Bisphenol A
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IUPAC name 4,4'-(propane-2,2-diyl)diphenol | |
| Other names BPA, p,p'-Isopropylidenebisphenol, 2,2-Bis(4-hydroxyphenyl)propane | |
| Identifiers | |
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ChEBI |
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DrugBank |
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ECHA InfoCard | 100.001.133 |
EC Number | 201-245-8 |
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PubChem CID |
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RTECS number | SL6300000 |
UNII |
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UN number | 2430 |
CompTox Dashboard (EPA) |
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| Properties | |
Chemical formula | C15H16O2 |
Molar mass | 7002228291000000000♠228.291 g·mol−1 |
| Appearance | White solid |
Density | 1.20 g/cm³ |
Melting point | 158 to 159 °C (316 to 318 °F; 431 to 432 K) |
Boiling point | 220 °C (428 °F; 493 K) 4 mmHg |
Solubility in water | 120–300 ppm (21.5 °C) |
Vapor pressure | 5×10−6 Pa (25 °C)[1] |
| Hazards | |
R-phrases (outdated) | R36 R37 R38 R43 |
S-phrases (outdated) | S24 S26 S37 |
NFPA 704 |  1 3 0 |
Flash point | 227 °C (441 °F; 500 K) |
Autoignition temperature | 600 °C (1,112 °F; 873 K) |
| Related compounds | |
Related phenols | Bisphenol S |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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Infobox references | |
Bisphenol A (BPA) is an organic synthetic compound with the chemical formula (CH3)2C(C6H4OH)2 belonging to the group of diphenylmethane derivatives and bisphenols, with two hydroxyphenyl groups. It is a colorless solid that is soluble in organic solvents, but poorly soluble in water (0.344 wt % at 83 °C[2]).
BPA is a starting material for the synthesis of plastics, primarily certain polycarbonates and epoxy resins, as well as some polysulfones and certain niche materials. BPA-based plastic is clear and tough, and is made into a variety of common consumer goods, such as plastic bottles including water bottles, sports equipment, CDs, and DVDs. Epoxy resins containing BPA are used to line water pipes, as coatings on the inside of many food and beverage cans and in making thermal paper such as that used in sales receipts.[3] In 2015, an estimated 4 million tonnes of BPA chemical were produced for manufacturing polycarbonate plastic, making it one of the highest volume of chemicals produced worldwide.[4]
BPA is a xenoestrogen, exhibiting estrogen-mimicking, hormone-like properties[5] that raise concern about its suitability in some consumer products and food containers. Since 2008, several governments have investigated its safety, which prompted some retailers to withdraw polycarbonate products. The U.S. Food and Drug Administration (FDA) has ended its authorization of the use of BPA in baby bottles and infant formula packaging, based on market abandonment, not safety.[6] The European Union and Canada have banned BPA use in baby bottles.
Contents
1 Production
2 Uses
2.1 Polycarbonates
2.2 Epoxy and vinyl ester resins
2.3 Specialized derivatives
3 Identification in plastics
4 History
5 Health effects
5.1 BPA substitutes
6 Environmental effects
7 Toxicity
8 References
9 Further reading
Production
World production capacity of BPA was 1 million tons in the 1980s,[2] and more than 2.2 million tons in 2009.[7] It is a high production volume chemical. This compound is synthesized by the condensation of acetone (hence the suffix A in the name)[8] with two equivalents of phenol. The reaction is catalyzed by a strong acid, such as hydrochloric acid (HCl) or a sulfonated polystyrene resin. Industrially, a large excess of phenol is used to ensure full condensation; the product mixture of the cumene process (acetone and phenol) may also be used as starting material:[2]
Numerous ketones undergo analogous condensation reactions.[2]
Uses
Bisphenol A is primarily used to make plastics, such as this polycarbonate water bottle.
In 2003, U.S. consumption was 856,000 tons, 72% of which used to make polycarbonate plastic and 21% going into epoxy resins.[9] In the U.S., less than 5% of the BPA produced is used in food contact applications,[10] but remains in the canned food industry and printing applications such as sales receipts.[11][12]
Polycarbonates
Bisphenol A and phosgene react to give polycarbonate. The reaction is conducted under biphasic conditions; the hydrochloric acid is scavenged with aqueous base:[13]
Million tonnes (8 billion pounds) of BPA are consumed for this purpose yearly.[14]
Epoxy and vinyl ester resins
It is a precursor in production of major classes of resins, specifically the vinyl ester resins. This application usually begins with alkylation of BPA with epichlorohydrin.[15]
Typical "vinyl ester" derived from bisphenol A diglycidyl ether, sometimes called BADGE. Free-radical polymerization gives a highly crosslinked polymer.[16]
Specialized derivatives
BPA is a versatile building block from which many derivatives have been prepared. Nitration give dinitrobisphenol A. Bromination gives tetrabromobisphenol A (TBBPA), which exhibits fire retardant properties.[17]
BPA is also used in the synthesis of polysulfones and some Polyether ether ketones. It is an antioxidant in some plasticizers, and as a polymerization inhibitor in PVC.[citation needed]
Several drug candidates have been developed from bisphenol A, including Ralaniten, #Ralaniten acetate, and EPI-001.
Identification in plastics
Some type 7 plastics may contain bisphenol A
In the U.S., plastic packaging is split into seven broad classes for recycling purposes by a Plastic identification code. As of 2014 there are no BPA labeling requirements for plastics in the U.S. "In general, plastics that are marked with Resin Identification Codes 1, 2, 4, 5, and 6 are very unlikely to contain BPA. Some, but not all, plastics that are marked with the Resin Identification Code 7 may be made with BPA."[18] Type 7 is the catch-all "other" class, and some type 7 plastics, such as polycarbonate (sometimes identified with the letters "PC" near the recycling symbol) and epoxy resins, are made from bisphenol A monomer.[2][19] Type 3 (PVC) may contain bisphenol A as an antioxidant in "flexible PVC" softened by plasticizers,[2] but not rigid PVC such as pipe, windows, and siding.
History
Bisphenol A was discovered in 1891 by Russian chemist Aleksandr Dianin.[20]
In 1934 workers at I.G. Farbenindustrie reported the coupling of BPA and epichlorohydrin. Over the following decade, coatings and resins derived from similar materials were described by workers at the companies of DeTrey Freres in Switzerland and DeVoe and Raynolds in the US. This early work underpinned the development of epoxy resins, which in turn motivated production of BPA.[16] The utilization of BPA further expanded with discoveries at Bayer and General Electric on polycarbonate plastics. These plastics first appeared in 1958, being produced by Mobay and General Electric, and Bayer.[21]
In terms of the endocrine disruption controversy, the British biochemist Edward Charles Dodds tested BPA as an artificial estrogen in the early 1930s. He found BPA to be 1 / 37,000 as effective as estradiol.[22][23][24] Dodds eventually developed a structurally similar[25] compound, diethylstilbestrol (DES), which was used as a synthetic estrogen drug in women and animals until it was banned due to its risk of causing cancer; the ban on use of DES in humans came in 1971 and in animals, in 1979.[22] BPA was never used as a drug.[22] BPA's ability to mimic the effects of natural estrogen derive from the similarity of phenol groups on both BPA and estradiol, which enable this synthetic molecule to trigger estrogenic pathways in the body.[26] Typically phenol-containing molecules similar to BPA are known to exert weak estrogenic activities, thus it is also considered an endocrine disrupter (ED) and estrogenic chemical.[27] Xenoestrogens is another category the chemical BPA fits under because of its capability to interrupt the network that regulates the signals which control the reproductive development in humans and animals.[28]
Health effects
The largest exposure humans have to BPA is by mouth from such sources as food packaging, the epoxy lining of metal food and beverage cans, and plastic bottles.[29][30]
BPA has been found to bind to both of the nuclear estrogen receptors (ERs), ERα and ERβ.[25] It is 1000- to 2000-fold less potent than estradiol.[25] BPA can both mimic the action of estrogen and antagonize estrogen, indicating that it is a selective estrogen receptor modulator (SERM) or partial agonist of the ER.[25] At high concentrations, BPA also binds to and acts as an antagonist of the androgen receptor (AR).[25] In addition to receptor binding, the compound has been found to affect Leydig cell steroidogenesis, including affecting 17α-hydroxylase/17,20 lyase and aromatase expression and interfering with LH receptor-ligand binding.[25]
In 1997, adverse effects of low-dose BPA exposure in laboratory animals were first proposed.[31] Modern studies began finding possible connections to health issues caused by exposure to BPA during pregnancy and during development. See US public health regulatory history and Chemical manufacturers reactions to bans. As of 2014, research and debates are ongoing as to whether BPA should be banned or not.
A 2007 study investigated the interaction between bisphenol A's and estrogen-related receptor γ (ERR-γ). This orphan receptor (endogenous ligand unknown) behaves as a constitutive activator of transcription. BPA seems to bind strongly to ERR-γ (dissociation constant = 5.5 nM), but only weakly to the ER.[32] BPA binding to ERR-γ preserves its basal constitutive activity.[32] It can also protect it from deactivation from the SERM 4-hydroxytamoxifen (afimoxifene).[32] This may be the mechanism by which BPA acts as a xenoestrogen.[32] Different expression of ERR-γ in different parts of the body may account for variations in bisphenol A effects. BPA has also been found to act as an agonist of the GPER (GPR30).[33]
According to the European Food Safety Authority "BPA poses no health risk to consumers of any age group (including unborn children, infants and adolescents) at current exposure levels".[34] But in 2017 the European Chemicals Agency concluded that BPA should be listed as a substance of very high concern due to its properties as an endocrine disruptor.[35]
In 2012, the United States' Food and Drug Administration (FDA) banned the use of BPA in baby bottles.[36]
The Environmental Protection Agency (EPA) also holds the position that BPA is not a health concern. In 2011, Andrew Wadge, the chief scientist of the United Kingdom's Food Standards Agency, commented on a 2011 U.S. study on dietary exposure of adult humans to BPA,[37] saying, "This corroborates other independent studies and adds to the evidence that BPA is rapidly absorbed, detoxified, and eliminated from humans – therefore is not a health concern."[38]
The Endocrine Society said in 2015 that the results of ongoing laboratory research gave grounds for concern about the potential hazards of endocrine-disrupting chemicals – including BPA – in the environment, and that on the basis of the precautionary principle these substances should continue to be assessed and tightly regulated.[39] A 2016 review of the literature said that the potential harms caused by BPA were a topic of scientific debate and that further investigation was a priority because of the association between BPA exposure and adverse human health effects including reproductive and developmental effects and metabolic disease.[40]
BPA substitutes
Concerns about the health effects of BPA have led many manufacturers to replace BPA with substitutes such as bisphenol S (BPS) and diphenyl sulfone. However, health concerns have been raised about these substitutes as well.[41]
Environmental effects
In 2010, the U.S. Environmental Protection Agency reported that over one million pounds of BPA are released into the environment annually.[42] BPA can be released into the environment by both pre-consumer and post-consumer leaching. Common routes of introduction from the pre-consumer perspective into the environment are directly from chemical plastics, coat and staining manufacturers, foundries who use BPA in casting sand, or transport of BPA and BPA-containing products.[43][44] Post-consumer BPA waste comes from effluent discharge from municipal wastewater treatment plants, irrigation pipes used in agriculture, ocean-borne plastic trash, indirect leaching from plastic, paper, and metal waste in landfills, and paper or material recycling companies.[43][44][45] Despite a rapid soil and water half-life of 4.5 days, and an air half-life of less than one day, BPA's ubiquity makes it an important pollutant. BPA has a low rate of evaporation from water and soil, which presents issues, despite its biodegradability and low concern for bio-accumulation. BPA has low volatility in the atmosphere and a low vapor pressure between 5.00 and 5.32 Pascals. Aqueous solutions of BPA absorbs at wavelengths greater than 250 nm.[46]
The ubiquitous nature of BPA makes the compound an important pollutant. It interferes with nitrogen fixation at the roots of leguminous plants associated with the bacterial symbiont Sinorhizobium meliloti.[47] BPA affects soybean seedlings with respect to root growth, nitrate production, ammonium production, and the activities of nitrate reductase and nitrite reductase. At low doses of BPA, the growth of roots were improved, the amount of nitrate in roots increased, the amount of ammonium in roots decreased, and the nitrate and nitrite reductase activities remained unchanged. However, at considerably higher concentrations of BPA, the opposite effects were seen for all but an increase in nitrate concentration and a decrease in nitrite and nitrate reductase activities.[48] Nitrogen is both a plant nutritional substance, but also the basis of growth and development in plants.
The amount of absorbed BPA on sediment was also seen to decrease with increases in temperature, as demonstrated by a study in 2006 with various plants from the Xiangjiang River in Central-South China. In general, as temperature increases, the water solubility of a compound increases. Therefore, the amount of sorbate that enters the solid phase will lower at the equilibrium point. It was also observed that the adsorption process of BPA on sediment is exothermic, the molar formation enthalpy, ΔH°, was negative, the free energy ΔG°, was negative, and the molar entropy, ΔS°, was positive. This indicates that the adsorption of BPA is driven by enthalpy. The adsorption of BPA has also been observed to decrease with increasing pH.[49]
A 2005 study conducted in the United States had found that 91–98% of BPA may be removed from water during treatment at municipal water treatment plants.[50] A more detailed explanation of aqueous reactions of BPA can be observed in the Degradation of BPA section below. Nevertheless, a 2009 meta-analysis of BPA in the surface water system showed BPA present in surface water and sediment in the U.S. and Europe.[51] According to Environment Canada in 2011, "BPA can currently be found in municipal wastewater. […]initial assessment shows that at low levels, bisphenol A can harm fish and organisms over time."[52]
BPA affects growth, reproduction, and development in aquatic organisms. Among freshwater organisms, fish appear to be the most sensitive species. Evidence of endocrine-related effects in fish, aquatic invertebrates, amphibians, and reptiles has been reported at environmentally relevant exposure levels lower than those required for acute toxicity. There is a widespread variation in reported values for endocrine-related effects, but many fall in the range of 1μg/L to 1 mg/L.[10]
A 2009 review of the biological impacts of plasticizers on wildlife published by the Royal Society with a focus on aquatic and terrestrial annelids, molluscs, crustaceans, insects, fish and amphibians concluded that BPA affects reproduction in all studied animal groups, impairs development in crustaceans and amphibians and induces genetic aberrations.[53]
Toxicity
BPA exhibits very low acute toxicity as indicated by its LD50 of 4 g/kg (mouse).[2]
References
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^ See:
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- Reprinted in condensed form in: A. Dianin (1892) "Condensationsproducte aus Ketonen und Phenolen" (Condensation products of ketones and phenols), Berichte der Deutschen chemischen Gesellschaft zu Berlin, 25, part 3 : 334-337.
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^ "Bisphenol A Fact Sheet". Government of Canada. Archived from the original on 23 April 2011. Retrieved 1 February 2012.
^ Oehlmann J, Schulte-Oehlmann U, Kloas W, Jagnytsch O, Lutz I, Kusk KO, Wollenberger L, Santos EM, Paull GC, Van Look KJ, Tyler CR (2009). "A critical analysis of the biological impacts of plasticizers on wildlife". Philosophical Transactions of the Royal Society B: Biological Sciences. 364 (1526): 2047–62. doi:10.1098/rstb.2008.0242. PMC 2873012. PMID 19528055.
Further reading
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Kabiersch G, Rajasärkkä J, Ullrich R, Tuomela M, Hofrichter M, Virta M, Hatakka A, Steffen K (April 2011). "Fate of bisphenol A during treatment with the litter-decomposing fungi Stropharia rugosoannulata and Stropharia coronilla". Chemosphere. 83 (3): 226–32. Bibcode:2011Chmsp..83..226K. doi:10.1016/j.chemosphere.2010.12.094. PMID 21295326.
Myers JP, vom Saal FS, Akingbemi BT, Arizono K, Belcher S, Colborn T, Chahoud I, Crain DA, Farabollini F, Guillette LJ, Hassold T, Ho SM, Hunt PA, Iguchi T, Jobling S, Kanno J, Laufer H, Marcus M, McLachlan JA, Nadal A, Oehlmann J, Olea N, Palanza P, Parmigiani S, Rubin BS, Schoenfelder G, Sonnenschein C, Soto AM, Talsness CE, Taylor JA, Vandenberg LN, Vandenbergh JG, Vogel S, Watson CS, Welshons WV, Zoeller RT (March 2009). "Why public health agencies cannot depend on good laboratory practices as a criterion for selecting data: the case of bisphenol A". Environ. Health Perspect. 117 (3): 309–15. doi:10.1289/ehp.0800173. PMC 2661896. PMID 19337501.
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