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Betanin
Betanin
Betanin
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Betanin
Names
IUPAC name
(2S)-1-{2-[(2S)-2,6-dicarboxy-2,3-dihydropyridin-4(1H)-ylidene]ethylidene}-5-(β-d-glucopyranosyloxy)-6-hydroxy-2,3-dihydro-1H-indol-1-ium-2-carboxylate
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.028.753 Edit this at Wikidata
E number E162 (colours)
KEGG
UNII
  • InChI=1S/C24H26N2O13/c27-8-17-18(29)19(30)20(31)24(39-17)38-16-6-10-5-14(23(36)37)26(13(10)7-15(16)28)2-1-9-3-11(21(32)33)25-12(4-9)22(34)35/h1-3,6-7,12,14,17-20,24,27,29-31H,4-5,8H2,(H4,28,32,33,34,35,36,37)/t12-,14-,17+,18+,19-,20+,24+/m0/s1 ☒N
    Key: DHHFDKNIEVKVKS-FMOSSLLZSA-N ☒N
  • InChI=1/C24H26N2O13/c27-8-17-18(29)19(30)20(31)24(39-17)38-16-6-10-5-14(23(36)37)26(13(10)7-15(16)28)2-1-9-3-11(21(32)33)25-12(4-9)22(34)35/h1-3,6-7,12,14,17-20,24,27,29-31H,4-5,8H2,(H4,28,32,33,34,35,36,37)/t12-,14-,17+,18+,19-,20+,24+/m0/s1
    Key: DHHFDKNIEVKVKS-FMOSSLLZBW
  • InChI=1/C24H26N2O13/c27-8-17-18(29)19(30)20(31)24(39-17)38-16-6-10-5-14(23(36)37)26(13(10)7-15(16)28)2-1-9-3-11(21(32)33)25-12(4-9)22(34)35/h1-3,6-7,12,14,17-20,24,27-31H,4-5,8H2,(H,32,33)(H,34,35)(H,36,37)/b2-1+/t12?,14-,17+,18+,19-,20+,24+/m0/s1
    Key: CTMLKIKAUFEMLE-BOKBUZBTBZ
  • OCC1[C@@H](O)[C@@H](O)[C@H](O)[C@@H](OC2=C(O)C=C(/[N+]([C@@H]([C@]([O-])=O)C4)=C/C=C3\C[C@H]([C@](O)=O)NC(C(O)=O)=C3)C4=C2)O1
Properties
C24H26N2O13
Molar mass 550.47 g/mol
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 ?)

Betanin, or beetroot red, is a red glycosidic food dye obtained from beets; its aglycone, obtained by hydrolyzing the glucose molecule, is betanidin. As a food additive, its E number is E162.[1] As a food additive, betanin has no safety concerns.[1]

The color of betanin depends on pH; between pH four and five, it is bright bluish-red, becoming blue-violet as the pH increases. Once the pH reaches alkaline levels, betanin degrades by hydrolysis, resulting in a yellow-brown color.[citation needed]

Betanin is a betalain pigment, together with isobetanin and other betacyanins.[2]

Sources

[edit]

Betanin is usually obtained from the extract of beet juice; the concentration of betanin in red beet can reach 300–600 mg/kg. Other dietary sources of betanin and other betalains include the Opuntia cactus, Swiss chard, and the leaves of some strains of amaranth.[citation needed]

Uses

[edit]

The most common uses of betanins are in coloring ice cream and powdered soft drink beverages; other uses are in some sugar confectionery, e.g. fondants, sugar strands, sugar coatings, and fruit or cream fillings. In hot processed candies, it can be used if added at the final part of the processing. Betanin is also used in soups as well as tomato and bacon products. Betanin has "not been implicated as causing clinical food allergy when used as a coloring agent".[3]

Betanin has also shown to have antimicrobial activity and can be used as a natural antimicrobial agent in food preservation.[4]

Degradation and stability

[edit]

Betanin degrades when subjected to light, heat, and oxygen; therefore, it is used in frozen products, products with a short shelf life, or products sold in dry state. Betanin can survive pasteurization when in products with high sugar content. Its sensitivity to oxygen is highest in products with a high water content and/or containing metal cations (e.g. iron and copper); antioxidants like ascorbic acid and sequestrants can slow this process down, together with suitable packaging. In dry form betanin is stable in the presence of oxygen.[5]

Safety

[edit]

Use of betanin and other betacyanins as food coloring has a long history in Europe.[1] A scientific panel for the European Food Safety Authority found that acute or chronic toxicity and carcinogenicity studies were too limited to make conclusive safety evaluations, and that the amounts added to foods were similar to those with naturally occurring betanin.[1] The panel also concluded that there was insufficient information to assign an acceptable daily intake level for beetroot red.[1]

See also

[edit]

References

[edit]

Further reading

[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia

Betanin

View on Grokipedia
from Grokipedia
Betanin is a naturally occurring reddish-violet classified as a betacyanin within the family of water-soluble, nitrogen-containing compounds, primarily responsible for the vibrant red color of (Beta vulgaris). It consists of a betalamic acid core conjugated with cyclo-DOPA and a glucose moiety, with the molecular formula C₂₄H₂₆N₂O₁₃ and a molecular weight of 550.5 g/mol. Chemically known as the 5-O-β-glucoside of betanidin, betanin exhibits an absorption maximum at 536 nm, producing shades from pink to violet, and is approved as a colorant under the designation E162 or Beet Red by regulatory bodies such as the and FDA. Betanin is biosynthesized from the amino acid in plants of the order, where it accumulates in vacuoles. Its primary natural source is red , where concentrations can reach 200–2100 mg/kg fresh weight, but it also occurs in dragon fruit (Hylocereus polyrhizus), prickly pear cactus (), ( spp.), and species. It is extracted via aqueous methods from and used industrially as a colorant in foods, , and pharmaceuticals, with emerging applications in biosensors and dye-sensitized solar cells. Betanin shows activity (TEAC ≈ 3–4) and potential health benefits including and anticancer effects, though its ability to cross the blood-brain barrier for neurodegenerative applications remains uncertain as of 2025. Recent studies (2025) explore its use as an .

Chemistry

Structure and properties

Betanin is a betacyanin pigment belonging to the family, which comprises nitrogen-containing compounds synthesized exclusively in of the order and certain fungi. Unlike anthocyanins, which are flavonoid-based and oxygen-containing, betalains feature a central betalamic acid moiety linked via an bond, providing their characteristic coloration. Betanin specifically is the predominant betacyanin in red , classified as a vacuolar chromoalkaloid due to its water-soluble nature and localization in cell vacuoles. The molecular formula of betanin is C24H26N2O13, with a molecular weight of 550.47 g/mol. It exists as a of the aglycone betanidin, where betanidin results from the spontaneous condensation of betalamic acid—a derivative of —with cyclo-3,4-dihydroxyphenylalanine (cyclo-DOPA), forming a resonating dihydropyridine . A β-D-glucose unit is attached via a at the 5-position of the cyclo-DOPA-derived moiety, enhancing its and stability. This structure can be visualized as a bicyclic core with the betalamic acid contributing the , the cyclo-DOPA providing the phenolic rings, and the glucose pendant influencing polarity; the overall configuration includes chiral centers at C-2, C-15, and the glucose anomeric carbon. Physically, betanin imparts a hue to solutions, arising from its conjugated π-electron system that absorbs visible light. It is highly water-soluble and also soluble in polar organic solvents such as , reflecting its polar ionic groups including carboxylates and hydroxyls. In neutral aqueous solutions ( 4–7), betanin exhibits maximum absorption at 538 nm, corresponding to its visible color intensity, with a secondary band around 280 nm due to aromatic rings. Chemically, it possesses pKa values of approximately 3.4 for the groups and 8.5 for the phenolic hydroxyl, influencing its state and color stability across ranges—remaining between 3.5 and 7 before shifting to at higher . The structure of betanin was first isolated from and fully elucidated in 1960 by researchers including Tom J. Mabry and Hans Wyler at the , using classical chemical degradation and spectroscopic methods to confirm the novel immonium-linked architecture distinct from known plant pigments. This discovery established betalains as a unique class, paving the way for subsequent biochemical studies.

Biosynthesis

Betanin, the predominant betacyanin in plants such as beets, is biosynthesized through a tyrosine-derived pathway that branches from the shikimate pathway. The process initiates with the conversion of L-tyrosine to L-3,4-dihydroxyphenylalanine (L-DOPA) via hydroxylation. L-DOPA then undergoes extradiol cleavage by a dioxygenase to form betalamic acid, the chromophore central to all betalains. Concurrently, L-DOPA spontaneously cyclizes to form cyclo-DOPA, which serves as the second key intermediate. Betalamic acid spontaneously condenses with cyclo-DOPA to yield betanidin, the aglycone of betanin; glucosylation at the 5-position of betanidin, or alternatively at cyclo-DOPA prior to condensation, produces betanin. The core enzymes driving this pathway include CYP76AD1, a monooxygenase that catalyzes the committed first step of tyrosine to , with isoforms such as CYP76AD6 contributing in certain . 4,5-dioxygenase (DODA), belonging to the α-ketoglutarate-dependent dioxygenase family, performs the ring-opening of to generate betalamic acid. Glycosyltransferases, notably cyclo-DOPA 5-O-glucosyltransferase (cDOPA5GT) and betanidin 5-O-glucosyltransferase (B5GT), facilitate the addition of glucose to yield the stable, vacuole-sequestered betanin. These enzymes are encoded by lineage-specific genes that have undergone duplications to enable efficient flux through the pathway. Betalain biosynthesis, including that of betanin, evolved through a single origin in the angiosperm order Caryophyllales approximately 60-80 million years ago, coinciding with the diversification of core Caryophyllales lineages. This innovation involved neofunctionalization of duplicated genes in the CYP76AD1 and DODA families, enabling the production of betalamic acid and its conjugates. In betalain-producing taxa, this pathway supplants anthocyanin pigmentation, with mutual exclusivity enforced by the loss or pseudogenization of anthocyanin pathway genes and vice versa, reflecting an adaptive shift in pigmentation strategy within the order. The regulation of betanin biosynthesis is governed by genetic elements such as MYB transcription factors that positively activate core pathway genes like CYP76AD1 and DODA. Environmental stresses, including , , , and , modulate expression of these genes, often upregulating production as a protective response against oxidative damage and UV radiation. For instance, abiotic stresses induce transcriptional changes in genes, enhancing betanin accumulation to bolster resilience.

Natural sources

Occurrence in plants

Betanin, a red-violet betacyanin pigment, occurs in plants belonging to the order Caryophyllales and certain fungi, where it serves as one of the primary classes of visible pigments alongside or replacing anthocyanins in other plant lineages. This distribution is phylogenetically restricted, appearing in most families of the order except Caryophyllaceae and Molluginaceae, and reflects an evolutionary adaptation unique to this group. Prominent examples include Beta vulgaris (beetroot), Amaranthus species (amaranth), Opuntia ficus-indica (prickly pear), Hylocereus polyrhizus (red dragon fruit), and Portulaca species, which accumulate betanin in specialized tissues for ecological functions. In these plants, betanin primarily functions as a coloration agent in flowers and fruits, providing vibrant red hues that attract pollinators and frugivores to facilitate reproduction and . Beyond visual signaling, it contributes to photoprotection by acting as a light-screening shield in epidermal tissues, reducing and oxidative damage under high . Additionally, betanin plays a role in responses, such as tolerance to UV radiation and , by scavenging and mitigating cellular damage during environmental challenges. Betanin is typically localized in vacuoles of roots, fruits, and flowers, with notable accumulation in the hypocotyls and storage roots of , the edible fruits of and , and the inflorescences of Amaranthus species; it is rarely observed in leaves. Global cultivation of betalain-producing plants is predominantly centered on for its pigment-rich roots, accounting for nearly all commercial production of betanin sources due to its widespread agricultural adaptation and high yield potential.

Content in beetroot and other foods

Betanin concentrations in red ( L.) varieties typically range from 50 to 300 mg per 100 g of fresh weight, with the highest levels observed in the peels and outer layers of the root. These levels can vary significantly due to differences in , soil conditions, and root maturity at harvest. In other edible sources, betanin content is generally lower but still notable. Red dragon fruit (Hylocereus polyrhizus) contains approximately 10 mg of betacyanins (primarily betanin equivalents) per 100 g of fresh weight, with higher concentrations in the peel compared to the flesh. Amaranth leaves (Amaranthus spp.) can reach up to 100 mg of total betacyanins per 100 g of fresh weight in pigmented varieties, though levels vary by genotype. Prickly pear (Opuntia ficus-indica) fruits exhibit 10 to 100 mg of betanin per 100 g of fresh weight, concentrated mainly in the peel of red cultivars. Food processing methods, such as , can concentrate betanin by removing insoluble and water, leading to higher levels per unit volume in the resulting compared to the whole . Factors influencing betanin content include genetic selection for high-pigment cultivars in beets, which has been used to develop lines with elevated concentrations. Seasonal and geographical variations also play a role, with cooler climates and earlier harvest times often yielding higher levels due to reduced heat stress during growth.

Extraction and production

Extraction methods

Betanin, the primary betacyanin pigment in red , is extracted primarily from the roots of through various laboratory and industrial techniques aimed at maximizing yield while preserving its stability. Traditional methods rely on solvent-based extractions, such as or dilute solutions, which solubilize the water-soluble betalains from the matrix. For example, extraction using at 40°C can achieve up to 96.3% recovery of betanins, though yields are generally lower at around 17.07 mg/L for betacyanins without optimization. Acidified , such as 0.1% at 50°C and 2, enhances and yields approximately 6.09 mg/100 mL of betanins by disrupting cell walls and preventing enzymatic degradation. Solvent mixtures like 20-50% in are also common, with 30% providing 7.24 mg/g dry weight of betacyanins due to improved penetration into the tissue. Advanced techniques have been developed to improve efficiency, reduce extraction time, and minimize solvent use, often achieving higher yields through enhanced . Ultrasound-assisted extraction, operating at 20-40 kHz for 30-60 minutes at 30°C, increases betacyanin yields to 4.45 mg/g by cavitational disruption of cell walls. Microwave-assisted extraction, using 100-600 W power for 1-5 minutes at around 50°C, can extract up to 202.08 mg/100 g of total betalains, offering rapid heating that accelerates while limiting thermal exposure. Supercritical CO2 extraction, conducted at 10-30 MPa and 40-60°C with co-solvents like , provides a green alternative for selective isolation, though it is less common for highly polar betanin and typically requires modifiers to achieve effective yields. Enzyme-aided methods, employing or at pH 4-5 and 40-50°C with 25 U/g enzyme dosage, boost extraction by 15-25% through targeted breakdown of cellulosic barriers, yielding 14.67 mg/L betacyanins at 25°C. Optimization of extraction parameters is crucial to balance yield and integrity, as betanin is sensitive to environmental conditions. Ideal ranges from 4-6, where stability is maximized and extraction efficiency peaks, avoiding extremes that promote or . Temperatures should be maintained below 60°C, with optimal ranges of 20-50°C for most methods to prevent degradation above 73°C; for instance, exceeding 60°C in extraction can reduce yields by promoting . Modern techniques, when optimized, can achieve up to 90% recovery, such as methods yielding 20-30% higher than conventional approaches. Post-extraction purification is essential to isolate high-purity betanin from impurities like sugars, proteins, and other pigments. Membrane , including or , effectively concentrates extracts by reducing total soluble solids from 12° to 6.4° while retaining betalains in the permeate. Chromatographic techniques, such as ion-exchange chromatography, (HPLC), or ion-pair high-speed counter-current chromatography (IP-HSCCC), provide superior separation; for example, ion-exchange methods achieve the highest purity levels by selectively binding betanin based on charge. These steps ensure betanin concentrations suitable for analytical or industrial applications, with HPLC often used for final polishing to obtain purity exceeding 95%.

Commercial production

Commercial production of betanin primarily utilizes processing waste from red beetroots (Beta vulgaris), including , peels, and juice residues from the and food industries, to extract the pigment efficiently and sustainably. Key producers are concentrated in , such as Doehler in and GNT Group in the , and in the United States, including , DDW The Color House, and . Industrial processes begin with aqueous extraction of betalains from beet waste, followed by filtration to remove solids, ultrafiltration for purification, and concentration via evaporation. The resulting liquid is then transformed into stable forms through spray-drying with carriers like maltodextrin to yield powders, or maintained as concentrates for direct use. In the European Union, betanin is approved as the natural food colorant E162, which must meet specifications for identity and purity. While traditional extraction dominates, emerging fermentation-based methods using genetically engineered yeasts like Yarrowia lipolytica are being developed for higher yields and reduced environmental impact, with titers up to 1.3 g/L achieved as of 2023, though they remain at pilot scale. Quality control in commercial production ensures betanin content of at least 0.4% in the final product, with rigorous testing for (e.g., lead below 2 mg/kg), , and microbial contaminants to comply with regulations. Market prices typically range from $8.5 to $61 per kg, varying by concentration, form (powder vs. liquid), and regional factors. Historically, betanin accelerated in the mid-20th century with beet powders introduced in the 1970s for applications, evolving to purified extracts after 2000 to improve and dosage efficiency in formulations.

Applications

As a food colorant

Betanin serves as a natural food colorant, approved under the designation E162 and approved as a color additive exempt from certification by the (FDA) under 21 CFR 73.40, with an (ADI) designated as "not specified" by the Joint FAO/WHO Expert Committee on Food Additives (JECFA). It is typically used at concentrations of 0.01–0.2% to achieve vibrant hues in products with a range of 3–7, where its stability is optimal for maintaining color intensity. This pigment provides a bluish- to violet- coloration depending on the exact and formulation, making it suitable for a variety of acidic to neutral matrices. In the , betanin finds widespread application in dairy products like yogurts and ice creams, beverages such as soft drinks and juices, confections including candies, and meat products like sausages and meat substitutes, where it imparts an appealing red color without the need for synthetic alternatives. It effectively replaces synthetic red dyes such as Allura Red (FD&C Red No. 40), offering a clean-label option that aligns with consumer preferences for natural ingredients while delivering comparable vibrancy in these products. The primary advantages of betanin as a colorant include its origin from , which avoids the potential health concerns associated with artificial dyes, and its inherent properties that can extend the of foods by inhibiting oxidation and microbial growth. However, at higher concentrations, it may introduce a subtle beet-like earthy flavor, which can influence sensory profiles in delicate applications. Betanin is commercially formulated as concentrates or spray-dried powders for ease of incorporation, and it is frequently blended with other colorants like anthocyanins or to enhance thermal and stability in complex food systems.

Other uses

Betanin finds application in cosmetics as a natural red-violet pigment, providing pigmentation in products such as lipsticks and creams where stable, plant-derived colorants are preferred over synthetic alternatives. In pharmaceuticals, betanin serves as a marker dye and colorant in non-ingestible formulations, such as topical preparations and diagnostic aids, due to its water-soluble nature and vibrant hue. It is also utilized in nutraceutical supplements for its coloring properties, where encapsulation techniques enhance its stability in neutral to slightly alkaline pH ranges common in such products. Analytically, betanin functions as a owing to its color transitions: it appears in acidic conditions ( 4–6) and shifts to at higher values (>7), making it suitable for biochemical assays and endpoints. This property has been exploited in colorimetric methods for detecting ions and metabolites, with detection limits as low as 0.84 μM for in aqueous samples using beet-derived extracts. In fluorescence-based assays, betanin enables metal ion sensing (e.g., Cu²⁺ and Eu³⁺) through reversible spectral changes, facilitating applications in . Emerging uses of betanin include textile dyeing, where it offers an eco-friendly alternative to synthetic dyes for cotton and wool fabrics, achieving durable red shades via ultrasound-assisted mordanting techniques. Research has also explored its potential in inks and sensors, such as ammonia-responsive films for quality detection, leveraging its pH sensitivity for non-invasive monitoring in industrial settings. Additionally, bioengineered production of betanin is being investigated for sustainable dye-sensitized solar cells and antimicrobial textiles.

Stability and degradation

Factors affecting stability

Betanin exhibits optimal stability within a range of 4 to 6, where the retains its characteristic color due to the integrity of its aldimine linkage, remaining stable from 3 to 7; outside this range, degradation accelerates, with exposure to below 3 causing and above 7 leading to conversion into yellow betaxanthins. This sensitivity arises from the betanin's molecular structure, which includes a glycosylated betanidin core vulnerable to or at extreme levels. Thermal stability of betanin is governed by Arrhenius kinetics, following degradation with activation energies typically around 80-100 kJ/mol, resulting in a of approximately 35 minutes at 80°C in aqueous solutions, while stability improves significantly below 50°C, where extend to days or weeks under refrigerated conditions (e.g., over 20 days at ). Higher temperatures promote and cleavage of the , exacerbating color loss in processed foods or extracts. Exposure to light, particularly UV wavelengths, induces by exciting electrons in the betanin , reducing to hours under continuous illumination, whereas storage in darkness preserves up to 90% of the pigment over weeks. Oxygen further destabilizes betanin through oxidative mechanisms, with aerobic conditions halving stability compared to anaerobic environments; this effect is intensified by transition metals such as Fe³⁺, which catalyze formation, though chelators like EDTA can mitigate it. High humidity or (a_w > 0.6) accelerates hydrolytic degradation by facilitating nucleophilic attacks on the pigment's bonds, shortening in moist environments, as evidenced by half-lives dropping from 236 days at a_w = 0.23 to under 4 days at a_w = 0.64 during storage at 50°C. Interactions with other molecules can modulate stability: sugars like in encapsulation matrices enhance resistance to heat and oxygen by forming protective barriers, increasing up to 17-fold compared to free betanidin, while certain proteins may stabilize through hydrogen bonding or destabilize via aggregation in complex food systems.

Degradation mechanisms

Betanin undergoes thermal degradation primarily through of the and subsequent , leading to the formation of 2-decarboxybetanin and other decarboxylated derivatives such as 2,15-bidecarboxy-betanin. This process is characterized by first-order kinetics, with involving the breaking of C–O and C–C bonds in the groups, often accompanied by rearrangement to yield neobetanin (14,15-dehydrobetanin). At temperatures above 50 °C, such as 75–85 °C, the degradation rate increases, resulting in products like betalamic acid and cyclo-DOPA-5-O-glycoside, with half-lives for example 2.3 hours at 75 °C and 4. Dehydrogenation is linked to these events at positions C-2 and C-17 of betanin and its isomers, particularly at 3–4. Oxidative degradation of betanin involves cleavage of the aldimine bond by (ROS), accelerated by molecular oxygen and leading to dehydrogenated derivatives such as neobetanin. This aerobic process deviates from strict first-order kinetics and produces betalamic acid and cyclo-dopa derivatives, with potential formation of yellow betaxanthins like vulgaxanthin through of betalamic acid with amines. Further oxidation can result in brown polymeric compounds via of degradation intermediates. enhances resistance to oxidation, extending the of the betanidin core up to 17-fold compared to the aglycone form. Photolytic degradation occurs under UV or visible light exposure, initiating of betanin to isobetanin and subsequent ring opening of the chromophore. This oxygen-dependent process leads to hydrolyzed and decarboxylated products, including neobetanin and other cleavage fragments, with degradation rates enhanced by photochemical reactions. Rate constants for are on the order of 10^{-3} min^{-1} in aqueous solutions, reflecting rapid color loss in light-exposed environments. pH-induced degradation proceeds via or of betanin's functional groups, promoting to the betanidin aglycone, particularly in acidic conditions below 3. This leads to isomerization (e.g., to isobetanin) and , yielding products such as 5,6-dihydroxyindole-2-carboxylic acid and methylpyridine-2,6-dicarboxylic acid. In alkaline environments above 7, cleavage of the aldimine bond dominates, with kinetics observed across pH ranges 3–8, though stability is optimal near neutral . for degradation decreases with increasing pH in the 3–5 range, but overall rates are minimized at 4–6.

Biological effects

Health benefits

Betanin exhibits significant activity primarily through its ability to scavenge free radicals, facilitated by the phenolic hydroxy groups in its structure. These groups enable betanin to donate hydrogen atoms or electrons to neutralize (ROS), such as and hydroxyl radicals, thereby preventing oxidative damage to cellular components. Studies using electron spin (ESR) have confirmed betanin's direct interaction with free radicals, highlighting its role in mitigating . It indicates a high potential to inhibit and protect against ROS-induced cellular injury. Betanin also demonstrates anti-inflammatory properties, particularly by inhibiting the nuclear factor kappa-B () pathway in cellular models. In experiments with lipopolysaccharide-stimulated macrophages have shown that betanin suppresses activation, leading to reduced production of pro-inflammatory cytokines such as tumor necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6). This inhibition occurs through betanin's interference with the phosphorylation and degradation of , a key regulator of translocation to the nucleus. Furthermore, in rodent models of , such as carrageenan-induced paw , betanin has exhibited potential to alleviate by enhancing antioxidant enzyme activities, including and , suggesting broader therapeutic implications for inflammatory conditions. Beyond these effects, betanin shows anticancer potential by inducing in various tumor cell lines. In human cells, betanin-enriched extracts have induced and autophagic cell death without significant toxicity to non-cancerous cells. Similar apoptotic effects have been observed in colon cancer cells, where betanin upregulates pro-apoptotic genes like BAD and while downregulating anti-apoptotic Bcl-2. Recent studies (as of 2025) have also highlighted betanin's neuroprotective potential in preventing neurodegenerative diseases like Alzheimer's, anti-adipogenic effects by reducing PPARγ and FAS levels to mitigate risk, and promotion of to improve endothelial function for cardiovascular health. Preliminary evidence suggests that beetroot, rich in betanin and nitrates, may support brain health and cognitive function in older adults. Nitrates from beetroot are converted to nitric oxide, which can improve cerebral blood flow and oxygenation, potentially enhancing task performance; for instance, a high-nitrate diet has been shown to increase regional perfusion in frontal lobe white matter, an area associated with executive function. However, longer-term supplementation with nitrate-rich beetroot juice has not consistently improved cognitive function or cerebral blood flow in overweight and obese older adults over 13 weeks. In laboratory studies, betanin reduces oxidation and inhibits beta-amyloid protein aggregation, a key process in Alzheimer's disease pathogenesis. Despite these promising preclinical findings, human evidence is limited and preliminary; small studies show mixed results, with no conclusive proof that beetroot prevents or treats Alzheimer's disease. Ongoing clinical trials are investigating the feasibility of beetroot juice supplementation in Alzheimer's patients, but results are not yet available. Beetroot contributes to a healthy diet through its antioxidants, potassium, and fiber, which may support overall brain health alongside exercise, blood pressure management, and adequate sleep, but it does not substitute for medical treatments. Individuals with memory issues or at risk for cognitive decline should consult a neurologist. For cardiovascular benefits, clinical trials in the involving juice supplementation—rich in betanin—have reported reductions in systolic by 4-8 mmHg in hypertensive individuals, attributed in part to betanin's modulation of endothelial function, independent of effects. The of betanin supports its physiological effects, as it is absorbed intact in the . Human pharmacokinetic studies indicate that betanin reaches peak plasma concentrations 2-3 hours after oral ingestion of juice, with detectable levels persisting up to 12 hours. Absorption efficiency is low, with human trials reporting 0.5-1% of ingested betanin appearing in plasma and , primarily due to limited intestinal uptake and rapid by . Despite this, the absorbed fraction is sufficient to exert systemic and actions.

Safety and toxicity

Betanin is generally regarded as safe for consumption as a food colorant. The Joint FAO/WHO Expert Committee on Food Additives (JECFA) has established an (ADI) of "not specified" for beet red, the primary source of betanin, indicating no identifiable to when used at levels conforming to . Similarly, the (EFSA) concluded in its 2015 re-evaluation that beetroot red (E 162), of which betanin is the main component, poses no safety concern at reported use levels across food categories. Available toxicological data, including short-term and long-term studies, support this assessment, with no evidence of or carcinogenicity observed in limited but relevant animal models. Allergic reactions to betanin are rare, primarily linked to underlying sensitivities to beetroot. In sensitive individuals, consumption may trigger histamine-like effects, such as urticaria or, in exceptional cases, with . Only isolated reports of directly to betanin exist, underscoring its low allergenic potential compared to other colorants. Acute toxicity studies demonstrate betanin's low hazard profile, with an oral LD50 exceeding 5,000 mg/kg body weight in rats, far above typical dietary exposure levels. Regarding potential risks from degradation, while betanin itself is stable under normal conditions, beet extracts may contain nitrates that could theoretically form nitrosamines under high-heat processing or in the presence of amines; however, regulatory controls minimize this risk to negligible levels in approved uses. Regulatory frameworks affirm betanin's safety profile. In the , it is authorized as E 162 for use in foods and other categories at , with strict limits on content (e.g., ≤200 mg/kg in certain products) to prevent exceedance of the nitrate ADI. residues in betanin extracts are monitored and regulated under EU (EC) No 396/2005, ensuring levels remain below maximum residue limits to protect vulnerable populations like .

References

  1. https://pmc.ncbi.nlm.nih.gov/articles/PMC8123435/
  2. https://pubchem.ncbi.nlm.nih.gov/compound/Betanin
  3. https://onlinelibrary.wiley.com/doi/10.1002/jmri.70158
  4. https://pubs.acs.org/doi/10.1021/jf010456f
  5. https://pubs.rsc.org/en/content/articlehtml/2021/np/d1np00018g
  6. https://www.chemicalbook.com/ChemicalProductProperty_EN_CB3459292.htm
  7. https://currentprotocols.onlinelibrary.wiley.com/doi/pdf/10.1002/0471142913.faf0301s00
  8. https://hal.science/hal-00577387v1/document
  9. https://journals.sagepub.com/doi/pdf/10.1177/1934578X0700201001
  10. https://opendata.uni-halle.de/bitstream/1981185920/9990/1/prom.pdf
  11. https://pmc.ncbi.nlm.nih.gov/articles/PMC10433459/
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