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Ferric EDTA

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Identification
Molecular formula
C10H12FeN2O8
CAS number
21265-50-9
IUPAC name
ferric;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxymethyl)amino]acetate
State
State

Ferric EDTA is commonly found in a solid state at room temperature. When utilized in industrial or agricultural applications, it can also be present in solution form, typically dissolved in water.

Melting point (Celsius)
250.00
Melting point (Kelvin)
523.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
374.11g/mol
Molar mass
374.1090g/mol
Density
1.8450g/cm3
Appearence

Ferric EDTA typically appears as a dark brown or reddish-brown solid. It may sometimes be found in liquid form as a brown solution, depending on its formulation and intended use. It has a characteristic appearance due to the ferric ion and the EDTA complex.

Comment on solubility

Solubility of Ferric 2-[2-[Bis(carboxylatomethyl)amino]ethyl-(carboxymethyl)amino]acetate

The solubility of ferric 2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxymethyl)amino]acetate in various solvents is quite fascinating and can vary significantly based on its interactions with the solvent molecules.

Key Factors Affecting Solubility:

  • pH Levels: The solubility can be highly dependent on the pH of the solution due to the presence of carboxylate groups, which can protonate or deprotonate, affecting solubility.
  • Solvent Polarity: Polar solvents like water may dissolve this compound effectively, while non-polar solvents may not.
  • Ionic Strength: The ionic strength of the solution plays a role; higher ionic strength can sometimes increase solubility due to screening effects.

In general, complexes with metal ions and numerous functional groups often exhibit enhanced solubility due to their ability to form multiple interactions with the solvent. For ferric 2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxymethyl)amino]acetate, one might expect good solubility in aqueous solutions, particularly in slightly alkaline conditions where the coordination environment enhances solubility.

As a result, it may be beneficial to approach experimental investigations by examining solubility under varied conditions to achieve optimal results. Such analysis will not only enhance the understanding of its solubility behavior but can also impact its applications in various fields.

Interesting facts

Interesting Facts about Ferric 2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxymethyl)amino]acetate

Ferric 2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxymethyl)amino]acetate is an intriguing compound that combines the essential element iron with a complex chelating agent. This compound serves a significant role in various biochemical and environmental applications. Here are some exciting facts:

  • Iron's Vital Role: Iron is an essential trace element in many biological systems, particularly in oxygen transport and electron transfer reactions. This compound effectively utilizes iron in its ferric (Fe3+) state.
  • Coordination Chemistry: The structure of this compound involves coordination between the iron ion and the multiple carboxylate and amino groups. This creates a unique complex that stabilizes the iron, enhancing its reactivity and bioavailability.
  • Applications in Medicine: Compounds like ferric 2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxymethyl)amino]acetate are studied for their potential in drug delivery systems and as contrast agents in magnetic resonance imaging (MRI).
  • Environmental Impact: This compound can also play a role in bioremediation processes, where it can help detoxify heavy metals and improve soil quality by chelating metal ions.
  • Comparative Analysis: By examining similar ferric complexes, researchers can draw parallels in stability and reactivity, contributing to a greater understanding of metal-ligand interactions in coordination chemistry.

In summary, Ferric 2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxymethyl)amino]acetate stands out not just for its chemical composition but also for its broad potential applications in both medicine and environmental sciences. The compound exemplifies how the complexity of coordination chemistry can lead to significant breakthroughs in various fields.

Synonyms
Ferric-EDTA
monoferric edetate
CLEWAT FEH
Hydrogen [[N,N'-ethylenebis[N-(carboxymethyl)glycinato]](4-)-N,N',O,O',ON,ON']ferrate(1-)
Hydrogen ((N,N'-ethylenebis(N-(carboxymethyl)glycinato))(4-)-N,N',O,O',ON,ON')ferrate(1-)
Ferrate(1-), ((N,N'-1,2-ethanediylbis(N-(carboxymethyl)glycinato))(4-)-N,N',O,O',ON,ON')-, hydrogen, (OC-6-21)-
FERRATE(1-), ((N,N'-1,2-ETHANEDIYLBIS(N-((CARBOXY-.KAPPA.O)METHYL)GLYCINATO-.KAPPA.N,.KAPPA.O))(4-))-, HYDROGEN (1:1), (OC-6-21)-
Ferrate(1-), ((N,N'-1,2-ethanediylbis(N-((carboxy-kappaO)methyl)glycinato-kappaN,kappaO))(4-))-, hydrogen (1:1), (OC-6-21)-
Ferrate(1-), [[N,N'-1,2-ethanediylbis[N-(carboxymethyl)glycinato]](4-)-N,N',O,O',ON,ON']-, hydrogen, (OC-6-21)-
Ferrate(1-), [[N,N'-1,2-ethanediylbis[N-[(carboxy-.kappa.O)methyl]glycinato-.kappa.N,.kappa.O]](4-)]-, hydrogen (1:1), (OC-6-21)-
Ferric EDTA
17099-81-9
KJ3C78Y22Z
Ferrate(1-), ((ethylenedinitrilo)tetraacetato)-, hydrogen
2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxymethyl)amino]acetate;iron(3+)
hydrogen ((ethylenedinitrilo)tetraacetato)ferrate(III)
EINECS 241-171-3
Ferric ethylenediaminetetraacetic acid
UNII-KJ3C78Y22Z
Ethylenediaminetetraacetic acid, Fe(III) chelate
Acetic acid, (ethylenedinitrilo)tetra-, iron salt
Ethylenediamine tetraacetic acid, iron (III) salt
Ferrate(1-), ((N,N'-1,2-ethanediylbis(N-((carboxy-kappaO)methyl)glycinato-kappaN,kappaO))(4-))-, hydrogen, (OC-6-21)-
SCHEMBL1092743
DTXSID0066163
IRON, (HYDROGEN(ETHYLENEDINITRILO)TETRAACETATO)-
UOMQUZPKALKDCA-UHFFFAOYSA-K