TRISODIUM HEDTA

Details

Stereochemistry	ACHIRAL
Molecular Formula	C10H15N2O7.3Na
Molecular Weight	344.2046
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

[Na+].[Na+].[Na+].OCCN(CCN(CC([O-])=O)CC([O-])=O)CC([O-])=O

InChI

InChIKey=WHNXAQZPEBNFBC-UHFFFAOYSA-K

InChI=1S/C10H18N2O7.3Na/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);;;/q;3*+1/p-3

HIDE SMILES / InChI

Molecular Formula	Na
Molecular Weight	22.9898
Charge	1
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Molecular Formula	C10H15N2O7
Molecular Weight	275.2353
Charge	-3
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/22251571 | https://www.ncbi.nlm.nih.gov/pubmed/22575537

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

Title	Date	PubMed
Biodegradability of ethylenediamine-based complexing agents and related compounds.	2001 Aug	11482674
Inhibition of CaT1 channel activity by a noncompetitive IP3 antagonist.	2001 Jan 12	11162491
Biodegradability of ethylenediamine-based complexing agents.	2001 Jun	11337848
Determination of strong binding chelators and their metal complexes by anion-exchange chromatography and inductively coupled plasma mass spectrometry.	2002 Feb 22	11883654
Direct modulation of volume-regulated anion channels by Ca(2+) chelating agents.	2002 Jun 19	12067708
Preparation of Gd3+-containing polymer complex as a novel magnetic resonance signal-enhancing coating material.	2003 Mar	15348476
Inactivation of human glutamate dehydrogenase by aluminum.	2003 Nov	14625697
Functional and structural study on chelator-induced suppression of S2/S1 FTIR spectrum in photosynthetic oxygen-evolving complex.	2003 Oct 1	14512202
The excitation cascade of Limulus ventral photoreceptors: guanylate cyclase as the link between InsP3-mediated Ca2+ release and the opening of cGMP-gated channels.	2004 Feb 26	15053840
The [Ru(Hedta)NO](0.1-) system: structure, chemical reactivity and biological assays.	2004 Nov	15522418
Equilibrium, kinetic and solvent effect studies on the reactions of [RuIII(Hedta)(H2O)] with thiols.	2005 Dec 21	16311647
Potential of Hemidesmus indicus for phytoextraction of lead from industrially contaminated soils.	2005 Jan	15620742
Macrocyclic lanthanide complexes as artificial nucleases and ribonucleases: effects of pH, metal ionic radii, number of coordinated water molecules, charge, and concentrations of the metal complexes.	2005 Sep 19	16156622
Effects of lead and chelators on growth, photosynthetic activity and Pb uptake in Sesbania drummondii grown in soil.	2006 Nov	16522347
Separation of chelating agents as copper complexes by capillary zone electrophoresis using quaternary ammonium bromides as additives in N-methylformamide.	2006 Oct 27	17723760
Confirmation of vanadium complex formation using electrospray mass spectrometry and determination of vanadium speciation by sample stacking capillary electrophoresis.	2007 Feb 28	17386644
A dendrite-autonomous mechanism for direction selectivity in retinal starburst amacrine cells.	2007 Jul	17622194
Influence of soil type on the mobility and bioavailability of chelated zinc.	2007 May 2	17407310
Homeostatic control of slow vacuolar channels by luminal cations and evaluation of the channel-mediated tonoplast Ca2+ fluxes in situ.	2008	18832189
Polyamine-polycarboxylate metal complexes with different biological effectiveness as nitric oxide scavengers. Clues for drug design.	2008 Jun 12	18484716

Substance Class	Chemical Created by `admin` on `Fri Dec 15 15:23:15 GMT 2023` Edited by `admin` on `Fri Dec 15 15:23:15 GMT 2023`
Record UNII	K3E0U7O8KI
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

TRISODIUM HEDTA

Official Name

English

N-(HYDROXYETHYL)-N,N',N'-ETHYLENEDIAMINETRIACETIC ACID TRISODIUM SALT

Common Name

English

GLYCINE, N-(2-(BIS(CARBOXYMETHYL)AMINO)ETHYL)-N-(2-HYDROXYETHYL)-, TRISODIUM SALT

Common Name

English

TRISODIUM N-HYDROXYETHYLETHYLENEDIAMINETRIACETATE

Common Name

English

N-(2-(BIS(CARBOXYMETHYL)AMINO)ETHYL)-N-(2-HYDROXYETHYL)GLYCINE TRISODIUM SALT

Common Name

English

TRISODIUM HEDTA [II]

Common Name

English

TRISODIUM HEDTA [INCI]

Common Name

English

SODIUM HEDTA

Common Name

English

TRISODIUM HYDROXYETHYLETHYLENEDIAMINETRIACETATE

Common Name

English

VERSENOL [MI]

Common Name

English

TRISODIUM N-HYDROXYETHYLETHYLENEDIAMINETRIACETATE [HSDB]

Common Name

English

NSC-148338

Code

English

TRISODIUM 2-(CARBOXYLATOMETHYL(2-HYDROXYETHYL)AMINO)ETHYLIMINODI(ACETATE)

Systematic Name

English

Classification Tree Code System Code

EPA PESTICIDE CODE

39109