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street name for lysergic acid diethylamide (同)back breaker, battery-acid, dose, dot, Elvis, loony toons, Lucy in the sky with diamonds, pane, superman, window pane, Zen
any of various water-soluble compounds having a sour taste and capable of turning litmus red and reacting with a base to form a salt
having the characteristics of an acid; "an acid reaction"

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酸性の / 酸味のある,すっぱい(sour) / (言葉・態度などが)厳しい,しんらつな / 酸 / すっぱいもの / 《俗》=LSD

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/11/04 21:57:46」(JST)

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Ethylenediaminetetraacetic acid, widely abbreviated as EDTA (for other names, see Table), is an aminopolycarboxylic acid and a colourless, water-soluble solid. Its conjugate base is named ethylenediaminetetraacetate. It is widely used to dissolve limescale. Its usefulness arises because of its role as a hexadentate ("six-toothed") ligand and chelating agent, i.e., its ability to "sequester" metal ions such as Ca²⁺ and Fe³⁺. After being bound by EDTA, metal ions remain in solution but exhibit diminished reactivity. EDTA is produced as several salts, notably disodium EDTA and calcium disodium EDTA.

It is on the World Health Organization's List of Essential Medicines, the most important medications needed in a basic health system.^[2]

1 Uses
- 1.1 Industry
- 1.2 Medicine
- 1.3 Alternative medicine
- 1.4 Cosmetics
- 1.5 Laboratory applications
2 Side effects
3 Synthesis
4 Nomenclature
5 Coordination chemistry principles
6 Environmental fate
- 6.1 Abiotic degradation
- 6.2 Biodegradation
7 Alternatives to EDTA
- 7.1 Iminodisuccinic acid (IDS)
- 7.2 Polyaspartic acid
- 7.3 Ethylenediamine-N,N’-disuccinic acid (EDDS)
- 7.4 Methylglycinediacetic acid (MGDA)
- 7.5 L-glutamic acid N,N-diacetic acid, tetra sodium salt (GLDA)
8 Methods of detection and analysis
9 References
10 External links

Uses

Industry

In industry, EDTA is mainly used to sequester metal ions in aqueous solution. In the textile industry, it prevents metal ion impurities from modifying colors of dyed products. In the pulp and paper industry, EDTA inhibits the ability of metal ions, especially Mn²⁺, from catalyzing the disproportionation of hydrogen peroxide, which is used in "chlorine-free bleaching." In a similar manner, EDTA is added to some food as a preservative or stabilizer to prevent catalytic oxidative decoloration, which is catalyzed by metal ions.^[3] In soft drinks containing ascorbic acid and sodium benzoate, EDTA mitigates formation of benzene (a carcinogen).^[4]

The reduction of water hardness in laundry applications and the dissolution of scale in boilers both rely on EDTA and related complexants to bind Ca²⁺, Mg²⁺, as well as other metal ions. Once bound to EDTA, these metal centers tend not to form precipitates or to interfere with the action of the soaps and detergents. For similar reasons, cleaning solutions often contain EDTA.

The solubilization of ferric ions, at or below near neutral pH can be accomplished using EDTA. This property is useful in agriculture including hydroponics. However, given the pH dependence of ligand formation, EDTA is not helpful for improving Fe solubility in above neutral soils.^[5] Otherwise, at near-neutral pH and above, iron(III) forms insoluble salts, which are less bioavailable to susceptible plant species. Aqueous [Fe(edta)]⁻ is used for removing ("scrubbing") hydrogen sulfide from gas streams. This conversion is achieved by oxidizing the hydrogen sulfide to elemental sulfur, which is non-volatile:

2 [Fe(edta)]⁻ + H₂S → 2 [Fe(edta)]²⁻ + S + 2 H⁺

In this application, the ferric center is reduced to its ferrous derivative, which can then be reoxidized by air. In similar manner, nitrogen oxides are removed from gas streams using [Fe(edta)]²⁻. The oxidizing properties of [Fe(edta)]⁻ are also exploited in photography, where it is used to solubilize silver particles.^[6]

EDTA was used in the separation of the lanthanide metals by ion-exchange chromatography. Perfected by F.H. Spedding et al. in 1954, the method relies on the steady increase in stability constant of the lanthanide EDTA complexes with atomic number. Using sulfonated polystyrene beads and copper(II) as a retaining ion, EDTA causes the lanthanides to migrate down the column of resin while separating into bands of pure lanthanide. The lanthanides elute in order of decreasing atomic number. Due to the expense of this method, relative to counter-current solvent extraction, ion-exchange is now used only to obtain the highest purities of lanthanide (typically greater than 4N, 99.99%).^{[citation needed]}

Medicine

EDTA is used to bind metal ions in the practice of chelation therapy, e.g., for treating mercury and lead poisoning.^[7] It is used in a similar manner to remove excess iron from the body. This therapy is used to treat the complication of repeated blood transfusions, as would be applied to treat thalassaemia. The U.S. FDA approved the use of EDTA for lead poisoning^[8] on July 16, 1953, under the brand name of Versenate,^[9] which was licensed to the pharmaceutical company Riker.

From 2003 to 2005, deaths of 3 individuals as a result of cardiac arrest caused by hypocalcemia during chelation therapy with EDTA were reported to the Centers for Disease Control and Prevention.^[10]

Dentists and endodontists use EDTA solutions to remove inorganic debris (smear layer) and lubricate the canals in endodontics. This procedure helps prepare root canals for obturation. Furthermore, EDTA solutions with the addition of a surfactant loosen up calcifications inside a root canal and allow instrumentation (canals shaping) and facilitate apical advancement of a file in a tight/calcified root canal towards the apex. It serves as a preservative (usually to enhance the action of another preservative such as benzalkonium chloride or thiomersal) in ocular preparations and eyedrops. In evaluating kidney function, the complex [Cr(edta)]⁻ is administered intravenously and its filtration into the urine is monitored. This method is useful for evaluating glomerular filtration rate.^[11]

EDTA is used extensively in the analysis of blood. It is an anticoagulant for blood samples for CBC/FBEs.

EDTA is a slime dispersant, and has been found to be highly effective in reducing bacterial growth during implantation of intraocular lenses (IOLs).^[12]

Alternative medicine

Some alternative practitioners believe EDTA acts as an antioxidant, preventing free radicals from injuring blood vessel walls, therefore reducing atherosclerosis.^[7] These ideas are as yet unsupported by rigorous scientific studies, and seem to contradict some currently accepted principles.^[13] The U.S. FDA has not approved it for the treatment of atherosclerosis.^[14]

Cosmetics

In shampoos, cleaners and other personal care products EDTA salts are used as a sequestering agent to improve their stability in air.^[15]

Laboratory applications

In the laboratory, EDTA is widely used for scavenging metal ions: In biochemistry and molecular biology, ion depletion is commonly used to deactivate metal-dependent enzymes, either as an assay for their reactivity or to suppress damage to DNA or proteins.^[16] In analytical chemistry, EDTA is used in complexometric titrations and analysis of water hardness or as a masking agent to sequester metal ions that would interfere with the analyses. EDTA finds many specialized uses in the biomedical laboratories, such as in veterinary ophthalmology as an anticollagenase to prevent the worsening of corneal ulcers in animals. In tissue culture EDTA is used as a chelating agent that binds to calcium and prevents joining of cadherins between cells, preventing clumping of cells grown in liquid suspension, or detaching adherent cells for passaging. In histopathology, EDTA can be used as a decalcifying agent making it possible to cut sections using a microtome once the tissue sample is demineralised. EDTA is also known to inhibit a range of metallopeptidases, the method of inhibition occurs via the chelation of the metal ion required for catalytic activity.^[17] EDTA can also be used to test for bioavailability of heavy metals in sediments. However, EDTA may influence the bioavailability of metals in solution, which may pose concerns regarding its effects in the environment, especially given its widespread uses and applications.

Side effects

EDTA exhibits low acute toxicity with LD₅₀ (rat) of 2.0 – 2.2 g/kg.^[6] It has been found to be both cytotoxic and weakly genotoxic in laboratory animals. Oral exposures have been noted to cause reproductive and developmental effects.^[15] The same study by Lanigan^[15] also found that both dermal exposure to EDTA in most cosmetic formulations and inhalation exposure to EDTA in aerosolized cosmetic formulations would produce exposure levels below those seen to be toxic in oral dosing studies.

Synthesis

The compound was first described in 1935 by Ferdinand Münz, who prepared the compound from ethylenediamine and chloroacetic acid.^[18] Today, EDTA is mainly synthesised from ethylenediamine (1,2-diaminoethane), formaldehyde, and sodium cyanide.^[19] This route yields the sodium salt, which can be converted in a subsequent step into the acid forms:

H₂NCH₂CH₂NH₂ + 4 CH₂O + 4 NaCN + 4 H₂O → (NaO₂CCH₂)₂NCH₂CH₂N(CH₂CO₂Na)₂ + 4 NH₃

(NaO₂CCH₂)₂NCH₂CH₂N(CH₂CO₂Na)₂ + 4 HCl → (HO₂CCH₂)₂NCH₂CH₂N(CH₂CO₂H)₂ + 4 NaCl

This process is used to produce about 80 thousand tonnes each year. Impurities cogenerated by this route include glycine and nitrilotriacetic acid; they arise from reactions of the ammonia coproduct.^[6]

Nomenclature

To describe EDTA and its various protonated forms, chemists distinguish between EDTA⁴⁻, the conjugate base that is the ligand, and H₄EDTA, the precursor to that ligand. At very low pH (very acidic conditions) the fully protonated H₆EDTA²⁺ form predominates, whereas at very high pH or very basic condition, the fully deprotonated EDTA⁴⁻ form is prevalent. In this article, the term EDTA is used to mean H_4-xEDTA^x−, whereas in its complexes EDTA⁴⁻ stands for the tetra-deprotonated ligand.

Coordination chemistry principles

Metal-EDTA chelate

In coordination chemistry, EDTA⁴⁻ is a member of the aminopolycarboxylic acid family of ligands. EDTA⁴⁻ usually binds to a metal cation through its two amines and four carboxylates. Many of the resulting coordination compounds adopt octahedral geometry. Although of little consequence for its applications, these octahedral complexes are chiral. The anion [Co(EDTA)]⁻ has been resolved into enantiomers.^[20] Many complexes of EDTA⁴⁻ adopt more complex structures due to either the formation of an additional bond to water, i.e. seven-coordinate complexes, or the displacement of one carboxylate arm by water. Ferric complex of EDTA is seven-coordinate.^[21] Early work on the development of EDTA was undertaken by Gerold Schwarzenbach in the 1940s.^[22] EDTA forms especially strong complexes with Mn(II), Cu(II), Fe(III), Pb (II) and Co(III).^[23]

Several features of EDTA's complexes are relevant to its applications. First, because of its high denticity, this ligand has a high affinity for metal cations:

[Fe(H₂O)₆]³⁺ + H₄EDTA [Fe(EDTA)]⁻ + 6 H₂O + 4 H⁺ (K_eq = 10^25.1)

Written in this way, the equilibrium quotient shows that metal ions compete with protons for binding to EDTA. Because metal ions are extensively enveloped by EDTA, their catalytic properties are often suppressed. Finally, since complexes of EDTA⁴⁻ are anionic, they tend to be highly soluble in water. For this reason, EDTA is able to dissolve deposits of metal oxides and carbonates.

Environmental fate

Abiotic degradation

EDTA is in such widespread use that questions have been raised whether it is a persistent organic pollutant. While EDTA serves many positive functions in different industrial, pharmaceutical and other avenues, the longevity of EDTA can pose serious issues in the environment. The degradation of EDTA is slow. It mainly occurs abiotically in the presence of sunlight.^[24]

The most important process for the elimination of EDTA from surface waters is direct photolysis at wavelengths below 400 nm.^[25] Depending on the light conditions, the photolysis half-lives of Fe(III)EDTA in surface waters can range as low as 11.3 minutes up to more than 100 hours.^[26] Degradation of FeEDTA, but not EDTA itself, produces Fe complexes of ED3A, EDDA, and EDMA- 92% of EDDA and EDMA biodegrades in 20 hours while ED3A displays significantly higher resistance. Many environmentally-abundant EDTA species (e.g., Mg²⁺, Ca²⁺) are more persistent.

Biodegradation

In many industrial wastewater treatment plants, EDTA elimination can be achieved at about 80% using microorganisms.^[27] Resulting byproducts are ED3A and IDA – suggesting that both the backbone and acetyl groups were attacked. Some microorganisms have even been discovered to form nitrates out of EDTA but degrade optimally at moderately alkaline conditions of pH 9.0–9.5.^[28]

Several bacterial strains isolated from sewage treatment plants efficiently degrade EDTA. Specific strains include Agrobacterium radiobacter ATCC 55002^[29] and the sub-branches of Proteobacteria like BNC1, BNC2 ^[30] and strain DSM 9103.^[31] The three strains share similar properties of aerobic respiration and are classified as gram-negative bacteria. Unlike photolysis, the chelated species is not exclusive to Fe(III) in order to be degraded. Rather, each strain uniquely consumes varying metal-EDTA complexes through several enzymatic pathways. Agrobacterium radiobacter only degrades Fe(III) EDTA ^[30] while BNC1 and DSM 9103 are not capable of degrading Fe(III) EDTA and are more suited for CaEDTA, BaEDTA, MgEDTA and MnEDTA.^[32] EDTA complexes require dissociation before degradation .

Alternatives to EDTA

Interest in environmental safety has brought up concerns about biodegradability in aminopolycarboxylates such as EDTA. For example, under the International Organization for Standardization 28-day 7827 test Austrian paper and pulp industries must use chelating agents that have biodegradation levels over 70–80%.^[33] An increased interest in safety has led to the development and research of alternative chelating ligands which can still bind strongly to metal ions but also have a higher biodegradability and a lower content of nitrogen.^[33]

Iminodisuccinic acid (IDS)

Commercially used since 1998, iminodisuccinic (IDS) acid biodegrades about 80% after only 7 days. IDS binds to calcium exceptionally well and forms stable compounds with other heavy metal ions. In addition to having a lower toxicity after chelation, the production of IDS is environment-friendly.^[33] Specifically, IDS is degraded through the use of IDS-epimerase and C-N lyase found in Agrobacterium tumefaciens (BY6) which can be harvested on a large scale. Additionally, the reactions catalyzed by both enzymes do not require any cofactors and can thus be applied directly.^[34]

Polyaspartic acid

Polyaspartic acid, like IDS binds to calcium and other heavy metal ions. It has a higher value of 7.2 meq/g than does EDTA, which only has 6.0 meq/g.^[33] While it has a higher theoretical capacity, in practical applications it exhibits low efficiency in lower ion concentration solutions. It has many practical applications including corrosion inhibitors, waste water additives, and agricultural polymers. A Polyaspartic acid-based laundry detergent was the first laundry detergent in the world to receive the EU flower ecolabel.^[33]

Ethylenediamine-N,N’-disuccinic acid (EDDS)

As a structural isomer of EDTA, ethylenediamine-N,N’-disuccinic acid can exist three isomers: (S,S), (R,S)/(S,R) and (R,R), but only the S,S-isomer is readily biodegradable. EDDS exhibits a surprisingly high rate biodegradation at 83% in 20 days. Biodegradation rates also varies the different metal ions chelated. For example, the complexes of lead and zinc with EDDS have relatively the same stability but the lead complex is biodegrades more efficiently than the zinc complex.^[33] As of 2002, EDDS has been commercially prominent in Europe on a large scale with an estimated demand rate increase of about 15% each year.^[33]

Methylglycinediacetic acid (MGDA)

Produced from BASF, methylglycinediacetic acid (MGDA) is produced from glycine.^[33] MGDA has a high rate of biodegradation >68%, but unlike many other chelating agents can degrade without the assistance of adapted bacteria. Additionally, unlike EDDS or IDS, MGDA can withstand higher temperatures while maintaining a high stability as well as the entire pH range. As a result, the chelating strength of MGDA is stronger than many commercial chelating agents.^[33]

L-glutamic acid N,N-diacetic acid, tetra sodium salt (GLDA)

Aminopolycarboxylate-based chelates control metal ions in water-based systems.

Methods of detection and analysis

The most sensitive method of detecting and measuring EDTA in biological samples is selected-reaction-monitoring capillary-electrophoresis mass-spectrometry (abbreviation SRM-CE/MS), which has a detection limit of 7.3 ng/mL in human plasma and a quantitation limit of 15 ng/mL.^[35] This method works with sample volumes as small as ~7–8 nL.^[35]

EDTA has also been measured in non-alcoholic beverages using high performance liquid chromatography (HPLC) at a level of 2.0 μg/mL.^[36]^[37]

References

^ Substance Name: Sodium calcium edetate. NIH.gov
^ "WHO Model List of EssentialMedicines" (PDF). World Health Organization. October 2013. Retrieved 22 April 2014.
^ Furia T (1964). "EDTA in Foods – A technical review". Food Technology 18 (12): 1874–1882.
^ US Food and Drug Administration: Center for Food Safety and Applied Nutrition Questions and Answers on the Occurrence of Benzene in Soft Drinks and Other Beverages
^ Norvell, W. A.; Lindsay, W. L. (1969). "Reactions of EDTA Complexes of Fe, Zn, Mn, and Cu with Soils". Soil Science Society of America Journal 33: 86. doi:10.2136/sssaj1969.03615995003300010024x.
^ ^a ^b ^c Hart, J. Roger (2005) "Ethylenediaminetetraacetic Acid and Related Chelating Agents" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim. doi:10.1002/14356007.a10_095
^ ^a ^b DeBusk, Ruth; et al. (2002). "Ethylenediaminetetraacetic acid (EDTA)". University of Maryland Medical Center.
^ "Calcium Disodium Versenate (Edetate Calcium Disodium) Injection [Graceway Pharmaceuticals, Llc]". Dailymed.nlm.nih.gov. Retrieved 2013-01-01.
^ "Drugs@FDA: FDA Approved Drug Products". Accessdata.fda.gov. Retrieved 2013-01-01.
^ Brown, M. J.; Willis, T.; Omalu, B.; Leiker, R. (2006). "Deaths Resulting from Hypocalcemia After Administration of Edetate Disodium: 2003-2005" (Full free text). Pediatrics 118 (2): e534. doi:10.1542/peds.2006-0858. PMID 16882789.
^ Shirley, D.G.; Walter, S.J.; Noormohamed, F.H. (2002). "Natriuretic effect of caffeine: assessment of segmental sodium reabsorption in humans". Clinical Science 103 (5): 461–466. doi:10.1042/CS20020055. PMID 12401118.
^ Kadry, A. A.; Fouda, S. I.; Shibl, A. M.; Abu El-Asrar, A. A. (2009). "Impact of slime dispersants and anti-adhesives on in vitro biofilm formation of Staphylococcus epidermidis on intraocular lenses and on antibiotic activities". Journal of Antimicrobial Chemotherapy 63 (3): 480. doi:10.1093/jac/dkn533. PMID 19147522.
^ Green, Saul; Wallace Sampson (December 14, 2002). "EDTA Chelation Therapy for Atherosclerosis And Degenerative Diseases: Implausibility and Paradoxical Oxidant Effects". Quackwatch. Retrieved 16 December 2009.
^ "Postmarket Drug Safety Information for Patients and Providers > Questions and Answers on Edetate Disodium (marketed as Endrate and generic products)". U.S. Food and Drug Administration.
^ ^a ^b ^c Lanigan RS and Yamarik TA (2002). "Final report on the safety assessment of EDTA, calcium disodium EDTA, diammonium EDTA, dipotassium EDTA, disodium EDTA, TEA-EDTA, tetrasodium EDTA, tripotassium EDTA, trisodium EDTA, HEDTA, and trisodium HEDTA". Int J Toxicol. 21 Suppl 2 (5): 95–142. doi:10.1080/10915810290096522. PMID 12396676.
^ Dominguez, K; Ward, WS (December 2009). "A novel nuclease activity that is activated by Ca²⁺ chelated to EGTA". Systems Biology in Reproductive Medicine 55 (5–6): 193–99. doi:10.3109/19396360903234052.
^ Auld, D. S. (1995). "Removal and replacement of metal ions in metallopeptidases". Methods in enzymology 248: 228–42. PMID 7674923.
^ Münz, F. (1938) "Polyamino carboxylic acids to I. G. Farbenindustrie, U.S. Patent 2,130,505, DE 718 981, 1935.
^ Industrial Synthesis of EDTA. chm.bris.ac.uk
^ Kirchner, S; Gyarfas, Eleonora C. (1957). "Barium (Ethylenediaminetetracetato) Cobalt(III) 4-Hydrate". Inorganic Syntheses. Inorganic Syntheses 5: 186–188. doi:10.1002/9780470132364.ch52. ISBN 9780470132364.
^ López-Alcalá, J. M.; Puerta-Vizcaíno, M. C.; González-Vílchez, F.; Duesler, E. N.; Tapscott, R. E. (1984). "A redetermination of sodium aqua[ethylenediaminetetraacetato(4-)]ferrate(III) dihydrate, Na[Fe(C₁₀H₁₂N₂O₈)(H₂O)]·2H₂O". Acta Cryst C40 (6): 939–941. doi:10.1107/S0108270184006338.
^ Sinex, Scott A. EDTA – A Molecule with a Complex Story. chm.bris.ac.uk
^ Holleman, A. F.; Wiberg, E. (2001). Inorganic Chemistry. San Diego: Academic Press. ISBN 0-12-352651-5.
^ Bucheli-Witschel, M.; Egli, T. (2001), "DAB: Environmental Fate and Microbial Degradation of Aminopolycarboxylic Acids", FEMS Microbiology Reviews 25 (1): 69–106, doi:10.1111/j.1574-6976.2001.tb00572.x, PMID 11152941
^ Kari, F.G (1994). Umweltverhalten von Ethylenediaminetetraacetate (EDTA) under spezieller Berucksuchtigung des photochemischen Ab-baus. (Ph.D). Swiss Federal Institute of Technology.
^ Frank, R; Rau, H (1989). "Photochemical transformation in aqueous solution and possible environmental fate of Ethylenediaminetetraacetatic acid (EDTA)". Ecotoxicology and Environmental Safety 19 (1): 55–63. doi:10.1016/0147-6513(90)90078-j. PMID 2107071.
^ Kaluza, U; Klingelhofer, P; K, Taeger (1998). "Microbial degradation of EDTA in an industrial wastewater treatment plant". Water Research 32 (9): 2843–2845. doi:10.1016/S0043-1354(98)00048-7.
^ VanGinkel, C.G; Vandenbroucke, K.L; C.A, Troo (1997). "Biological removal of EDTA in conventional activated-sludge plants operated under alkaline conditions". Bioresources Technology 32 (2–3): 2843–2845. doi:10.1016/S0960-8524(96)00158-7.
^ Lauff, J.J.; Steele, D.B; Coogan, L.A; Breitfeller, J.M (1990). "Degradation of the ferric chelate of EDTA by a pure culture of an Agrobacterium sp.". Applied Environmental Microbiology 56 (11): 3346–3353. PMC 184952. PMID 16348340.
^ ^a ^b Nortemannl, B (1992). "Total degradation of EDTA by mixed culturesand a bacterial isolate" (PDF). Applied Environmental Microbiology 58 (2): 671–676. PMC 195300. PMID 16348653.
^ Witschel, M., Weilemann, H.-U and Egli, T. (1995). Degradation of EDTA by a bacterial isolate. Poster presented at the 45th Annual Meeting of the Swiss Society for Microbiology (Speech). Lugano, Switzerland.
^ Hennekenl, L; Nortemann, B; Hempel, D.C (1995). "Influence of physiological conditions on EDTA degradation". Applied Environmental Microbiology 44: 190–197. doi:10.1007/bf00164501.
^ ^a ^b ^c ^d ^e ^f ^g ^h ⁱ "Chelating Agents of a New Generation as an Alternative to Conventional Chelators for Heavy Metal Ions Removal from Different Waste Waters" (PDF). InTech. Retrieved 2013-12-12.
^ Cokesa, Z.; Knackmuss, H.; Rieger P. (2004), "Biodegradation of All Stereoisomers of the EDTA Substitute Iminodisuccinate by Agrobacterium Tumefaciens BY6 Requires an Epimerase and a Stereoselective C-N Lyase", Appl. Environ Microbiol. 70 (7): 3941–3947, doi:10.1128/aem.70.7.3941-3947.2004, PMC 444814, PMID 15240267
^ ^a ^b Sheppard, R. L.; Henion, J. (1997). "Peer Reviewed: Determining EDTA in Blood". Analytical Chemistry 69 (15): 477A. doi:10.1021/ac971726p. PMID 9253241.
^ Loyaux-Lawniczak, S.; Douch, J.; Behra, P. (1999). "Optimisation of the analytical detection of EDTA by HPLC in natural waters". Fresenius' Journal of Analytical Chemistry 364 (8): 727. doi:10.1007/s002160051422.
^ Cagnasso, C. E.; López, L. B.; Rodríguez, V. G.; Valencia, M. E. (2007). "Development and validation of a method for the determination of EDTA in non-alcoholic drinks by HPLC". Journal of Food Composition and Analysis 20 (3–4): 248. doi:10.1016/j.jfca.2006.05.008.

External links

The MEROPS online database for peptidases and their inhibitors: EDTA
Lanigan RS; Yamarik TA (2002). "Final report on the safety assessment of EDTA, calcium disodium EDTA, diammonium EDTA, dipotassium EDTA, disodium EDTA, TEA-EDTA, tetrasodium EDTA, tripotassium EDTA, trisodium EDTA, HEDTA, and trisodium HEDTA". Int. J. Toxicol. 21 Suppl 2 (5): 95–142. doi:10.1080/10915810290096522. PMID 12396676.
EDTA: Molecule of the Month
EDTA Determination of Total Water Hardness
EDTA: the chelating agent under environmental scrutiny, Química Nova, Nov.-Dec., 2003 (text version)
EDTA: the chelating agent under environmental scrutiny, Química Nova, Nov.-Dec., 2003 (PDF version)

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★リンクテーブル★

リンク元	「エチレンジアミン四酢酸」「エデト酸」
拡張検索	「ethylenediaminetetraacetic acid infusion test」

「エチレンジアミン四酢酸」

Ethylenediaminetetraacetic acid
	; Disodium EDTA
Names
	Systematic IUPAC name 2-({2-[Bis(carboxymethyl)amino]ethyl}(carboxymethyl)amino)acetic acid
	Other names Diaminoethane-tetraacetic acid; Edetic acid; Ethylenedinitrilo-tetraacetic acid; Versene;
Identifiers
CAS Registry Number	60-00-4
Abbreviations	EDTA, H4EDTA
Beilstein Reference	1716295
ChEBI	CHEBI:42191
ChEMBL	ChEMBL858
ChemSpider	5826
EC number	200-449-4
Gmelin Reference	144943
	InChI InChI=1S/C10H16N2O8/c13-7(14)3-11(4-8(15)16)1-2-12(5-9(17)18)6-10(19)20/h1-6H2,(H,13,14)(H,15,16)(H,17,18)(H,19,20) ; Key: KCXVZYZYPLLWCC-UHFFFAOYSA-N ;
Jmol-3D images	Image; Image
KEGG	D00052
MeSH	Edetic+Acid
PubChem	6049
RTECS number	AH4025000
	SMILES [o]:c(:[oH])CN(CCN(Cc(:[o]):[oH])Cc(:[o]):[oH])Cc(:[o]):[oH] ; OC(=O)CN(CCN(CC(O)=O)CC(O)=O)CC(O)=O ;
UNII	9G34HU7RV0
UN number	3077
Properties
Chemical formula	C10H16N2O8
Molar mass	292.24 g·mol−1
Appearance	Colourless crystals
Density	860 mg mL−1 (at 20 °C)
log P	−0.836
Acidity (pKa)	1.782
Basicity (pKb)	12.215
Thermochemistry
Std enthalpy of; formation (ΔfHo298)	−1.7654–−1.7580 MJ mol−1
Std enthalpy of; combustion (ΔcHo298)	−4.4617–−4.4545 MJ mol−1
Pharmacology
ATC code	S01XA05; V03AB03 (salts)
DrugBank	DB00974
Routes of; administration	Intramuscular; Intravenous;
Hazards
GHS pictograms
GHS signal word	WARNING
GHS hazard statements	H319
GHS precautionary statements	P305+351+338
EU classification (DSD)	Xi
R-phrases	R36
S-phrases	(S2), S26
NFPA 704	0 1 0
	Lethal dose or concentration (LD, LC):
LD50 (Median dose)	1000 mg/kg (oral, rat)
Related compounds
Related alkanoic acids	Daminozide; Octopine;
Related compounds	Triethylenetetramine; Tetraacetylethylenediamine; PMDTA; Bis-tris propane;
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	verify (what is: /?)
	Infobox references

　　[★]

英: ethylenediaminetetraacetate, ethylenediaminetetraacetic acid ethylenediamine tetra acetic acid, EDTA
同: エデト酸 edetic acid、エデト酸二ナトリウムカルシウム edetate calcium disodium、CaNa2EDTA、エダタミル edathamil
商: ブライアン
関: Versenate

二価金属イオンをキレートする
血液の抗凝固薬　←　Ca2+をキレートしてfree Ca2+が減少するため
金属中毒の治療？

例えば、鉛中毒治療薬

「エデト酸」

　　[★]

英: edeticacid
関: エチレンジアミン四酢酸; calcium disodium edetate、disodium edetate、edetate、edetate calcium disodium、EDTA、ethylenediaminetetraacetic acid、sodium calcium edetate、sodium edetate

多価カチオンを補足するキレート剤

「ethylenediaminetetraacetic acid infusion test」

　　[★] エチレンジアミン四酢酸負荷試験

[1] Substance Name: Sodium calcium edetate. NIH.gov

[2] "WHO Model List of EssentialMedicines" (PDF). World Health Organization. October 2013. Retrieved 22 April 2014.

[furia1964-3] Furia T (1964). "EDTA in Foods – A technical review". Food Technology 18 (12): 1874–1882.

[4] US Food and Drug Administration: Center for Food Safety and Applied Nutrition Questions and Answers on the Occurrence of Benzene in Soft Drinks and Other Beverages

[5] Norvell, W. A.; Lindsay, W. L. (1969). "Reactions of EDTA Complexes of Fe, Zn, Mn, and Cu with Soils". Soil Science Society of America Journal 33: 86. doi:10.2136/sssaj1969.03615995003300010024x.

[Ullmann-6] Hart, J. Roger (2005) "Ethylenediaminetetraacetic Acid and Related Chelating Agents" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim. doi:10.1002/14356007.a10_095

[r1-7] DeBusk, Ruth; et al. (2002). "Ethylenediaminetetraacetic acid (EDTA)". University of Maryland Medical Center.

[8] "Calcium Disodium Versenate (Edetate Calcium Disodium) Injection [Graceway Pharmaceuticals, Llc]". Dailymed.nlm.nih.gov. Retrieved 2013-01-01.

[9] "Drugs@FDA: FDA Approved Drug Products". Accessdata.fda.gov. Retrieved 2013-01-01.

[10] Brown, M. J.; Willis, T.; Omalu, B.; Leiker, R. (2006). "Deaths Resulting from Hypocalcemia After Administration of Edetate Disodium: 2003-2005" (Full free text). Pediatrics 118 (2): e534. doi:10.1542/peds.2006-0858. PMID 16882789.

[11] Shirley, D.G.; Walter, S.J.; Noormohamed, F.H. (2002). "Natriuretic effect of caffeine: assessment of segmental sodium reabsorption in humans". Clinical Science 103 (5): 461–466. doi:10.1042/CS20020055. PMID 12401118.

[12] Kadry, A. A.; Fouda, S. I.; Shibl, A. M.; Abu El-Asrar, A. A. (2009). "Impact of slime dispersants and anti-adhesives on in vitro biofilm formation of Staphylococcus epidermidis on intraocular lenses and on antibiotic activities". Journal of Antimicrobial Chemotherapy 63 (3): 480. doi:10.1093/jac/dkn533. PMID 19147522.

[13] Green, Saul; Wallace Sampson (December 14, 2002). "EDTA Chelation Therapy for Atherosclerosis And Degenerative Diseases: Implausibility and Paradoxical Oxidant Effects". Quackwatch. Retrieved 16 December 2009.

[14] "Postmarket Drug Safety Information for Patients and Providers > Questions and Answers on Edetate Disodium (marketed as Endrate and generic products)". U.S. Food and Drug Administration.

[lanigan2002-15] Lanigan RS and Yamarik TA (2002). "Final report on the safety assessment of EDTA, calcium disodium EDTA, diammonium EDTA, dipotassium EDTA, disodium EDTA, TEA-EDTA, tetrasodium EDTA, tripotassium EDTA, trisodium EDTA, HEDTA, and trisodium HEDTA". Int J Toxicol. 21 Suppl 2 (5): 95–142. doi:10.1080/10915810290096522. PMID 12396676.

[16] Dominguez, K; Ward, WS (December 2009). "A novel nuclease activity that is activated by Ca²⁺ chelated to EGTA". Systems Biology in Reproductive Medicine 55 (5–6): 193–99. doi:10.3109/19396360903234052.

[17] Auld, D. S. (1995). "Removal and replacement of metal ions in metallopeptidases". Methods in enzymology 248: 228–42. PMID 7674923.

[18] Münz, F. (1938) "Polyamino carboxylic acids to I. G. Farbenindustrie, U.S. Patent 2,130,505, DE 718 981, 1935.

[19] Industrial Synthesis of EDTA. chm.bris.ac.uk

[20] Kirchner, S; Gyarfas, Eleonora C. (1957). "Barium (Ethylenediaminetetracetato) Cobalt(III) 4-Hydrate". Inorganic Syntheses. Inorganic Syntheses 5: 186–188. doi:10.1002/9780470132364.ch52. ISBN 9780470132364.

[21] López-Alcalá, J. M.; Puerta-Vizcaíno, M. C.; González-Vílchez, F.; Duesler, E. N.; Tapscott, R. E. (1984). "A redetermination of sodium aqua[ethylenediaminetetraacetato(4-)]ferrate(III) dihydrate, Na[Fe(C₁₀H₁₂N₂O₈)(H₂O)]·2H₂O". Acta Cryst C40 (6): 939–941. doi:10.1107/S0108270184006338.

[22] Sinex, Scott A. EDTA – A Molecule with a Complex Story. chm.bris.ac.uk

[23] Holleman, A. F.; Wiberg, E. (2001). Inorganic Chemistry. San Diego: Academic Press. ISBN 0-12-352651-5.

[24] Bucheli-Witschel, M.; Egli, T. (2001), "DAB: Environmental Fate and Microbial Degradation of Aminopolycarboxylic Acids", FEMS Microbiology Reviews 25 (1): 69–106, doi:10.1111/j.1574-6976.2001.tb00572.x, PMID 11152941

[25] Kari, F.G (1994). Umweltverhalten von Ethylenediaminetetraacetate (EDTA) under spezieller Berucksuchtigung des photochemischen Ab-baus. (Ph.D). Swiss Federal Institute of Technology.

[26] Frank, R; Rau, H (1989). "Photochemical transformation in aqueous solution and possible environmental fate of Ethylenediaminetetraacetatic acid (EDTA)". Ecotoxicology and Environmental Safety 19 (1): 55–63. doi:10.1016/0147-6513(90)90078-j. PMID 2107071.

[27] Kaluza, U; Klingelhofer, P; K, Taeger (1998). "Microbial degradation of EDTA in an industrial wastewater treatment plant". Water Research 32 (9): 2843–2845. doi:10.1016/S0043-1354(98)00048-7.

[28] VanGinkel, C.G; Vandenbroucke, K.L; C.A, Troo (1997). "Biological removal of EDTA in conventional activated-sludge plants operated under alkaline conditions". Bioresources Technology 32 (2–3): 2843–2845. doi:10.1016/S0960-8524(96)00158-7.

[29] Lauff, J.J.; Steele, D.B; Coogan, L.A; Breitfeller, J.M (1990). "Degradation of the ferric chelate of EDTA by a pure culture of an Agrobacterium sp.". Applied Environmental Microbiology 56 (11): 3346–3353. PMC 184952. PMID 16348340.

[Nortemannl_1992_671.E2.80.93676-30] Nortemannl, B (1992). "Total degradation of EDTA by mixed culturesand a bacterial isolate" (PDF). Applied Environmental Microbiology 58 (2): 671–676. PMC 195300. PMID 16348653.

[31] Witschel, M., Weilemann, H.-U and Egli, T. (1995). Degradation of EDTA by a bacterial isolate. Poster presented at the 45th Annual Meeting of the Swiss Society for Microbiology (Speech). Lugano, Switzerland.

[32] Hennekenl, L; Nortemann, B; Hempel, D.C (1995). "Influence of physiological conditions on EDTA degradation". Applied Environmental Microbiology 44: 190–197. doi:10.1007/bf00164501.

[intech-33] ^ ^a ^b ^c ^d ^e ^f ^g ^h ⁱ "Chelating Agents of a New Generation as an Alternative to Conventional Chelators for Heavy Metal Ions Removal from Different Waste Waters" (PDF). InTech. Retrieved 2013-12-12.

[34] Cokesa, Z.; Knackmuss, H.; Rieger P. (2004), "Biodegradation of All Stereoisomers of the EDTA Substitute Iminodisuccinate by Agrobacterium Tumefaciens BY6 Requires an Epimerase and a Stereoselective C-N Lyase", Appl. Environ Microbiol. 70 (7): 3941–3947, doi:10.1128/aem.70.7.3941-3947.2004, PMC 444814, PMID 15240267

[sheppard-35] Sheppard, R. L.; Henion, J. (1997). "Peer Reviewed: Determining EDTA in Blood". Analytical Chemistry 69 (15): 477A. doi:10.1021/ac971726p. PMID 9253241.

[36] Loyaux-Lawniczak, S.; Douch, J.; Behra, P. (1999). "Optimisation of the analytical detection of EDTA by HPLC in natural waters". Fresenius' Journal of Analytical Chemistry 364 (8): 727. doi:10.1007/s002160051422.

[37] Cagnasso, C. E.; López, L. B.; Rodríguez, V. G.; Valencia, M. E. (2007). "Development and validation of a method for the determination of EDTA in non-alcoholic drinks by HPLC". Journal of Food Composition and Analysis 20 (3–4): 248. doi:10.1016/j.jfca.2006.05.008.

Names

Disodium EDTA
Systematic IUPAC name 2-({2-[Bis(carboxymethyl)amino]ethyl}(carboxymethyl)amino)acetic acid
Other names Diaminoethane-tetraacetic acid Edetic acid Ethylenedinitrilo-tetraacetic acid Versene
Identifiers
CAS Registry Number	60-00-4^Y
Abbreviations	EDTA, H₄EDTA
Beilstein Reference	1716295
ChEBI	CHEBI:42191^Y
ChEMBL	ChEMBL858^Y
ChemSpider	5826^Y
EC number	200-449-4
Gmelin Reference	144943
InChI InChI=1S/C10H16N2O8/c13-7(14)3-11(4-8(15)16)1-2-12(5-9(17)18)6-10(19)20/h1-6H2,(H,13,14)(H,15,16)(H,17,18)(H,19,20)^Y Key: KCXVZYZYPLLWCC-UHFFFAOYSA-N^Y
Jmol-3D images	Image Image
KEGG	D00052^Y
MeSH	Edetic+Acid
PubChem	6049
RTECS number	AH4025000
SMILES [o]:c(:[oH])CN(CCN(Cc(:[o]):[oH])Cc(:[o]):[oH])Cc(:[o]):[oH] OC(=O)CN(CCN(CC(O)=O)CC(O)=O)CC(O)=O
UNII	9G34HU7RV0^Y
UN number	3077
Properties
Chemical formula	C₁₀H₁₆N₂O₈
Molar mass	292.24 g·mol⁻¹
Appearance	Colourless crystals
Density	860 mg mL⁻¹ (at 20 °C)
log P	−0.836
Acidity (pK_a)	1.782
Basicity (pK_b)	12.215
Thermochemistry
Std enthalpy of formation (Δ_fH^o₂₉₈)	−1.7654–−1.7580 MJ mol−1
Std enthalpy of combustion (Δ_cH^o₂₉₈)	−4.4617–−4.4545 MJ mol−1
Pharmacology
ATC code	S01XA05 V03AB03 (salts)
DrugBank	DB00974^Y
Routes of administration	Intramuscular Intravenous
Hazards
GHS pictograms
GHS signal word	WARNING
GHS hazard statements	H319
GHS precautionary statements	P305+351+338
EU classification (DSD)	Xi
R-phrases	R36
S-phrases	(S2), S26
NFPA 704	0 1 0
Lethal dose or concentration (LD, LC):
LD₅₀ (Median dose)	1000 mg/kg (oral, rat)^[1]
Related compounds
Related alkanoic acids	Daminozide Octopine
Related compounds	Triethylenetetramine Tetraacetylethylenediamine PMDTA Bis-tris propane
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is: Y/N?)
Infobox references

匿名

検索

案内

ethylenediaminetetraacetic acid