Dieldrin

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Dieldrin
Dieldrin-3D-balls.png
Dieldrin.svg
Names
IUPAC name
(1aR,2R,2aS,3S,6R,6aR,7S,7aS)-3,4,5,6,9,9-hexachloro-1a,2,2a,3,6,6a,7,7a-octahydro-2,7:3,6-dimethanonaphtho[2,3-b]oxirene
Other names
Dieldrin, HEOD
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.000.440 Edit this at Wikidata
KEGG
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C12H8Cl6O/c13-8-9(14)11(16)5-3-1-2(6-7(3)19-6)4(5)10(8,15)12(11,17)18/h2-7H,1H2/t2-,3+,4+,5-,6-,7+,10+,11- checkY
    Key: DFBKLUNHFCTMDC-PICURKEMSA-N checkY
  • InChI=1/C12H8Cl6O/c13-8-9(14)11(16)5-3-1-2(6-7(3)19-6)4(5)10(8,15)12(11,17)18/h2-7H,1H2/t2-,3+,4+,5-,6-,7+,10+,11-
    Key: DFBKLUNHFCTMDC-PICURKEMBL
SMILES
  • ClC5(Cl)[C@]3(Cl)C(\Cl)=C(\Cl)[C@@]5(Cl)[C@H]4[C@H]1C[C@H]([C@@H]2O[C@H]12)[C@@H]34
Properties
Chemical formula
 C12H8Cl6O
Molar mass 380.91 g/mol
Appearance colorless to light tan crystals
Density 1.75 g/cm3
Melting point 176 to 177 °C (349 to 351 °F; 449 to 450 K)
Boiling point 385 °C (725 °F; 658 K)
Solubility in water
 0.02%[1]
Hazards
Main hazards potential carcinogen[1]
Flash point noncombustible [1]
Lethal dose or concentration (LD, LC):
LD50 (median dose)
 45 mg/kg (oral, rabbit)
49 mg/kg (oral, guinea pig)
38 mg/kg (oral, mouse)
65 mg/kg (oral, dog)
38 mg/kg (oral, rat)[2]
LC50 (median concentration)
 80 mg/m3 (cat, 4 hr)
13 mg/m3 (rat, 4 hr)[2]
NIOSH (US health exposure limits):
PEL (Permissible)
 TWA 0.25 mg/m3 [skin][1]
REL (Recommended)
 Ca TWA 0.25 mg/m3 [skin][1]
IDLH (Immediate danger)
 Ca [50 mg/m3][1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N  (what is checkY☒N ?)
Infobox references

Dieldrin is an organochloride originally produced in 1948 by J. Hyman & Co, Denver, as an insecticide. Dieldrin is closely related to aldrin, which reacts further to form dieldrin. Aldrin is not toxic to insects; it is oxidized in the insect to form dieldrin which is the active compound. Both dieldrin and aldrin are named after the Diels-Alder reaction which is used to form aldrin from a mixture of norbornadiene and hexachlorocyclopentadiene.

Originally developed in the 1940s as an alternative to DDT, dieldrin proved to be a highly effective insecticide and was very widely used during the 1950s to early 1970s. Endrin is a stereoisomer of dieldrin.

However, it is an extremely persistent organic pollutant; it does not easily break down. Furthermore, it tends to biomagnify as it is passed along the food chain. Long-term exposure has proven toxic to a very wide range of animals including humans, far greater than to the original insect targets. For this reason, it is now banned in most of the world.

It has been linked to health problems such as Parkinson's, breast cancer, and immune, reproductive, and nervous system damage. It is also an endocrine disruptor, acting as an estrogen and antiandrogen, and can adversely affect testicular descent in the fetus if a pregnant woman is exposed to it.[3]

Synthesis[]

Dieldrin can be formed from the Diels-Alder reaction of hexachloro-1,3-cyclopentadiene with norbornadiene followed by epoxidation of the addition product with a peroxy acid such as peracetic acid as shown below. [4]

Synthesis of dieldrin

Metabolism[]

The metabolism of Dieldrin occurs by various routes. Hydration of the epoxy group leads to formation of the trans diol and to the dicarboxylic acid. The diol is the most important metabolite produced by the rabbit. In the rat, the primary route of metabolism is hydroxylation of the CH2 group leading to production of the alcohol. There is hydrogen bonding between the OH and the epoxy group. It is excreted in the faeces. It is likely that this is an example of enterohepatic recirculation, for bile contains the glucronide. This is probably cleaved by gut microflora. There is an interesting metabolite in rat urine, first described by Klein. The methylene group of the dieldrin links to one end of the CiC:CCl group to form a cage structure. The other end of the original ClC:CCl is converted to a ketone. The same metabolite is produced from the photoisomer of Dieldrin, in which the same cage structure is produced, but the other end of the original chlorinated double bond forms a CHCl group.

Legislation and history[]

The chemicals dieldrin and aldrin were widely applied in agricultural areas throughout the world. Both are toxic and bioaccumulative. Aldrin does break down to dieldrin in living systems, but dieldrin is known to resist bacterial and chemical breakdown processes in the environment.

Aldrin was used to control soil pests (namely termites) on corn and potato crops. Dieldrin was an insecticide used on fruit, soil, and seed. It persists in the soil with a half-life of five years at temperate latitudes. Both aldrin and dieldrin may be volatilized from sediment and redistributed by air currents, contaminating areas far from their sources. They have been measured in Arctic wildlife, suggesting long range transport from southern agricultural regions.[5]

Both aldrin and dieldrin have been banned in most developed countries, but aldrin is still used as a termiticide in Malaysia, Thailand, Venezuela and parts of Africa. In Canada, their sale was restricted in the mid-1970s, with the last registered use of the compounds in Canada being withdrawn in 1984.[6]

IPCS quotes the World Health Organization as stating dieldrin is prohibited for use in agriculture in, among others, Brazil, Ecuador, Finland, the German Democratic Republic, Singapore, Sweden, Yugoslavia, and the USSR. The European Community legislation prohibits the marketing of phytopharmaceutical products containing dieldrin. In Argentina, Canada, Chile, the Federal Republic of Germany, Hungary, and the USA, its use is prohibited, with some exceptions. The use of dieldrin is restricted in India, Mauritius, Togo, and the United Kingdom. Its use in industry is prohibited in Switzerland and its manufacture and use in Japan is under government control. In Finland, the only accepted use for dieldrin is as a termiticide in one glue mixture for exported plywood. India requires registration and licences for all importation, manufacture, sale, or storage.

Australia[]

Organochlorines and other chemicals were originally developed in the 1930s for use as insecticides and pesticides. DDT became famous worldwide in 1939 after its use in overcoming a typhus infestation in Naples. The use of organochlorines increased during the 1950s and peaked in the 1970s. Their use in Australia was dramatically lowered between the mid 1970s and the early 1980s. The first restrictions on the use of dieldrin and related chemicals in Australia were introduced in 1961-2, with registration required for their use on produce animals, such as cattle and chickens. This coincided with increasing concerns worldwide about the long-term effects of persistent pesticides. The publication of Silent Spring (an account of the environmental and health effects of pesticides) by Rachel Carson in 1962 was a key driving force in raising this concern. The phase-out process was driven by government bans and deregistration, in turn promoted by changing public perceptions that food containing residues of these chemicals was less acceptable and possibly hazardous to health. [7]

Throughout this time, continuous pressure was maintained by relevant committees, for example the Technical Committee on Agricultural Chemicals (TCAC), to reduce approved organochlorine use. By 1981, the use of dieldrin worldwide was limited to sugarcane and bananas, and these uses were deregistered by 1985. In 1987, a nationwide recall system was put into place, and in December of that year, the government prohibited all imports of these chemicals into Australia without express ministerial approval. In 1994, the National Registration Authority for Agricultural and Veterinary Chemicals published a use of organochlorines in termite control, recommending the phase-out of organochlorines used in termite control upon development of viable alternatives. The same year, the Agriculture and Resource Management Council of Australia and New Zealand decided to phase out remaining organochlorine uses by 30 June 1995, with the exception of the Northern Territory. In November 1997, the use of all organochlorines other than mirex was phased out in Australia. Remaining stocks of mirex are to be used only for contained baits for termites in plantations of young trees in the Northern Territory until stocks run out, which is expected in the near future. [7]

The recognition of negative impacts on health has stimulated the implementation of multiple legislative policies in regards to the use and disposal of organochlorine pesticides. For example, the Environment Protection (Marine) Policy 1994 became operational in May 1995 in South Australia. It dictated the acceptable concentration of toxicants such as dieldrin in marine waters and the manner in which these levels must be tested and tried. [7]

Momentum against organochlorine and similar molecules continued to grow internationally, leading, to negotiations which matured as the Stockholm Convention on the use of persistent organic pollutants (POPs). POPs are defined as hazardous and environmentally persistent substances which can be transported between countries by the earth's oceans and atmosphere.

Most POPs (including dieldrin) bioaccumulate in the fatty tissues of humans and other animals. The Stockholm Convention banned 12 POPs, nicknamed "the dirty dozen". These include: aldicarb, toxaphene, chlordane and heptachlor, chlordimeform, chlorobenzilate, DBCP, DDT, "drins" (aldrin, dieldrin and endrin), EDB, HCH and lindane, paraquat, parathion and methyl parathion, pentachlorophenol, and 2,4,5-T. This took force on 17 May 2004. Australia ratified the Convention only three days later and became a party to it in August that year.[7]

Well before this, Australia had been well advanced in meeting the measures agreed upon under the Convention. Production, import and use of aldrin, chlordane, DDT, dieldrin, hexachlorobenzene (HCB), heptachlor, endrin, and toxaphene are not permitted in Australia. Production and importation of polychlorinated biphenyls (PCBs) are not permitted in Australia, with the phase-out of existing PCBs being managed under the National Strategy for the Management of Scheduled Waste. This strategy also addresses how Australia will manage HCB waste and organochlorine pesticides.

Legislation in Australia on the import, use and disposal of dieldrin and other organochlorines has been extensive and covers mainly environmental and potential health impacts on the population. [7]

In Popular Culture[]

Dieldrin is mentioned in conjunction with DDT in the 1971 mockumentary The Hellstrom Chronicle, as having been used by a California farmer to deal with locusts, but therewith he ended up contaminating his crop.

References[]

  1. ^ a b c d e f NIOSH Pocket Guide to Chemical Hazards. "#0206". National Institute for Occupational Safety and Health (NIOSH).
  2. ^ a b "Dieldrin". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
  3. ^ Raun Andersen, Helle; Vinggaard, Anne Marie; Høj Rasmussen, Thomas; Gjermandsen, Irene Marianne; Cecilie Bonefeld-Jørgensen, Eva (2002). "Effects of Currently Used Pesticides in Assays for Estrogenicity, Androgenicity, and Aromatase Activity in Vitro". Toxicology and Applied Pharmacology. 179 (1): 1–12. doi:10.1006/taap.2001.9347. ISSN 0041-008X. PMID 11884232.
  4. ^ Jubb, A. H. (1975). Basic Organic Chemistry, Part 5 Industrial products. London: Wiley. ISBN 978-0-471-85014-4.
  5. ^ (Orris et al. 2000)
  6. ^ Environment Canada. "Descriptions of some toxic contaminants found in the Pacific and Yukon Region". Ecoinfo. Archived from the original on 13 March 2012.
  7. ^ a b c d e "Dieldrin and Breast Cancer: a Literature Review" (PDF). 10 November 2008. Retrieved 3 September 2020.

External links[]

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