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Cited by 200

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Oxidizing intermediates in the reaction of ferrous EDTA with hydrogen peroxide. Reactions with organic molecules and ferrocytochrome c.

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Rush, J D, Koppenol, W H·1986·Journal of Biological Chemistry

Abstract

The reaction between hydrogen peroxide and ferrous EDTA generates an oxidizing intermediate (I1) which is not the hydroxyl radical. It oxidizes ferrocytochrome c and also reacts with hydrogen peroxide (k5 = 3.2 X 10(3) M-1 S-1) to form a second oxidizing transient (I2). I1 is not scavenged by t-butyl alcohol whereas I2 is. I1 is found to be significantly less reactive than the hydroxyl radical toward benzoate ion, t-butyl alcohol, acetate ion, arginine, and serine, but is scavenged by compounds with readily oxidizable functional groups such as ethanol and isopropyl alcohol. This indicates that I1 does not undergo the characteristic reactions of the hydroxyl radical but shows a pattern of reactivity more associated with a metal ion oxidant like a ferryl (FeO2+)-EDTA complex.

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Metadata

Authors
Rush, J. D., & Koppenol, W. H.
Venue
Journal of Biological Chemistry
Publisher
Elsevier BV
Published
1986-05
Volume
261
Issue
15
Pages
6730-6733
ISSN
0021-9258 (ISSN-L)
OpenAlex
W1508450059
Cited by
200
References
1
FWCI
13.23
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Oxidizing intermediates in the reaction of ferrous EDTA with hydrogen peroxide. Reactions with organic molecules and ferrocytochrome c. https://app.cochat.ai/papers/10.1016/s0021-9258(19)62677-3
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Rush, J. D., & Koppenol, W. H. (1986). Oxidizing intermediates in the reaction of ferrous EDTA with hydrogen peroxide. Reactions with organic molecules and ferrocytochrome c. Journal of Biological Chemistry. https://doi.org/10.1016/s0021-9258(19)62677-3

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