Ethylenediaminetetraacetic Acid (EDTA) can be used for coronary artery disease and neural system disease research.
Ethylenediaminetetraacetic Acid (EDTA) is used for research use only.
Ethylenediaminetetraacetic Acid (EDTA) is widely used in industry.
CAS Number: 60-00-4 (free acid)
6381-92-6 (dihydrate disodium salt)
EC Number: 200-449-4
MDL number: MFCD00003541
Linear Formula: (HO2CCH2)2NCH2CH2N(CH2CO2H)2
Molecular Formula : C10H16N2O8
Molecular Weight: 292.244 g·mol−1
SYNONYMS:
2,2',2'',2'''-(Ethane-1,2-diyldinitrilo)tetraacetic acid, Dissolvine Z, 2-({2-[bis(carboxymethyl)amino]ethyl}(carboxymethyl)amino)acetic acid, Diaminoethane-tetraacetic acid, Edetic acid, Ethylenedinitrilo-tetraacetic acid, Versene, EDTA, Edetic Acid, N,N'-1,2-Ethane diylbis-(N-(carboxymethyl)glycine), Diaminoethanetetra-acetic acid, Glycine, N,N'-1,2-ethanediylbis[N-(carboxymethyl)-, Acetic acid, (ethylenedinitrilo)tetra-, Acide ethylenediaminetetracetique, Celon A, Celon ATH, Cheelox, Cheelox BF acid, Chemcolox 340, Complexon II, 3,6-Diazaoctanedioic acid, 3,6-bis(carboxymethyl)-, Edathamil, Edta, Edta acid, Endrate, Ethylenediamine-N,N,N',N'-tetraacetic acid, Ethylenedinitrilotetraacetic acid, Hamp-ene acid, Havidote, Komplexon ii, Kyselina ethylendiamintetraoctova, Metaquest A, Nervanaid B acid, Nullapon B acid, Nullapon BF acid, Perma kleer 50 acid, Questex 4H, SEQ 100, Sequestrene AA, Sequestric acid, Sequestrol, Tetrine acid, Titriplex, Tricon bw, Trilon BW, Versene, Versene acid, Vinkeil 100, Warkeelate acid, (Ethylenedintrilo)tetraacetic acid, EDTA, free base, EDTA, free acid, Trilon BS, ([2-(Bis-carboxymethyl-amino)-ethyl]-carboxymethyl-amino)-acetic acid, Titriplex II, YD 30, Quastal Special, Acetic acid, 2,2',2'',2'''-(1,2-ethanediyldinitrilo)tetrakis-, Gluma Cleanser, EDTA (chelating agent), Chelest 3A, ICRF 185, (Ethylenedinitrilo)tetraacetic acid, EDTA, Edathamil, Ethylenedinitrilotetraacetic acid, Edathamil, (Ethylenedinitrilo)tetraacetic acid, Ethylenedinitrilotetraacetic acid, EDTA, EDTA, Edetic acid, Ethylenediaminetetraacetic acid, 60-00-4, Edathamil, Sequestrol, Versene, Havidote, Titriplex, EDTA acid, Versene acid, Endrate, Cheelox, Gluma cleanser, Sequestrene aa, Sequestric acid, Warkeelate acid, Komplexon ii, Tetrine acid, Quastal Special, Metaquest A, Trilon bw, Titriplex II, Hamp-ene acid, Cheelox BF acid, Trilon BS, Celon A, Celon ATH, Chelest 3A, Questex 4H, (Ethylenedinitrilo)tetraacetic acid, Chemcolox 340, Universne acid, EDTA (chelating agent), Dissolvine E, Vinkeil 100, Nullapon B acid, Nullapon bf acid, Nervanaid B acid, Perma kleer 50 acid, Clewat TAA, Ethylenedinitrilotetraacetic acid, Acide edetique, Acido edetico, Acidum edeticum, Caswell No. 438, Versenate, ICRF 185, Calcium disodium versenate, Ethylenebisiminodiacetic acid, Ethylenediamine-N,N,N',N'-tetraacetic acid, SEQ 100, YD 30, Disodium EDTA, CCRIS 946, Chelaton 3, Ethylenebis(iminodiacetic acid), HSDB 809, Acide ethylenediaminetetracetique, ETHYLENEDIAMINE TETRAACETIC ACID, Cheladrate, Edetate calcium, Edetate disodium, Acide edetique [INN-French], Acido edetico [INN-Spanish], Acidum edeticum [INN-Latin], Acetic acid, (ethylenedinitrilo)tetra-, EPA Pesticide Chemical Code 039101, Ethylenediaminetetraacetate, Kyselina ethylendiamintetraoctova, Tricon bw, Acid, Edetic, AI3-17181, H4edta, 3,6-Diazaoctanedioic acid, 3,6-bis(carboxymethyl)-, Glycine, N,N'-1,2-ethanediylbis[N-(carboxymethyl)-, 470462-56-7, EINECS 200-449-4, UNII-9G34HU7RV0, Edetate, BRN 1716295, Edta disodium, Versene-13C4, 9G34HU7RV0, Disodium edetate, Disodium versene, Endrate disodium, Sodium versenate, Edetic acid disodium salt, Kyselina ethylendiamintetraoctova [Czech], Acetic acid, 2,2',2'',2'''-(1,2-ethanediyldinitrilo)tetrakis-, Acide ethylenediaminetetracetique [French], Disodium edetate dihydrate, DTXSID6022977, Metaquest B, N,N'-1,2-Ethanediylbis(N-(carboxymethyl)glycine), CHEBI:42191, ethylene diamine tetraacetic acid, Kiresuto B, Chelaplex III, Diso-Tate, Titriplex III, 2-[2-[bis(carboxymethyl)amino]ethyl-(carboxymethyl)amino]acetic acid, Chelaton III, Glycine, N,N'-1,2-ethanediylbis(N-(carboxymethyl)-, N,N'-1,2-Ethane diylbis-(N-(carboxymethyl)glycine), Versene NA, Triplex III, Disodium versenate, Edathamil disodium, Trilon BD, Versene Na2, Disodium sequestrene, Disodium tetracemate, EDTA disodium salt, MFCD00003541, EDTA, ion(4-), CHEMBL858, Sequestrene sodium 2, 2,2',2'',2'''-(ethane-1,2-diylbis(azanetriyl))tetraacetic acid, 2-({2-[bis(carboxymethyl)amino]ethyl}(carboxymethyl)amino)acetic acid, {[-(BIS-CARBOXYMETHYL-AMINO)-ETHYL]-CARBOXYMETHYL-AMINO}-ACETIC ACID, Disodium salt of EDTA, ethylenediamine tetracetic acid, DTXCID902977, Perma Kleer Di Crystals, (ethylenedinitrilo)tetraacetic acid, ion(4-), Calcium disodium versenate (TN), ethylene-diamine tetraacetic acid, 2,2',2'',2'''-(ethane-1,2-diyldinitrilo)tetraacetic acid, EC 200-449-4, 4-04-00-02449 (Beilstein Handbook Reference), EDT, Ethylenediaminetetraacetic acid disodium salt, Edetate calcium disodium (USP), Sequestrene Na2, Trilon B, Selekton B2, Disodium ethylenediaminetetraacetate, (ethane-1,2-diyldinitrilo)tetraacetic acid, EDETIC ACID (II), EDETIC ACID [II], Perma kleer 50 crystals disodium salt, Disodium (ethylenedinitrilo)tetraacetate, Disodium ethylenediaminetetraacetic acid, EDETIC ACID (MART.), EDETIC ACID [MART.], CaEDTA, N,N'-1,2-ethanediylbis[N-(carboxymethyl)glycine], CBC 50152966, DR-16133, Ethylenediaminetetraacetate, disodium salt, EDETIC ACID (USP-RS), EDETIC ACID [USP-RS], ANTICOAGULANT ETHYLENEDIAMINE TETRAACETIC ACID, Disodium diacid ethylenediaminetetraacetate, D'E.d.t.a. disodique, Disodium (ethylenedinitrilo)tetraacetic acid, 2,2',2'',2'''-(ethane-1,2-diyldinitrilo)tetraacetate, Disodium dihydrogen ethylenediaminetetraacetate, Ethylenediaminetetraacetic acid, disodium salt, ANTICOAGULANT ETHYLENEDIAMINE TETRAACETIC ACID (EDTA), Disodium ethylenediamine-N,N,N',N'-tetraacetate, EDETIC ACID (EP MONOGRAPH), EDETIC ACID [EP MONOGRAPH], Disodium dihydrogen(ethylenedinitrilo)tetraacetate, 139-33-3, C10H16N2O8, NSC2760, NCGC00159485-02, 6381-92-6, disodium-edta, Edetic, Edetic acid [INN:BAN:NF], ((-(bis-carboxymethyl-amino)-ethyl)-carboxymethyl-amino)-acetic acid, (Ethylenedinitrilo)tetraacetic acid, disodium salt, Versenic Acid, Acid, Ethylenediaminetetraacetic, ([2-(Bis-carboxymethyl-amino)-ethyl]-carboxymethyl-amino)-acetic acid, {[2-(Bis-carboxymethyl-amino)-ethyl]-carboxymethyl-amino}-acetic acid, 2-(2-[bis(carboxymethyl)amino]ethylamino)acetic acid, Calcium Disodium Edetate (JAN), ethylenediamine tetra-acetic acid, Techrun DO, Acid, Ethylenedinitrilotetraacetic, EDTA, anhydrous, Zonon AO, EDTA, free acid, EDTA, free base, ACETIC ACID, (ETHYLENEDINITRILO)TETRA-, DISODIUM SALT, Versene acid (TN), ethylenediaminetetraacetic acid (edta), Caswell No 438, Glycine, N,N'-1,2-ethanediylbis(N-(carboxymethyl))-, Ethylenediamine-tetraacetic acid (EDTA), Acroma DH 700, Spectrum_001018, Edetic acid (NF/INN), EDTA [VANDF], Spectrum2_000003, Spectrum3_000412, Spectrum4_000531, Spectrum5_000955, EDTA [INCI], Edetic acid [BAN:INN], EDETIC ACID [INN], EDTA [MI], EDETIC ACID [HSDB], EDTA, anhydrous ACS grade, ethylenediaminetetracetic acid, BSPBio_001964, Diaminoethanetetra-acetic acid, KBioGR_001161, KBioSS_001498, ethylenediaminetetraacetic-acid, MLS001249457, BIDD:ER0565, DivK1c_000777, EDETIC ACID [WHO-DD], SPBio_000005, ethylenediamine-tetraacetic acid, CHEBI:4735, KBio1_000777, KBio2_001498, KBio2_004066, KBio2_006634, KBio3_001184, (Ethylenedintrilo)tetraacetic acid, ethylen-ediamine tetra-acetic acid, ethylene diamine tetra acetic acid, NINDS_000777, (ethylenedinitrilo) tetraacetic acid, CS-B1827, HY-Y0682, STR08855, Tox21_202736, BDBM50330325, HB5135, s6350, AKOS001574475, Glycine, (N,N'-1,2-ethanediylbis(N-(carboxymethyl)-, labeled with carbon-14, (ethane-1,2-diyldinitrilo)tetraacetate, DB00974, CAS-60-00-4, IDI1_000777, USEPA/OPP Pesticide Code: 039101, ETHYLENE BIS (IMINODIACETIC ACID), NCGC00159485-03, NCGC00159485-04, NCGC00260284-01, 688-55-1, AC-10615, SMR000058776, SBI-0051360.P003, E0084, Ethylenediaminetetraacetic acid, 2Na (EDTA), Ethylenediaminetetraacetic acid, LR, >=98%, NS00003929, EN300-71613, C00284, D00052, ethylene-N,N'-biscarboxymethyl-N,N'-diglycine, Ethylenediaminetetraacetic acid, p.a., 98.0%, AB00053468_03, Ethylenediaminetetraacetic acid, >=98.0% (KT), A832566, N,N'-1,2-Ethanediylbis(N-carboxymethyl)-glycine, N,N'-1,2-Ethanediylbis[N-(carboxymethyl)]glycine, N,N-1,2-Ethanediylbis[N-(carboxymethyl)]glycine, Q408032, SR-01000883946, Ethylenediaminetetraacetic Acid Sodium Salt Solution, Ethylenediaminetetraacetic acid, Cell Culture Reagent, J-610078, N, N-1,2-Ethanediylbis(N-(Carboxymethyl)Glycine), SR-01000883946-1, 3,6-Diazooctanedioic Acid, 3,6-bis(Carboxymethyl)-, 37C3C5E7-D921-445F-82D6-FEBF1AE5AEF5, Ethylenediaminetetraacetic acid, Electrophoresis Grade, Glycine, N, N'-1,2-Ethanediylbis-N-(Carboxymethyl), Z2588038976, Ethylenediaminetetraacetic acid, BioUltra, >=99.0% (KT), Ethylenediaminetetraacetic acid, 99.995% trace metals basis, Ethylenediaminetetraacetic acid, SAJ special grade, >=99.0%, Ethylenediaminetetraacetic acid, Vetec(TM) reagent grade, 98%, [{2-[bis(carboxymethyl)amino]ethyl}(carboxymethyl)amino]acetic acid, edta disodium salt, cal-ex decalcifier, buffer solution, ph 10.00, sodium di ethylenediamine tetraacetate dihydrate, ethylenediamine tetraacetic acid, disodium salt dihydrate, ethylenediamine tetraacetic acid, disodium salt, standard solution, sodium di ethylenediamine tetraacetate standard solution, ethylenedinitrilo tetraacetic acid disodium, dihydrate, reagent, Edetic Acid, N,N'-1,2-Ethane diylbis-(N-(carboxymethyl)glycine), Diaminoethanetetra-acetic acid, Glycine, N,N'-1,2-ethanediylbis[N-(carboxymethyl)-, Acetic acid, (ethylenedinitrilo)tetra-, Acide ethylenediaminetetracetique, Celon A, Celon ATH, Cheelox, Cheelox BF acid, Chemcolox 340, Complexon II, 3,6-Diazaoctanedioic acid, 3,6-bis(carboxymethyl)-, Edathamil, Edta, Edta acid, Endrate, Ethylenediamine-N,N,N',N'-tetraacetic acid, Ethylenedinitrilotetraacetic acid, Hamp-ene acid, Havidote, Komplexon ii, Kyselina ethylendiamintetraoctova, Metaquest A, Nervanaid B acid, Nullapon B acid, Nullapon BF acid, Perma kleer 50 acid, Questex 4H, SEQ 100, Sequestrene AA, Sequestric acid, Sequestrol, Tetrine acid, Titriplex, Tricon bw, Trilon BW, Versene, Versene acid, Vinkeil 100, Warkeelate acid, (Ethylenedintrilo)tetraacetic acid, EDTA, free base, EDTA, free acid, Trilon BS, ([2-(Bis-carboxymethyl-amino)-ethyl]-carboxymethyl-amino)-acetic acid, Titriplex II, YD 30, Quastal Special, Acetic acid, 2,2',2'',2'''-(1,2-ethanediyldinitrilo)tetrakis-, Gluma Cleanser, EDTA (chelating agent), Chelest 3A, ICRF 185, 2,2',2'',2'''-(Ethane-1,2-diyldinitrilo)tetraacetic acid, Dissolvine Z, 2-({2-[bis(carboxymethyl)amino]ethyl}(carboxymethyl)amino)acetic acid, Diaminoethane-tetraacetic acid, Edetic acid, Ethylenedinitrilo-tetraacetic acid, Versene, EDTA, 2,2'',2'''',2''''''-(ethane-1,2-diylbis(azanetriyl))tetraacetic acid, Ethylenediaminetetraacetic acid, BioUltra, anhydrous, >=99% (titration), Glycine, N,N'-1, {2-ethanediylbis[N-(carboxymethyl)-,} disodium salt, {[2-(Bis-carboxymethyl-amino)-ethyl]-carboxymethyl-amino}-acetic acid(EDTA), 2-[2-[bis(2-hydroxy-2-oxoethyl)amino]ethyl-(2-hydroxy-2-oxoethyl)amino]ethanoic acid, Ethylenediaminetetraacetic acid, anhydrous, free-flowing, Redi-Dri(TM), >=98%, Ethylenediamine-N,N,N inverted exclamation mark ,N inverted exclamation mark -tetraacetic Acid-13C4 (|A-labels), Ethylenediaminetetraacetic acid, anhydrous, crystalline, BioReagent, suitable for cell culture, Ethylenediaminetetraacetic acid, anhydrous, free-flowing, powder, Redi-Dri(TM), ACS reagent, 99.4-100.6%, InChI=1/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, N,N′-(Ethane-1,2-diyl)bis[N-(carboxymethyl)glycine], 2,2′,2′′,2′′′-(Ethane-1,2-diyldinitrilo)tetraacetic acid, EthyleneDiamineTetraAcetic acid, Diaminoethane-tetraacetic acid, N,N′-(Ethane-1,2-diyl)bis[N-(carboxymethyl)glycine], 2,2′,2′′,2′′′-(Ethane-1,2-diyldinitrilo)tetraacetic acid, EthyleneDiamineTetraAcetic acid, Diaminoethane-tetraacetic acid, Edetic acid (conjugate base edetate) (INN, USAN), Versene, (Ethylenedinitrilo)tetraacetic acid, EDTA, Edathamil, Ethylenedinitrilotetraacetic acid
Ethylenediaminetetraacetic Acid (EDTA) (EDTA, edetate calcium disodium, calcium disodium versenate) is a chelation agent used for heavy metal toxicity.
Ethylenediaminetetraacetic Acid (EDTA), which was first synthesized in the mid-1930s, has non-pharmacologic and pharmacologic purposes.
Ethylenediaminetetraacetic Acid (EDTA), also called EDTA acid, is an aminopolycarboxylic acid with the formula [CH2N(CH2CO2H)2]2.
This white, slightly water-soluble solid, Ethylenediaminetetraacetic Acid (EDTA), is widely used to bind to iron (Fe2+/Fe3+) and calcium ions (Ca2+), forming water-soluble complexes even at neutral pH.
Ethylenediaminetetraacetic Acid (EDTA) is available as several salts, notably disodium EDTA, sodium calcium edetate, and tetrasodium EDTA, but these all function similarly.
Ethylenediaminetetraacetic Acid (EDTA) forms chelate complexes with Mg2+-ions and other bivalent metal cations.
Ethylenediaminetetraacetic Acid (EDTA) can therefore be applied as a general inhibitor for all enzymes which require such metal cations to function (e.g. DNases and metal proteases).
Ethylenediaminetetraacetic Acid (EDTA) is a kind of metal chelating agent (binds to bivalent and trivalent metal cations, including calcium).
Ethylenediamine tetraacetic acid is a colorless crystalline solid.
Ethylenediaminetetraacetic Acid (EDTA) is slightly soluble in water.
Immediate steps should be taken to limit Ethylenediaminetetraacetic Acid (EDTA)'s spread to the environment.
Ethylenediaminetetraacetic Acid (EDTA) is a tetracarboxylic acid, an ethylenediamine derivative and a polyamino carboxylic acid.
Ethylenediaminetetraacetic Acid (EDTA) has a role as an antidote, a geroprotector, a chelator, a copper chelator and an anticoagulant.
Ethylenediaminetetraacetic Acid (EDTA) is a conjugate acid of an EDTA(2-).
Ethylenediaminetetraacetic Acid (EDTA) is a chelating agent (chelating agents) that sequesters a variety of polyvalent cations.
Ethylenediaminetetraacetic Acid (EDTA) is a Lead Chelator and Anti-coagulant.
The mechanism of action of Ethylenediaminetetraacetic Acid (EDTA) is as a Lead Chelating Activity and Calcium Chelating Activity.
The physiologic effect of Ethylenediaminetetraacetic Acid (EDTA) is by means of Decreased Coagulation Factor Activity.
Ethylenediaminetetraacetic Acid (EDTA) has been reported in Perilla frutescens, Apis cerana, and other organisms with data available.
Ethylenediaminetetraacetic Acid (EDTA) is the acid form of edetate, a chelating agent with anti-hypercalcemic and anticoagulant properties.
Ethylenediaminetetraacetic Acid (EDTA) binds calcium and heavy metal ions, forming soluble stable complexes which are readily excreted by the kidneys.
This results in a decrease in serum calcium levels.
Ethylenediaminetetraacetic Acid (EDTA) is a chelating agent (chelating agents) that sequesters a variety of polyvalent cations.
Ethylenediaminetetraacetic Acid (EDTA) is a chelating agent that sequesters a variety of polyvalent cations such as CALCIUM.
Ethylenediaminetetraacetic Acid (EDTA) is a white odourless, colourless crystalline powder, with a melting point of 240C at which it decomposes.
Ethylenediaminetetraacetic Acid (EDTA) is insoluble in cold water, alcohol and general organic solvents, slightly soluble in water, soluble in sodium hydroxide, sodium carbonate and ammonia solution, soluble in boiling water.
The alkali metal salts are soluble in water.
Ethylenediaminetetraacetic Acid (EDTA) is an important complexing agent.
Ethylenediaminetetraacetic Acid (EDTA) is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 000 tonnes per annum.
Ethylenediaminetetraacetic Acid (EDTA) is a molecule called a chelating agent.
Ethylenediaminetetraacetic Acid (EDTA) is a chelating agent is a claw-like substance that can grab and stick to other molecules.
Some types of Ethylenediaminetetraacetic Acid (EDTA) stick to calcium.
Other types stick to metals, such as lead.
USES and APPLICATIONS of ETHYLENEDIAMINETETRAACETIC ACID (EDTA):
Ethylenediaminetetraacetic Acid (EDTA) is mainly used to bind metal ions in aqueous solution making EDTA useful in a wide variety of uses as a chelating agent.
Ethylenediaminetetraacetic Acid (EDTA) is widely used to dissolve limescale.
In shampoos, cleaners, and other personal care products Ethylenediaminetetraacetic Acid (EDTA) salts are used as stabilizers.
Ethylenediaminetetraacetic Acid (EDTA) is added to some food as a preservative or stabilizer to prevent catalytic oxidative decoloration, which is catalyzed by metal ions.
In the pulp and paper industry, Ethylenediaminetetraacetic Acid (EDTA) inhibits the ability of metal ions, especially Mn2+, from catalyzing the disproportionation of hydrogen peroxide, which is used in "chlorine-free bleaching."
Ethylenediaminetetraacetic Acid (EDTA) has antibacterial, anti-inflammatory, antioxidant, anti-hypercalcemia and anticoagulant activities.
Ethylenediaminetetraacetic Acid (EDTA) decreases the metal ion-catalyzed oxidative damage to proteins, and allows maintenance of reducing environment during protein purification.
Ethylenediaminetetraacetic Acid (EDTA) can alleviate the liver fibrosis.
Ethylenediaminetetraacetic Acid (EDTA) can be used for coronary artery disease and neural system disease research.
Ethylenediaminetetraacetic Acid (EDTA) is used for research use only.
Chelating agent, Ethylenediaminetetraacetic Acid (EDTA) is used in many enzyme buffers and, at higher concentrations, as an enzyme inactivator.
Ethylenediaminetetraacetic Acid (EDTA) is widely used in industry.
Ethylenediaminetetraacetic Acid (EDTA) also has applications in food preservation, medicine, cosmetics, water softening, in laboratories, and other fields.
Ethylenediaminetetraacetic Acid (EDTA) is thus used to dissolve Fe- and Ca-containing scale as well as to deliver iron ions under conditions where its oxides are insoluble.
As a pharmacologic agent, Ethylenediaminetetraacetic Acid (EDTA) is used as calcium disodium edetate, which prevents it from binding calcium in the body.
Cosmetics uses of Ethylenediaminetetraacetic Acid (EDTA): In shampoos, cleaners, and other personal care products, Ethylenediaminetetraacetic Acid (EDTA) salts are used as a sequestering agent to improve their stability in air.
Dentistry: Ethylenediaminetetraacetic Acid (EDTA) is used in dentistry as a chelating agent for smear layer removal from root canal walls.
The oxidising properties of [Fe(EDTA)]− are used in photography to solubilise silver particles.
Ethylenediaminetetraacetic Acid (EDTA) is also used to remove crud (corroded metals) from fuel rods in nuclear reactors.
Ethylenediaminetetraacetic Acid (EDTA) is used in pharmaceutical manufacturing and as a food additive.
Ethylenediaminetetraacetic Acid (EDTA) is used in chemical analysis, to make detergents and cleaning compounds, and for many other uses.
Ethylenediaminetetraacetic Acid (EDTA) is also used as an anticoagulant for blood specimens and is applied as a treatment of lead poisoning.
Ethylenediaminetetraacetic Acid (EDTA) is a small molecule drug with a maximum clinical trial phase of III.
Ethylenediaminetetraacetic Acid (EDTA) is used in pharmaceutical manufacturing and as a food additive.
Industrial Applications: Ethylenediaminetetraacetic Acid (EDTA) is used in water treatment to sequester metal ions, preventing scale formation and corrosion.
Food Industry: Ethylenediaminetetraacetic Acid (EDTA) acts as a preservative and stabilizer, preventing metal-catalyzed oxidation in products like mayonnaise and soft drinks.
Pharmaceuticals: Ethylenediaminetetraacetic Acid (EDTA) serves as a chelating agent in medications to treat metal poisoning and as a stabilizer in certain drug formulations.
Cosmetics: Ethylenediaminetetraacetic Acid (EDTA) is incorporated into personal care products to enhance stability by binding metal ions that could cause degradation.
Laboratory Use: Ethylenediaminetetraacetic Acid (EDTA) is employed in biochemistry and molecular biology to sequester divalent cations, inhibiting enzymatic activities that require metal cofactors.
Ethylenediaminetetraacetic Acid (EDTA) is widely used, can be used for processing colour photographic materials bleach fixing bath washing, dyeing auxiliaries, textile processing auxiliaries, detergent, stabiliser, synthetic rubber and polymerization initiator.
Uses for Ethylenediaminetetraacetic Acid (EDTA): Agricultural Formulations, Bleaching (Pulp), Cleaning (Hard Surface),
Cleaning (Industrial), Cleaning (Institutional), Cleaning (Metal), Cleaning (Offshore), Drilling/Completion Fluids, Industrial Cleaning, Offshore Cleaning, Oilfield, Photography, and Textile.
Ethylenediaminetetraacetic Acid (EDTA) is predominantly used in agriculture, water treatment, pulp and paper industries and also used in the manufacture of cleaners and detergents.
Ethylenediaminetetraacetic Acid (EDTA) is used chelating agents bind or capture trace amounts of iron, copper, manganese, calcium and other metals that occur naturally in many materials.
Such naturally occurring metals can cause chemical degradation, discoloration, scaling, instability, rancidity, ineffective cleaning performance and other problems.
In Metalworking industries Ethylenediaminetetraacetic Acid (EDTA) is used for surface preparation, metal cleaning, metal plating, and in metalworking fluids.
In Cleaning products Ethylenediaminetetraacetic Acid (EDTA) is employed to remove hard water scale, soap film, and inorganic scales.
Ethylenediaminetetraacetic Acid (EDTA) is commonly used in a wide variety of cleaning products and formulations, including hard surface cleaners, laundry detergents, bactericidal cleaners, vehicle washes etc.
Ethylenediaminetetraacetic Acid (EDTA) is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.
Ethylenediaminetetraacetic Acid (EDTA) is used in the following products: washing & cleaning products, coating products, polishes and waxes, biocides (e.g. disinfectants, pest control products), adhesives and sealants, fillers, putties, plasters, modelling clay, non-metal-surface treatment products, photo-chemicals, air care products, metal surface treatment products and textile treatment products and dyes.
Other release to the environment of Ethylenediaminetetraacetic Acid (EDTA) is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters), outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids), outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials), indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment), indoor use in long-life materials with high release rate (e.g. release from fabrics, textiles during washing, removal of indoor paints) and outdoor use in long-life materials with high release rate (e.g. tyres, treated wooden products, treated textile and fabric, brake pads in trucks or cars, sanding of buildings (bridges, facades) or vehicles (ships)).
Other release to the environment of Ethylenediaminetetraacetic Acid (EDTA) is likely to occur from: indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment), indoor use in long-life materials with high release rate (e.g. release from fabrics, textiles during washing, removal of indoor paints) and outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials).
Ethylenediaminetetraacetic Acid (EDTA) can be found in complex articles, with no release intended: vehicles, machinery, mechanical appliances and electrical/electronic products (e.g. computers, cameras, lamps, refrigerators, washing machines) and electrical batteries and accumulators.
Ethylenediaminetetraacetic Acid (EDTA) can be found in products with material based on: stone, plaster, cement, glass or ceramic (e.g. dishes, pots/pans, food storage containers, construction and isolation material), fabrics, textiles and apparel (e.g. clothing, mattress, curtains or carpets, textile toys), leather (e.g. gloves, shoes, purses, furniture), metal (e.g. cutlery, pots, toys, jewellery), paper (e.g. tissues, feminine hygiene products, nappies, books, magazines, wallpaper), rubber (e.g. tyres, shoes, toys), wood (e.g. floors, furniture, toys) and plastic (e.g. food packaging and storage, toys, mobile phones).
Ethylenediaminetetraacetic Acid (EDTA) is intended to be released from scented: clothes, eraser, toys, paper products and CDs.
Ethylenediaminetetraacetic Acid (EDTA) is intended to be released from: packaging material for metal parts (releasing grease/corrosion inhibitors).
Ethylenediaminetetraacetic Acid (EDTA) is used in the following products: fertilisers.
Ethylenediaminetetraacetic Acid (EDTA) is used in the following areas: agriculture, forestry and fishing and formulation of mixtures and/or re-packaging.
Release to the environment of Ethylenediaminetetraacetic Acid (EDTA) can occur from industrial use: in processing aids at industrial sites, in the production of articles, as processing aid and of substances in closed systems with minimal release.
Other release to the environment of Ethylenediaminetetraacetic Acid (EDTA) is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters) and outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids).
Ethylenediaminetetraacetic Acid (EDTA) is used in the following products: fertilisers and pH regulators and water treatment products.
Release to the environment of Ethylenediaminetetraacetic Acid (EDTA) can occur from industrial use: formulation of mixtures and formulation in materials.
Ethylenediaminetetraacetic Acid (EDTA) is used in the following products: pH regulators and water treatment products.
Ethylenediaminetetraacetic Acid (EDTA) is used in the following areas: mining, scientific research and development and health services.
Ethylenediaminetetraacetic Acid (EDTA) is used for the manufacture of: and chemicals.
Release to the environment of Ethylenediaminetetraacetic Acid (EDTA) can occur from industrial use: as processing aid, in processing aids at industrial sites, in the production of articles and of substances in closed systems with minimal release.
Other release to the environment of Ethylenediaminetetraacetic Acid (EDTA) is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use, indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters) and outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids).
Release to the environment of Ethylenediaminetetraacetic Acid (EDTA) can occur from industrial use: manufacturing of the substance and formulation of mixtures.
Ethylenediaminetetraacetic Acid (EDTA) is used in pharmaceutical manufacturing and as a food additive.
-Industrial uses of Ethylenediaminetetraacetic Acid (EDTA):
Ethylenediaminetetraacetic Acid (EDTA) is mainly used to sequester (bind or confine) metal ions in aqueous solution.
In the textile industry, Ethylenediaminetetraacetic Acid (EDTA) prevents metal ion impurities from modifying colours of dyed products.
In the pulp and paper industry, Ethylenediaminetetraacetic Acid (EDTA) inhibits the ability of metal ions, especially Mn2+, from catalysing the disproportionation of hydrogen peroxide, which is used in chlorine-free bleaching.
-Gas scrubbing uses of Ethylenediaminetetraacetic Acid (EDTA):
Aqueous [Fe(EDTA)]− is used for removing ("scrubbing") hydrogen sulfide from gas streams.
This conversion is achieved by oxidising 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 iron(III) centre is reduced to its iron(II) derivative, which can then be reoxidised by air.
In a similar manner, nitrogen oxides are removed from gas streams using [Fe(EDTA)]2−.
-Food uses of Ethylenediaminetetraacetic Acid (EDTA):
In a similar manner, Ethylenediaminetetraacetic Acid (EDTA) is added to some food as a preservative or stabiliser to prevent catalytic oxidative decolouration, which is catalysed by metal ions.
-Water softener uses of Ethylenediaminetetraacetic Acid (EDTA):
The reduction of water hardness in laundry applications and the dissolution of scale in boilers both rely on Ethylenediaminetetraacetic Acid (EDTA) and related complexants to bind Ca2+, Mg2+, as well as other metal ions.
Once bound to Ethylenediaminetetraacetic Acid (EDTA), these metal complexes are less likely to form precipitates or to interfere with the action of the soaps and detergents.
For similar reasons, cleaning solutions often contain Ethylenediaminetetraacetic Acid (EDTA).
In a similar manner Ethylenediaminetetraacetic Acid (EDTA) is used in the cement industry for the determination of free lime and free magnesia in cement and clinkers.
The solubilisation of Fe3+ ions at or below near neutral pH can be accomplished using Ethylenediaminetetraacetic Acid (EDTA).
This property is useful in agriculture including hydroponics.
However, given the pH dependence of ligand formation, Ethylenediaminetetraacetic Acid (EDTA) is not helpful for improving iron solubility in above neutral soils.
Otherwise, at near-neutral pH and above, iron(III) forms insoluble salts, which are less bioavailable to susceptible plant species.
-Application of Ethylenediaminetetraacetic Acid (EDTA):
Stock solution: 0.5 M in water, pH 8.5.
Recommended final concentration for enzyme inhibition 1-10 mM.
The disodium salt of Ethylenediaminetetraacetic Acid (EDTA) only dissolves when the pH-value is around 8.0.
Ethylenediaminetetraacetic Acid (EDTA) is used for molecular biology and biochemistry.
-Ion-exchange chromatography uses of Ethylenediaminetetraacetic Acid (EDTA):
Ethylenediaminetetraacetic Acid (EDTA) was used in 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 Ethylenediaminetetraacetic Acid (EDTA) complexes with atomic number.
Using sulfonated polystyrene beads and Cu2+ as a retaining ion, Ethylenediaminetetraacetic Acid (EDTA) causes the lanthanides to migrate down the column of resin while separating into bands of pure lanthanides.
The lanthanides elute in order of decreasing atomic number.
Due to the expense of this method, relative to countercurrent solvent extraction, ion exchange is now used only to obtain the highest purities of lanthanides (typically greater than 99.99%).
-Medicine uses of Ethylenediaminetetraacetic Acid (EDTA):
Sodium calcium edetate, an Ethylenediaminetetraacetic Acid (EDTA) derivative, is used to bind metal ions in the practice of chelation therapy, such as for treating mercury and lead poisoning.
Ethylenediaminetetraacetic Acid (EDTA) 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.
-In testing uses of Ethylenediaminetetraacetic Acid (EDTA):
In medical diagnosis and organ function tests (here, kidney function test), the chromium(III) complex [Cr(EDTA)]− (as radioactive chromium-51 (51Cr)) is administered intravenously and its filtration into the urine is monitored.
This method is useful for evaluating glomerular filtration rate (GFR) in nuclear medicine.
Ethylenediaminetetraacetic Acid (EDTA) is used extensively in the analysis of blood.
Ethylenediaminetetraacetic Acid (EDTA) is an anticoagulant for blood samples for CBC/FBCs, where the Ethylenediaminetetraacetic Acid (EDTA) chelates the calcium present in the blood specimen, arresting the coagulation process and preserving blood cell morphology.
Tubes containing Ethylenediaminetetraacetic Acid (EDTA) are marked with lavender (purple) or pink tops.
Ethylenediaminetetraacetic Acid (EDTA) is also in tan top tubes for lead testing and can be used in royal blue top tubes for trace metal testing.
Ethylenediaminetetraacetic Acid (EDTA) is a slime dispersant, and has been found to be highly effective in reducing bacterial growth during implantation of intraocular lenses (IOLs).
-Dentistry uses of Ethylenediaminetetraacetic Acid (EDTA):
Dentists and endodontists use Ethylenediaminetetraacetic Acid (EDTA) solutions to remove inorganic debris (smear layer) and lubricate the root canals in endodontics.
This procedure helps prepare root canals for obturation.
Furthermore, Ethylenediaminetetraacetic Acid (EDTA) solutions with the addition of a surfactant loosen up calcifications inside a root canal and allow instrumentation (canal shaping) and facilitate apical advancement of a file in a tight or calcified root canal towards the apex.
-Eyedrops uses of Ethylenediaminetetraacetic Acid (EDTA):
Ethylenediaminetetraacetic Acid (EDTA) serves as a preservative (usually to enhance the action of another preservative such as benzalkonium chloride or thiomersal) in ocular preparations and eyedrops.
-Alternative medicine uses of Ethylenediaminetetraacetic Acid (EDTA):
Some alternative practitioners believe Ethylenediaminetetraacetic Acid (EDTA) acts as an antioxidant, preventing free radicals from injuring blood vessel walls, therefore reducing atherosclerosis.
These ideas are unsupported by scientific studies, and seem to contradict some currently accepted principles.
The U.S. FDA has not approved Ethylenediaminetetraacetic Acid (EDTA) for the treatment of atherosclerosis.
-Laboratory applications of Ethylenediaminetetraacetic Acid (EDTA):
In the laboratory, Ethylenediaminetetraacetic Acid (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, proteins, and polysaccharides.
Ethylenediaminetetraacetic Acid (EDTA) also acts as a selective inhibitor against dNTP hydrolyzing enzymes (Taq polymerase, dUTPase, MutT), liver arginase and horseradish peroxidase independently of metal ion chelation.
These findings urge the rethinking of the utilisation of Ethylenediaminetetraacetic Acid (EDTA) as a biochemically inactive metal ion scavenger in enzymatic experiments.
In analytical chemistry, Ethylenediaminetetraacetic Acid (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.
Ethylenediaminetetraacetic Acid (EDTA) finds many specialised uses in the biomedical labs, such as in veterinary ophthalmology as an anticollagenase to prevent the worsening of corneal ulcers in animals.
In tissue culture, Ethylenediaminetetraacetic Acid (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, Ethylenediaminetetraacetic Acid (EDTA) can be used as a decalcifying agent making it possible to cut sections using a microtome once the tissue sample is demineralised.
Ethylenediaminetetraacetic Acid (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.
Ethylenediaminetetraacetic Acid (EDTA) can also be used to test for bioavailability of heavy metals in sediments.
However, Ethylenediaminetetraacetic Acid (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.
-Digoxin toxicity uses of Ethylenediaminetetraacetic Acid (EDTA):
Ethylenediaminetetraacetic Acid (EDTA) has also been used to treat digoxin toxicity, although most doctors prefer to use other methods.
In this case, Ethylenediaminetetraacetic Acid (EDTA) helps remove excess levels of digoxin, a medication that is used to treat abnormal rhythms of the heart.
-Atherosclerosis uses of Ethylenediaminetetraacetic Acid (EDTA):
Evidence that Ethylenediaminetetraacetic Acid (EDTA) chelation therapy is effective for heart disease is mixed.
Proponents believe Ethylenediaminetetraacetic Acid (EDTA) may help people with atherosclerosis (hardening of the arteries) or peripheral vascular disease (decreased blood flow to the legs) by clearing clogged arteries and improving blood flow.
However, the few studies that show Ethylenediaminetetraacetic Acid (EDTA) may help have been poorly designed, making the results questionable.
The theory that Ethylenediaminetetraacetic Acid (EDTA) clears clogged arteries and improves blood flow is based on an outdated model about what causes heart disease.
Newer theories include the possibility that Ethylenediaminetetraacetic Acid (EDTA) functions like an antioxidant, preventing damaging molecules known as free radicals from injuring blood vessel walls and allowing plaque to build up.
In fact, studies suggest that Ethylenediaminetetraacetic Acid (EDTA) chelation therapy in combination with oral high-dose vitamins and minerals significantly reduced the occurrence of cardiac events compared to placebo.
Other studies suggest Ethylenediaminetetraacetic Acid (EDTA) chelation reduces further cardiac events among people who have diabetes, who have already had a heart attack.
-Chelation therapy is a treatment that involves repeated intravenous (IV) administration of a chemical solution of Ethylenediaminetetraacetic Acid (EDTA).
Ethylenediaminetetraacetic Acid (EDTA) is used to treat acute and chronic lead poisoning by pulling toxins (including heavy metals such as lead, cadmium, and mercury) from the bloodstream.
The word "chelate" comes from the Greek root chele, which means "to claw."
Ethylenediaminetetraacetic Acid (EDTA) has a claw-like molecular structure that binds to heavy metals and other toxins.
The U.S. Food and Drug Administration (FDA) approved Ethylenediaminetetraacetic Acid (EDTA) chelation therapy as a treatment for lead and heavy metal poisoning.
Ethylenediaminetetraacetic Acid (EDTA) is also used as an emergency treatment for hypercalcemia (excessive calcium levels) and the control of ventricular arrhythmias (abnormal heart rhythms) associated with digitalis toxicity.
Studies by the National Academy of Sciences/National Research Council in the late 1960s suggested that Ethylenediaminetetraacetic Acid (EDTA) might be effective in the treatment of arteriosclerosis (blocked arteries).
However, most well-designed studies have found that Ethylenediaminetetraacetic Acid (EDTA) is not effective for heart disease.
In fact, many medical organizations, including the National Institutes of Health (NIH), the American Medical Association (AMA), the American Heart
Association (AHA), and the American College of Cardiology (ACC), have publicly criticized and denounced the practice of Ethylenediaminetetraacetic Acid (EDTA) chelation therapy for heart disease.
Proponents of chelation therapy for heart disease claim that Ethylenediaminetetraacetic Acid (EDTA), combined with oral vitamins and minerals, helps dissolve plaques and mineral deposits associated with atherosclerosis (hardening of the arteries).
Most reports about using chelation therapy for heart disease have been based on case studies and a few animal studies that may not apply to people.
Also, several large-scale clinical trials published in peer-reviewed journals have found that Ethylenediaminetetraacetic Acid (EDTA) chelation therapy is no better than placebo in improving symptoms of heart disease.
Some medical experts note that theories about why chelation might help treat atherosclerosis depend on an outdated understanding of how heart disease develops.
Finally, and probably most importantly, the safety of Ethylenediaminetetraacetic Acid (EDTA) chelation therapy for people with heart disease is not known.
-Uses of Ethylenediaminetetraacetic Acid (EDTA):
*Lead poisoning and heavy metal toxicity
*Chelation therapy using Ethylenediaminetetraacetic Acid (EDTA) is the medically-accepted treatment for lead poisoning.
Injected intravenously and once in the bloodstream, Ethylenediaminetetraacetic Acid (EDTA) traps lead and other metals, forming a compound that the body can eliminate in the urine.
The process generally takes 1 to 3 hours.
Other heavy metal poisonings treated with chelation include mercury, arsenic, aluminum, chromium, cobalt, manganese, nickel, selenium, zinc, tin, and thallium.
*Chelating agents other than Ethylenediaminetetraacetic Acid (EDTA) are also used to clear several of these substances from the bloodstream.
-Other key applications for Ethylenediaminetetraacetic Acid (EDTA) include:
In Photography as a bleach in photographic film processing.
In the manufacturing of paper to maximize bleaching efficiency during pulping, prevent brightness reversion, and protect bleach potency.
In Scale removal and prevention - to clean calcium and other types of scale from boilers, evaporators, heat exchangers, filter cloths, and glass-lined kettles.
Water treatment - to control water hardness and scale-forming calcium and magnesium ions and to prevent scale formation.
BENEFITS OF ETHYLENEDIAMINETETRAACETIC ACID (EDTA):
*Metal Ion Sequestration:
Effectively binds to a variety of metal ions, enhancing the stability and efficacy of products.
*Versatility:
Applicable in numerous industries due to its broad-spectrum chelating abilities.
*Stability:
Ethylenediaminetetraacetic Acid (EDTA) enhances the shelf-life and quality of products by preventing metal-induced degradation.
WHY DO PEOPLE TAKE ETHYLENEDIAMINETETRAACETIC ACID (EDTA)?
Ethylenediaminetetraacetic Acid (EDTA) is sometimes prescribed by doctors to clean toxic metals, such as lead, from the blood.
Doctors have used the molecule for decades to treat heavy metal poisoning.
In those cases, Ethylenediaminetetraacetic Acid (EDTA) is given through an IV.
Ethylenediaminetetraacetic Acid (EDTA) is also an ingredient in some prescription cancer-fighting medicines.
Supplement makers claim that over-the-counter forms of Ethylenediaminetetraacetic Acid (EDTA) can be taken by mouth to "detox" the body and make your gastrointestinal tract healthier.
There is no scientific evidence to support this.
Preliminary studies show that intravenous Ethylenediaminetetraacetic Acid (EDTA) therapy under physician supervision may help patients who have had a heart attack, particularly if they have diabetes.
However, more study is needed to prove this.
Some people take Ethylenediaminetetraacetic Acid (EDTA) to try to treat:
*Diabetes
*Peripheral vascular disease
*Alzheimer's disease
However, evidence is lacking that Ethylenediaminetetraacetic Acid (EDTA) works for those conditions.
HOW TO TAKE ETHYLENEDIAMINETETRAACETIC ACID (EDTA):
*Pediatric
For the treatment of lead poisoning: A doctor may give EDTA intravenously (IV) in a clinic or hospital.
The dose depends on the amount of lead in the child's blood, as well as the child's height and weight.
Daily treatment for up to 5 days may be required.
*Adult
For heavy metal toxicity:
Ethylenediaminetetraacetic Acid (EDTA) chelation therapy is often given intravenously with calcium, magnesium, and vitamins B and C over a period of 1 to 3 hours.
The recommended adult dosage of Ethylenediaminetetraacetic Acid (EDTA) varies depending on the size of the person and the amount of lead or other metal in the body.
The amount of Ethylenediaminetetraacetic Acid (EDTA) used would be determined in a hospital setting.
AVAILABLE FORMS OF ETHYLENEDIAMINETETRAACETIC ACID (EDTA):
Ethylenediaminetetraacetic Acid (EDTA) is a synthetic chemical and not found naturally.
Because there is concern that EDTA may deplete important vitamins and minerals, Ethylenediaminetetraacetic Acid (EDTA) chelation therapy is often given with essential nutrients (including calcium, B vitamins, vitamin C, and magnesium).
There are advertisements for oral chelating agents available on the market, some of which contain Ethylenediaminetetraacetic Acid (EDTA).
However, they have not been studied in clinical trials.
Some manufacturers promote topical Ethylenediaminetetraacetic Acid (EDTA) solutions as well.
These also lack substantial research.
Speak with your physician.
PHYSICAL and CHEMICAL PROPERTIES of ETHYLENEDIAMINETETRAACETIC ACID (EDTA):
IUPAC Name: 2,2',2'',2'''-(Ethane-1,2-diyldinitrilo)tetraacetic acid
CAS Number: 60-00-4
EC Number: 200-449-4
Molecular Formula: C₁₀H₁₆N₂O₈
Molecular Weight: 292.24 g/mol
CAS No. 60-00-4
EC No. 200-449-4
Formula: (HO2CCH2)2NCH2CH2N(CH2CO2H)2
Molecular weight: 292.24
Appearance: white crystalline solid.
Relative density: 0.86 g/cm3
Melting Point: 220C (428F)
Solubility: Very slightly soluble in cold water.
pH (1%): 2.5
Physical state: liquid
Color: No data available
Odor: No data available
Melting point/freezing point: No data available
Initial boiling point and boiling range: No data available
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: Not applicable
Autoignition temperature: Not applicable
Decomposition temperature: No data available
pH: No data available
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: No data available
Partition coefficient: n-octanol/water: No data available
Vapor pressure: No data available
Density: No data available
Relative density: No data available
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: Not classified as explosive.
Oxidizing properties: none
Other safety information: No data available
CAS Number: 60-00-4
Molecular Weight: 292.24
Beilstein: 1716295
EC Number: 200-449-4
MDL Number: MFCD00003541
Physical State: Powder
Color: White
Odor: Odorless
Melting Point/Freezing Point: Melting point/range: 250 °C - dec.
Initial Boiling Point and Boiling Range: No data available
Flammability (solid, gas): No data available
Upper/Lower Flammability or Explosive Limits: No data available
Flash Point: Not applicable
Autoignition Temperature: No data available
Decomposition Temperature: > 220 °C
pH: 2.5 at 10 g/l at 23 °C
Viscosity:
Kinematic Viscosity: No data available
Dynamic Viscosity: No data available
Water Solubility: 0.4 g/l at 20 °C
Partition Coefficient (n-octanol/water): No data available
Vapor Pressure: No data available
Density: 1.46 g/cm³ at 20 °C
Relative Density: No data available
Relative Vapor Density: No data available
Particle Characteristics: No data available
Explosive Properties: No data available
Oxidizing Properties: None
Other Safety Information:
Dissociation constant: 8.85 - 10.44 at 20 °C
Molecular Weight: 292.24 g/mol
XLogP3-AA: -5.9
Hydrogen Bond Donor Count: 4
Hydrogen Bond Acceptor Count: 10
Rotatable Bond Count: 11
Exact Mass: 292.09066547 g/mol
Monoisotopic Mass: 292.09066547 g/mol
Topological Polar Surface Area: 156 Ų
Heavy Atom Count: 20
Formal Charge: 0
Complexity: 316
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
CAS No. 60-00-4
EC No. 200-449-4
Formula: (HO2CCH2)2NCH2CH2N(CH2CO2H)2
Molecular weight: 292.24
Appearance: white crystalline solid.
Relative density: 0.86 g/cm3
Melting Point: 220C (428F)
Solubility: Very slightly soluble in cold water.
pH (1%): 2.5
Chemical Formula: C10H16N2O8
Molar Mass: 292.244 g·mol⁻¹
Appearance: Colorless crystals
Density: 0.860 g cm⁻³ (at 20 °C)
Log P: -0.836
Acidity (pKa): 2.0, 2.7, 6.16, 10.26
Thermochemistry:
Standard Enthalpy of Formation (ΔfH⦵298): -1765.4 to -1758.0 kJ mol⁻¹
Standard Enthalpy of Combustion (ΔcH⦵298): -4461.7 to -4454.5 kJ mol⁻¹
CAS Number: 65501-24-8
Packing: 500g/bottle
Appearance: White crystal powder
Chemical Properties: Odorless, soluble in water, easy to absorb moisture
pH Value: 7.3±1 (5% aqueous solution, g/ml)
Solubility in Water: ≥60% (g/ml, 25℃)
Validity Period: 3 years
Storage Conditions: Dry and sealed at room temperature.
Chemical formula: C10H16N2O8
Molar mass: 292.244 g·mol−1
Appearance: Colourless crystals
Density: 0.860 g cm−3 (at 20 °C)
log P: −0.836
Acidity (pKa): 2.0, 2.7, 6.16, 10.26
Thermochemistry
Std enthalpy of formation (ΔfH⦵298): −1765.4 to −1758.0 kJ mol−1
Std enthalpy of combustion (ΔcH⦵298): −4461.7 to −4454.5 kJ mol−1
Molecular Weight: 292.24 g/mol
XLogP3-AA: -5.9
Hydrogen Bond Donor Count: 4
Hydrogen Bond Acceptor Count: 10
Rotatable Bond Count: 11
Exact Mass: 292.09066547 Da
Monoisotopic Mass: 292.09066547 Da
Topological Polar Surface Area: 156 Ų
Heavy Atom Count: 20
Formal Charge: 0
Complexity: 315
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
FIRST AID MEASURES of ETHYLENEDIAMINETETRAACETIC ACID (EDTA):
-Description of first-aid measures:
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed:
No data available
ACCIDENTAL RELEASE MEASURES of ETHYLENEDIAMINETETRAACETIC ACID (EDTA):
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.
FIRE FIGHTING MEASURES of ETHYLENEDIAMINETETRAACETIC ACID (EDTA):
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Suppress (knock down) gases/vapors/mists with a water spray jet.
Prevent fire extinguishing water from contaminating surface water or the ground water system.
EXPOSURE CONTROLS/PERSONAL PROTECTION of ETHYLENEDIAMINETETRAACETIC ACID (EDTA):
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Skin protection:
Full contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,11 mm
Break through time: 480 min
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter type P2
-Control of environmental exposure:
Do not let product enter drains.
HANDLING and STORAGE of ETHYLENEDIAMINETETRAACETIC ACID (EDTA):
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.
STABILITY and REACTIVITY of ETHYLENEDIAMINETETRAACETIC ACID (EDTA):
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature) .
-Conditions to avoid:
no information available