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Fe(II)-EDTA, also known as ferrous ethylenediaminetetraacetate, is a chelating agent that is commonly used as a fertilizer additive to provide iron to plants. It is composed of iron (Fe) in its +2 oxidation state (Fe(II)) and the chelating agent EDTA. Chelating agents like EDTA are able to form stable complexes with metal ions, which allows for the controlled release and uptake of the metal by plants. Fe(II)-EDTA is highly soluble in water, making it easy to apply to soil, and is readily absorbed by plants, making it an effective source of iron for iron-deficient crops.

15651-72-6

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15651-72-6 Usage

Uses

Used in Agriculture:
Fe(II)-EDTA is used as a fertilizer additive for providing iron to plants, particularly for iron-deficient crops. It helps in the controlled release and uptake of iron by plants, promoting their growth and development.
However, there are concerns about the environmental impact of Fe(II)-EDTA, as it can persist in the soil and contribute to metal pollution. Therefore, it is essential to use it responsibly and consider alternative methods of providing iron to plants when necessary.

Check Digit Verification of cas no

The CAS Registry Mumber 15651-72-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,6,5 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15651-72:
(7*1)+(6*5)+(5*6)+(4*5)+(3*1)+(2*7)+(1*2)=106
106 % 10 = 6
So 15651-72-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H16N2O8.Fe/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);/q;+2/p-2

15651-72-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethylenediaminetetraacetatoferrate(2-)

1.2 Other means of identification

Product number -
Other names Edta Fe(II)

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:15651-72-6 SDS

15651-72-6Relevant academic research and scientific papers

Unidirectional Electron Transfer at Self-Assembled Monolayers of 11-Ferrocenyl-1-undecanethiol on Gold

Sato, Yukari,Itoigawa, Hiroyuki,Uosaki, Kohei

, p. 1032 - 1037 (1993)

The electron-exchange reaction between the ferrocenyl group of self-assembled monolayers of 11-ferrocenyl-1-undecanethiol on gold electrodes and Fe(III) species in solution is studied.The monolayer acts as an effective electron-transfer mediator for the r

MECHANISM OF Fe-EDTA CATALYZED SUPEROXIDE DISMUTATION.

Bull,McClune,Fee

, p. 5290 - 5300 (2007/10/02)

The catalysis of superoxide dismutation (2O//2 plus 2H** plus yields O//2 plus H//2O//2) by Fe**3** plus -EDTA and Fe**2** plus -EDTA has been examined. Potentiometric and spectrophotometric titrations of Fe**3** plus -EDTA revealed an ionization at pK//a equals 7. 6 consistent with the ionization of a bound water molecule. No other ionizations were detected below pH 10. 7. Potentiometric titration of Fe**2** plus -EDTA revealed no ionizations in the pH range 5-11. A mechanism has been derived for reaction 6 which accounts for the pH dependence of the individual rate constants, general-acid catalysis, and the pH dependence of the formation constant. The breakdown of the peroxo complex is catalyzed by both specific and general acids, and k// minus //6/ left bracket H** plus right bracket approximately equals 10**1**0 M** minus **1 s** minus **1 in the absence of general acids. The rate of formation of the peroxo complex is independent of pH but is increased by general acids.

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