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Sodium iminodiacetate

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Identification
Molecular formula
C4H9NO4Na
CAS number
16721-71-2
IUPAC name
sodium;2-[formyl(hydroxy)amino]acetate
State
State

At room temperature, sodium iminodiacetate exists as a solid. It is commonly used in its solid form for chelation and other chemical applications.

Melting point (Celsius)
292.00
Melting point (Kelvin)
565.15
Boiling point (Celsius)
400.00
Boiling point (Kelvin)
673.15
General information
Molecular weight
145.07g/mol
Molar mass
145.0660g/mol
Density
1.5600g/cm3
Appearence

Sodium iminodiacetate typically appears as a white crystalline solid. It may appear as a powder or small crystalline fragments, and it is highly soluble in water, lending to its utility in various chemical reactions and processes.

Comment on solubility

Solubility of Sodium 2-[Formyl(hydroxy)amino]acetate

Sodium 2-[formyl(hydroxy)amino]acetate, often referred to by its more common name, exhibits interesting solubility characteristics that are crucial for its applications in various fields. This compound typically displays the following solubility features:

  • Highly soluble in water: The presence of the sodium ion contributes to its excellent solubility in aqueous solutions due to ionic interactions.
  • pH-dependent solubility: Its solubility can vary with changes in pH, often becoming more soluble in alkaline conditions.
  • Complex formation: It has a tendency to form complexes with other ions or molecules, which may further enhance or impede its solubility depending on the counter ions.
  • Temperature effects: Solubility may also be influenced by temperature, with higher temperatures generally leading to increased solubility for many salts.

In conclusion, the solubility of sodium 2-[formyl(hydroxy)amino]acetate is characterized by a strong affinity for water and sensitivity to environmental conditions such as pH and temperature. Its ability to dissolve readily makes it an important compound in various chemical processes.

Interesting facts

Interesting Facts about Sodium 2-[Formyl(hydroxy)amino]acetate

Sodium 2-[formyl(hydroxy)amino]acetate, commonly referred to in scientific literature for its functional groups, boasts several intriguing characteristics. This compound serves as a significant participant in biochemical pathways and is worth noting for various reasons:

  • Biochemical Utility: This compound plays a role in the synthesis of amino acids, which are the building blocks of proteins.
  • Hydroxyl Group Advantage: The presence of a hydroxyl group enhances the compound's ability to engage in hydrogen bonding, making it valuable in organic synthesis and medicinal chemistry.
  • Environmental Impact: Sodium 2-[formyl(hydroxy)amino]acetate may have potential applications in environmentally benign reactions due to its water-soluble nature.
  • Research Applications: It has been studied for its role in various research applications, particularly in the field of drug discovery.
  • Status in Education: Students often encounter this compound in organic chemistry, where they learn about its functional groups and applications.

To further emphasize its significance, it’s fascinating to note that compounds like sodium 2-[formyl(hydroxy)amino]acetate are not only pivotal in laboratory settings but are also essential in understanding biochemical systems and advancing pharmaceutical research. As a wise quote from chemist Linus Pauling states, "The best way to have a good idea is to have lots of ideas." Exploring compounds like this may very well lead to revolutionary discoveries!