlorine pesticides—such as DDE—are neurotoxic, cause oxidative stress, and damage the brain's dopaminergic system.[17]

Some studies have indicated that DDE is an endocrine disruptor[14] and contributes to breast cancer, but more recent studies provide strong evidence that there is no relationship between DDE exposure and breast cancer.[15] What is more clear is that DDE is a weak antiandrogen.[16]

The biological mechanism for the thinning is not entirely known, but it is believed that p,p'-DDE impairs the shell gland's ability to excrete calcium carbonate onto the developing egg.[7][9][10][11][12] Multiple mechanisms may be at work, or different mechanisms may operate in different species.[7] Some studies have shown that although DDE levels have fallen dramatically, eggshell thickness remains 10–12 percent thinner than before DDT was first used.[13]


DDE has been shown to be toxic to rats at 79.6 mg/kg.[4] DDE and its parent, DDT, are reproductive toxicants for certain birds species, and major reasons for the decline of the bald eagle,[5] brown pelican[6] peregrine falcon, and osprey.[7] These compounds cause egg shell thinning in susceptible species, which leads to the birds’ crushing their eggs instead of incubating them, due to the latter’s lack of resistance.[8] Birds of prey, waterfowl, and song birds are more susceptible to eggshell thinning than chickens and related species, and DDE appears to be more potent than DDT.[7]


Degradation of DDT to form DDE by an elimination of HCl

DDE is created by dehydrohalogenation of DDT. The loss of HCl results in a double bond on the central (previously quaternary) carbon atoms.


  • Synthesis 1
  • Toxicity 2
  • Mechanism 3
  • See Also 4
  • References 5


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