Dichlorodiphenyldichloroethane

Dichlorodiphenyldichloroethane

Names
IUPAC names 1-chloro-4-[2,2-dichloro-1-(4- chlorophenyl)ethyl]benzene
Identifiers
CAS Number	72-54-8 Y
3D model (Jmol)	Interactive image
Abbreviations	DDD
Beilstein Reference	4-05-00-01884
ChEBI	CHEBI:27841 Y
ChEMBL	ChEMBL196590 Y
ChemSpider	6057 Y
ECHA InfoCard	100.000.712
EC Number	200-783-0
KEGG	C06636 Y
MeSH	DDD
PubChem	6294
InChI InChI=1S/C14H10Cl4/c15-11-5-1-9(2-6-11)13(14(17)18)10-3-7-12(16)8-4-10/h1-8,13-14H Y Key: AHJKRLASYNVKDZ-UHFFFAOYSA-N Y InChI=1/C14H10Cl4/c15-11-5-1-9(2-6-11)13(14(17)18)10-3-7-12(16)8-4-10/h1-8,13-14H Key: AHJKRLASYNVKDZ-UHFFFAOYAJ
SMILES Clc1ccc(cc1)C(c2ccc(Cl)cc2)C(Cl)Cl
Properties
Chemical formula	C14H10Cl4
Molar mass	320.04
Appearance	Colorless and crystalline
Density	1.476 g/cm3
Melting point	109.5 °C (229.1 °F; 382.6 K)
Boiling point	350 °C (662 °F; 623 K)
Solubility in water	0.09 mg/L
log P	6.02 (octanol-water)
Vapor pressure	1.35×10−6mm Hg
Henry's law constant (kH)	6.6×10−6atm ∙ m3/mol
Atmospheric OH rate constant	4.34×10−12 cm3/molecule ∙ s
Related compounds
Related compounds	DDE, DDT, mitotane, perthane
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y  (what is YN ?)
Infobox references

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.

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.

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.

The following are synonyms for DDD: