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DDT

File:P,p'-dichlorodiphenyltrichloroethane.svg · Wikimedia Commons · See Wikimedia Commons

EntityQ163648· pop 70· linked from 2,174 articles

Also known as dichlorodiphenyltrichloroethane, p,p'-DDT, 1,1-bis(4-chlorophenyl)-2,2,2-trichloroethane, 1,1'-(2,2,2-trichloroethylidene)bis[4-chlorobenzene], alpha,alpha-bis(p-chlorophenyl)-beta,beta,beta-trichlorethane, p,p'-dichlorodiphenyltrichloroethane, clofenotane, 4,4'-DDT

Dichlorodiphenyltrichloroethane (DDT) is a colorless, tasteless, and almost odorless crystalline chemical compound, an organochloride. Originally developed as an insecticide, it became infamous for its environmental impacts. DDT was first synthesized in 1874 by the Austrian chemist Othmar Zeidler. DDT's insecticidal action was discovered by the Swiss chemist Paul Hermann Müller in 1939. DDT was used in the second half of World War II to limit the spread of the insect-borne diseases malaria and typhus among civilians and troops. Müller was awarded the Nobel Prize in Physiology or Medicine in 19

OverviewAI-generated

DDT is a chemical compound with the formula C₁₄H₉Cl₅. Its IUPAC name is 1-chloro-4-[2,2,2-trichloro-1-(4-chlorophenyl)ethyl]benzene. The substance has a density of 0.99 and a mass of 351.914688688. Physical properties include a melting point of 227, a decomposition point of 230, and a flash point of 171. The vapor pressure is 0.0000002.

Safety data indicates an immediately dangerous to life or health level of 500 and a time-weighted average exposure limit of 1. The compound has a charge of 0, with no hydrogen bond donors or acceptors. Its topological polar surface area is 0, and its xlogp value is 6.9. DDT is referenced by 2,174 other encyclopedia articles.

Synthesized by Vinony from 25 facts across 4 sources: Wikidata, PubChem, PubMed, Vinony graph. Generated from structured data (not the Wikipedia text) and checked against those facts — may still contain errors.

Chemical data

Formula
C14H9Cl5
Molecular weight
354.5 g/mol
IUPAC name
1-chloro-4-[2,2,2-trichloro-1-(4-chlorophenyl)ethyl]benzene
SMILES
C1=CC(=CC=C1C(C2=CC=C(C=C2)Cl)C(Cl)(Cl)Cl)Cl
InChIKey
YVGGHNCTFXOJCH-UHFFFAOYSA-N
XLogP
6.9
Polar surface area
0 Ų
H-bond donors
0
H-bond acceptors
0
Formal charge
0

via PubChem

Research

21,488 papers

via PubMed

~49 min read

Encyclopedic overview

28 sections
Contents
  • Properties and chemistry
  • Isomers and related compounds
  • Production and use
  • Mechanism of insecticide action
  • History
  • Use in the 1940s and 1950s
  • United States ban
  • International usage restrictions
  • Environmental impact
  • Eggshell thinning{{anchor|Effects_on_wildlife_and_eggshell_thinning}}
  • Human health
  • Acute toxicity
  • Chronic toxicity
  • Carcinogenicity
  • Breast cancer
  • Malaria control{{anchor|Use_against_malaria}}
  • Initial effectiveness
  • Mosquito resistance
  • Residents' concerns
  • Human exposure
  • Criticism of restrictions on DDT use
  • Alternatives
  • Insecticides
  • Non-chemical vector control
  • See also
  • References
  • Further reading
  • External links

Dichlorodiphenyltrichloroethane (DDT) is a colorless, tasteless, and almost odorless crystalline chemical compound, an organochloride. Originally developed as an insecticide, it became infamous for its environmental impacts. DDT was first synthesized in 1874 by the Austrian chemist Othmar Zeidler. DDT's insecticidal action was discovered by the Swiss chemist Paul Hermann Müller in 1939. DDT was used in the second half of World War II to limit the spread of the insect-borne diseases malaria and typhus among civilians and troops. Müller was awarded the Nobel Prize in Physiology or Medicine in 1948 "for his discovery of the high efficiency of DDT as a contact poison against several arthropods". The World Health Organization's (WHO) anti-malaria campaign of the 1950s and 1960s relied heavily on DDT and the results were promising, though there was a resurgence in developing countries afterwards.

The widespread use of DDT after World War II soon raised environmental concerns, highlighted in the United States by Rachel Carson's 1962 book Silent Spring, which helped spur public opposition and contributed to the 1972 US ban on its agricultural use. The restrictions by governments worldwide that followed were also driven by growing evidence of environmental, wildlife and health harm, and the evolution of insect resistance to DDT. These measures aided the recovery of endangered species. Agricultural use was later largely banned worldwide under the Stockholm Convention on Persistent Organic Pollutants of 2004, although limited public-health use for malaria control remains permitted under WHO guidelines.

Excerpted from Wikipedia’s “DDT” article, available under the CC BY-SA 4.0 licence.

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