Rahul Sharma (Editor)

Dichlorodiphenyldichloroethane

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Abbreviations
  
DDD

Density
  
1.476 g/cm³

Solubility in water
  
0.00009 kg/m³

Boiling point
  
350 °C

Melting point
  
109.5 °C

Appearance
  
Colorless and crystalline

Dichlorodiphenyldichloroethane httpsuploadwikimediaorgwikipediacommonsthu

Atmospheric OH rate constant
  
4.34×10 cm/molecule ∙ s

Related compounds
  
DDE, DDT, mitotane, perthane

Dichlorodiphenyldichloroethane (DDD) is an organochlorine insecticide that is slightly irritating to the skin. DDD is a metabolite of DDT. DDD is colorless and crystalline; it is closely related chemically and is similar in properties to DDT, but it is considered to be less toxic to animals than DDT. The molecular formula for DDD is (ClC6H4)2CHCHCl2 or C14H10Cl4, whereas the formula for DDT is (ClC6H4)2CHCCl3 or C14H9Cl5.

Contents

DDD is in the “Group B2” classification, meaning that it is a probable human carcinogen. This is based on an increased incidence of lung tumors in male and female mice, liver tumors in male mice, and thyroid tumors in male rats. Further basis is that DDD is so similar to and is a metabolite of DDT, another probable human carcinogen.

DDD is no longer registered for agricultural use in the United States, but the general population continues to be exposed to it due to its long persistence time. The primary source of exposure is oral ingestion of food.

1946 is the date of the earliest recorded use in English of the abbreviation “DDD” to stand for dichlorodiphenyldichloroethane, as far as could be determined.

Mitotane

Interestingly enough, if one of the p-chlorines in DDD is switched to ortho-position, then we get a useful chemotherapeutic agent, mitotane. This is an example of a positional isomer.

Table of names

The following are synonyms for DDD:

References

Dichlorodiphenyldichloroethane Wikipedia