Organophosphate

In organic chemistry, organophosphates (also known as phosphate esters, or OPEs) are a class of organophosphorus compounds with the general structure O=P(OR)
3, a central phosphate molecule with alkyl or aromatic substituents.[1] They can be considered as esters of phosphoric acid. Organophosphates are best known for their use as pesticides.

Like most functional groups, organophosphates occur in a diverse range of forms,[2] with important examples including key biomolecules such as DNA, RNA and ATP, as well as many insecticides, herbicides, nerve agents and flame retardants. OPEs have been widely used in various products as flame retardants, plasticizers, and performance additives to engine oil. The low cost of production and compatibility to diverse polymers made OPEs to be widely used in industry including textile, furniture, electronics as plasticizers and flame retardants. These compounds are added to the final product physically rather than by chemical bond.[3] Due to this, OPEs leak into the environment more readily through volatilization, leaching, and abrasion.[4] OPEs have been detected in diverse environmental compartments such as air, dust, water, sediment, soil and biota samples at higher frequency and concentration.[1][4]

The popularity of OPEs as flame retardants came as a substitution for the highly regulated brominated flame retardants.[5]

## Contents

* 1 Forms
* 2 Synthesis
* 2.1 Alcoholysis of POCl3
* 2.2 Esterification of phosphoric acid and P2O5
* 2.3 Oxidation of phosphite esters
* 2.4 Phosphorylation
* 2.5 Laboratory methods
* 3 Properties
* 3.1 Bonding
* 3.2 Acidity
* 3.3 Water solubility
* 4 Industrial materials
* 4.1 Pesticides
* 4.2 Flame retardants
* 4.3 Plasticisers
* 4.4 Hydraulic fluids and lubricant additives
* 4.5 Metal extractants
* 4.6 Surfactants
* 4.7 Nerve agents
* 5 In nature
* 6 References

## Forms

Organophosphates are a class of compounds encompassing a number of distinct but closely related function groups. These are primarily the esters of phosphoric acid and can be mono‑esters, di‑esters or tri‑esters depending on the number of attached organic groups (abbreviated as 'R' in the image below). In general man‑made organophosphates are most often triesters, while biological organophosphates are usually mono- or di-esters. The hydrolysis of triesters can form diesters and monoesters.[6]

400px

In the context of pesticides, derivatives of organophosphates such as organothiophosphates (P=S) or phosphorodiamidates (P-N) are included as being organophosphates. The reason is that these compound are converted into organophosphates biologically.

300px

In biology the esters of diphosphoric acid and triphosphoric acid are generally included as organophosphates. The reason is again a practical one, as many cellular processes involve the mono-, di- and tri- phosphates of the same compound. For instance, the phosphates of adenosine (AMP, ADP, ATP) play a key role in many metabolic processes.

475px

## Synthesis

### Alcoholysis of POCl

Phosphorus oxychloride reacts readily with alcohols to give organophosphates. This is the dominant industrial route and is responsible for almost all organophosphate production. Aluminum trichloride or magnesium chloride are often employed as catalysts.

O=PCl
3 \+ 3 ROH → O=P(OR)
3 \+ 3 HCl

When aliphatic alcohols are used the HCl by-product can react with the phosphate esters to give organochlorides and a lower ester.

O=P(OR)
3 \+ HCl → O=P(OR)
2OH + RCl

This reaction is usually undesirable and is exacerbated by high reaction temperatures. It can be inhibited by the use of a base or the removal of HCl through sparging.

### Esterification of phosphoric acid and P2O5

Esterifications of phosphoric acid with alcohols proceed less readily than the more common carboxylic acid esterifications, with the reactions rarely proceeding much further than the phosphate mono-ester. The reaction requires high temperatures, under which the phosphoric acid can dehydrate to form poly-phosphoric acids. These are exceedingly viscous and their linear polymeric structure renders them less reactive than phosphoric acid.[7] Despite these limitations the reaction does see industrial use for the formation of monoalkyl phosphates, which are used as surfactants.[8] A major appeal of this route is the low cost of phosphoric acid compared to phosphorus oxychloride.

OP(OH)
3 \+ ROH → OP(OH)
2(OR) + H

P2O5 is the anhydride of phosphoric acid and acts similarly. The reaction yields equimolar amounts of di- and monoesters with no phosphoric acid. The process is mostly limited to primary alcohols, as secondary alcohols are prone to undesirable side reactions such as dehydration.[7]

### Oxidation of phosphite esters

Organophosphites can be easily oxidised to give organophosphates. This is not a common industrial route, however large quantities of organophosphites are manufactured as antioxidant stabilisers for plastics. The gradual oxidation of these generates organophosphates in the human environment.[9][10][11]

P(OR)
3 \+ [O] → OP(OR)

### Phosphorylation

Main article: Biology:Phosphorylation

The formation of organophosphates is an important part of biochemistry and living systems achieve this using a variety of enzymes. Phosphorylation is essential to the processes of both anaerobic and aerobic respiration, which involve the production of adenosine triphosphate (ATP), the "high-energy" exchange medium in the cell. Protein phosphorylation is the most abundant post-translational modification in eukaryotes. Many enzymes and receptors are switched "on" or "off" by phosphorylation and dephosphorylation.

### Laboratory methods

Various specialised methods have been developed on the laboratory-scale for scientific investigations. These are rarely employed in bulk manufacturing. Examples include the Atherton-Todd reaction, which converts a dialkyl phosphite to a phosphoryl chloride. This can then react with an alcohol to give an organophosphate and HCl.

## Properties

### Bonding

The bonding in organophosphates has been a matter of prolonged debate; the phosphorus atom is classically hypervalent, as it possesses more bonds than the octet rule should allow.[12] The focus of debate is usually on the nature of the phosphoryl P=O bond, which displays (in spite of the common depiction) non-classical bonding, with a bond order somewhere between 1 and 2. Early papers explained the hypervalence in terms of d-orbital hybridisation, with the energy penalty of promoting electrons into the higher energy orbitals being off-set by the stabilisation of additional bonding.[13] Later advances in computational chemistry showed that d-orbitals played little significant role in bonding.[14][15] Current models rely on either negative hyperconjugation,[16] or a more complex arraignment with a dative-type bond from P to O, combined with back-donation from an oxygen 2p orbital.[15][17] These models agree with the experimental observations of the phosphoryl as being shorter than P-OR bonds[18] and much more polarised. It has been argued that a more accurate depiction is dipolar (i.e. (RO)3P+-O−),[19] which is similar to the depiction of phosphorus ylides such as methylenetriphenylphosphorane. However, in contrast to ylides, the phosphoryl group is unreactive and organophosphates are poor nucleophiles, despite the high concentration of charge on the phosphoryl oxygen. The polarisation accounts in part for the higher melting points of phosphates when compared to their corresponding phosphites. Bonding in the structurally related iminophosphoranes has also been a matter of prelonged debate, however the penta-coordinate phosphoranes (i.e. P(OR)5) are entirely different and involve three-center four-electron bonds.

### Acidity

Phosphate esters bearing P-OH groups are acidic. The pKa of the first OH group is typically between 1-2, while the second OH deprotonates at a pKa between 6-7.[20] As such, phosphate mono- and di-esters are negatively charged at physiological pH.[21] This is of great practical importance, as it makes these compounds far more resistant to degradation by hydrolysis or other forms of nucleophilic attack, due to electrostatic repulsion between negative charges.[22] This effects nearly all organophosphate biomolecules, such as DNA and RNA and accounts in-part for their high stability.[22] The presence of this negative charge also makes these compounds much more water-soluble.

### Water solubility

The water solubility of organophosphates is an important characteristic in biological, industrial and environmental settings. The wide variety of substitutes used in organophosphate esters results in great variations in physical properties. OPEs exhibit a wide range of octanol/water partition coefficients where log Kow values range from -0.98 up to 10.6.[5] Mono- and di- esters are usually water-soluble, particularity biomolecules. Tri-esters such as flame retardants and plasticisers have positive log Kow values ranging between 1.44 and 9.49, signifying hydrophobicity.[5][23][4][24] Hydrophobic OPEs are more likely to be bioaccumulated and biomagnified in aquatic ecosystems.[3] Halogenated organophosphates tend to be denser than water and sink, causing them to accumulate in sediments.[25]

## Industrial materials

### Pesticides

Malathion, one of the first organophosphate insecticides. It remains important as a Vector control agent.

Organophosphates are best known for their use as pesticides. The vast majority are insecticides and are used either to protect crops, or as vector control agents to reduce the transmission of diseases spread by insects, such as mosquitoes. Health concerns have seen their use significantly decrease since the turn of the century.[26][27] Glyphosate is sometimes called an organophosphate, but is in-fact a phosphonate. Its chemistry, mechanism of toxicity and end-use as a herbicide are different from the organophosphate insecticides.

The development of organophosphate insecticides dates back to the 1930s and is generally credited to Gerhard Schrader.[28] At the time pesticides were largely limited to arsenic salts (calcium arsenate, lead arsenate and Paris green)[29] or pyrethrin plant extracts, all of which had major problems.[30] Schrader was seeking more effective agents, however while some organophosphates were found to be far more dangerous to insects than higher animals,[31] the potential effectiveness of others as chemical weapons did not go unnoticed. The development of organophosphate insecticides and the earliest nerve agents was conjoined, with Schrader also developing the nerve agents tabun and sarin. Organophosphate pesticides were not commercialised until after WWII. Parathion was among the first marketed, followed by malathion and azinphosmethyl . Although organophosphates were used in considerable quantities they were originally less important than organochlorine insecticides such as DDT, dieldrin, and heptachlor. When many of the organochlorines were banned in the 1970s, following the publishing of Silent Spring, organophosphates became the most important class of insecticides globally. Nearly 100 were commercialised, with the following being a varied selection:

* Acephate
* Azinphos-methyl
* Bensulide
* Chlorethoxyfos
* Coumaphos
* Diazinon
* Dichlorvos
* Dicrotophos
* Dimethoate
* Disulfoton
* Ethion
* Ethoprop
* Ethyl parathion
* Fenamiphos
* Fenitrothion
* Fonofos
* Isoxathion
* Malathion
* Methamidophos
* Methidathion
* Mevinphos
* Naled
* Phosmet
* Profenofos
* Propetamphos
* Quinalphos
* Sulfotep
* Tebupirimfos
* Temephos
* Terbufos
* Tetrachlorvinphos
* Triazofos

Organophosphate insecticides are acetylcholinesterase inhibitors, which disrupt the transmission of nerve signals in exposed organisms, with fatal results. The risk of human death through organophosphate poisoning[32] was obvious from the start and led to efforts to lower toxicity against mammals while not reducing efficacy against insects.[33][34]

The majority of organophosphate insecticides are organothiophosphates (P=S) or phosphorodiamidates (P-N), both of which are significantly weaker acetylcholinesterase inhibitors than the corresponding phosphates (P=O). They are 'activated' biologically by the exposed organism, via oxidative conversion of P=S to P=O,[35] hydroxylation,[36][37] or other related process which see them transformed into organophosphates. In mammals these transformations occur almost exclusively in the liver,[38] while in insects they take place in the gut and fat body.[39][40][41] As the transformations are handled by different enzymes in different classes of organism it is possible to find compounds which activate more rapidly and completely in insects, and thus display more targeted lethal action.

This selectivity is far from perfect and organophosphate insecticides remain acutely toxic to humans, with many thousands estimated to be killed each year due to intentional (suicide)[42] or unintentional poisoning. Beyond their acute toxicity, long-term exposure to organophosphates is associated with a number of heath risks, including organophosphate-induced delayed neuropathy (muscle weakness) and developmental neurotoxicity.[28][43][44] There is limited evidence that certain compounds cause cancer, including malathion and diazinon.[45] Children[46] and farmworkers[47] are considered to be at greater risk.

Pesticide regulation in the United States and the regulation of pesticides in the European Union have both been increasing restrictions on organophosphate pesticides since the 1990s, particularly when used for crop protection. The use of organophosphates has decreased considerably since that time, having been replaced by pyrethroids and neonicotinoids, which are effective at much lower levels.[26] Reported cases of organophosphate poisoning in the US have reduced during this period.[48][49] Regulation in the global south can be less extensive.[50][51]

In 2015, only 3 of the 50 most common crop-specific pesticides used in the US were organophosphates (Chlorpyrifos, Bensulide, Acephate).[52] No new organophosphate pesticides have been commercialised in the 21st century.[53] The situation in vector control is fairly similar, despite different risk trade-offs,[54] with the global use of organophosphate insecticides falling by nearly half between 2010 and 2019.[27] Even so, Pirimiphos-methyl, Malathion and Temefos are still important, primarily for the control of malaria in the Asia-Pacific region.[27] The continued use of these agents is being challenged by the emergence of insecticide resistance.[55]

### Flame retardants

Bisphenol A diphenyl phosphate, a common organophosphate flame retardant

Flame retardants are added to materials to prevent combustion and to delay the spread of fire after ignition. Organophosphate flame retardants are part of a wider family of phosphorus-based agents which include organic phosphonate and phosphinate esters, in addition to inorganic salts.[56][57] When some prominent brominated flame retardant were banned in the early 2000s phosphorus-based agents were promoted as safer replacements. This has led to a large increase in their use, with an estimated 1 million tonnes of organophosphate flame retardants produced in 2018.[58] Safety concerns have subsequently been raised about some of these reagents,[59][60] with several under regulatory scrutiny.[61][62]

Organophosphate flame retardants were first developed in the first half of the twentieth century in the from of triphenyl phosphate, tricresyl phosphate and tributyl phosphate for use in plastics like cellulose nitrate and cellulose acetate.[63] Use in cellulose products is still significant, but the largest area of application is now in plasticized vinyl polymers, primarily PVC. The more modern organophosphate flame retardants come in 2 major types; chlorinated aliphatic compounds or aromatic diphosphates.[56] The chlorinated compounds TDCPP, TCPP and TCEP are all involatile liquids, of which TCPP is perhaps the most important. They are used in polyurethane (insulation, soft furnishings), PVC (wire and cable) phenolic resins and epoxy resins (varnishes, coatings and adhesives). The most important of the diphosphates is bisphenol-A bis(diphenyl phosphate), with related analogues based around resorcinol and hydroquinone. These are used in polymer blends of engineering plastics, such as PPO/HIPS and PC/ABS,[64] which are commonly used to make casing for electrical items like TVs, computers and home appliances.

Organophosphates act multifunctionally to retard fire in both the gas phase and condensed (solid) phase. Halogenated organophosphates are more active overall as their degradation products interfere with combustion directly in the gas phase. All organophosphates have activity in the condensed phase, by forming phosphorus acids which promote char formation, insulating the surface from heat and air.

Organophosphates were originally thought to be a safe replacements for brominated flame retardants, however many are now coming under regulatory pressure due to their apparent health risks.[62][59][60] The chlorinated organophosphates may be carcinogenic, while others such as tricresyl phosphate have necrotoxic properties.[65] Bisphenol-A bis(diphenyl phosphate) can hydrolyse to form Bisphenol-A which is under significant scrutiny as potential endocrine-disrupting chemical. Although their names imply that they are a single chemical, some (but not all) are produced as complex mixtures. For instance, commercial grade TCPP can contain 7 different isomers,[66] while tricresyl phosphate can contain up to 10.[67] This makes their safety profiles harder to ascertain, as material from different producers can have different compositions.[68]

### Plasticisers

Main article: Chemistry:Plasticizer

2-Ethylhexyl diphenyl phosphate an alkyl diaryl organophosphate used as both a plasticizer and flame retardant in PVC

Plasticisers are added to polymers and plastics to improve their flexibility and processability, giving a softer more easily deformable material. In this way brittle polymers can be made more durable. The most frequently plasticised polymers are the vinyls (PVC, PVB, PVA and PVCA), as well as cellulose plastics (cellulose acetate, nitrocellulose and cellulose acetate butyrate).[69] PVC dominates the market, consuming 80-90% of global plasticiser production.[69][70] PVC can accept large amounts of plasticiser; it is common for products to be 0-50% plasticiser by mass, but loadings can be as high as 70-80% in the case of plastisols.[71]

Pure PVC is more than 60% chlorine by mass and is difficult to burn, but its flammability increases the more it is plasticised.[72] Organophosphates find use because they are multifunctional; primarily plasticising but also imparting flame resistance. Compounds are typically triaryl or alkyl diaryl phosphates, with cresyl diphenyl phosphate and 2-ethylhexyl diphenyl phosphate being important examples respectively.[73] These are both liquids with high boiling points. Organophosphates are more expensive than traditional plasticisers and so tend be used in combination with other plasticisers and flame retardants.[74]

### Hydraulic fluids and lubricant additives

Similar to their use as plastisiers, organophosphates are well suited to use as hydraulic fluids due to their low freezing points and high boiling points, fire-resistance, non-corrosiveness, excellent boundary lubrication properties and good general chemical stability. The triaryl phosphates are the most important group, with tricresyl phosphate being the first to be commercialised in the 1940s, with trixylyl phosphate following shortly after. Butylphenyl diphenyl phosphate and propylphenyl diphenyl phosphate became available after 1960.[75]

In addition to their use as hydraulic base-stock, organophosphates (tricresyl phosphate) and metal organothiophosphates (zinc dithiophosphate) are used as both an antiwear additives and extreme pressure additives in lubricants, where they remain effective even at high temperatures.[76][77][78]

### Metal extractants

Organophosphates have long been used in the field of extractive metallurgy to liberate valuable rare earth metals from their ores.[79] Di(2-ethylhexyl)phosphoric acid and tributyl phosphate are used for the liquid–liquid extraction of these elements from the acidic mixtures form by the leaching of mineral deposits.[80] The same compounds are also used in nuclear reprocessing, as part of the PUREX process.[81]

### Surfactants

Mono- and di- phosphate esters of alcohols (or alcohol ethoxylates) act as surfactants (detergents).[82] Although they are very common in biology as phospholipids, their industrial use is largely limited to certain niche areas. Compared to the more common sulfur-based anionic surfactants (such as LAS or SLES), phosphate ester surfactants are more expensive and generate less foam.[82] Benefits include high stability at extremes of pH, low skin irritation and a high tolerance to dissolved salts.[7] In agricultural settings monoesters of fatty alcohol ethoxylates are used, which are able to disperse poorly miscible or insoluble pesticides into water. As they are low-foaming these mixtures can be sprayed effectively onto fields, while a high salt tolerance allows co-spraying of pesticides and inorganic fertilisers.[83] Low-levels of phosphate mono-esters, such as potassium cetyl phosphate, find use in cosmetic creams and lotions.[84] These in oil-in-water formulations are primarily based on non-ionic surfactants, with the anionic phosphate acting as emulsion-stabilisers. Phosphate tri-esters such as tributyl phosphate are used as anti-foaming agent in paints and concrete.

### Nerve agents

Although the first phosphorus compounds observed to act as cholinesterase inhibitors were organophosphates,[85] the vast majority of nerve agents are instead phosphonates containing a P-C bond. Only a handful of organophosphate nerve agents were developed between the 1930s and 1960s, including diisopropylfluorophosphate, VG and NPF. Between 1971 and 1993 the Soviet Union developed many new potential nerve agents, commonly known as the Novichok agents.[86] Some of these can be considered organophosphates (in a broad sense), being derivatives of fluorophosphoric acid. Examples include A-232, A-234, A-262, C01-A035 and C01-A039. The most notable of these is A-234, which was claimed to be responsible for the poisoning of Sergei and Yulia Skripal in Salisbury (UK) 2018.[87]

## In nature

The detection of OPEs in the air as far away as Antarctica at concentrations around 1 ng/m3 suggests their persistence in air, and their potential for long-range transport.[24] OPEs were measured in high frequency in air and water and widely distributed in northern hemisphere.[88][89] The chlorinated OPEs (TCEP, TCIPP, TDCIPP) in urban sampling sites and non-halogenated like TBOEP in rural areas respectively were frequently measured in the environment across multiple sites. In the Laurentian Great Lakes total OPEs concentrations were found to be 2–3 orders of magnitude higher than concentrations of brominated flame retardants measured in similar air.[89] Waters from rivers in Germany, Austria, and Spain have been consistently recorded for TBOEP and TCIPP at highest concentrations.[24] From these studies, it is clear that OPE concentrations in both air and water samples are often orders of magnitude higher than other flame retardants, and that concentrations are largely dependent on sampling location, with higher concentrations in more urban, polluted locations.

## References

1. ↑ 1.0 1.1 Greaves, Alana K.; Letcher, Robert J.; Chen, Da; McGoldrick, Daryl J.; Gauthier, Lewis T.; Backus, Sean M. (2016-10-01). "Retrospective analysis of organophosphate flame retardants in herring gull eggs and relation to the aquatic food web in the Laurentian Great Lakes of North America" (in en). Environmental Research 150: 255–263. doi:10.1016/j.envres.2016.06.006. ISSN 0013-9351. PMID 27322497. Bibcode: 2016ER....150..255G. http://www.sciencedirect.com/science/article/pii/S0013935116302389.
2. ↑ Ung, Sosthène P.-M.; Li, Chao-Jun (2023). "From rocks to bioactive compounds: a journey through the global P( v ) organophosphorus industry and its sustainability". RSC Sustainability 1 (1): 11–37. doi:10.1039/D2SU00015F.
3. ↑ 3.0 3.1 Wang, Xiaolei; Zhong, Wenjue; Xiao, Bowen; Liu, Qing; Yang, Liping; Covaci, Adrian; Zhu, Lingyan (2019-04-01). "Bioavailability and biomagnification of organophosphate esters in the food web of Taihu Lake, China: Impacts of chemical properties and metabolism" (in en). Environment International 125: 25–32. doi:10.1016/j.envint.2019.01.018. ISSN 0160-4120. PMID 30690428. Bibcode: 2019EnInt.125...25W.
4. ↑ 4.0 4.1 4.2 Wei, Gao-Ling; Li, Ding-Qiang; Zhuo, Mu-Ning; Liao, Yi-Shan; Xie, Zhen-Yue; Guo, Tai-Long; Li, Jun-Jie; Zhang, Si-Yi et al. (January 2015). "Organophosphorus flame retardants and plasticizers: Sources, occurrence, toxicity and human exposure" (in en). Environmental Pollution 196: 29–46. doi:10.1016/j.envpol.2014.09.012. PMID 25290907. Bibcode: 2015EPoll.196...29W.
5. ↑ 5.0 5.1 5.2 Veen, Ike van der; Boer, Jacob de (2012). "Phosphorus flame retardants: Properties, production, environmental occurrence, toxicity and analysis" (in en-GB). Chemosphere 88 (10): 1119–1153. doi:10.1016/j.chemosphere.2012.03.067. PMID 22537891. Bibcode: 2012Chmsp..88.1119V. https://www.mendeley.com/catalogue/7d985eb2-32e4-30e4-9157-1941d4a1b324/.
6. ↑ Liu, Yaxin; Gong, Shuai; Ye, Langjie; Li, Jianhua; Liu, Chunsheng; Chen, Da; Fang, Mingliang; Letcher, Robert J. et al. (October 2021). "Organophosphate (OP) diesters and a review of sources, chemical properties, environmental occurrence, adverse effects, and future directions". Environment International 155. doi:10.1016/j.envint.2021.106691. PMID 34146766. Bibcode: 2021EnInt.15506691L.
7. ↑ 7.0 7.1 7.2 Arora, Pinklesh; Singh, Rakhi; Seshadri, Geetha; Tyagi, Ajay Kumar (16 July 2018). "Synthesis, Properties and Applications of Anionic Phosphate Ester Surfactants: A Review". Tenside Surfactants Detergents 55 (4): 266–272. doi:10.3139/113.110570.
8. ↑ Tracy, David J.; Reierson, Robert L. (April 2002). "Commercial synthesis of monoalkyl phosphates". Journal of Surfactants and Detergents 5 (2): 169–172. doi:10.1007/s11743-002-0218-9.
9. ↑ Liu, Runzeng; Mabury, Scott A. (19 February 2019). "Organophosphite Antioxidants in Indoor Dust Represent an Indirect Source of Organophosphate Esters". Environmental Science & Technology 53 (4): 1805–1811. doi:10.1021/acs.est.8b05545. PMID 30657667. Bibcode: 2019EnST...53.1805L.
10. ↑ Bi, Ruifeng; Meng, Weikun; Su, Guanyong (July 2023). "Organophosphate esters (OPEs) in plastic food packaging: non-target recognition, and migration behavior assessment". Environment International 177. doi:10.1016/j.envint.2023.108010. PMID 37307603. Bibcode: 2023EnInt.17708010B.
11. ↑ Gong, Xinying; Zhang, Wenjun; Zhang, Shuyi; Wang, Yu; Zhang, Xinyi; Lu, Yuan; Sun, Hongwen; Wang, Lei (1 June 2021). "Organophosphite Antioxidants in Mulch Films Are Important Sources of Organophosphate Pollutants in Farmlands". Environmental Science & Technology 55 (11): 7398–7406. doi:10.1021/acs.est.0c08741. PMID 33754709. Bibcode: 2021EnST...55.7398G.
12. ↑ Fugel, Malte; Malaspina, Lorraine A.; Pal, Rumpa; Thomas, Sajesh P.; Shi, Ming W.; Spackman, Mark A.; Sugimoto, Kunihisa; Grabowsky, Simon (7 May 2019). "Revisiting a Historical Concept by Using Quantum Crystallography: Are Phosphate, Sulfate and Perchlorate Anions Hypervalent?". Chemistry – A European Journal 25 (26): 6523–6532. doi:10.1002/chem.201806247. PMID 30759315. Bibcode: 2019ChEuJ..25.6523F.
13. ↑ Cundari, Thomas R. (2013). "Chemical bonding involving d-orbitals". Chemical Communications 49 (83): 9521–9525. doi:10.1039/c3cc45204b. PMID 24013652.
14. ↑ Magnusson, Eric (October 1990). "Hypercoordinate molecules of second-row elements: d functions or d orbitals?". Journal of the American Chemical Society 112 (22): 7940–7951. doi:10.1021/ja00178a014. Bibcode: 1990JAChS.112.7940M.
15. ↑ 15.0 15.1 Gamoke, Benjamin; Neff, Diane; Simons, Jack (14 May 2009). "Nature of PO Bonds in Phosphates". The Journal of Physical Chemistry A 113 (19): 5677–5684. doi:10.1021/jp810014s. PMID 19378976. Bibcode: 2009JPCA..113.5677G.
16. ↑ Rajani, Puchakayala; Gopakumar, Gopinadhanpillai; Nagarajan, Sivaraman; Brahmmananda Rao, Cherukuri Venkata Siva (July 2021). "Does the basicity of phosphoryl oxygen change with alkyl chain length in phosphate ligands?". Chemical Physics Letters 775. doi:10.1016/j.cplett.2021.138641. Bibcode: 2021CPL...77538641R.
17. ↑ Chesnut, D. B. (1 May 2003). "Atoms-in-Molecules and Electron Localization Function Study of the Phosphoryl Bond". The Journal of Physical Chemistry A 107 (21): 4307–4313. doi:10.1021/jp022292r. Bibcode: 2003JPCA..107.4307C.
18. ↑ Corbridge, Derek E. C. (1971). "The structural chemistry of phosphates". Bulletin de la Société française de Minéralogie et de Cristallographie 94 (3): 271–299. doi:10.3406/bulmi.1971.6534.
19. ↑ Rai, Uma S.; Symons, Martyn C. R. (1994). "EPR data do not support the P=O representation for trialkyl phosphates and phosphine oxides or sulfides". J. Chem. Soc., Faraday Trans. 90 (18): 2649–2652. doi:10.1039/FT9949002649.
20. ↑ Kumler, W. D.; Eiler, John J. (December 1943). "The Acid Strength of Mono and Diesters of Phosphoric Acid. The n-Alkyl Esters from Methyl to Butyl, the Esters of Biological Importance, and the Natural Guanidine Phosphoric Acids". Journal of the American Chemical Society 65 (12): 2355–2361. doi:10.1021/ja01252a028. Bibcode: 1943JAChS..65.2355K.
21. ↑ Davis, Bernard D. (December 1958). "On the importance of being ionized". Archives of Biochemistry and Biophysics 78 (2): 497–509. doi:10.1016/0003-9861(58)90374-6. PMID 13618032.
22. ↑ 22.0 22.1 Westheimer, F. H. (6 March 1987). "Why Nature Chose Phosphates". Science 235 (4793): 1173–1178. doi:10.1126/science.2434996. PMID 2434996. Bibcode: 1987Sci...235.1173W.
23. ↑ Möller, A.; Sturm, R.; Xie, Z.; Cai, M.; He, J.; Ebinghaus, R. (2012). "Organophosphorus Flame Retardants and Plasticizers in Airborne Particles over the Northern Pacific and Indian Ocean toward the Polar Regions: Evidence for Global Occurrence". Environmental Science and Technology 46 (6): 3127–3134. doi:10.1021/es204272v. PMID 22332897. Bibcode: 2012EnST...46.3127M.
24. ↑ 24.0 24.1 24.2 Greaves, Alana K.; Letcher, Robert J. (January 2017). "A Review of Organophosphate Esters in the Environment from Biological Effects to Distribution and Fate". Bulletin of Environmental Contamination and Toxicology 98 (1): 2–7. doi:10.1007/s00128-016-1898-0. PMID 27510993. Bibcode: 2017BuECT..98....2G.
25. ↑ McDonough, Carrie A.; De Silva, Amila O.; Sun, Caoxin; Cabrerizo, Ana; Adelman, David; Soltwedel, Thomas; Bauerfeind, Eduard; Muir, Derek C. G. et al. (2018-06-05). "Dissolved Organophosphate Esters and Polybrominated Diphenyl Ethers in Remote Marine Environments: Arctic Surface Water Distributions and Net Transport through Fram Strait" (in en). Environmental Science & Technology 52 (11): 6208–6216. doi:10.1021/acs.est.8b01127. ISSN 0013-936X. PMID 29787253. Bibcode: 2018EnST...52.6208M. https://pubs.acs.org/doi/10.1021/acs.est.8b01127.
26. ↑ 26.0 26.1 World Health Organisation (WHO) (2022). Status and Trends of Pesticide Use. World Health Organization, & Food and Agriculture Organization of the United Nations. https://wedocs.unep.org/20.500.11822/40351.
27. ↑ 27.0 27.1 27.2 van den Berg, Henk; da Silva Bezerra, Haroldo Sergio; Al-Eryani, Samira; Chanda, Emmanuel; Nagpal, Bhupender N.; Knox, Tessa B.; Velayudhan, Raman; Yadav, Rajpal S. (13 December 2021). "Recent trends in global insecticide use for disease vector control and potential implications for resistance management". Scientific Reports 11 (1): 23867. doi:10.1038/s41598-021-03367-9. PMID 34903838. Bibcode: 2021NatSR..1123867V.
28. ↑ 28.0 28.1 Costa, Lucio G (1 March 2018). "Organophosphorus Compounds at 80: Some Old and New Issues". Toxicological Sciences 162 (1): 24–35. doi:10.1093/toxsci/kfx266. PMID 29228398.
29. ↑ "Pinpointing Trends In Pesticide Use. Limited data indicate that pesticide use has dropped since the 1970s". Chemical & Engineering News (ACS) 87 (7). 2009. ISSN 0009-2347. https://cen.acs.org/articles/87/i7/Pinpointing-Trends-Pesticide-Use.html.
30. ↑ Costa, Lucio G. (1987). "Toxicology of Pesticides: A Brief History". Toxicology of Pesticides (NATO ASI Series). pp. 1–10. doi:10.1007/978-3-642-70898-5_1. ISBN 978-3-642-70900-5.
31. ↑ Richmond, Martha (2021). "Discovery and Commercial Introduction and Mode of Action of Parathion, Malathion, Diazinon, Tetrachlorvinphos, and Glyphosate". Cancer Hazards: Parathion, Malathion, Diazinon, Tetrachlorvinphos and Glyphosate. AESS Interdisciplinary Environmental Studies and Sciences Series. pp. 3–11. doi:10.1007/978-3-030-81953-8_1. ISBN 978-3-030-81952-1.
32. ↑ Peter, J. V.; Sudarsan, T. I.; Moran, J. L. (2014). "Clinical features of organophosphate poisoning: A review of different classification systems and approaches". Indian Journal of Critical Care Medicine 18 (11): 735–745. doi:10.4103/0972-5229.144017. PMID 25425841.
33. ↑ O'Brien, R. D.; Thorn, G. D.; Fisher, R. W. (1 October 1958). "New Organophosphate Insecticides Developed on Rational Principles1". Journal of Economic Entomology 51 (5): 714–718. doi:10.1093/jee/51.5.714.
34. ↑ Salgado, Vincent L; David, Michael D (April 2017). "Chance and design in proinsecticide discovery". Pest Management Science 73 (4): 723–730. doi:10.1002/ps.4502. PMID 27976502. Bibcode: 2017PMSci..73..723S.
35. ↑ Gage, J. C. (1 June 1953). "A cholinesterase inhibitor derived from OO -diethyl O - p -nitrophenyl thiophosphate in vivo". Biochemical Journal 54 (3): 426–430. doi:10.1042/bj0540426. PMID 13058919.
36. ↑ Heath, D. F.; Lane, D. W. J.; Park, P. O. (22 December 1955). "The decomposition of some organophosphorus insecticides and related compounds in plants". Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences 239 (663): 191–214. doi:10.1098/rstb.1955.0009. Bibcode: 1955RSPTB.239..191H.
37. ↑ Spencer, E. Y.; O'Brien, R. D.; White, R. W. (February 1957). "Metabolism of Insecticides, Permanganate Oxidation Products of Schradan". Journal of Agricultural and Food Chemistry 5 (2): 123–127. doi:10.1021/jf60072a004. Bibcode: 1957JAFC....5..123S.
38. ↑ Davison, A. N. (1 June 1955). "Return of cholinesterase activity in the rat after inhibition by organophosphorus compounds. 2. A comparative study of true and pseudo cholinesterase". Biochemical Journal 60 (2): 339–346. doi:10.1042/bj0600339. PMID 14389245.
39. ↑ Metcalf, Robert L.; March, Ralph B. (1 March 1953). "Further Studies1 on the Mode of Action of Organic Thionophosphate Insecticides". Annals of the Entomological Society of America 46 (1): 63–74. doi:10.1093/aesa/46.1.63.
40. ↑ Spencer, E. Y.; O'Brien, R. D. (August 1953). "Schradan, Enhancement of Anticholinesterase Activity in Octamethylpyrophosphoramide by Chlorine". Journal of Agricultural and Food Chemistry 1 (11): 716–720. doi:10.1021/jf60011a003. Bibcode: 1953JAFC....1..716S.
41. ↑ O'Brien, R. D. (1 May 1961). "The effect of SKF 525A (2-diethylaminoethyl 2:2-diphenylvalerate hydrochloride) on organophosphate metabolism in insects and mammals". Biochemical Journal 79 (2): 229–235. doi:10.1042/bj0790229. PMID 13730019.
42. ↑ Mew, Emma J.; Padmanathan, Prianka; Konradsen, Flemming; Eddleston, Michael; Chang, Shu-Sen; Phillips, Michael R.; Gunnell, David (September 2017). "The global burden of fatal self-poisoning with pesticides 2006-15: Systematic review". Journal of Affective Disorders 219: 93–104. doi:10.1016/j.jad.2017.05.002. PMID 28535450.
43. ↑ Jokanović, Milan; Oleksak, Patrik; Kuca, Kamil (January 2023). "Multiple neurological effects associated with exposure to organophosphorus pesticides in man". Toxicology 484. doi:10.1016/j.tox.2022.153407. PMID 36543276. Bibcode: 2023Toxgy.48453407J.
44. ↑ World Health Organization (WHO) (March 2022). "The environmental, human health and economic impacts of pesticides". United Nations Environment Programme [UNEP]. https://wedocs.unep.org/bitstream/handle/20.500.11822/40354/Pesticides_Ch5.pdf.
45. ↑ IARC Working Group on the Evaluation of Carcinogenic Risks to Humans (2017). "Some Organophosphate Insecticides and Herbicides". IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. (International Agency for Research on Cancer) 12: 464. PMID 31829533.
46. ↑ Muñoz-Quezada, María Teresa; Lucero, Boris A.; Barr, Dana B.; Steenland, Kyle; Levy, Karen; Ryan, P. Barry; Iglesias, Veronica; Alvarado, Sergio et al. (December 2013). "Neurodevelopmental effects in children associated with exposure to organophosphate pesticides: A systematic review". NeuroToxicology 39: 158–168. doi:10.1016/j.neuro.2013.09.003. PMID 24121005. Bibcode: 2013NeuTx..39..158M.
47. ↑ Muñoz-Quezada, María Teresa; Lucero, Boris Andrés; Iglesias, Verónica Paz; Muñoz, María Pía; Cornejo, Claudia Alejandra; Achu, Eduardo; Baumert, Brittney; Hanchey, Arianna et al. (2 January 2016). "Chronic exposure to organophosphate (OP) pesticides and neuropsychological functioning in farm workers: a review". International Journal of Occupational and Environmental Health 22 (1): 68–79. doi:10.1080/10773525.2015.1123848. PMID 27128815.
48. ↑ Clune, Alison L.; Ryan, P. Barry; Barr, Dana Boyd (April 2012). "Have Regulatory Efforts to Reduce Organophosphorus Insecticide Exposures Been Effective?". Environmental Health Perspectives 120 (4): 521–525. doi:10.1289/ehp.1104323. PMID 22251442. Bibcode: 2012EnvHP.120..521C.
49. ↑ Stone, David L; Sudakin, Daniel L; Jenkins, Jeffrey J (December 2009). "Longitudinal trends in organophosphate incidents reported to the National Pesticide Information Center, 1995–2007". Environmental Health 8 (1): 18. doi:10.1186/1476-069X-8-18. PMID 19379510. Bibcode: 2009EnvHe...8...18S.
50. ↑ Souza, Marília Cristina Oliveira; Cruz, Jonas Carneiro; Cesila, Cibele Aparecida; Gonzalez, Neus; Rocha, Bruno Alves; Adeyemi, Joseph A.; Nadal, Marti; Domingo, José L. et al. (July 2023). "Recent trends in pesticides in crops: A critical review of the duality of risks-benefits and the Brazilian legislation issue". Environmental Research 228. doi:10.1016/j.envres.2023.115811. PMID 37030406. Bibcode: 2023ER....22815811S.
51. ↑ Galt, Ryan E. (October 2008). "Beyond the circle of poison: Significant shifts in the global pesticide complex, 1976–2008". Global Environmental Change 18 (4): 786–799. doi:10.1016/j.gloenvcha.2008.07.003. Bibcode: 2008GEC....18..786G. https://escholarship.org/content/qt1d88g9fw/qt1d88g9fw.pdf.
52. ↑ Maggi, Federico; Tang, Fiona H. M.; la Cecilia, Daniele; McBratney, Alexander (12 September 2019). "PEST-CHEMGRIDS, global gridded maps of the top 20 crop-specific pesticide application rates from 2015 to 2025". Scientific Data 6 (1): 170. doi:10.1038/s41597-019-0169-4. PMID 31515508. Bibcode: 2019NatSD...6..170M.
53. ↑ Umetsu, Noriharu; Shirai, Yuichi (20 May 2020). "Development of novel pesticides in the 21st century". Journal of Pesticide Science 45 (2): 54–74. doi:10.1584/jpestics.D20-201. PMID 33132734.
54. ↑ Gray, George M.; Hammitt, James K. (October 2000). "Risk/Risk Trade-offs in Pesticide Regulation: An Exploratory Analysis of the Public Health Effects of a Ban on Organophosphate and Carbamate Pesticides". Risk Analysis 20 (5): 665–680. doi:10.1111/0272-4332.205060. PMID 11110213. Bibcode: 2000RiskA..20..665G.
55. ↑ Siegfried, Blair D.; Scharf, Michael E. (2001). "Mechanisms of Organophosphate Resistance in Insects". Biochemical Sites of Insecticide Action and Resistance. pp. 269–291. doi:10.1007/978-3-642-59549-3_13. ISBN 978-3-540-67625-6.
56. ↑ 56.0 56.1 van der Veen, Ike; de Boer, Jacob (August 2012). "Phosphorus flame retardants: Properties, production, environmental occurrence, toxicity and analysis". Chemosphere 88 (10): 1119–1153. doi:10.1016/j.chemosphere.2012.03.067. PMID 22537891. Bibcode: 2012Chmsp..88.1119V.
57. ↑ Schmitt, Elmar (May 2007). "Phosphorus-based flame retardants for thermoplastics". Plastics, Additives and Compounding 9 (3): 26–30. doi:10.1016/S1464-391X(07)70067-3.
58. ↑ He, Huan; Gao, Zhanqi; Zhu, Donglin; Guo, Jiehong; Yang, Shaogui; Li, Shiyin; Zhang, Limin; Sun, Cheng (December 2017). "Assessing bioaccessibility and bioavailability of chlorinated organophosphorus flame retardants in sediments". Chemosphere 189: 239–246. doi:10.1016/j.chemosphere.2017.09.017. PMID 28942249. Bibcode: 2017Chmsp.189..239H.
59. ↑ 59.0 59.1 Blum, Arlene; Behl, Mamta; Birnbaum, Linda S.; Diamond, Miriam L.; Phillips, Allison; Singla, Veena; Sipes, Nisha S.; Stapleton, Heather M. et al. (12 November 2019). "Organophosphate Ester Flame Retardants: Are They a Regrettable Substitution for Polybrominated Diphenyl Ethers?". Environmental Science & Technology Letters 6 (11): 638–649. doi:10.1021/acs.estlett.9b00582. PMID 32494578. Bibcode: 2019EnSTL...6..638B.
60. ↑ 60.0 60.1 Du, Jia; Li, Huanxuan; Xu, Shaodan; Zhou, Qingwei; Jin, Meiqing; Tang, Junhong (August 2019). "A review of organophosphorus flame retardants (OPFRs): occurrence, bioaccumulation, toxicity, and organism exposure". Environmental Science and Pollution Research 26 (22): 22126–22136. doi:10.1007/s11356-019-05669-y. PMID 31243659. Bibcode: 2019ESPR...2622126D.
61. ↑ "ECHA identifies certain brominated flame retardants as candidates for restriction". European Chemicals Agency. https://echa.europa.eu/-/echa-identifies-certain-brominated-flame-retardants-as-candidates-for-restriction.
62. ↑ 62.0 62.1 "Regulatory strategy for flame retardant". European Chemicals Agency. https://echa.europa.eu/documents/10162/2082415/flame_retardants_strategy_en.pdf/. doi:10.2823/854233
63. ↑ Weil, E.D.; Levchik, S.V. (26 January 2001). "Phosphorus Flame Retardants". Kirk-Othmer Encyclopedia of Chemical Technology: 1–34. doi:10.1002/0471238961.1608151923050912.a01.pub3. ISBN 978-0-471-48494-3.
64. ↑ Pawlowski, Kristin H; Schartel, Bernhard (November 2007). "Flame retardancy mechanisms of triphenyl phosphate, resorcinol bis(diphenyl phosphate) and bisphenol A bis(diphenyl phosphate) in polycarbonate/acrylonitrile–butadiene–styrene blends". Polymer International 56 (11): 1404–1414. doi:10.1002/pi.2290.
65. ↑ Barth, Mary L.; Craig, Peter H. (October 1999). "Evaluation of the hazards of industrial exposure to tricresyl phosphate:a review and interpretation of the literature". Journal of Toxicology and Environmental Health, Part B 2 (4): 281–300. doi:10.1080/109374099281142. PMID 10596299. Bibcode: 1999JTEHB...2..281P.
66. ↑ Truong, Jimmy W.; Diamond, Miriam L.; Helm, Paul A.; Jantunen, Liisa M. (December 2017). "Isomers of tris(chloropropyl) phosphate (TCPP) in technical mixtures and environmental samples". Analytical and Bioanalytical Chemistry 409 (30): 6989–6997. doi:10.1007/s00216-017-0572-7. PMID 29147747. Bibcode: 2017ABiCh.409.6989T.
67. ↑ Amiri, Roshanak; Bissram, Meera J.; Hashemihedeshi, Mahin; Dorman, Frank L.; Megson, David; Jobst, Karl J. (5 April 2023). "Differentiating Toxic and Nontoxic Tricresyl Phosphate Isomers Using Ion–Molecule Reactions with Oxygen". Journal of the American Society for Mass Spectrometry 34 (4): 640–648. doi:10.1021/jasms.2c00334. PMID 36942790. Bibcode: 2023JASMS..34..640A. https://e-space.mmu.ac.uk/631735/5/Amiri et al_TCP_JASMS_FINAL_clean.pdf.
68. ↑ Duarte, Daniel J.; Rutten, Joost M.M.; van den Berg, Martin; Westerink, Remco H.S. (March 2017). "In vitro neurotoxic hazard characterization of different tricresyl phosphate (TCP) isomers and mixtures". NeuroToxicology 59: 222–230. doi:10.1016/j.neuro.2016.02.001. PMID 26851706. Bibcode: 2017NeuTx..59..222D.
69. ↑ 69.0 69.1 "Plasticizers". Ullmann's Encyclopedia of Industrial Chemistry 27: 613–614. 15 June 2000. doi:10.1002/14356007.a20_439. ISBN 3-527-30673-0.
70. ↑ Rahman, M; Brazel, C (December 2004). "The plasticizer market: an assessment of traditional plasticizers and research trends to meet new challenges". Progress in Polymer Science 29 (12): 1223–1248. doi:10.1016/j.progpolymsci.2004.10.001.
71. ↑ "3.13 Plasticizers". Plastics additives handbook (6. ed.). Munich: Carl Hanser Verlag. 2009. pp. 485–511. ISBN 978-3-446-40801-2.
72. ↑ William Coaker, A. (September 2003). "Fire and flame retardants for PVC". Journal of Vinyl and Additive Technology 9 (3): 108–115. doi:10.1002/vnl.10072.
73. ↑ Grossman, Richard F (2008-05-02). Handbook of Vinyl Formulating. John Wiley & Sons. p. 289. ISBN 978-0-470-25354-0.
74. ↑ Levchik, Sergei V.; Weil, Edward D. (October 2005). "Overview of the recent literature on flame retardancy and smoke suppression in PVC". Polymers for Advanced Technologies 16 (10): 707–716. doi:10.1002/pat.645.
75. ↑ Rudnick, L.R. (2013). "Chapter 4: Neutral Phosphate Esters". Synthetics, Mineral Oils, and Bio-Based Lubricants: Chemistry and Technology, Second Edition. Chemical Industries. CRC Press. pp. 81–104. doi:10.1201/9781315158150-4. ISBN 978-1-4398-5538-6. https://books.google.com/books?id=9YXRBQAAQBAJ&pg=PA81. Retrieved 2024-01-07.
76. ↑ Guan, Bihan; Pochopien, Bernadeta A.; Wright, Dominic S. (August 2016). "The chemistry, mechanism and function of tricresyl phosphate (TCP) as an anti-wear lubricant additive". Lubrication Science 28 (5): 257–265. doi:10.1002/ls.1327.
77. ↑ Johnson, David; Hils, John (18 December 2013). "Phosphate Esters, Thiophosphate Esters and Metal Thiophosphates as Lubricant Additives". Lubricants 1 (4): 132–148. doi:10.3390/lubricants1040132.
78. ↑ Li, Haogang; Zhang, Yanbin; Li, Changhe; Zhou, Zongming; Nie, Xiaolin; Chen, Yun; Cao, Huajun; Liu, Bo et al. (May 2022). "Extreme pressure and antiwear additives for lubricant: academic insights and perspectives". The International Journal of Advanced Manufacturing Technology 120 (1–2): 1–27. doi:10.1007/s00170-021-08614-x.
79. ↑ Hidayah, Nur Nadiatul; Abidin, Sumaiya Zainal (June 2018). "The evolution of mineral processing in extraction of rare earth elements using liquid-liquid extraction: A review". Minerals Engineering 121: 146–157. doi:10.1016/j.mineng.2018.03.018. Bibcode: 2018MiEng.121..146H.
80. ↑ Xie, Feng; Zhang, Ting An; Dreisinger, David; Doyle, Fiona (February 2014). "A critical review on solvent extraction of rare earths from aqueous solutions". Minerals Engineering 56: 10–28. doi:10.1016/j.mineng.2013.10.021. Bibcode: 2014MiEng..56...10X.
81. ↑ Paiva, A. P.; Malik, P. (2004). "Recent advances on the chemistry of solvent extraction applied to the reprocessing of spent nuclear fuels and radioactive wastes". Journal of Radioanalytical and Nuclear Chemistry 261 (2): 485–496. doi:10.1023/B:JRNC.0000034890.23325.b5. Bibcode: 2004JRNC..261..485P.
82. ↑ 82.0 82.1 Farn, R.J. (2008). Chemistry and Technology of Surfactants. Wiley. pp. 122–124. ISBN 978-1-4051-7179-3. https://books.google.com/books?id=CCn81pnPrgwC&pg=PP2. Retrieved 2023-05-27.
83. ↑ Kaneko, T.M.; Spicer, L.D. (1985). Pesticide Formulations and Application Systems: Fourth Symposium: a Symposium Sponsored by ASTM Committee E-35 on Pesticides, New Orleans, La., 2-3 Nov. 1983. ASTM special technical publication. ASTM. pp. 5–14. ISBN 978-0-8031-0413-6. https://books.google.com/books?id=NSvmvgBsn8cC&pg=PA5. Retrieved 2023-05-27.
84. ↑ Miller, Dennis; Wiener, Eva-Maria; Turowski, Angelika; Thunig, Christine; Hoffmann, Heinz (July 1999). "O/W emulsions for cosmetics products stabilized by alkyl phosphates — rheology and storage tests". Colloids and Surfaces A: Physicochemical and Engineering Aspects 152 (1–2): 155–160. doi:10.1016/S0927-7757(98)00630-X.
85. ↑ 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.
86. ↑ Chai, Peter R.; Hayes, Bryan D.; Erickson, Timothy B.; Boyer, Edward W. (January 2018). "Novichok agents: a historical, current, and toxicological perspective". Toxicology Communications 2 (1): 45–48. doi:10.1080/24734306.2018.1475151. PMID 30003185.
87. ↑ Vale, J. Allister; Marrs, Timothy C.; Maynard, Robert L. (2 November 2018). "Novichok: a murderous nerve agent attack in the UK". Clinical Toxicology 56 (11): 1093–1097. doi:10.1080/15563650.2018.1469759. PMID 29757015.
88. ↑ Salamova, Amina; Ma, Yuning; Venier, Marta; Hites, Ronald A. (2014-01-14). "High Levels of Organophosphate Flame Retardants in the Great Lakes Atmosphere". Environmental Science & Technology Letters 1 (1): 8–14. doi:10.1021/ez400034n. Bibcode: 2014EnSTL...1....8S.
89. ↑ 89.0 89.1 Venier, Marta; Dove, Alice; Romanak, Kevin; Backus, Sean; Hites, Ronald (2014-08-19). "Flame Retardants and Legacy Chemicals in Great Lakes' Water" (in en). Environmental Science & Technology 48 (16): 9563–9572. doi:10.1021/es501509r. ISSN 0013-936X. PMID 25045802. Bibcode: 2014EnST...48.9563V. https://pubs.acs.org/doi/10.1021/es501509r.

* v
* t
* e

Organophosphorus

Only P-O bonds|

| P(III)|

* Phosphite/Organophosphite

|

P(V)|

* Phosphate/Organophosphate

With P-C bonds|

| One P-C bonds|

| P(III)|

* Phosphonite

|

P(V)|

* Phosphonate

Two P-C bonds|

| P(III)|

* Phosphinite

|

P(V)|

* Phosphinate

Three P-C bonds|

| P(III)|

* Phosphine

|

P(V)|

* Phosphine oxide

With P-N bonds|

| One P-N bond|

| P(III)|

* Phosphoramidite
* e.g. Nucleoside phosphoramidite

|

P(V)|

* Phosphoramidate
* e.g. Phosphocreatine

Two P-N bond|

| P(III)|

* Phosphorodiamidite

|

P(V)|

* Phosphorodiamidate
* e.g. Morpholino
* Cyclophosphamide

Three P-N bond|

| P(V)|

* Phosphoramide
* e.g. Hexamethylphosphoramide
* Metepa

|

With P-C and P-N bonds|

| One P-C bond and one P-N bond|

| P(V)|

* Phosphonamidate

|

One P-C bond and two P-N bond|

| P(V)|

* Phosphonamide

|

Two P-C bond and one P-N bond|

| P(V)|

* Phosphinamide

|

With P-S bonds|

| One P-S bond|

| P(III)|

* Phosphorothioite

|

P(V)|

* Phosphorothioate

Two P-S bond|

| P(III)|

* Phosphorodithioite

|

P(V)|

* Phosphorodithioate

* v
* t
* e

Pest control: Insecticides

Carbamates|

* Aldicarb
* Bendiocarb
* Carbaryl
* Carbofuran
* Ethienocarb
* Fenobucarb
* Oxamyl
* Methomyl
* Propoxur

Inorganic compounds|

* Aluminium phosphide
* Boric acid
* Chromated copper arsenate
* Copper(II) arsenate
* Copper(I) cyanide
* Cryolite
* Diatomaceous earth
* Lead hydrogen arsenate
* Paris Green
* Scheele's Green

Insect growth regulators|

* Benzoylureas
* Diflubenzuron
* Flufenoxuron
* Hydroprene
* Lufenuron
* Methoprene
* Pyriproxyfen

Neonicotinoids|

* Acetamiprid
* Clothianidin
* Dinotefuran
* Imidacloprid
* Nitenpyram
* Nithiazine
* Thiacloprid
* Thiamethoxam

Organochlorides|

* Aldrin
* Beta-HCH
* Carbon tetrachloride
* Chlordane
* Cyclodiene
* 1,2-DCB
* 1,4-DCB
* 1,1-DCE
* 1,2-DCE
* DDD
* DDE
* DDT
* Dicofol
* Dieldrin
* Endosulfan
* Endrin
* Heptachlor
* Kepone
* Lindane
* Methoxychlor
* Mirex
* Tetradifon
* Toxaphene

Organophosphorus|

* Acephate
* Azamethiphos
* Azinphos-methyl
* Bensulide
* Chlorethoxyfos
* Chlorfenvinphos
* Chlorpyrifos
* Chlorpyrifos-methyl
* Coumaphos
* Demeton-S-methyl
* Diazinon
* Dichlorvos
* Dicrotophos
* Diisopropyl fluorophosphate
* Dimefox
* Dimethoate
* Dioxathion
* Disulfoton
* Ethion
* Ethoprop
* Fenamiphos
* Fenitrothion
* Fenthion
* Fosthiazate
* Isoxathion
* Malathion
* Methamidophos
* Methidathion
* Mevinphos
* Mipafox
* Monocrotophos
* Naled
* Omethoate
* Oxydemeton-methyl
* Parathion
* Parathion-methyl
* Phenthoate
* Phorate
* Phosalone
* Phosmet
* Phoxim
* Pirimiphos-methyl
* Quinalphos
* Schradan
* Temefos
* Tebupirimfos
* Terbufos
* Tetrachlorvinphos
* Tribufos
* Trichlorfon

Pyrethroids|

* Acrinathrin
* Allethrins
* Bifenthrin
* Bioallethrin
* Cyfluthrin
* Cyhalothrin
* Cypermethrin
* Cyphenothrin
* Deltamethrin
* Empenthrin
* Esfenvalerate
* Etofenprox
* Fenpropathrin
* Fenvalerate
* Flumethrin
* Imiprothrin
* Metofluthrin
* Permethrin
* Phenothrin
* Prallethrin
* Pyrethrin (I, II; chrysanthemic acid)
* Pyrethrum
* Resmethrin
* Silafluofen
* Tefluthrin
* Tetramethrin
* Tralomethrin
* Transfluthrin

Ryanoids|

* Chlorantraniliprole
* Cyantraniliprole
* Flubendiamide
* Ryanodine
* Ryanodol

Other chemicals|

* Afoxolaner
* Amitraz
* Azadirachtin
* Buprofezin
* Chlordimeform
* Chlorfenapyr
* Cyromazine
* Fenazaquin
* Fenoxycarb
* Fipronil
* Fluralaner
* Hydramethylnon
* Indoxacarb
* Limonene
* Lotilaner
* Pyridaben
* Pyriprole
* Ryanodine
* Sarolaner
* Sesamex
* Spinosad
* Sulfluramid
* Tebufenozide
* Tebufenpyrad
* Veracevine
* Xanthone
* Metaflumizone

Metabolites|

* Oxon
* Malaoxon
* Paraoxon
* TCPy

Biopesticides|

* Bacillus thuringiensis
* Baculovirus
* Beauveria bassiana
* Beauveria brongniartii
* Metarhizium acridum
* Metarhizium anisopliae
* Nomuraea rileyi
* Lecanicillium lecanii
* Paecilomyces fumosoroseus
* Paenibacillus popilliae
* Purpureocillium lilacinum

* v
* t
* e

Health issues of plastics and polyhalogenated compounds (PHCs)

Plasticizers: Phthalates|

* DIBP
* DBP
* BBP (BBzP)
* DIHP
* DEHP (DOP)
* DIDP
* DINP

Miscellaneous plasticizers|

* Organophosphates
* Adipates (DEHA
* DOA)

Monomers|

* Bisphenol A (BPA, in Polycarbonates)
* Vinyl chloride (in PVC)

Miscellaneous additives incl. PHCs|

* PBDEs
* PCBs
* Organotins
* PFCs
* Perfluorooctanoic acid

Health issues|

* Teratogen
* Carcinogen
* Endocrine disruptor
* Diabetes
* Obesity
* Obesogen
* Polymer fume fever

Pollution|

* Plastic pollution
* Rubber pollution
* Great Pacific garbage patch
* Persistent organic pollutant
* Dioxins
* List of environmental health hazards

Regulations|

* California Proposition 65
* European REACH regulation
* Japan Toxic Substances Law
* Toxic Substances Control Act

Acetylcholine receptor modulators

* v
* t
* e

Muscarinic acetylcholine receptor modulators

mAChRs|

| Agonists|

* 77-LH-28-1
* AC-42
* AC-260,584
* Aceclidine
* Acetylcholine
* AF30
* AF150(S)
* AF267B
* Alvameline
* AQRA-741
* Arecoline
* Bethanechol
* Bevonium
* Butyrylcholine
* Carbachol
* CDD-0034
* CDD-0078
* CDD-0097
* CDD-0098
* CDD-0102
* Cevimeline
* Choline
* cis-Dioxolane
* Clozapine
* Desmethylclozapine (norclozapine)
* Ethoxysebacylcholine
* Itameline
* LY-593,039
* L-689,660
* LY-2,033,298
* McNA343
* Methacholine
* Milameline
* Muscarine
* NGX-267
* Ocvimeline
* Oxotremorine
* PD-151,832
* Pilocarpine
* RS86
* Sabcomeline
* SDZ 210-086
* Sebacylcholine
* Suberyldicholine
* Talsaclidine
* Tazomeline
* Thiopilocarpine
* Vedaclidine
* VU-0029767
* VU-0090157
* VU-0152099
* VU-0152100
* VU-0238429
* WAY-132,983
* Xanomeline
* YM-796

|

Antagonists|

* 3-Quinuclidinyl benzilate
* 4-DAMP
* Aclidinium bromide (+formoterol)
* Abediterol
* AF-DX 250
* AF-DX 384
* Ambutonium bromide
* Anisodamine
* Anisodine
* Antihistamines (first-generation) (e.g., brompheniramine, buclizine, captodiame, chlorphenamine (chlorpheniramine), cinnarizine, clemastine, cyproheptadine, dimenhydrinate, [[Chemistry:Dimetdimetindene, Diphenhydramine|diphenhydramine]], doxylamine, meclizine, mepyramine (pyrilamine), mequitazine, perlapine, phenindamine, pheniramine, Phenyltoloxamine|Phenyltoloxamine]]]], promethazine, propiomazine, triprolidine)
* AQ-RA 741
* Atropine
* Atropine methonitrate
* Atypical antipsychotics (e.g., clozapine, Chemistry:Fluperlapine

Precursors
(and prodrugs)|

* Acetyl-coA
* Adafenoxate
* Choline (lecithin)
* Citicoline
* Cyprodenate
* Dimethylethanolamine
* Glycerophosphocholine
* Meclofenoxate (centrophenoxine)
* Phosphatidylcholine
* Phosphatidylethanolamine
* Phosphorylcholine
* Pirisudanol

See also: Receptor/signaling modulators • Nicotinic acetylcholine receptor modulators • Acetylcholine metabolism/transport modulators

* v
* t
* e

Nicotinic acetylcholine receptor modulators

nAChRs|

| Agonists
(and PAMs)|

* 5-HIAA
* A-84,543
* A-366,833
* A-582,941
* A-867,744
* ABT-202
* ABT-418
* ABT-560
* ABT-894
* Acetylcholine
* Altinicline
* Anabasine
* Anatoxin-a
* AR-R17779
* Bephenium hydroxynaphthoate
* Butinoline
* Butyrylcholine
* Carbachol
* Choline
* Cotinine
* Cytisine
* Decamethonium
* Desformylflustrabromine
* Dianicline
* Dimethylphenylpiperazinium
* Epibatidine
* Epiboxidine
* Ethanol (alcohol)
* Ethoxysebacylcholine
* EVP-4473
* EVP-6124
* Galantamine
* GTS-21
* Ispronicline
* Ivermectin
* JNJ-39393406
* Levamisole
* Lobeline
* MEM-63,908 (RG-3487)
* Morantel
* Nicotine (tobacco)
* NS-1738
* PHA-543,613
* PHA-709,829
* PNU-120,596
* PNU-282,987
* Pozanicline
* Pyrantel
* Rivanicline
* RJR-2429
* Sazetidine A
* SB-206553
* Sebacylcholine
* SIB-1508Y
* SIB-1553A
* SSR-180,711
* Suberyldicholine
* Suxamethonium (succinylcholine)
* Suxethonium (succinyldicholine)
* TC-1698
* TC-1734
* TC-1827
* TC-2216
* TC-5214
* TC-5619
* TC-6683
* Tebanicline
* Tribendimidine
* Tropisetron
* UB-165
* Varenicline
* WAY-317,538
* XY-4083

|

Antagonists
(and NAMs)|

* 18-MAC
* 18-MC
* α-Neurotoxins (e.g., α-bungarotoxin, α-cobratoxin, α-conotoxin, many others)
* ABT-126
* Alcuronium
* Allopregnanolone
* Amantadine
* Anatruxonium
* AQW051
* Atracurium
* Barbiturates (e.g., pentobarbital, sodium thiopental)
* BNC-210
* Bungarotoxins (e.g., α-bungarotoxin, κ-bungarotoxin)
* Bupropion
* BW284C51
* BW-A444
* Candocuronium iodide (chandonium iodide)
* Chlorisondamine
* Cisatracurium
* Coclaurine
* Coronaridine
* Curare
* Cyclopropane
* Dacuronium bromide
* Decamethonium
* Dehydronorketamine
* Desflurane
* Dextromethorphan
* Dextropropoxyphene
* Dextrorphan
* Diadonium
* DHβE
* Dihydrochandonium
* Dimethyltubocurarine (metocurine)
* Dioscorine
* Dipyrandium
* Dizocilpine (MK-801)
* Doxacurium
* Encenicline
* Enflurane
* Erythravine
* Esketamine
* Fazadinium
* Gallamine
* Gantacurium chloride
* Halothane
* Hexafluronium
* Hexamethonium (benzohexonium)
* Hydroxybupropion
* Hydroxynorketamine
* Ibogaine
* Isoflurane
* Ketamine
* Kynurenic acid
* Laudanosine
* Laudexium (laudolissin)
* Levacetylmethadol
* Levomethadone
* Malouetine
* ME-18-MC
* Mecamylamine
* Memantine
* Methadone
* Methorphan (racemethorphan)
* Methyllycaconitine
* Metocurine
* Mivacurium
* Morphanol (racemorphan)
* Neramexane
* Nitrous oxide
* Norketamine
* Pancuronium bromide
* Pempidine
* Pentamine
* Pentolinium
* Phencyclidine
* Pipecuronium bromide
* Progesterone
* Promegestone
* Radafaxine
* Rapacuronium bromide
* Reboxetine
* Rocuronium bromide
* Sevoflurane
* Stercuronium iodide
* Surugatoxin
* Thiocolchicoside
* Toxiferine
* Tramadol
* Trimetaphan camsilate (trimethaphan camsylate)
* Tropeinium
* Tubocurarine
* Vanoxerine
* Vecuronium bromide
* Xenon

Precursors
(and prodrugs)|

* Acetyl-coA
* Adafenoxate
* Choline (lecithin)
* Citicoline
* Cyprodenate
* Dimethylethanolamine
* Glycerophosphocholine
* Meclofenoxate (centrophenoxine)
* Phosphatidylcholine
* Phosphatidylethanolamine
* Phosphorylcholine
* Pirisudanol

See also: Receptor/signaling modulators • Muscarinic acetylcholine receptor modulators • Acetylcholine metabolism/transport modulators

0.00

(0 votes)

Original source: https://en.wikipedia.org/wiki/Organophosphate. Read more

|

Retrieved from "https://handwiki.org/wiki/index.php?title=Chemistry:Organophosphate&oldid=4245634"
*[v]: View this template
*[t]: Discuss this template
*[e]: Edit this template
*[mAChRs]: Muscarinic acetylcholine receptors
*[nAChRs]: Nicotinic acetylcholine receptors
*[PAMs]: positive allosteric modulators
*[NAMs]: negative allosteric modulators