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Details

Stereochemistry ACHIRAL
Molecular Formula C6H11NO5
Molecular Weight 177.1552
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-(2-HYDROXYETHYL)IMINODIACETIC ACID

SMILES

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

InChI

InChIKey=JYXGIOKAKDAARW-UHFFFAOYSA-N
InChI=1S/C6H11NO5/c8-2-1-7(3-5(9)10)4-6(11)12/h8H,1-4H2,(H,9,10)(H,11,12)

HIDE SMILES / InChI

Molecular Formula C6H11NO5
Molecular Weight 177.1552
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Mobility of radionuclides in soil/groundwater system: comparing the influence of EDTA and four of its degradation products.
2010-10
Determination of alternative and conventional chelating agents as copper(II) complexes by capillary zone electrophoresis--the first use of didecyldimethylammonium bromide as a flow reversal reagent.
2007-02-12
Enhanced Fenton's destruction of non-aqueous phase perchloroethylene in soil systems.
2006-06
Enhanced chemical oxidation of aromatic hydrocarbons in soil systems.
2005-11
Enhanced uptake of As, Zn, and Cu by Vetiveria zizanioides and Zea mays using chelating agents.
2005-09
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:50:46 GMT 2025
Edited
by admin
on Mon Mar 31 22:50:46 GMT 2025
Record UNII
BPQ4R5AF5K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CHELEST EA
Preferred Name English
N-(2-HYDROXYETHYL)IMINODIACETIC ACID
Systematic Name English
GLYCINE, N-(CARBOXYMETHYL)-N-(2-HYDROXYETHYL)-
Systematic Name English
ETHANOLDIGLYCINE
Common Name English
NSC-18474
Code English
ACETIC ACID, ((2-HYDROXYETHYL)IMINO)DI-
Common Name English
2-HYDROXYETHYLAMINODIACETIC ACID
Common Name English
ETHANOLAMINE-N,N-DIACETIC ACID
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 39104
Created by admin on Mon Mar 31 22:50:46 GMT 2025 , Edited by admin on Mon Mar 31 22:50:46 GMT 2025
Code System Code Type Description
ECHA (EC/EINECS)
202-263-9
Created by admin on Mon Mar 31 22:50:46 GMT 2025 , Edited by admin on Mon Mar 31 22:50:46 GMT 2025
PRIMARY
EPA CompTox
DTXSID4042177
Created by admin on Mon Mar 31 22:50:46 GMT 2025 , Edited by admin on Mon Mar 31 22:50:46 GMT 2025
PRIMARY
NSC
18474
Created by admin on Mon Mar 31 22:50:46 GMT 2025 , Edited by admin on Mon Mar 31 22:50:46 GMT 2025
PRIMARY
CHEBI
143268
Created by admin on Mon Mar 31 22:50:46 GMT 2025 , Edited by admin on Mon Mar 31 22:50:46 GMT 2025
PRIMARY
CAS
93-62-9
Created by admin on Mon Mar 31 22:50:46 GMT 2025 , Edited by admin on Mon Mar 31 22:50:46 GMT 2025
PRIMARY
FDA UNII
BPQ4R5AF5K
Created by admin on Mon Mar 31 22:50:46 GMT 2025 , Edited by admin on Mon Mar 31 22:50:46 GMT 2025
PRIMARY
PUBCHEM
7152
Created by admin on Mon Mar 31 22:50:46 GMT 2025 , Edited by admin on Mon Mar 31 22:50:46 GMT 2025
PRIMARY