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68391-67-3

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68391-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68391-67-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,3,9 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 68391-67:
(7*6)+(6*8)+(5*3)+(4*9)+(3*1)+(2*6)+(1*7)=163
163 % 10 = 3
So 68391-67-3 is a valid CAS Registry Number.

68391-67-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[carboxylatomethyl(carboxymethyl)amino]acetate,iron(2+)

1.2 Other means of identification

Product number -
Other names ferrous nitrilotriacetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:68391-67-3 SDS

68391-67-3Upstream product

68391-67-3Downstream Products

68391-67-3Relevant articles and documents

Reactions of FeIInta and FeIIedda with Hydrogen Peroxide

Rush, J. D.,Koppenol, W. H.

, p. 4957 - 4963 (1988)

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.

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