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EDTA

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Identification
Molecular formula
C10H16N2O8S
CAS number
60-00-4
IUPAC name
2-amino-5-[[2-(carboxymethylamino)-2-oxo-1-(sulfomethyl)ethyl]amino]-5-oxo-pentanoic acid
State
State

At room temperature, EDTA is typically in a white solid state.

Melting point (Celsius)
250.00
Melting point (Kelvin)
523.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
273.15
General information
Molecular weight
292.24g/mol
Molar mass
292.2430g/mol
Density
1.8000g/cm3
Appearence

EDTA is a white, crystalline powder.

Comment on solubility

Solubility of 2-amino-5-[[2-(carboxymethylamino)-2-oxo-1-(sulfomethyl)ethyl]amino]-5-oxo-pentanoic acid

The compound 2-amino-5-[[2-(carboxymethylamino)-2-oxo-1-(sulfomethyl)ethyl]amino]-5-oxo-pentanoic acid, represented by the formula C10H16N2O8S, exhibits notable solubility characteristics due to its complex structure and functional groups. Key points regarding its solubility include:

  • Hydrophilicity: The presence of multiple carboxylic acid and amino functional groups leads to enhanced hydrophilicity, contributing to good solubility in polar solvents like water.
  • Salt Formation: The functionality within the compound can also allow for protonation and deprotonation, further enhancing its solubility in aqueous solutions when in the form of salts.
  • pH Dependence: Solubility may vary with pH; at different pH levels, the ionization state of the amino and carboxyl groups changes, which can either increase or decrease solubility.
  • Temperature Influence: As with many compounds, solubility can improve with an increase in temperature, allowing for greater dissolution rates in aqueous environments.

This compound's unique combination of several polar groups enhances its potential to interact with solvents, making it soluble under a variety of conditions. Therefore, when working with this chemical, it is essential to consider its behavior in different solvent systems and environmental conditions.

Interesting facts

Interesting Facts about 2-amino-5-[[2-(carboxymethylamino)-2-oxo-1-(sulfomethyl)ethyl]amino]-5-oxo-pentanoic acid

This compound, often referred to in the literature as a complex amino acid derivative, is known for its multifaceted role in biochemical processes. Here are some noteworthy aspects:

  • Diverse Functionality: The presence of multiple functional groups allows this compound to interact with various biological molecules, potentially influencing metabolic pathways.
  • Biological Relevance: It may play a role in the synthesis of proteins and enzymes, as amino acids are fundamental building blocks for most biological structures.
  • Research Applications: Scientists are investigating its potential use in drug design, particularly in creating molecules that canmodulate metabolic activity or serve as therapeutic agents targeting specific diseases.
  • Analytical Techniques: To study this compound, techniques such as NMR and mass spectrometry are often employed, providing insights into its structural characteristics and behaviors in different environments.
  • Role in Nutrition: Understanding the interaction of this amino acid derivative in nutritional studies may yield information on its role in human health and its potential as a dietary supplement.

As with many compounds in organic chemistry, the exploration of 2-amino-5-[[2-(carboxymethylamino)-2-oxo-1-(sulfomethyl)ethyl]amino]-5-oxo-pentanoic acid can lead to discovering new pathways in both synthetic and biological chemistry. Its study not only sheds light on fundamental biochemical processes but can also pave the way for innovative applications in medicine and beyond.

Synonyms
glutathione sulfonic acid
2-amino-5-[[1-(carboxymethylamino)-1-oxo-3-sulfopropan-2-yl]amino]-5-oxopentanoic acid
SCHEMBL10935016
DTXSID00274401
NSC621989
NSC-621989
FG166997
SR-01000883743
N-(N-.gamma.-L-glutamyl-3-sulfo-L-alanyl)glycine
SR-01000883743-1