File:P,p'-dichlorodiphenyltrichloroethane.svg · Wikimedia Commons · See Wikimedia Commons
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
DDT is a chemical insecticide that was developed in the 1930s and widely used during World War II to control disease-carrying insects like mosquitoes and lice. While it was effective at preventing malaria and typhus, DDT later became notorious for causing significant environmental damage, leading to restrictions on its use in many countries.
AI-generated from the Wikipedia summary — may 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- DDT.JAMA · 1974Jukes TH
- Dichlorodiphenyltrichloroethane (DDT): ubiquity, persistence, and risks.ReviewEnvironmental health perspectives · 2002Turusov V, Rakitsky V, Tomatis LDOI: 10.1289/ehp.02110125
- DDT and breast cancer in young women: new data on the significance of age at exposure.Environmental health perspectives · 2007Cohn BA, Wolff MS, Cirillo PM et al.DOI: 10.1289/ehp.10260
- Apparent Khat chewers exposure to DDT in Ethiopia and its potential toxic effects: A scoping review.Regulatory toxicology and pharmacology : RTP · 2024Ali SA, Destaye AGDOI: 10.1016/j.yrtph.2023.105555
- DDT residues in marine phytoplankton.ReviewResidue reviews · 1972Cox JLDOI: 10.1007/978-1-4615-8491-9_2
- Should DDT be banned by international treaty?ReviewParasitology today (Personal ed.) · 2000Curtis CF, Lines JDDOI: 10.1016/s0169-4758(99)01605-1
- DDT.El Farmaceutico · 1945SIMMONS JS
- [Dichlorodiphenyltrichloroethane (DDT) and its metabolites: hormone-like and carcinogenic properties].ReviewVoprosy onkologii · 2003Turusov VS, Rakitskiĭ VN, Tomatis L
via PubMed
Wikidata facts
- Mass
- 351.914688688
- Image
- DDT chemical on watch glass.png
Show 11 more facts
- Commons category
- DDT
- NIOSH Pocket Guide ID
- 0174
- density
- 0.99
- immediately dangerous to life or health
- 500
- melting point
- 108.30000000000001
- decomposition point
- 230
- flash point
- 162
- vapor pressure
- 0.0000002
- time-weighted average exposure limit
- 0.5
- canonical SMILES
- C1=CC(=CC=C1C(C2=CC=C(C=C2)Cl)C(Cl)(Cl)Cl)Cl
- chemical formula
- C₁₄H₉Cl₅
Sources (6)
via Wikidata · CC0
~49 min read
Article
28 sectionsContents
- 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.
Gallery (31)
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