Ferric EDTA

Ferric EDTA

Names
Other names (ethylenedinitrilo)tetraacetatoferrate
Identifiers
CAS Number	15275-07-7
3D model (JSmol)	Interactive image
ChemSpider	26311
EC Number	241-171-3
PubChem CID	28283
CompTox Dashboard (EPA)	DTXSID0066163
InChI InChI=1S/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;+3/p-3 Key: UOMQUZPKALKDCA-UHFFFAOYSA-K
SMILES C(CN(CC(=O)[O-])CC(=O)[O-])N(CC(=O)O)CC(=O)[O-].[Fe+3]
Properties
Chemical formula	C10H12FeN2O8
Molar mass	344.057 g·mol−1
Appearance	yellow
Hazards
GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H315, H319
Precautionary statements	P264, P280, P302+P352, P305+P351+P338, P321, P332+P313, P337+P313, P362
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Ferric EDTA is the coordination complex formed from ferric ions and EDTA. EDTA has a high affinity for ferric ions. It gives yellowish aqueous solutions.^[1]

Synthesis and structure

Solutions of Fe(III)-EDTA are produced by combining ferrous salts and aqueous solutions of EDTA known as Jacobson's solution (cf. chemical equation (1) under Table (1)).^[2]

Near neutral pH, the principal complex is [Fe(EDTA)(H₂O)]⁻, although most sources ignore the aquo ligand. The [Fe(EDTA)(H₂O)]⁻ anion has been crystallized with many cations, e.g., the trihydrate Na[Fe(EDTA)(H₂O)]^.2H₂O.^[3] The salts as well as the solutions are yellow-brown. Provided the nutrient solution in which the [Fe(EDTA)(H₂O)]⁻ complex will be used has a pH of at least 5.5, all the uncomplexed iron, as a result of incomplete synthesis reaction, will still change into the chelated ferric form.^[4]

Uses

EDTA is used to solubilize iron(III) in water. In the absence of EDTA or similar chelating agents, ferric ions form insoluble solids and are thus not bioavailable.^[1]

Together with pentetic acid (DTPA), EDTA is widely used for sequestering metal ions. Otherwise these metal ions catalyze the decomposition of hydrogen peroxide, which is used to bleach pulp in papermaking. Several million kilograms EDTA are produced for this purpose annually.^[5]

Iron chelate is commonly used for agricultural purposes to treat chlorosis, a condition in which leaves produce insufficient chlorophyll. Iron and ligand are absorbed separately by the plant roots whereby the highly stable ferric chelate is first reduced to the less stable ferrous chelate.^[6] In horticulture, iron chelate is often referred to as 'sequestered iron' and is used as a plant tonic, often mixed with other nutrients and plant foods (e.g. seaweed). It is recommended in ornamental horticulture for feeding ericaceous plants like Rhododendrons if they are growing in calcareous soils. The sequestered iron is available to the ericaceous plants, without adjusting the soil's pH, and thus, lime-induced chlorosis is prevented.

Ferric EDTA can be used as a component for the Hoagland solution or the Long Ashton Nutrient Solution.^[7] According to Jacobson (1951),^[2] the stability of ferric EDTA was tested by adding 5 ppm iron, as the complex, to Hoagland's solution at various pH values. No loss of iron occurred below pH 6. In addition to Jacobson's original recipe and a modified protocol by Steiner and van Winden (1970),^[4] an updated version for producing the ferric EDTA complex by Nagel et al. (2020)^[8] is presented in Table (1).

Jacobson's solution

Table (1) to prepare the ferric EDTA stock solution

The formation of Fe(III)-EDTA (FeY)⁻ can be described as follows:

FeSO₄∙7H₂O + K₂H₂Y + 1/4 O₂ → K[FeY(H₂O)]^.H₂O + KHSO₄ + 5.5 H₂O (1)^[8]

Iron chelate has also been used as a bait in the chemical control of slugs, snails and slaters in agriculture in Australia and New Zealand. They have advantages over other more generally poisonous substances used as their toxicity is more specific to molluscs.^[9]

Ferric EDTA is used as a photographic bleach to convert silver metal into silver salts, that can later be removed.

Iron EDTA preparation methods

Iron EDTA can also be prepared using different sources of carbonates, chlorides and sulfates.

Iron(II)-EDTA using carbonates

Combination of iron carbonate, EDTA acid and sodium hydroxide gives the iron EDTA:

FeCO₃ + C₁₀H₁₆N₂O₈ + 2 NaOH → C₁₀H₁₂FeNa₂N₂O₈ • 2 H₂O + CO₂ + H₂O

With this reaction % Fe can achieve 12.0 minimum in chelated form.

Iron(III)-EDTA using chlorides

Combination of iron chloride, EDTA acid and sodium hydroxide gives the iron EDTA:

FeCl₃ + C₁₀H₁₆N₂O₈ + 4 NaOH → C₁₀H₁₂FeNaN₂O₈ + 3 NaCl + 4 H₂O

This results in getting % Fe = 9.0 and to enrich the iron content sodium chloride to be separated using crystallization method and for this twice of iron chloride and seeding with iron EDTA powder after cooling to 40 °C results iron EDTA powder.

Iron(II)-EDTA using sulfates

Combination of iron sulfate, EDTA acid and sodium hydroxide gives the iron EDTA:

FeSO₄ + C₁₀H₁₆N₂O₈ + 4 NaOH → C₁₀H₁₂FeNa₂N₂O₈ + Na₂SO₄ + 2 H₂O

This combination gives % Fe about 9.5.

Related derivatives

Aside from EDTA, the chelating agent EDDHA is used to solubilize iron in water. It also can be used for the purposes of agriculture, accessible to plants.^[10]

In iron chelation therapy, deferoxamine, has been used to treat excess iron stores, i.e. haemochromatosis.^[11]

See also

• DTPA
• EDDHA
• Tartrate
• Citrate

References

This page was last edited on 18 January 2024, at 13:23