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Ethoxyquin
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Ethoxyquin[1]
Ethoxyquin
Ethoxyquin
Names
Preferred IUPAC name
6-Ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.001.887 Edit this at Wikidata
E number E324 (antioxidants, ...)
UNII
  • InChI=1S/C14H19NO/c1-5-16-11-6-7-13-12(8-11)10(2)9-14(3,4)15-13/h6-9,15H,5H2,1-4H3 checkY
    Key: DECIPOUIJURFOJ-UHFFFAOYSA-N checkY
  • InChI=1/C14H19NO/c1-5-16-11-6-7-13-12(8-11)10(2)9-14(3,4)15-13/h6-9,15H,5H2,1-4H3
    Key: DECIPOUIJURFOJ-UHFFFAOYAT
  • O(c2ccc1c(\C(=C/C(N1)(C)C)C)c2)CC
Properties
C14H19NO
Molar mass 217.312 g·mol−1
Melting point < 25 °C (77 °F; 298 K)
Boiling point 123–125 °C (253–257 °F; 396–398 K) at 2 mmHg
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Ethoxyquin (EMQ) is a quinoline-based antioxidant used as a food preservative in certain countries and originally to control scald on pears after harvest (under commercial names such as "Stop-Scald").[2] It is used as a preservative in some pet foods to slow the development of rancidity of fats. Ethoxyquin is also used in some spices to prevent color loss due to oxidation of the natural carotenoid pigments.[3]

Regulation

[edit]

Ethoxyquin was initially registered as a pesticide in 1965 as an antioxidant used as a deterrent of scald in pears through post-harvest indoor application via a drench and/or impregnated wrap.[3]

As an antioxidant to control the browning of pears, ethoxyquin is approved in the United States[3] and in the European Union.[2]

In the United States, it is approved for use as an animal feed additive[4] and is limited as a food additive to use only in the spices chili powder, paprika, and ground chili.[5] Ethoxyquin is not permitted for use as food additive in Australia[citation needed] nor within the European Union.[6]

Ethoxyquin is allowed in the fishing industry in Norway and France as a feed stabilizer, so is commonly used in food pellets fed to farmed salmon.[7]

Norway made this practice illegal when the EU suspended authorization in 2017 and in accordance with the suspension utilized a transition period which allowed the sale of feed containing ethoxyquin until December 31, 2019, after this date it was illegal to sell feed containing ethoxyquin. Feed containing ethoxyquin had to be used by June 20, 2020.[8]

Ethoxyquin is used in pellets fed to chickens on chicken farms.[9]

In 2017, the EU suspended authorization for use as a feed additive, with various dates between 2017 and 2019 for final allowance of sale of goods so that alternatives may be phased in.[10]

Safety

[edit]

Some speculation exists that ethoxyquin in pet foods might be responsible for multiple health problems. To date, the U.S. Food and Drug Administration has only found a verifiable connection between ethoxyquin and buildup of protoporphyrin IX in the liver, as well as elevations in liver-related enzymes in some animals, but no health consequences from these effects are known.[11] In 1997, the Center for Veterinary Medicine asked pet food manufacturers to voluntarily limit ethoxyquin levels to 75 ppm until further evidence is reported.[11] However, most pet foods that contain ethoxyquin have never exceeded this amount.[11]

In 2017, reports from the Swiss Department for regional affairs laboratory, service of consummation and veterinary affairs showed that farmed salmon often exceeded the set limits for ethoxyquin contamination by several orders of magnitude and that health effects of the chemical on the human body were not studied in sufficient detail.[12] In 2013, researchers at the Department of General Genetics, Molecular Biology and Plant Biotechnology, Faculty of Biology and Environmental Protection, University of Łódź, Poland, summarized the health effects of animals and humans exposed to varying levels of ethoxyquin observed in scientific studies. The summary includes: loss of weight, changes in liver, kidney, alimentary duct, urinary bladder and mitochondria, anemia, lethargy, discolored urine, skin, or fur, increase in mortality, detrimental effect on immunity, condition factor of final body weight in relation to body length of fish and inducement of allergies (contact exposure).[13]

2015 EFSA review

[edit]

A 2015 review by the European Food Safety Authority indicated that data to assess the safety of ethoxyquin as a feed additive for target animals, or its safety for consumers and the environment are lacking.[14] The agency found one of its metabolites, ethoxyquin quinone imine, to be possibly genotoxic, and p-phenetidine, an impurity that could be present from the manufacturing process, to be possibly mutagenic.[2] In response, feed manufacturers have taken steps to significantly reduce the amount of p-phenetidine in their products.[15]

See also

[edit]

References

[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia

Ethoxyquin

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from Grokipedia
Ethoxyquin, chemically known as 6-ethoxy-1,2-dihydro-2,2,4-trimethylquinoline with the molecular formula C₁₄H₁₉NO and CAS number 91-53-2, is a synthetic primarily utilized as a feed additive to prevent in feeds rich in polyunsaturated fats, such as fishmeal and pet foods. Developed in the mid-20th century, it effectively stabilizes fats and vitamins against oxidative degradation at low concentrations, thereby extending and maintaining in compounded feeds. In the United States, the (FDA) authorizes its inclusion in feeds with mandatory labeling to presence and concentrations do not exceed safe-use limits, typically up to 150 mg/kg in complete feeds. Regulatory evaluations by the (EFSA) affirm its safety for meat-producing animals like , pigs, , rabbits, and certain at levels up to 50 mg/kg complete feed, citing no evidence of or carcinogenicity from the additive itself, though residues pose concerns for , , and some aquaculture products. Despite its efficacy, ethoxyquin has encountered controversies over potential impurities, bioaccumulation in food chains, and incomplete data, prompting temporary suspensions in the EU and ongoing scrutiny in global markets, balanced against empirical demonstrations of its role in averting feed spoilage and related economic losses.

Chemical Properties

Molecular Structure and Synthesis

Ethoxyquin possesses the molecular formula C₁₄H₁₉NO and a molar mass of 217.31 g/mol. Its systematic name is 6-ethoxy-1,2-dihydro-2,2,4-trimethyl, featuring a partially saturated quinoline core with methyl groups at the 2-position, an additional methyl at the 4-position, and an ethoxy substituent on the ring at the 6-position. The includes a secondary at the 1-position and a between carbons 3 and 4 in the heterocyclic ring, contributing to its properties through radical scavenging. The compound is synthesized via acid-catalyzed condensation of p-phenetidine (4-ethoxyaniline) with acetone. This reaction proceeds through initial formation followed by cyclization and dehydration to form the dihydroquinoline ring, often employing iodine or other catalysts to facilitate the process. Industrial production typically involves under vacuum to purify the resulting viscous liquid, which solidifies into a glass-like state upon cooling. Variations may incorporate analogues of acetone or alternative catalysts, but the p-phenetidine-acetone route remains the standard method due to its efficiency and accessibility of precursors.

Physical and Chemical Characteristics

Ethoxyquin is a viscous, pale yellow to amber liquid at , with a faint amine-like . Its molecular formula is C14H19NO, and the molecular weight is 217.31 g/mol. The compound has a below 0 °C and a of 123–125 °C at 2 mmHg (approximately 0.0027 atm). Density measures 1.03 g/mL at 20 °C, with a of 1.569–1.571. Vapor pressure is low at 0.035 Pa (25 °C), indicating minimal volatility under standard conditions. Ethoxyquin exhibits low solubility in water, less than 1 mg/mL at 20 °C, but is miscible with many organic solvents, including acetone, ethanol, and chloroform, as well as fats and oils. Chemically, ethoxyquin is stable under normal storage conditions but sensitive to light and air, where it may darken, polymerize, or form dimers upon prolonged exposure; hazardous polymerization can occur above 160 °C.
PropertyValue
Molecular formulaC14H19NO
Molecular weight217.31 g/mol
AppearanceViscous yellow-amber
Melting point< 0 °C
Boiling point123–125 °C at 2 mmHg
Density (20 °C)1.03 g/mL
Water solubility (20 °C)< 1 mg/mL

Historical Development

Discovery and Initial Research

Ethoxyquin (6-ethoxy-1,2-dihydro-2,2,4-trimethylquinoline) was first synthesized in 1921 by German chemist Emil Knoevenagel through a condensation reaction involving aniline and acetone or related carbonyl compounds, though this early preparation did not immediately lead to practical applications. Its recognition as a potent antioxidant emerged later, with initial commercial development in the mid-20th century by Monsanto Chemical Company, which identified its efficacy in preventing oxidative degradation of isoprene polymers in the rubber industry. Monsanto's early research demonstrated ethoxyquin's ability to act as a radical-trapping agent, inhibiting chain reactions of free radicals that cause polymer cracking and deterioration under exposure to oxygen and heat. Building on these findings, Monsanto expanded research in the 1950s to explore ethoxyquin's broader stabilizing properties, refining its formulation for cost-effective industrial use while confirming low volatility and high thermal stability compared to other quinoline derivatives. Initial toxicity assessments in laboratory animals, including dogs, indicated minimal acute effects at dietary levels intended for feed preservation, supporting its transition from rubber stabilization to potential food and agricultural applications. These studies emphasized ethoxyquin's lipophilic nature, enabling it to partition into lipid phases and quench peroxyl radicals effectively, a mechanism validated through peroxide value measurements in oxidized fats. By the early 1960s, Monsanto's research culminated in patent filings for tetrahydroquinoline antioxidants, including analogs, which detailed synthetic methods and stabilization performance in organic materials. This groundwork led to its 1965 registration by the U.S. Environmental Protection Agency as a pesticide for post-harvest treatment of pears, where it prevented scald by suppressing enzymatic browning and lipid oxidation during storage, marking the first approved agricultural use based on field trials showing reduced fruit loss rates of up to 50%.

Commercial Introduction and Expansion

Ethoxyquin was developed by Monsanto Chemical Company in the 1950s as a synthetic antioxidant, with initial commercial applications focusing on preventing oxidation in animal feeds and rubber products before expanding to agricultural uses such as post-harvest treatment of pears. Its efficacy in stabilizing fats against peroxidation prompted early adoption in livestock and pet feeds, where it was reported in use by 1959 to extend shelf life and maintain nutritional quality. A key milestone came with U.S. Patent 2,989,963 granted to on June 27, 1961, covering agricultural processes involving ethoxyquin, which facilitated broader commercialization. The compound received initial U.S. pesticide registration in 1965 for controlling scald in pears, but its primary market growth occurred through animal feed preservation, driven by rising demand for processed feeds in poultry, aquaculture, and pet nutrition industries. By 1970, ethoxyquin was authorized as a feed additive in the European Union under early regulatory frameworks, supporting its integration into dehydrated forage and fish meal to mitigate lipid rancidity. Production scaled rapidly, reaching up to 1,000,000 pounds annually in the U.S. by 1977 across three manufacturing plants, reflecting expanded use amid growing global animal agriculture. Further expansion in the late 20th century aligned with surges in pet food markets and intensive farming, where ethoxyquin's cost-effectiveness and potency as a quinoline-based stabilizer outperformed some natural alternatives in high-fat feeds. This period saw its routine inclusion at levels up to 150 ppm in U.S. feeds, bolstering supply chain stability for exported products like rendered fats and meals, though production data post-1977 remains less granular in public records.

Applications and Efficacy

Use in Animal Feed and Pet Food

Ethoxyquin serves as a synthetic antioxidant in animal feed to prevent lipid peroxidation, particularly in ingredients prone to oxidation such as fish meal, poultry fat, and vegetable oils. It is incorporated during feed manufacturing to stabilize fats and vitamins, thereby extending shelf life and preserving nutritional value. The U.S. Food and Drug Administration (FDA) permits its use in animal feeds under 21 CFR 573.380 and 573.400, specifying safe incorporation levels based on feed type and animal species. In practice, ethoxyquin is commonly applied to fish meal cargoes during international shipping to comply with International Maritime Organization requirements, which mandate at least 100 mg/kg of ethoxyquin or an equivalent antioxidant to inhibit spontaneous combustion and rancidity. Studies demonstrate its efficacy in fish meal, where it reduces peroxide values and maintains protein quality, outperforming some alternatives in oxidative stability tests. For complete animal feeds, typical inclusion rates range from 50 to 150 mg/kg, with the (EFSA) assessing it as efficacious and safe at 50 mg/kg for all species, supporting its role in mitigating feed degradation under storage conditions. For pet food, ethoxyquin is utilized similarly to safeguard rendered fats and fish-derived proteins in dry kibble and canned formulations, where oxidation can lead to off-flavors and nutrient loss. The FDA sets a maximum of 150 mg/kg (ppm) in pet foods, though the Center for Veterinary Medicine has encouraged voluntary reduction to below 75 ppm, a level most manufacturers adhere to. Research confirms its antioxidant performance in pet food matrices, correlating with lower thiobarbituric acid reactive substances (TBARS) values indicative of reduced rancidity. Despite efficacy, its application in pet foods has prompted scrutiny, with some producers opting for natural alternatives amid consumer preferences, though regulatory approvals affirm its functionality at approved doses.

Other Industrial and Agricultural Uses

Ethoxyquin was originally developed in the mid-20th century by the rubber industry as an antioxidant to inhibit the oxidation of , thereby preventing cracking and degradation in rubber products. It functions as an anti-degradation agent by scavenging free radicals and stabilizing polymer chains against oxidative breakdown, a role that persists in some industrial formulations despite shifts toward alternative stabilizers. Historical production data indicate its application in tire manufacturing and other elastomer processing, where concentrations up to 1-2% were employed to extend material lifespan under thermal and oxidative stress. In agriculture, ethoxyquin has been utilized as a post-harvest treatment to control superficial scald in apples and pears, applied as a dip or drench at concentrations of 1000-3000 ppm to inhibit ethylene-induced oxidation of alpha-farnesene in fruit skin. This pesticidal application, registered by the U.S. Environmental Protection Agency for indoor processing of pears, targets enzymatic browning and storage disorders without leaving significant residues on edible portions when used per good agricultural practices. Earlier formulations also served as a herbicide and pesticide, though these uses have been largely superseded by more selective compounds since the 1980s due to efficacy limitations and regulatory scrutiny. Current agricultural deployment remains limited to specific fruit preservation protocols, with efficacy demonstrated in reducing scald incidence by up to 90% in controlled storage trials.

Demonstrated Benefits in Oxidation Prevention

Ethoxyquin acts as a potent synthetic antioxidant in animal feeds by scavenging free radicals and chelating metal ions that catalyze lipid peroxidation, thereby interrupting the oxidative chain reactions that degrade unsaturated fats. Its efficacy stems from the quinoline ring structure, which donates hydrogen atoms to stabilize peroxyl radicals formed during fat oxidation. In practical applications, ethoxyquin prevents rancidity in high-fat feeds like those containing fish meal or rendered animal fats, maintaining palatability and nutritional integrity over extended storage periods of up to several months under ambient conditions. For instance, inclusion at levels of 125-150 mg/kg feed has been shown to significantly lower thiobarbituric acid (TBA) values and peroxide numbers in poultry and swine diets, indicating reduced secondary oxidation products compared to unsupplemented controls. Ethoxyquin also stabilizes fat-soluble vitamins and carotenoids; it retards the degradation of vitamin E (tocopherols), vitamin A precursors like carotenes, and xanthophyll pigments, preserving their bioavailability in feeds exposed to heat, light, or air during pelleting and transport. Comparative trials in extruded pet foods demonstrate that ethoxyquin outperforms or matches natural alternatives in extending oxidative stability indices (OSI) by 20-50%, particularly in omega-3 rich formulations prone to rapid peroxidation. Notably, ethoxyquin's oxidation metabolites, such as ethoxyquin dimer (EQDM) and quinoline imine (QI), retain 69% and 80% of the parent compound's antioxidative potency, respectively, providing sustained protection even as the additive partially degrades. This residual activity contributes to its effectiveness in preventing protein oxidation alongside lipids, as evidenced by lower carbonyl content in treated feed samples stored for 12 weeks.

Regulatory History

Approvals in the United States

Ethoxyquin is regulated by the United States Food and Drug Administration (FDA) as a permitted food additive for animal feed under Title 21 of the Code of Federal Regulations (CFR), specifically § 573.380, which authorizes its use to retard oxidation of carotene, xanthophylls, and vitamins A and E. The regulation specifies that it may be safely incorporated into complete animal feeds at concentrations not exceeding 150 parts per million (ppm), with additional allowances up to 200 ppm in fish feed prior to pelleting and in certain dehydrated forage products under § 573.400. Labeling of feeds containing ethoxyquin is mandatory, requiring declaration as "Ethoxyquin, a preservative" or the phrase "ethoxyquin added to retard the oxidative destruction of carotene, xanthophylls, and vitamins A and E." Residues of ethoxyquin in edible tissues and products from treated animals are subject to FDA-established tolerances to ensure human food safety, including 5 ppm in uncooked fat from cattle, sheep, and swine (excluding poultry), 3 ppm in poultry fat and liver, 0.5 ppm in eggs and muscle meat, and 0 ppm in milk. These tolerances reflect evaluations of potential carryover from feed to animal-derived foods, with the FDA determining that approved use levels do not pose unacceptable risks based on available toxicological data. In 1977, the FDA requested voluntary reduction of maximum ethoxyquin levels in certain feeds following industry-submitted data from Monsanto Company tests, though the core approval framework remained intact. By 1990, the FDA nominated ethoxyquin for further carcinogenicity testing due to emerging questions about long-term effects, but subsequent reviews affirmed its safety for approved uses without altering authorization. As of January 2024, ethoxyquin retains full FDA approval for these applications, with no suspensions or bans implemented, distinguishing U.S. policy from more restrictive international measures.

European Union Assessments and Restrictions

In 2015, the (EFSA) conducted an assessment of ethoxyquin as a feed additive and concluded that insufficient data existed to evaluate its safety for target animals, consumers, or the environment, citing gaps in toxicological studies and residue data. This led to recommendations for further research on genotoxicity, carcinogenicity, and long-term effects. Following the EFSA's inconclusive findings, the European Commission issued Implementing Regulation (EU) 2017/962 on June 28, 2017, suspending 's authorization as a feed additive for all animal species and categories pending submission of supplementary safety data by the applicant. The suspension allowed transitional measures for existing stocks until August 2020, after which use in feed production was prohibited. EFSA revisited the additive in a 2022 opinion, determining that ethoxyquin at a maximum of 50 mg/kg complete feed posed no direct risk to most animal species (except certain sensitive groups like fish and rabbits, where data remained inadequate) but could not conclude on consumer safety due to uncertainties in residue metabolism and potential impurities like p-phenetidine. Environmental risks were also unresolvable without additional exposure modeling. On August 8, 2022, Commission Implementing Regulation (EU) 2022/1375 repealed the 2017 suspension but refused reauthorization, confirming a permanent prohibition on ethoxyquin in animal feed across the EU due to unresolved data deficiencies despite the applicant's submissions. This decision aligned with the EU's precautionary approach under Regulation (EC) No 1831/2003, prioritizing comprehensive safety validation over historical use patterns. Post-2020, enforcement has included monitoring residues in imported feeds, with violations noted in some seafood products exceeding prior limits.

International Variations and Bans

In the European Union, the authorization of ethoxyquin as a feed additive for all animal species was suspended in June 2017 under Commission Implementing Regulation (EU) 2017/962, following concerns raised by the European Food Safety Authority regarding data gaps in toxicological assessments. This suspension was made permanent in August 2022 via Commission Implementing Regulation (EU) 2022/1375, which refused reauthorization due to insufficient evidence demonstrating safety for users, consumers, and the environment, effectively prohibiting its use in animal feed, including imported fish meal. The United Kingdom aligned with these restrictions post-Brexit, rejecting fish and fish products containing detectable ethoxyquin residues. Vietnam implemented a ban on ethoxyquin in aquaculture feeds in January 2020, as announced by the Ministry of Agriculture and Rural Development, to mitigate potential residue accumulation in seafood products amid heightened food safety scrutiny. This measure tightened controls on preservatives in aquafeeds, reflecting localized concerns over long-term exposure risks in farmed species. Regulatory approaches vary significantly elsewhere, with ethoxyquin remaining authorized in numerous jurisdictions for feed preservation, particularly in fish meal to prevent oxidation during storage and transport. In Australia, it is permitted as a feed additive subject to maximum residue limits in domestically sold products, though exports to the EU and UK face rejection risks if residues exceed zero tolerance. Canada allows its inclusion in pet foods and feeds, as evidenced by export certification guidelines addressing EU import barriers without domestic prohibitions. Japan, along with China, South Korea, and the United States, continues to permit ethoxyquin in fish meal production, facilitating global trade in preserved marine ingredients despite EU restrictions. These permissions often hinge on established maximum residue levels and historical efficacy data, contrasting with the EU's precautionary suspension amid unresolved impurity and metabolite concerns.
Country/RegionStatusKey Details
European UnionProhibitedSuspension June 2017; refusal August 2022; zero tolerance for imports.
United KingdomProhibitedAligned with EU; rejects residues in fish imports.
VietnamProhibited in aquacultureBan effective January 2020 on aquafeed use.
AustraliaPermittedAllowed with MRLs for domestic feed; export cautions to EU/UK.
CanadaPermittedAuthorized in feeds; EU export notes highlight denial elsewhere.
JapanPermittedUsed in fish meal; no reported bans.
Such divergences have prompted trade frictions, with EU import controls necessitating residue testing for fish meal from permitting countries, potentially increasing costs and limiting supply chains reliant on ethoxyquin-stabilized products.

Safety and Toxicology

Key Studies on Animal and Human Effects

In sub-chronic oral toxicity studies in rats and dogs, ethoxyquin exposure led to pathological changes primarily in the liver and kidneys, with increased organ weights and hepatocellular hypertrophy observed at doses exceeding 100 mg/kg body weight per day. A one-year chronic toxicity study in dogs, which formed part of the basis for initial FDA approval, identified no adverse effects at dietary levels up to 150 mg/kg feed, though higher doses were associated with reduced body weight gain and mild liver enzyme elevations. In a two-year combined chronic toxicity and carcinogenicity study in F344 rats fed ethoxyquin at 0, 160, 800, or 4000 ppm, the no-observed-adverse-effect level (NOAEL) was determined to be 160 ppm (approximately 8 mg/kg body weight per day), with urinary bladder tumors noted only in female rats at the highest dose of 4000 ppm, suggesting potential carcinogenic risk under extreme exposure conditions not reflective of typical feed use. The Joint FAO/WHO Expert Committee on Food Additives (JMPR) evaluated these data in 1998 and established a NOEL of 125 ppm (6 mg/kg body weight per day) from rat studies, with no evidence of carcinogenicity at relevant doses. Reproductive and developmental toxicity assessments, including a two-generation study in beagle dogs at doses up to 300 mg/kg body weight per day, showed no effects on fertility, gestation, or offspring viability, supporting a NOAEL of 100 mg/kg body weight per day. The European Food Safety Authority (EFSA) in 2015 concluded that ethoxyquin itself is neither genotoxic nor carcinogenic and does not induce developmental toxicity, deriving a lowest NOAEL of 2 mg/kg body weight per day across rat and dog studies for consumer safety extrapolations. A 2022 EFSA re-evaluation affirmed safety for animal species at 50 mg/kg complete feed, though impurities like p-phenetidine raised concerns for margins of safety in target animals. Human effects data are sparse, with no direct epidemiological studies linking ethoxyquin exposure to adverse outcomes, as it is not intended for human consumption. An in vitro study on human peripheral lymphocytes exposed to ethoxyquin concentrations of 0.1–1 mM reported dose-dependent DNA damage via comet assay, indicating potential genotoxicity under isolated cellular conditions. However, regulatory assessments, including those by EFSA and the Norwegian Institute of Nutrition and Seafood Research, find no evidence of human health effects from typical dietary residues, attributing low risk to minimal exposure levels (e.g., below 0.01 mg/kg body weight per day via animal products). Biomonitoring efforts from 2000–2021 in European populations detected ethoxyquin metabolites in urine but correlated them with negligible toxicological concern, consistent with EPA findings of moderate acute oral toxicity (LD50 ~1–2 g/kg in rats) but no chronic human-relevant hazards at trace exposures.

Impurities and Residue Concerns

Ethoxyquin formulations may contain impurities such as p-phenetidine, a potential mutagen present at concentrations below 2.5 mg/kg in the additive, as identified in manufacturing specifications evaluated by regulatory bodies. Oxidation products and related transformation products (TPs) can also form during storage or processing, contributing to impurity profiles that require analytical monitoring, with the sum of ethoxyquin-related impurities often calculated by difference in quality assessments. Residues of ethoxyquin and its metabolites, including the dimer ethoxyquin dimer (EQDM), ethoxyquin imine (EQI), and dihydroethoxyquin (DHEQ), have been detected in edible tissues of animals fed ethoxyquin-supplemented diets. In piglets fed up to 150 mg/kg feed, residue levels reached 1,713 µg/kg in fat, 84 µg/kg in liver, and 71 µg/kg in muscle; similar patterns occur in cattle (231 µg/kg fat), laying hens (575 µg/kg fat, 46 µg/kg eggs), and salmon (294 µg/kg total EQ + EQDM in flesh). In swine tissues, these residues remain below levels posing consumer hazards even at higher feed inclusions, according to liquid chromatography analyses. United States regulations establish tolerances for ethoxyquin residues in animal-derived products, including 5 ppm in fat from treated animals and 0.5 ppm in uncooked eggs and liver, reflecting assessments that dietary exposure from approved uses poses low risk. However, the European Food Safety Authority (EFSA) has expressed inability to fully conclude on consumer safety due to toxicological data gaps on metabolites like EQDM—whose potential adverse effects remain undetermined—and insufficient residue studies for impurities such as p-phenetidine in dairy products. These uncertainties stem from limited genotoxicity data on certain metabolites, though ethoxyquin itself shows no genotoxic or carcinogenic effects in available studies. No widespread evidence links residues to human health harms at regulated levels, but ongoing monitoring addresses potential bioaccumulation in aquatic species.

Environmental and Long-Term Exposure Data

Limited data exist on the environmental persistence of ethoxyquin, with no quantitative information available on its degradation rates in soil or water bodies. Ecotoxicity assessments indicate moderate toxicity to fish (LC50 >10 mg/L for species such as ) and aquatic invertebrates (EC50 >10 mg/L for ), suggesting potential risks to aquatic ecosystems at elevated concentrations. In simulations, ethoxyquin introduction via industrial effluents has been shown to increase organic loading, potentially complicating microbial degradation processes and leading to incomplete removal. The (EFSA) has stated that insufficient data prevent conclusions on ethoxyquin's safety for the environment, particularly regarding in non-target organisms. Residues of ethoxyquin have been detected in wild and farmed aquatic species, including (Salmo salar), where it accumulates in muscle tissue following dietary exposure in feed, with depuration occurring over weeks post-exposure cessation. Studies on soil microbial communities exposed to ethoxyquin-contaminated pesticides report dissipation half-lives of 10-20 days under aerobic conditions, alongside transient shifts in microbial respiration and enzymatic activity, though long-term disruptions remain unquantified. Long-term exposure data in animals derive primarily from chronic feeding studies, where ethoxyquin at levels up to 1500 mg/kg diet showed no carcinogenic or reproductive effects in rats over 2 years, per U.S. EPA evaluations, supporting a reference dose (RfD) of 0.004 mg/kg body weight/day for chronic human exposure. In and models, dietary inclusions of 50-100 mg/kg feed over months elicited no observed adverse effects on organ function or growth, as assessed by EFSA in 2022, though impurities like p-phenetidine may contribute to minor at higher doses. Human from 2000 to 2021 reveals declining urinary metabolite levels (e.g., ethoxyquin dimer from 1.2 µg/g in 2000 to below detection limits by 2021), attributed to reduced use in animal feeds, with primary exposure routes via consumption of preserved meats and . No direct long-term human cohort studies exist, and regulatory assessments rely on animal extrapolations, noting absence of or developmental toxicity in available mammalian data.

Controversies and Debates

Allegations of Toxicity and Health Risks

Allegations of for ethoxyquin have primarily centered on its potential to cause liver damage, reproductive dysfunction, and carcinogenic effects in animals, particularly dogs and cats consuming preserved pet foods. Reports from dog breeders and owners since the late have linked chronic exposure to ethoxyquin-containing diets with and problems, allergies, autoimmune disorders, behavioral issues, and increased cancer incidence, though these claims often rely on anecdotal observations rather than controlled epidemiological . In dogs, the minimal effect level has been identified at 100 ppm (approximately 2.5 mg/kg body weight per day), where clinical signs and liver alterations, including elevations and accumulation, were observed. High-dose studies in laboratory animals have fueled further concerns about organ toxicity. In dogs, subchronic exposure at 20 mg/kg/day led to liver enzyme elevations, bile stasis, glycogen depletion, and histopathological changes such as necrosis, establishing this as a LOAEL with a NOAEL of 4 mg/kg/day for chronic effects. Rats exhibited kidney hyperplastic and preneoplastic tubules suggestive of carcinogenic potential, alongside increased liver weights and lesions at doses exceeding 250 mg/kg/day. Ethoxyquin and its dimer metabolite (EQDM) have demonstrated DNA damage and chromosome aberrations in human lymphocytes in vitro, with IC₅₀ values around 0.09 mM, raising genotoxicity alarms despite equivocal Ames test results. Carcinogenicity allegations persist due to findings of urinary tumors in rats at ≥1000 ppm (16% incidence at 2500 ppm), attributed to nongenotoxic tumor promotion rather than . The U.S. FDA nominated ethoxyquin for further carcinogenicity testing in 1998 based on equivocal data and reports of enhanced mutagenicity from known carcinogens like DMBA, though it also inhibits aflatoxin-induced liver lesions in some models. Impurities such as p-phenetidine, occasionally present, have been flagged for potential carcinogenicity, amplifying distrust among critics. These concerns have prompted calls for bans or label disclosures, particularly in pet foods where residues may accumulate from fishmeal preservatives.

Empirical Evidence Supporting Safe Use

Toxicological studies have demonstrated that ethoxyquin exhibits low acute oral in laboratory animals, with LD50 values exceeding 5,000 mg/kg body weight in rats and mice, indicating minimal risk at typical exposure levels. Ethoxyquin itself has been found not to be genotoxic, carcinogenic, or developmentally toxic based on and assays, including Ames tests, chromosomal aberration studies, and multi-generation reproduction trials in . These findings stem from controlled experiments evaluating DNA damage, mutagenicity, and tumor induction, where no adverse effects were observed attributable to the parent compound at doses up to the identified no-observed-adverse-effect levels (NOAELs). Subchronic and chronic feeding studies in rats and dogs established a NOAEL of 2 mg/kg body weight per day, the lowest value derived from histopathological examinations showing no significant organ damage, growth impairment, or clinical signs at this threshold. This NOAEL supports safe inclusion levels in , with the (EFSA) concluding in 2022 that ethoxyquin is safe for all target animal species at up to 50 mg/kg complete feed, based on margin-of-exposure calculations incorporating metabolism and residue data from , pigs, and trials. Similarly, the U.S. (FDA) permits ethoxyquin as a in animal feeds at a maximum of 150 parts per million, reflecting reviewed data affirming no unacceptable risks to or pets at these concentrations. Target animal tolerance studies, including those on chickens for fattening and salmonids, reported no adverse effects on performance, mortality, or organ when ethoxyquin was administered at proposed use levels, further corroborating its safety profile for preserving fats in high-unsaturated feed ingredients like fishmeal. These empirical results, derived from peer-reviewed regulatory assessments, underscore ethoxyquin's utility without eliciting toxicity endpoints in production animals under standard conditions.

Critiques of Regulatory Decisions

The suspension of ethoxyquin authorization as a feed additive across the via Commission Implementing Regulation (EU) 2017/962, effective from June 2017, has been critiqued by feed industry representatives for relying on the amid data gaps rather than affirmative evidence of harm. The European Feed Manufacturers' Federation (FEFAC) contends that the European Food Safety Authority's (EFSA) 2015 assessment affirmed ethoxyquin's safety for target animals at proposed use levels up to 150 mg/kg feed, deeming it non-genotoxic and non-carcinogenic, with subsequent concerns arising from impurities like p-phenetidine (limited to <2.5 mg/kg in approved products) and insufficient modern studies on transformation products, rather than direct toxicity observations. Industry analyses highlight ethoxyquin's proven track record since the 1950s in preventing in animal feeds, particularly fishmeal, where it maintains stability during global transport as required by guidelines (minimum 100 mg/kg ). Critics argue that the EU's approach imposes undue burdens by mandating retrospective data under contemporary standards for a substance with no documented incidents from residues, contrasting sharply with the U.S. Food and Drug Administration's (FDA) ongoing approval for use up to 150 ppm in animal feeds and ingredients, backed by evaluations showing no adverse effects at those levels. EFSA's 2022 reassessment resolved some concerns but retained inconclusiveness for long-living or reproductive animals, consumers via residues, and environmental endpoints due to lingering gaps, prompting continued restrictions despite no identified risks from monitored exposure levels. FEFAC and stakeholders criticize this as regulatory inertia, potentially disrupting feed supply chains by limiting access to stabilized imports while third-country products treated with ethoxyquin enter the market, thus yielding negligible safety gains at the expense of nutritional efficacy and economic viability. Proponents of stricter scrutiny, including some environmental groups, defend the framework for prioritizing comprehensive over historical use, yet detractors emphasize causal realism: absent empirical links between approved doses and outcomes in multi-decade applications, the decisions exemplify overregulation that favors hypothetical risks over verifiable benefits in feed preservation.

Alternatives and Market Dynamics

Synthetic and Natural Substitutes

Synthetic substitutes for ethoxyquin primarily consist of other phenolic antioxidants such as (BHA), (BHT), tertiary butylhydroquinone (TBHQ), and , which inhibit in animal feeds and fats. These compounds have been formulated into blended products like Extend-OX™ 10E and Noxyfeed, designed as direct 1:1 replacements for ethoxyquin in fishmeal and feeds, maintaining oxidative stability comparable to ethoxyquin at dosages of 100-150 ppm. Combinations including , lignosulfonic acid, and have demonstrated equivalent or superior protection against rancidity in EU-compliant feeds post-2017 ethoxyquin restrictions, with peroxide values remaining below 5 meq/kg after 6 months of storage under accelerated conditions. Natural alternatives emphasize plant-derived antioxidants, including mixed tocopherols (forms of ), rosemary extracts (rich in and rosmarinic acid), and polyphenols, which scavenge free radicals to preserve feed quality without synthetic residues. Mixed tocopherols at 200-400 ppm effectively stabilize omega-3-rich pet foods and fish oils, outperforming ethoxyquin in some shelf-life tests by reducing () by up to 70% over 12 weeks, though they require higher inclusion levels and increase costs by 2-5 times compared to synthetics. Partial substitution with polyphenols (from ) and in broiler feeds improved liver antioxidant enzyme activity ( up 25%) and feed stability, as evidenced by a poultry trial where oxidative indices were 15-20% lower than ethoxyquin controls after 42 days. Other botanical options, such as , extract, and , have shown promise in stabilizing rendered fats and kibble, with reducing oxidation in by 40-60% relative to controls in stability assays, though varies with matrix pH and moisture content. Plant feed additives broadly serve as viable ethoxyquin replacements in poultry nutrition, enhancing growth performance without synthetic drawbacks, per a 2021 meta-analysis of trials demonstrating reduced levels in meat by 10-30%. Despite these benefits, natural substitutes often underperform synthetics in high-heat processes or tropical storage, necessitating synergistic blends with chelators like for optimal results. The global ethoxyquin market, valued at USD 219.2 million in 2022, is predominantly driven by its role as a synthetic antioxidant in animal feed, where it prevents lipid peroxidation, rancidity, and nutrient degradation, thereby minimizing economic losses from feed spoilage estimated to affect up to 10-20% of stored fats in untreated feeds. This application supports cost efficiencies for livestock producers and pet food manufacturers by extending shelf life—often from weeks to months—and preserving high-value components like fishmeal and vegetable oils, with annual global feed production exceeding 1 billion tons where antioxidants like ethoxyquin comprise a low-cost additive at concentrations of 100-200 ppm. In regions with intensive animal agriculture, such as North America and Asia-Pacific, ethoxyquin's use correlates with reduced operational costs, contributing to market growth at a projected CAGR of 4.5-5.8% through 2030, fueled by rising meat and pet food demand. Regulatory restrictions pose significant economic challenges, including the European Union's 2022 ban on ethoxyquin in following 2017 EFSA toxicity concerns, which has compelled EU producers to reformulate feeds with alternatives, incurring transition costs estimated in millions for large-scale operations and disrupting supply chains for imported fishmeal. Outside the EU, continued approvals—such as FDA tolerance in the —sustain market viability, but global scrutiny over residues and environmental persistence may elevate compliance expenses, with some governments proposing usage limits that could shrink by 10-15% in affected regions by 2030. Future trends indicate moderated growth to USD 278-367 million by 2030-2033, tempered by a shift toward natural s like tocopherols and extracts amid consumer preferences for "clean label" products and mandates, potentially eroding ethoxyquin's cost advantage in premium pet foods. Innovations in hybrid preservatives and stricter residue monitoring may extend its niche in industrial feeds, but persistent debates could accelerate phase-outs in export-oriented markets, favoring diversified portfolios to mitigate regulatory risks.

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