16448-54-7 Usage
Uses
Used in Environmental Applications:
Ferric nitrilotriacetate is used as a chelating agent for the removal of heavy metals from wastewater and soil. Its ability to bind to metal ions, such as iron and copper, makes it useful in this application.
Used in Detergent and Cleaning Products:
Ferric nitrilotriacetate is used as a chelating agent in the formulation of detergents and cleaning products. It helps to bind and remove metal ions, enhancing the cleaning and degreasing properties of these products.
Used in Pharmaceutical and Agricultural Chemicals Synthesis:
Ferric nitrilotriacetate is used as a chelating agent in the synthesis of pharmaceuticals and agricultural chemicals. Its ability to bind to metal ions can improve the stability and effectiveness of these products.
Used in Medical Applications:
Ferric nitrilotriacetate has been studied for its potential use in the treatment of iron overload disorders. Its ability to bind to iron ions may help to reduce the levels of excess iron in the body.
However, it is important to handle ferric nitrilotriacetate with caution due to its potential health and environmental hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 16448-54-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,4 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16448-54:
(7*1)+(6*6)+(5*4)+(4*4)+(3*8)+(2*5)+(1*4)=117
117 % 10 = 7
So 16448-54-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H9NO6.Fe/c8-4(9)1-7(2-5(10)11)3-6(12)13;/h1-3H2,(H,8,9)(H,10,11)(H,12,13);/q;+3/p-3
16448-54-7Relevant academic research and scientific papers
Reactions of FeIInta and FeIIedda with Hydrogen Peroxide
Rush, J. D.,Koppenol, W. H.
, p. 4957 - 4963 (2007/10/02)
Reactions of ferrous nitrilotriacetate (nta) and ethylenediamine-N,N'-diacetate (edda) complexes with hydrogen peroxide at neutral pH in the presence of formate lead to transient intermediates characterized by absorptions near 280 and 400 nm as previously observed for hedta as a ligand.The decomposition of hydrogen peroxide by FeIIInta and-edda leads to ligand destruction, which is not inhibited by formate.During this process a reactive intermediate is scavenged by ABTS at concentrations of the latter that are much higher than expected if the hydroxyl radical were the reactive intermediate.This intermediate is not scavenged by the bromide ion.These stopped-flow and steady-state experiments give evidence for the following reactions (HL = nta, edda): (a) HLFeII + H2O2 -> HLFe(H2O2), (b) HLFe(H2O2) + HLFeII + 2H+ -> 2HLFeIII + 2H2O, (c) HLFe(H2O2) + HCO2- -> L.FeII + CO2.- + 2H2O, (d) HLFe(H2O2) + H+ -> L+FeII + 2H2O, (e) HLFe(H2O2) + ABTS + 2H+ -> HLFeIII + ABTS.+ + 2H2O.Reactions b-e are ascribed to a compound designated as HLFe(H2O2) in reaction a, which might be a hypervalent iron complex HLFeIV(OH-)2 but not a hydroxyl radical.The ability of the HLFe(H2O2) complex to oxidize ethanol but not bromide suggests a one-electron reduction potential greater than E0'(CH3.CHOH,H+/CH3CH2OH) = 1.2 V at pH 7 and smaller than E0(Br2.-/2Br- = 1.63 V.
