Chemistry:Tetraethyl pyrophosphate
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| Preferred IUPAC name
Tetraethyl diphosphate | |
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PubChem CID
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| UNII | |
| UN number | 3018 2783 |
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| Properties | |
| C8H20O7P2 | |
| Molar mass | 290.189 g·mol−1 |
| Appearance | colorless to amber liquid[1] |
| Odor | faint, fruity[1] |
| Density | 1.19 g/mL (20°C)[1] |
| Melting point | 0 °C; 32 °F; 273 K[1] |
| Boiling point | decomposes[1] |
| miscible[1] | |
| Vapor pressure | 0.0002 mmHg (20°C)[1] |
| Hazards | |
| GHS pictograms |  
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| GHS Signal word | Danger |
| H300, H310, H400 | |
| P262, P264, P270, P273, P280, P301+310, P302+350, P310, P321, P322, P330, P361, P363, P391, P405, P501 | |
| NFPA 704 (fire diamond) | |
| Lethal dose or concentration (LD, LC): | |
LDLo (lowest published)
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0.5 mg/kg (rat, oral) 2.3 mg/kg (guinea pig, oral) 3 mg/kg (mouse, oral)[2] |
| NIOSH (US health exposure limits): | |
PEL (Permissible)
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TWA 0.05 mg/m3 [skin][1] |
REL (Recommended)
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TWA 0.05 mg/m3 [skin][1] |
IDLH (Immediate danger)
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5 mg/m3[1] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
Tetraethyl pyrophosphate, abbreviated TEPP, is an organophosphate compound with the formula [(C
2H
5O)
2P(O)]
2O. It is the tetraethyl derivative of pyrophosphate (P2O74-). It is a colorless oil that solidifies near room temperature. It is used as an insecticide. The compound hydrolyzes rapidly.[3]
Applications
TEPP is an insecticide to aphids, mites, spiders, mealybugs, leafhoppers, lygus bugs, thrips, leafminers, and many other pests.[4] TEPP and other organophosphates are the most widely used pesticides in the U.S. due to their effectiveness and relative small impact on the environment because this organophosphate breaks down so easily.
TEPP has been used for treatment for myasthenia gravis, an autoimmune disease. The treatment would deliver an increase in strength.[5]
Synthesis
The synthesis by De Clermont and Moschnin was based on the earlier work by Alexander Williamson (who is well known for the Williamson-synthesis of ethers).[6] Their synthesis made use of ethyl iodide and silver salts to form esters in combination with pyrophosphate.[7]
- Ag
4P
2O
7 + 4EtI → [(EtO)
2P(O)]
2O + 4AgI
Commercial routes to TEPP often use methods developed by Schrader, Woodstock, and Toy. Triethyl phosphate reacts with phosphorus oxychloride (Schrader-method) or phosphorus pentoxide (Woodstock-method).[8][9] Alternatively, controlled hydrolysis of diethyl phosphorochloridate delivers the compound:[10][11]
- 2(EtO)
2P(O)Cl + H
2O → [(EtO)
2P(O)]
2O + 2HCl
The related tetrabenzylpyrophosphate is prepared by dehydration of dibenzylphosphoric acid:[12]
- 2(RO)
2P(O)OH → [(EtO)
2P(O)]
2O + H
2O
Hydrolysis
TEPP and most of the other organophosphates are susceptible to hydrolysis.[13] The product is diethyl phosphate.[13][14]
Toxicity
TEPP is bioactive as an acetylcholinesterase inhibitor. It reacts with the serine hydroxyl group at the active site, preventing this enzyme from acting on its normal substrate, the neurotransmitter acetyl choline.
TEPP is highly toxic for all warm-blooded animals, including humans.[15] There are three types of effects on these animals that have come forward during laboratory studies.
- DERMAL: LD50 = 2.4 mg/kg (male rat)
- ORAL: LD50 = 1.12 mg/kg (rat)[4]
Death is mostly due to either respiratory failure and in some cases cardiac arrest. The route of absorption might be responsible for the range of effect on certain systems.[16]
For cold-blooded animals the effects are slightly different. In a study with frogs, acute exposure caused a depression in the amount of erythrocytes in the blood. There was also a reduction of white bloodcells, especially the neutrophil granulocytes and lymphocytes. There was no visible damage to the bloodvessels to explain the loss of blood cells. Further there were no signs like hypersalivation or tears like in warm-blooded animals, though there was hypotonia leading to paralysis.[17]
History
It was first synthesized by Wladimir Moschnin in 1854 while working with Adolphe Wurtz. A fellow student Philippe de Clermont is often incorrectly credited as the discoverer of TEPP despite his recognition of the Moschnin primacy in two publications.[18]
The ignorance about the potential toxicity of TEPP is evidenced by De Clermont himself, who described the taste of TEPP as having a burning taste and a peculiar odor [6] Even though TEPP has repeatedly been synthesized by other chemists during the years that followed, not until the 1930s had any adverse effects been observed. Furthermore, Philippe de Clermont has never been reported ill by his family up to his passing at the age of 90. In the meantime, organophosphorus chemistry has really started developing with the help of A. W. von Hofmann, Carl Arnold August Michaelis and Aleksandr Arbuzov.[19]
It was not until 1932 before the first adverse effects of compounds similar to TEPP had been recognized. Willy Lange and Gerda von Krueger were the first to report such effects, about which the following statement was published in their article (in German):[20]
"Interestingly, we report the strong effect of monofluorophosphate phosphoric acid alkyl esters on the human organism. The vapor of these compounds have a pleasant odor and sharply aromatic. After only a few minutes of inhaling the vapor, there is a strong pressure on the larynx, associated with shortness of breath. Then comes decreased awareness, opacities, and dazzling phenomena causing painful sensitivity of the eye to light. Only after several hours is there relief from these phenomena. They are apparently not caused by acidic decomposition products of the ester, but they are probably due to the Dialkyl monofluorophosphates themselves. The effects are exerted by very small amounts."
Starting in 1935 the German government started gathering information about new toxic substances, of which some were to be classified as secret by the German Ministry of Defence.[19] Gerhard Schrader, who has become famous for his studies into organophosphorus insecticides and nerve gases, was one of the chemists who was also studying TEPP. In his studies, in particular his studies into the biological aspects, he noticed that this reagent could possibly be used as an insecticide. This would make the classification of the compound as secret disadvantageous for commercial firms .[19]
Around the beginning of the Second World War, TEPP was discovered to be an inhibitor of cholinesterases.[6] Schrader referred to the studies by Eberhard Gross, who was the first to recognize the mechanism of action for TEPP in 1939. More experiments were conducted including those of Hans Gremels, who confirmed Gross's work.[19] Gremels was also involved in the development of nerve gases at that time. His studies involved several species of animals and human volunteers. Around that same time, atropine was discovered as a possible antidote for the anticholinesterase activity of TEPP.
After the Second World War, Schrader was among many German scientists who were interrogated by English scientists, among others. During the war, the English had been developing chemical weapons of their own to surprise their enemies. In these interrogations the existence of TEPP and other insecticides were disclosed. The existence of nerve gases, however also being disclosed by Schrader, was kept secret by the military.[10]
References
- ↑ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 1.8 1.9 NIOSH Pocket Guide to Chemical Hazards. "#0590". National Institute for Occupational Safety and Health (NIOSH). https://www.cdc.gov/niosh/npg/npgd0590.html.
- ↑ "TEPP". Immediately Dangerous to Life and Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH). https://www.cdc.gov/niosh/idlh/107493.html.
- ↑ Robert L. Metcalf. "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a14_263.
- ↑ 4.0 4.1 Henderson, Chas. F.; Tilton, Elvin. W. (1955). "Tests with Acaricides against the Brown Wheat Mite12". Journal of Economic Entomology 48 (2): 157–161. doi:10.1093/jee/48.2.157.
- ↑ Marr, W.G.; Grob, David (1950-06-20). "Some Ocular Effects of a new Anticholinesterase Agent*". American Journal of Ophthalmology 33 (6): 904–908. doi:10.1016/0002-9394(50)91606-0. ISSN 0002-9394. https://doi.org/10.1016/0002-9394(50)91606-0.
- ↑ 6.0 6.1 6.2 Petroianu, G. A. (2009-04-01). "The synthesis of phosphor ethers: who was Franz Anton Voegeli?". Die Pharmazie 64 (4): 269–271. doi:10.1691/ph.2009.8244. ISSN 0031-7144. PMID 19435147.
- ↑ Petroianu, Georg (2015). "History of organophosphorus cholinesterase inhibitors & reactivators". Military Medical Science Letters 84 (4): 182–185. doi:10.31482/mmsl.2015.023.
- ↑ Sherma, Joseph; Zweig, Gunter (1973) (in en). Thin-Layer and Liquid Chromatography and Pesticides of International Importance: Analytical Methods for Pesticides and Plant Growth Regulators. 7. Academic Press. pp. 471–477. ISBN 978-1-4832-2084-0. https://books.google.com/books?id=icnYBAAAQBAJ.
- ↑ National Research Council (U S. ) Pesticide Residues Committee (1965) (in en). Report on "no Residue" and "zero Tolerance".. National Academies. pp. 3–4. https://books.google.com/books?id=s2QrAAAAYAAJ.
- ↑ 10.0 10.1 Toy, A. D. F. (1948). "The Preparation of Tetraethyl Pyrophosphate and Other Tetraalkyl Pyrophosphates". Journal of the American Chemical Society 70 (11): 3882–3886. doi:10.1021/ja01191a104. PMID 18102975.
- ↑ Steinberg, Geo. M. (1950). "Reactions of Dialkyl Phosphites. Synthesis of Dialkyl Chlorophosphates, Tetraalkyl Pyrophosphates, and Mixed Orthophosphate Esters". Journal of Organic Chemistry 15 (3): 637–47. doi:10.1021/jo01149a031.
- ↑ Todd D. Nelson; Jonathan D. Rosen; M. Bhupathy; James McNamara; Michael J. Sowa; Chad Rush; Louis S. Crocker (2003). "Tetrabenzyl Pyrophosphate". Organic Syntheses 80: 219. doi:10.15227/orgsyn.080.0219.
- ↑ 13.0 13.1 Sogorb, Miguel A; Vilanova, Eugenio (2002-03-10). "Enzymes involved in the detoxification of organophosphorus, carbamate and pyrethroid insecticides through hydrolysis". Toxicology Letters 128 (1–3): 215–228. doi:10.1016/S0378-4274(01)00543-4. PMID 11869832.
- ↑ Jokanović, Milan (2001-09-25). "Biotransformation of organophosphorus compounds". Toxicology 166 (3): 139–160. doi:10.1016/S0300-483X(01)00463-2. PMID 11543910.
- ↑ "Benfluralin - National Library of Medicine HSDB Database". http://toxnet.nlm.nih.gov/cgi-bin/sis/search/a?dbs+hsdb:@term+@DOCNO+407.
- ↑ Clarke, Myra L.; Harvey, Douglas Graham; Humphreys, David John (1988). Veterinary Toxicology (2 ed.). London, England: Bailliere Tindal. p. 157.
- ↑ Kaplan, Harold M.; Glaczenski, Sheila S. (1965-06-01). "Hematological effects of organophosphate insecticides in the frog (Rana pipiens)". Life Sciences 4 (12): 1213–1219. doi:10.1016/0024-3205(65)90335-8. PMID 4284682.
- ↑ Fest, Christa; Schmidt, Karl-Julius (1982). The Chemistry of Organophosphorus Pesticides. Springer. doi:10.1007/978-3-642-68441-8. ISBN 978-3-642-68443-2.The history of cholinesterase inhibitors: who was Moschnin(e)?
- ↑ 19.0 19.1 19.2 19.3 "9: "Structure-Activity Relationships of the Organophosphorus Anticholinesterase Agents, Historical development of organophosphorus cholinesterase inhibitors"" (in en). Cholinesterases and Anticholinesterase Agents. Handbook of Experimental Pharmacology. 15. Springer Science & Business Media. 1963. pp. 434–437. ISBN 978-3-642-99875-1. https://books.google.com/books?id=Je7rCAAAQBAJ.
- ↑ Petroianu, G. A. (2010-10-01). "Toxicity of phosphor esters: Willy Lange (1900-1976) and Gerda von Krueger (1907-after 1970)". Die Pharmazie 65 (10): 776–780. ISSN 0031-7144. PMID 21105582.
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