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دی‌کلرودی‌فنیل‌دی‌کلرواتیلن

Structure via PubChem · Public domain (PubChem)

EntityQ409592· pop 14· linked from 784 articles

دی‌کلرودی‌فنیل‌دی‌کلرواتیلن

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Also known as p,p'-DDE, 4,4'-DDE, p,p'-(dichlorodiphenyl)-2,2-dichloroethylene, p,p'-dichlorodiphenyldichloroethene, p,p'-dichlorodiphenyldichloroethylene, Dichlorodiphenyl Dichloroethylene

Dichlorodiphenyldichloroethylene (DDE) is a chemical compound formed by the loss of hydrogen chloride (dehydrohalogenation) from DDT, of which it is one of the more common breakdown products. Due to DDT's massive prevalence in society and agriculture during the mid 20th century, DDT and DDE are still widely seen in animal tissue samples. DDE is particularly dangerous because it is fat-soluble like other organochlorines; thus, it is rarely excreted from the body, and concentrations tend to increase throughout life. The major exception is the excretion of DDE in breast milk, which transfers a su

Chemical data

Formula
C14H8Cl4
Molecular weight
318 g/mol
IUPAC name
1-chloro-4-[2,2-dichloro-1-(4-chlorophenyl)ethenyl]benzene
SMILES
C1=CC(=CC=C1C(=C(Cl)Cl)C2=CC=C(C=C2)Cl)Cl
InChIKey
UCNVFOCBFJOQAL-UHFFFAOYSA-N
XLogP
7
Polar surface area
0 Ų
H-bond donors
0
H-bond acceptors
0
Formal charge
0

via PubChem

Drug data · ChEMBL

Molecule type
Small molecule

via ChEMBL · EBI

Research

6,411 papers

via PubMed

Wikidata facts

Mass
315.938010976
Show 3 more facts
Commons category
Dichlorodiphenyldichloroethylene
chemical formula
C₁₄H₈Cl₄
canonical SMILES
C1=CC(=CC=C1C(=C(Cl)Cl)C2=CC=C(C=C2)Cl)Cl
Sources (3)

via Wikidata · CC0

Gallery (2)