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Ethylenediaminetetraacetic acid

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Identification
Molecular formula
C10H16N2O8
CAS number
60-00-4
IUPAC name
2-[2-[2-[bis(carboxymethyl)amino]ethoxy]ethyl-(carboxymethyl)amino]acetic acid
State
State

At room temperature, ethylenediaminetetraacetic acid is typically in a solid state in the form of a crystalline powder.

Melting point (Celsius)
237.00
Melting point (Kelvin)
510.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
292.24g/mol
Molar mass
292.2430g/mol
Density
1.4503g/cm3
Appearence

Ethylenediaminetetraacetic acid (EDTA) is typically a white, crystalline powder.

It is also available in aqueous solution form as a colorless solution due to its solubility properties.

Comment on solubility

Solubility of 2-[2-[2-[bis(carboxymethyl)amino]ethoxy]ethyl-(carboxymethyl)amino]acetic acid

This compound, with its complex structure, exhibits notable solubility characteristics. Here are some key points to consider:

  • Polar Nature: The presence of multiple carboxymethyl groups results in a highly polar compound.
  • Hydrophilicity: Given its polar functional groups, this compound is expected to be highly soluble in water.
  • Intermolecular Interactions: Extensive hydrogen bonding can occur due to the carboxylic acid moieties, further enhancing solubility in aqueous solutions.
  • Buffering Capacity: The carboxylic groups contribute to the stability of the compound in various pH environments, indicating that it may remain soluble across a range of conditions.
  • Solvent Compatibility: While water is a preferred solvent, one might find reduced solubility in non-polar solvents due to the overall hydrophilic nature.

In summary, 2-[2-[2-[bis(carboxymethyl)amino]ethoxy]ethyl-(carboxymethyl)amino]acetic acid is characterized by its high solubility in polar solvents, particularly water, making it an interesting candidate for various applications in biochemical and pharmaceutical fields.

Interesting facts

Interesting Facts about 2-[2-[2-[bis(carboxymethyl)amino]ethoxy]ethyl-(carboxymethyl)amino]acetic acid

This remarkable compound, known for its complex structure and multifunctional properties, is a fascinating example of synthetic chemistry in action. It belongs to a category of compounds that play crucial roles in various biochemical pathways and applications, particularly in the fields of pharmaceuticals and biochemistry.

Key Features

  • Biocompatibility: This compound has been investigated for its compatibility with biological systems, making it a potential candidate for drug delivery systems and therapeutic applications.
  • Ion Exchange Properties: Its intricate structure allows for certain ion exchange capabilities, which can be exploited in various chemical processes, such as purification and separation techniques.
  • Role in Chelation: The presence of multiple carboxymethyl groups enhances its ability to chelate metal ions, offering valuable applications in removing heavy metals from biological systems.
  • Buffering Capacity: Due to its carboxylic acid groups, it can act as a buffering agent, maintaining pH levels in biological and chemical environments.

Chemical Applications

In the laboratory, chemists appreciate this compound for its versatility:

  • Used in the formulation of complex molecules for targeted drug delivery.
  • Serves as a key building block in the synthesis of larger and more complex molecular structures.
  • Investigated for its potential in developing biocompatible materials for tissue engineering.

Conclusion

Overall, 2-[2-[2-[bis(carboxymethyl)amino]ethoxy]ethyl-(carboxymethyl)amino]acetic acid is not just another chemical compound; it stands at the intersection of therapeutic innovation and applied chemistry. Its multifunctional nature presents students and researchers alike with exciting possibilities for exploration and study.

Synonyms
923-73-9
BAETA
Bis(2-aminoethyl) Ether N,N,N',N'-Tetraacetic Acid
2-[2-[2-[bis(carboxymethyl)amino]ethoxy]ethyl-(carboxymethyl)amino]acetic acid
Eedta
BADE
DDTE
Oxabis(ethyleniminodiacetic acid)
EINECS 213-099-2
BRN 1717019
2,2'-Oxydiethylenediaminetetra(acetic acid)
Bis(diaminoethyl ether)-N,N,N'N'-tetraacetic acid
Glycine, N,N'-(oxydi-2,1-ethanediyl)bis(N-(carboxymethyl)-
ACETIC ACID, OXYBIS(ETHYLENENITRILO)TETRA-
SCHEMBL620348
DTXSID70238959
SLVOVFVZZFUEAS-UHFFFAOYSA-N
AKOS037634480
oxybis(ethylenenitrilo)tetraacetic acid
NS00022875
Bis(2-aminoethyl)ether N,N,N',N'-tetraacetic acid
BIS(2-AMINOETHYL)ETHERN,N,N,N-TETRAACETICACID
6-Oxa-3,9-diazaundecanedioic acid, 3,9-bis(carboxymethyl)
2,2',2'',2'''-[Oxybis(2,1-ethanediylnitrilo)]tetraacetic acid