DDT does not occur naturally and is synthesised by consecutive Friedel–Crafts reactions between chloral ( CClģCHO) and two equivalents of chlorobenzene ( CĥCl), in the presence of an acidic catalyst. It is highly hydrophobic and nearly insoluble in water but has good solubility in most organic solvents, fats and oils. Properties and chemistry ĭDT is similar in structure to the insecticide methoxychlor and the acaricide dicofol.
Īlong with the passage of the Endangered Species Act, the United States ban on DDT is a major factor in the comeback of the bald eagle (the national bird of the United States) and the peregrine falcon from near-extinction in the contiguous United States. DDT still has limited use in disease vector control because of its effectiveness in killing mosquitos and thus reducing malarial infections, but that use is controversial due to environmental and health concerns. Ī worldwide ban on agricultural use was formalized under the Stockholm Convention on Persistent Organic Pollutants which has been in effect since 2004. Although Carson never directly called for an outright ban on the use of DDT, its publication was a seminal event for the environmental movement and resulted in a large public outcry that eventually led, in 1972, to a ban on DDT's agricultural use in the United States. The book cited claims that DDT and other pesticides caused cancer and that their agricultural use was a threat to wildlife, particularly birds. It talked about environmental impacts that correlated with the widespread use of DDT in agriculture in the United States, and it questioned the logic of broadcasting potentially dangerous chemicals into the environment with little prior investigation of their environmental and health effects. Opposition to DDT was focused by the 1962 publication of Rachel Carson's book Silent Spring. Although it was promoted by government and industry for use as an agricultural and household pesticide, there were also concerns about its use from the beginning. īy October 1945, DDT was available for public sale in the United States. 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". 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. DDT's insecticidal action was discovered by the Swiss chemist Paul Hermann Müller in 1939. DDT was first synthesized in 1874 by the Austrian chemist Othmar Zeidler.
Originally developed as an insecticide, it became infamous for its environmental impacts. Dichlorodiphenyltrichloroethane, commonly known as DDT, is a colorless, tasteless, and almost odorless crystalline chemical compound, an organochloride.
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