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About This Item
Linear Formula:
(HO2CCH2)2NCH2CH2N(CH2CO2H)2
CAS Number:
Molecular Weight:
292.24
Beilstein:
1716295
EC Number:
MDL number:
UNSPSC Code:
12352100
eCl@ss:
39030907
PubChem Substance ID:
NACRES:
NA.21
Quality Level
Assay
≥98.0% (KT)
form
powder
mp
250 °C (dec.) (lit.)
solubility
water: soluble 0.4 g/L at 20 °C
functional group
amine
carboxylic acid
SMILES string
OC(=O)CN(CCN(CC(O)=O)CC(O)=O)CC(O)=O
InChI
1S/C10H16N2O8/c13-7(14)3-11(4-8(15)16)1-2-12(5-9(17)18)6-10(19)20/h1-6H2,(H,13,14)(H,15,16)(H,17,18)(H,19,20)
InChI key
KCXVZYZYPLLWCC-UHFFFAOYSA-N
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General description
Ethylenediaminetetraacetic acid (EDTA, N,N,N′,N′-ethylenediaminetetraacetic acid) is a chelating agent. It forms complexes with rare earth metal ions and the stability constants of these complexes have been evaluated. Hydroxyl radicals generated pulse radiolytically in N2O- and N2O-O2-saturated solutions reacts with EDTA. Absorption spectrum of this reaction was recorded and maxima was observed at 275 and 480nm. EDTA is an excellent ligand for Cd(II) and forms stable Cd-EDTA complexes. 113Cd NMR studies of Cd-EDTA complexes have been reported.
Application
Ethylenediaminetetraacetic acid (EDTA) may be employed in a microtiter plate assay. In this assay, interaction between EDTA or lactoferrin and nisin, lysozyme, or monolaurin against Listeria monocytogenes, Escherichia coli, Salmonella enteritidis, and Pseudomonas fluorescens strains was investigated.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye 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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