| Identification | More | [Name]
Ethylenediaminetetraacetic acid | [CAS]
60-00-4 | [Synonyms]
1,2-DIAMINOETHANE-N,N,N',N'-TETRA-ACETIC ACID
BETZ 0640
COMPLEXONE II(R)
EDATHAMIL
EDETIC ACID
EDTA
EDTA ACID
EDTA DIHYDRATE
EDTA REAGENT
EDTA SOLUTION
EDTA TITRANT
ETHYLENEBIS(IMINODIACETIC ACID)
ETHYLENEDIAMINE-N,N,N',N'-TETRAACETIC ACID
ETHYLENEDIAMINETETRAACETIC ACID
ETHYLENEDIAMINETETRAACETIC ACID DIHYDRATE
ETHYLENEDIAMINETETRACETIC ACID
(ETHYLENEDINITRILO)TETRAACETIC ACID
(ETHYLENEDINITRILO)TETRAACETIC ACID DIHYDRATE
HAMPENE ACID
IDRANAL(R) | [EINECS(EC#)]
200-449-4 | [Molecular Formula]
C10H16N2O8 | [MDL Number]
MFCD00003541 | [Molecular Weight]
292.24 | [MOL File]
60-00-4.mol |
| Chemical Properties | Back Directory | [Definition]
An organic chelating agent. | [Appearance]
EDTA is a white, odorless, crystalline material or white powder | [Melting point ]
250 °C (dec.) (lit.) | [Boiling point ]
434.18°C (rough estimate) | [density ]
0,86 g/cm3 | [vapor pressure ]
<0.013 hPa (20 °C) | [refractive index ]
n20/D 1.363
| [Fp ]
>400°C DIN 51758 | [storage temp. ]
2-8°C
| [solubility ]
3 M NaOH: 100 mg/mL
| [form ]
crystalline
| [pka]
pKa 2 (Uncertain);10.26 (Uncertain) | [color ]
White to almost white | [Odor]
Odorless | [PH]
2.5 (10g/l, H2O, 23℃)(slurry) | [PH Range]
2.5 at 10 g/l at 23 °C | [Stability:]
Stable. Incompatible with copper, copper alloys, nickel, aluminium, strong oxidizing agents, strong bases | [Water Solubility ]
0.5 g/L (25 ºC) | [Decomposition ]
240 °C | [λmax]
λ: 280 nm Amax: ≤0.25 | [Merck ]
14,3517 | [BRN ]
1716295 | [LogP]
-0.836 (est) | [Uses]
Ethylenediaminetetraacetate (EDTA) is a sequestrant and chelating agent that functions in water but not in fats and oils. It is used to control the reaction of trace metals with some organic and inorganic components to prevent deterioration of color, texture, and development of precipitates, as well as to prevent oxidation which results in rancidity. The reactive sites of the metal ions are blocked, which prevents their normal reactions. The most common interfering metal ions in food products are iron and copper. It can be used in combination with the antioxidants bht and propyl gallate. It is used in margarine, mayonnaise, and spreads to prevent the vegetable oil from going rancid. It is used in canned corn prior to retorting to prevent discoloration caused by trace quantities of copper, iron, and chromium. It also inhibits copper-catalyzed oxidation of ascorbic acid. It occurs as disodium calcium and disodium dihydrogen . Its use is approved in specified foods, with an average usage level being in the range of 100–300 ppm. | [CAS DataBase Reference]
60-00-4(CAS DataBase Reference) | [NIST Chemistry Reference]
N,N'-1,2-Ethane diylbis-(N-(carboxymethyl)glycine)(60-00-4) | [EPA Substance Registry System]
60-00-4(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36:Irritating to the eyes.
R52/53:Harmful to aquatic organisms, may cause long-term adverse effects in the aquatic environment .
R36/37/38:Irritating to eyes, respiratory system and skin .
R36/38:Irritating to eyes and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S61:Avoid release to the environment. Refer to special instructions safety data sheet .
S37/39:Wear suitable gloves and eye/face protection .
S36:Wear suitable protective clothing . | [RIDADR ]
UN 3077 9 / PGIII | [WGK Germany ]
2
| [RTECS ]
AH4025000
| [F ]
3 | [Autoignition Temperature]
>200 °C | [TSCA ]
Yes | [HS Code ]
29224900 | [Safety Profile]
Poison by
intraperitoneal route. Experimental
teratogenic and reproductive effects.
Mutation data reported. A general-purpose
chelaung and complexing agent. When
heated to decomposition it emits toxic
fumes of NOx. | [Hazardous Substances Data]
60-00-4(Hazardous Substances Data) | [Toxicity]
LD50 orally in Rabbit: 2580 mg/kg |
| Hazard Information | Back Directory | [General Description]
Ethylenediamine tetraacetic acid is a colorless crystalline solid. EDTA(60-00-4) is slightly soluble in water. The primary hazard is the threat to the environment. Immediate steps should be taken to limit its spread to the environment. EDTA(60-00-4) is used in chemical analysis, to make detergents and cleaning compounds, and for many other uses. | [Reactivity Profile]
Behaves as a weak organic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in EDTA to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions | [Air & Water Reactions]
Slightly soluble in water. | [Potential Exposure]
EDTA is a white, odorless, crystalline material or white powder | [First aid]
If this chemical gets into the eyes, remove any
contact lenses at once and irrigate immediately for at least
15 minutes, occasionally lifting upper and lower lids. Seek
medical attention immediately. If this chemical contacts
the skin, remove contaminated clothing and wash immediately with soap and water. Seek medical attention immediately. If this chemical has been inhaled, remove from
exposure, begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has
stopped and CPR if heart action has stopped. Transfer
promptly to a medical facility. When this chemical
has been swallowed, get medical attention. Give large
quantities of water and induce vomiting. Do not make an
unconscious person vomit | [Shipping]
UN3082 Environmentally hazardous substances,
liquid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required | [Incompatibilities]
Incompatible with oxidizers (chlorates,
nitrates, peroxides, permanganates, perchlorates, chlorine,
bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases,
strong acids, oxoacids, epoxides, copper, copper alloys, and
nickel | [Description]
Ethylenediaminetetraacetic Acid (EDTA) is a common polydentate ligand. In EDTA, the hydrogen atoms are easily removed
in solution to produce anionic EDTA4-. In its anionic form Ethylenediaminetetraacetic Acid (EDTA) has six binding atoms, two
nitrogen and four oxygen.
Ethylenediaminetetraacetic Acid (EDTA) binds to a metal ion at the six binding sites, wrapping itself around the metal ion,
forming a very stable complex.the strong grasp of Ethylenediaminetetraacetic Acid (EDTA) on the metal ion is analogous
to a crab or lobster clamping down on an object with its claw, hence the name chelation.
Ethylenediaminetetraacetic Acid (EDTA) is such an effective chelating agent because it can deactivate a metal at up to six sites. | [Chemical Properties]
Edetic acid occurs as a white crystalline powder. | [Chemical Properties]
EDTA is a white, odorless, crystalline material or white powder | [Chemical Properties]
Ethylenediaminetetraacetic acid is a solid. | [Chemical Properties]
white crystals or powder | [History]
Ethylenediaminetetraacetic Acid (EDTA) was first synthesized in the early 1930s by the German chemist Ferdinand Münz
working for I. G. Farben. Münz, who was looking for a substitute for citric acid to use with
dye solutions in the textile industry, was the first to patent a process for Ethylenediaminetetraacetic Acid (EDTA) synthesis
in Germany in 1935. Münz subsequently applied for United States patents in 1936 and
1937 (U.S. Patent Number 2130505); his method involved reacting monochloroacetic acid
(C2H3ClO2) and ethylene diamine (C2H8N2). Concurrent with Münz’s work, Frederick C.
Bersworth in the United States synthesized Ethylenediaminetetraacetic Acid (EDTA) using different methods that gave greater
yields and made EDTA’s commercial production economically viable. Bersworth syntheses
involved reacting formaldehyde, amines, and hydrogen cyanide. Bersworth and Münz obtained
patents for Ethylenediaminetetraacetic Acid (EDTA) production in the 1940s (U.S. Patent Numbers 2407645 and 2461519). | [Production Methods]
Edetic acid may be prepared by the condensation of ethylenediamine
with sodium monochloroacetate in the presence of sodium
carbonate. An aqueous solution of the reactants is heated to about
90°C for 10 hours, then cooled, and hydrochloric acid is added to
precipitate the edetic acid.
Edetic acid may also be prepared by the reaction of ethylenediamine
with hydrogen cyanide and formaldehyde with subsequent
hydrolysis of the tetranitrile, or under alkaline conditions with
continuous extraction of ammonia. | [Brand name]
Versene Acid (Dow Chemical). | [Agricultural Uses]
EDTA is short for ethylenediamhetetraacetic acid, an amino polycarboxylic acid. It is a tetraprotic acid and is represented as H4Y with four carboxyl groups and two nitrogen atoms acting as ligand sites. Thus the compound is a hexadentate ligand. Ligands include ions such as Cl-, NO2-and CN- or neutral molecules like NH3 and H2O, which possess a lone pair of electrons that can be shared with a metal cation in coordinate covalent bonds.
The water solubility of EDTA is very low and, therefore, its di-sodium salt Na2H2Y.2H2O is commonly used in titrations. The Y4- forms very stable, one-to-one complexes with practically every metal ion in the Periodic Table. The reactions are carried out in a neutral or alkaline medium as the complex decomposes in acidic medium.
(and hence deterioration) of the food product, (d) to increase the storage life of whole blood by removing free calcium ions (Ca2+) to inhibit clotting, and (e) for extracting trace elements, especially copper. EDTA metal complexes, such as NaFeEDTA, MnEDTA, ZnEDTA and CuEDTA are used as fertilizers and foliar sprays. | [Pharmaceutical Applications]
Edetic acid and edetate salts are used in pharmaceutical formulations,
cosmetics, and foods as chelating agents. They form stable
water-soluble complexes (chelates) with alkaline earth and heavy
metal ions. The chelated form has few of the properties of the free
ion, and for this reason chelating agents are often described as
‘removing’ ions from solution; this process is also called sequestering.
The stability of the metal–edetate complex depends on the
metal ion involved and also on the pH. The calcium chelate is
relatively weak and will preferentially chelate heavy metals, such as
iron, copper, and lead, with the release of calcium ions. For this
reason, edetate calcium disodium is used therapeutically in cases of
lead poisoning.
Edetic acid and edetates are primarily used as antioxidant
synergists, sequestering trace amounts of metal ions, particularly
copper, iron, and manganese, that might otherwise catalyze
autoxidation reactions. Edetic acid and edetates may be used alone
or in combination with true antioxidants, the usual concentration
employed being in the range 0.005–0.1% w/v. Edetates have been
used to stabilize ascorbic acid; corticosteroids; epinephrine; folic
acid; formaldehyde; gums and resins; hyaluronidase; hydrogen
peroxide; oxytetracycline; penicillin; salicylic acid, and unsaturated
fatty acids. Essential oils may be washed with a 2% w/v solution of
edetate to remove trace metal impurities.
Edetic acid and edetates possess some antimicrobial activity but
are most frequently used in combination with other antimicrobial
preservatives owing to their synergistic effects. Many solutions used
for the cleaning, storage, and wetting of contact lenses contain
disodium edetate. Typically, edetic acid and edetates are used in
concentrations of 0.01–0.1% w/v as antimicrobial preservative
synergists.
Edetic acid and disodium edetate may also be used as water
softeners since they will chelate the calcium and magnesium ions
present in hard water; edetate calcium disodium is not effective.
Many cosmetic and toiletry products, e.g. soaps, contain edetic acid
as a water softener. | [Biological Activity]
Chelating agent; sequesters di- and trivalent metal ions. | [Biochem/physiol Actions]
Ethylenediaminetetraacetic acid (EDTA) is an anticoagulant, majorly used in preventing clotting of blood samples. EDTA may trigger aggregation of platelets resulting in pseudothrombocytopenia. EDTA along with tetracycline imparts serves as root conditioning agent and provides relief in gum infection. EDTA-tetracycline therapy decreases coronary artery calcium levels in atherosclerosis. Calcium Disodium EDTA administration is effective in slowing down the progression of chronic kidney disease. | [Safety]
Edetic acid and edetates are widely used in topical, oral, and
parenteral pharmaceutical formulations. They are also extensively
used in cosmetics and food products.
Edetic acid is generally regarded as an essentially nontoxic and
nonirritant material, although it has been associated with doserelated
bronchoconstriction when used as a preservative in
nebulizer solutions. It has therefore been recommended that
nebulizer solutions for bronchodilation should not contain edetic
acid.
Edetates, particularly disodium edetate and edetate calcium
disodium, are used in a greater number and variety of pharmaceutical
formulations than the free acid.
Disodium edetate, trisodium edetate, and edetic acid readily
chelate calcium and can, in large doses, cause calcium depletion
(hypocalcemia) if used over an extended period or if administered
too rapidly by intravenous infusion. If used in preparations for the
mouth, they can also leach calcium from the teeth. In contrast,
edetate calcium disodium does not chelate calcium.
Edetate calcium disodium is nephrotoxic and should be used
with caution in patients with renal impairment.
The WHO has set an estimated acceptable daily intake for
disodium edetate in foodstuffs at up to 2.5 mg/kg body-weight.
LD50 (mouse, IP): 0.25 g/kg
LD50 (rat, IP): 0.397 g/kg | [Environmental Fate]
EDTA can be very persistent in water, including wastewatertreatment
plants. EDTA is often found in the receiving waters of
many industrial areas, thus being classified as one of the major
organic pollutants discharged in waters. The available ecotoxicity
data for EDTA indicate that these compounds are slow to
degrade under typical environmental conditions but are not
expected to bioconcentrate. EDTA compounds range from
practically nontoxic to moderately toxic on an acute basis,
depending on the salt. Algae and invertebrates are among the
most sensitive species based on predictive modeling for acute
and chronic endpoints for EDTA, depending on the compound.
EDTA and its salts also do not appear to be very toxic for
terrestrial wild mammals, and adverse effects from reasonably
expected agricultural uses are not expected. | [storage]
Although edetic acid is fairly stable in the solid state, edetate salts
are more stable than the free acid, which decarboxylates if heated
above 150°C. Disodium edetate dihydrate loses water of crystallization
when heated to 120°C. Edetate calcium disodium is slightly
hygroscopic and should be protected from moisture.
Aqueous solutions of edetic acid or edetate salts may be sterilized
by autoclaving, and should be stored in an alkali-free container.
Edetic acid and edetates should be stored in well-closed
containers in a cool, dry place. | [Purification Methods]
Dissolve EDTA in aqueous KOH or ammonium hydroxide, and precipitate it twice with dilute HCl or HNO3. Boil it twice with distilled water to remove mineral acid, then recrystallise it from water or dimethylformamide. Dry it at 110o. It also recrystallises from boiling 1N HCl; wash the crystals with distilled H2O and dry them in vacuo. [Ma & Ray Biochemistry 19 751 1980, Beilstein 4 IV 2449.] | [Toxicity evaluation]
The principal toxicity of EDTA relates to the metal chelate,
especially in lead poisoning. Lead may be released from the
chelate in the kidneys, and then the lead may affect the tubules
and glomeruli of the kidneys. | [Regulatory Status]
Included in the FDA Inactive Ingredients Database (oral, otic, rectal,
and topical preparations; submucosal injection preparations).
Included in nonparenteral medicines licensed in the UK. Included
in the Canadian List of Acceptable Non-medicinal Ingredients. |
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