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 | |
| Names | |
|---|---|
| Preferred IUPAC name Tetraethyl diphosphate | |
| Identifiers | |
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3D model (JSmol) | |
| ChEBI | |
| ChEMBL | |
| ChemSpider |
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| ECHA InfoCard | 100.003.179 |
| EC Number |
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| KEGG | |
| RTECS number |
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| UNII | |
| UN number | 3018 2783 |
| |
| |
| 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 labelling: | |
  | |
| Danger | |
| H300,H310,H400 | |
| P262,P264,P270,P273,P280,P301+P310,P302+P350,P310,P321,P322,P330,P361,P363,P391,P405,P501 | |
| NFPA 704 (fire diamond) | |
| Lethal dose or concentration (LD, LC): | |
LDLo (lowest published) | 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) | TWA 0.05 mg/m3 [skin][1] |
REL (Recommended) | TWA 0.05 mg/m3 [skin][1] |
IDLH (Immediate danger) | 5 mg/m3[1] |
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). | |
Tetraethyl pyrophosphate, abbreviatedTEPP, is anorganophosphate compound with the formula[(C2H5O)2P(O)]2O. It is the tetraethyl derivative ofpyrophosphate (P2O74-). It is a colorless oil that solidifies near room temperature. It is used as aninsecticide. The compound hydrolyzes rapidly.[3]
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.[citation needed]
TEPP has been used for treatment for myasthenia gravis, anautoimmune disease. The treatment would deliver an increase in strength.[5]
The synthesis by De Clermont and Moschnin was based on the earlier work by Alexander Williamson (who is well known for theWilliamson ether synthesis).[6] Their synthesis made use ofethyl iodide and silver salts to form esters in combination with pyrophosphate.[7]
Commercial routes to TEPP often use methods developed by Schrader, Woodstock, and Toy.Triethyl phosphate reacts withphosphorus oxychloride (Schrader's method) orphosphorus pentoxide (Woodstock's method).[8][9] Alternatively, controlled hydrolysis ofdiethyl phosphorochloridate delivers the compound:[10][11]
The related tetrabenzylpyrophosphate is prepared by dehydration of dibenzylphosphoric acid:[12]
TEPP and most of the other organophosphates are susceptible to hydrolysis.[13] The product is diethyl phosphate.[13][14]
TEPP is bioactive as anacetylcholinesterase inhibitor. It reacts with theserine hydroxyl group at the active site, preventing this enzyme from acting on its normal substrate, the neurotransmitteracetyl choline.[citation needed]
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.
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]
It was first synthesized byWladimir Moschnin in 1854 while working withAdolphe Wurtz. A fellow studentPhilippe 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 potentialtoxicity 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 andAleksandr 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 theGerman 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 theSecond World War, TEPP was discovered to be aninhibitor 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 theanticholinesterase activity of TEPP.[citation needed]
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]
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