H8126
N-(2-Hydroxyethyl)ethylenediamine-N,N′,N′-triacetic acid
~98%
Synonym(s):
N-Carboxymethyl-N′-(2-hydroxyethyl)-N,N′-ethylenediglycine, HEDTA, HEEDTA
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About This Item
Linear Formula:
HOCH2CH2N(CH2CO2H)CH2CH2N(CH2CO2H)2
CAS Number:
Molecular Weight:
278.26
Beilstein:
1804795
EC Number:
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22
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Assay
~98%
Quality Level
form
powder
mp
212 °C (dec.) (lit.)
SMILES string
OCCN(CCN(CC(O)=O)CC(O)=O)CC(O)=O
InChI
1S/C10H18N2O7/c13-4-3-11(5-8(14)15)1-2-12(6-9(16)17)7-10(18)19/h13H,1-7H2,(H,14,15)(H,16,17)(H,18,19)
InChI key
URDCARMUOSMFFI-UHFFFAOYSA-N
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Application
N-(2-Hydroxyethyl)ethylenediamine-N,N′,N′-triacetic acid (HEDTA) can be used as an ionophore for the selective determination of Fe(III) ions by the potentiometric method. It is also used to form complexes with metal ions such as iron(II), copper (II), zinc(II), manganese(II), and uranium(VI) ions. Therefore, HEDTA plays an important role in the separation of f-elements and the treatment and disposal of nuclear waste.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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C Huang et al.
Plant physiology, 124(1), 415-422 (2000-09-12)
Phosphate (P) is taken up by plants through high-affinity P transporter proteins embedded in the plasma membrane of certain cell types in plant roots. Expression of the genes that encode these transporters responds to the P status of the plants
Swaran J S Flora et al.
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 134(3), 319-328 (2003-03-20)
Aluminum, a known neurotoxic substance, has been suggested as a contributing factor in the pathogenesis of Alzheimer's disease. Therapeutic efficacy of combined administration of citric acid (CA) and N-(2-hydroxyethyl) ethylenediaminetriacetic acid (HEDTA) was evaluated in decreasing blood and brain aluminum
Y M Tzou et al.
Chemosphere, 51(9), 993-1000 (2003-04-17)
The complexation of Fe(II) with organic ligand results in the decrease of redox potential, and enhances the reduction ability of Fe(II). An important example is the use of Fe(II)-organic complexes to accelerate Cr(VI) reduction. Dissolved O(2) and light can potentially
Patrícia Graça Zanichelli et al.
Journal of inorganic biochemistry, 98(11), 1921-1932 (2004-11-04)
The [Ru(II)(Hedta)NO(+)] complex is a diamagnetic species crystallizing in a distorted octahedral geometry, with the Ru-N(O) length 1.756(4) A and the RuNO angle 172.3(4) degrees . The complex contains one protonated carboxylate (pK(a)=2.7+/-0.1). The [Ru(II)(Hedta)NO(+)] complex undergoes a nitrosyl-centered one-electron
Ana Alvarez-Fernández et al.
Journal of the American Society for Mass Spectrometry, 18(1), 37-47 (2006-10-03)
A high-performance liquid chromatography-electrospray ionization/mass spectrometry (time of flight) method has been developed for the simultaneous determination of synthetic Fe(III)-chelates used as fertilizers. Analytes included the seven major Fe(III)-chelates used in agriculture, Fe(III)-EDTA, Fe(III)-DTPA, Fe(III)-HEDTA, Fe(III)-CDTA, Fe(III)-o,oEDDHA, Fe(III)-o,pEDDHA, and Fe(III)-EDDHMA
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