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Details

Stereochemistry ACHIRAL
Molecular Formula C10H18N2O7
Molecular Weight 278.2591
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HYDROXYETHYLETHYLENEDIAMINETRIACETIC ACID

SMILES

OCCN(CCN(CC(O)=O)CC(O)=O)CC(O)=O

InChI

InChIKey=URDCARMUOSMFFI-UHFFFAOYSA-N
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)

HIDE SMILES / InChI

Molecular Formula C10H18N2O7
Molecular Weight 278.2591
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

HYDROXYETHYLETHYLENEDIAMINETRIACETIC ACID (HEDTA) is used in cosmetics and care products. It’s a chelating agent, which in combination with selenium was effective in reducing the concentration of Al and level of DNA damage. In addition, experiments with rodents have shown that combination of HEDTA and propolis preserved histological features, mitigated oxidative stress and improved liver, kidney, and brain functions more profoundly.

Approval Year

PubMed

PubMed

TitleDatePubMed
Biodegradability of ethylenediamine-based complexing agents.
2001 Jun
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.
2002
On-column complexation and simultaneous separation of vanadium(IV) and vanadium(V) by capillary electrophoresis with direct UV detection.
2002 Oct
Effect of N-hydroxyethyl-ethylenediamine-triacetic acid (HEDTA) on Cr(VI) reduction by Fe(II).
2003 Jun
Aluminum-induced oxidative stress in rat brain: response to combined administration of citric acid and HEDTA.
2003 Mar
Biogeochemistry of fluoride in a plant-solution system.
2003 Nov-Dec
Equilibrium, kinetic and solvent effect studies on the reactions of [RuIII(Hedta)(H2O)] with thiols.
2005 Dec 21
Potential of Hemidesmus indicus for phytoextraction of lead from industrially contaminated soils.
2005 Jan
Effects of lead and chelators on growth, photosynthetic activity and Pb uptake in Sesbania drummondii grown in soil.
2006 Nov
Separation of chelating agents as copper complexes by capillary zone electrophoresis using quaternary ammonium bromides as additives in N-methylformamide.
2006 Oct 27
A dendrite-autonomous mechanism for direction selectivity in retinal starburst amacrine cells.
2007 Jul
Determination of sequestering agents in cosmetics and synthetic detergents by high-performance liquid chromatography with ultraviolet detection.
2007 Nov 9
Polyamine-polycarboxylate metal complexes with different biological effectiveness as nitric oxide scavengers. Clues for drug design.
2008 Jun 12
Limits of calcium clearance by plasma membrane calcium ATPase in olfactory cilia.
2009
The dystrophin complex controls bk channel localization and muscle activity in Caenorhabditis elegans.
2009 Dec
Speciation of Zn-aminopolycarboxylic complexes by electrospray ionization mass spectrometry and ion chromatography with inductively coupled plasma mass spectrometry.
2009 Feb
Interdomain interactions control Ca2+-dependent potentiation in the cation channel TRPV4.
2010 May 11
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:02:04 GMT 2023
Edited
by admin
on Fri Dec 15 15:02:04 GMT 2023
Record UNII
R79J91U341
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HYDROXYETHYLETHYLENEDIAMINETRIACETIC ACID
HSDB  
Common Name English
HEDTA
INCI  
INCI  
Official Name English
N-HYDROXYETHYL ETHYLENEDIAMINE TRIACETIC ACID
Systematic Name English
HYDROXYETHYLETHYLENEDIAMINETRIACETIC ACID [HSDB]
Common Name English
HEDTA [INCI]
Common Name English
N-(2-HYDROXYETHYL)ETHYLENEDIAMINETRIACETIC ACID
Common Name English
NSC-7341
Code English
N-(2-HYDROXYETHYL)ETHYLENEDIAMINE-N,N',N'-TRIACETIC ACID
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 39108
Created by admin on Fri Dec 15 15:02:04 GMT 2023 , Edited by admin on Fri Dec 15 15:02:04 GMT 2023
Code System Code Type Description
NSC
7341
Created by admin on Fri Dec 15 15:02:04 GMT 2023 , Edited by admin on Fri Dec 15 15:02:04 GMT 2023
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HSDB
5651
Created by admin on Fri Dec 15 15:02:04 GMT 2023 , Edited by admin on Fri Dec 15 15:02:04 GMT 2023
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RXCUI
1364568
Created by admin on Fri Dec 15 15:02:04 GMT 2023 , Edited by admin on Fri Dec 15 15:02:04 GMT 2023
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DAILYMED
R79J91U341
Created by admin on Fri Dec 15 15:02:04 GMT 2023 , Edited by admin on Fri Dec 15 15:02:04 GMT 2023
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CAS
150-39-0
Created by admin on Fri Dec 15 15:02:04 GMT 2023 , Edited by admin on Fri Dec 15 15:02:04 GMT 2023
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FDA UNII
R79J91U341
Created by admin on Fri Dec 15 15:02:04 GMT 2023 , Edited by admin on Fri Dec 15 15:02:04 GMT 2023
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MESH
C026060
Created by admin on Fri Dec 15 15:02:04 GMT 2023 , Edited by admin on Fri Dec 15 15:02:04 GMT 2023
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PUBCHEM
8773
Created by admin on Fri Dec 15 15:02:04 GMT 2023 , Edited by admin on Fri Dec 15 15:02:04 GMT 2023
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EPA CompTox
DTXSID1059737
Created by admin on Fri Dec 15 15:02:04 GMT 2023 , Edited by admin on Fri Dec 15 15:02:04 GMT 2023
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ECHA (EC/EINECS)
205-759-3
Created by admin on Fri Dec 15 15:02:04 GMT 2023 , Edited by admin on Fri Dec 15 15:02:04 GMT 2023
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WIKIPEDIA
Hydroxyethylethylenediaminetriacetic acid
Created by admin on Fri Dec 15 15:02:04 GMT 2023 , Edited by admin on Fri Dec 15 15:02:04 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
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ACTIVE MOIETY