CHEBI:24786 - iminodiacetic acid

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ChEBI Name iminodiacetic acid
Definition An amino dicarboxylic acid that is glycine in which one of the hydrogens attached to the nitrogen is substituted by a carboxymethyl group.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C4H7NO4
Net Charge 0
Average Mass 133.10270
Monoisotopic Mass 133.03751
InChI InChI=1S/C4H7NO4/c6-3(7)1-5-2-4(8)9/h5H,1-2H2,(H,6,7)(H,8,9)
Roles Classification
Chemical Role(s): chelator
A ligand with two or more separate binding sites that can bind to a single metallic central atom, forming a chelate.
Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
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ChEBI Ontology
Outgoing iminodiacetic acid (CHEBI:24786) has role chelator (CHEBI:38161)
iminodiacetic acid (CHEBI:24786) is a amino dicarboxylic acid (CHEBI:36164)
iminodiacetic acid (CHEBI:24786) is a glycine derivative (CHEBI:24373)
iminodiacetic acid (CHEBI:24786) is a non-proteinogenic α-amino acid (CHEBI:83925)
iminodiacetic acid (CHEBI:24786) is conjugate acid of iminodiacetate (CHEBI:24785)
Incoming N-(2-hydroxyethyl)iminodiacetic acid (CHEBI:143268) has functional parent iminodiacetic acid (CHEBI:24786)
N-(carboxymethyl)-L-alanine (CHEBI:149655) has functional parent iminodiacetic acid (CHEBI:24786)
iminodiacetate (CHEBI:24785) is conjugate base of iminodiacetic acid (CHEBI:24786)
2,2'-iminodiacetic acid
Synonyms Sources
2,2'-azanediyldiacetic acid IUPAC
2-[(carboxymethyl)amino]acetic acid IUPAC
aminodiacetic acid ChemIDplus
bis(carboxymethyl)amine NIST Chemistry WebBook
diglycine ChemIDplus
diglycocoll ChemIDplus
IDA ChemIDplus
iminobis(acetic acid) ChemIDplus
iminodiacetic acid ChemIDplus
iminodiethanoic acid ChemIDplus
N-(carboxymethyl)glycine ChemIDplus
Manual Xrefs Databases
c0558 UM-BBD
CPD-10189 MetaCyc
FDB028424 FooDB
HMDB0011753 HMDB
Iminodiacetic_acid Wikipedia
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Registry Numbers Types Sources
142-73-4 CAS Registry Number NIST Chemistry WebBook
142-73-4 CAS Registry Number ChemIDplus
878499 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
1735711 PubMed citation Europe PMC
21212492 PubMed citation Europe PMC
21488608 PubMed citation Europe PMC
21567989 PubMed citation Europe PMC
8892809 PubMed citation Europe PMC
9023192 PubMed citation Europe PMC
Last Modified
22 September 2020