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Aspartame

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Identification
Molecular formula
C14H18N2O5
CAS number
22839-47-0
IUPAC name
2-amino-3-(3-oxoprop-1-enyl)but-2-enedioic acid
State
State

At room temperature, aspartame is a solid.

Melting point (Celsius)
246.00
Melting point (Kelvin)
519.00
Boiling point (Celsius)
200.00
Boiling point (Kelvin)
473.00
General information
Molecular weight
294.30g/mol
Molar mass
294.3040g/mol
Density
1.3470g/cm3
Appearence

Aspartame appears as a white, odorless, crystalline powder. It is a dipeptide ester, consisting of phenylalanine and aspartic acid, which gives it a granulated structure.

Comment on solubility

Solubility of 2-amino-3-(3-oxoprop-1-enyl)but-2-enedioic acid

The solubility of 2-amino-3-(3-oxoprop-1-enyl)but-2-enedioic acid, with the chemical formula C14H18N2O5, is an intriguing aspect to consider due to the specific functional groups present in its structure. This compound features both amino and carbonyl groups, which play crucial roles in determining its solubility in various solvents.

Here are some important points regarding its solubility:

  • Polar Groups: The presence of polar amino (-NH2) and carbonyl (C=O) groups typically enhances solubility in polar solvents, such as water.
  • Hydrogen Bonding: These functional groups can engage in hydrogen bonding, which further increases the compound's solubility in aqueous environments.
  • Organic Solvents: The hydrophobic carbon backbone may limit solubility in nonpolar solvents, suggesting that 2-amino-3-(3-oxoprop-1-enyl)but-2-enedioic acid is preferentially soluble in polar solvents.
  • Solution Behavior: The overall solubility can be influenced by factors such as pH, temperature, and the presence of other solutes.

In conclusion, while 2-amino-3-(3-oxoprop-1-enyl)but-2-enedioic acid is expected to have favorable solubility in polar solvents due to its functional groups, the actual solubility would need to be quantified experimentally to provide definitive insights.

Interesting facts

Interesting Facts about 2-amino-3-(3-oxoprop-1-enyl)but-2-enedioic acid

2-amino-3-(3-oxoprop-1-enyl)but-2-enedioic acid, often referred to within the scientific community for its structural complexity and biological significance, is a unique compound that belongs to the family of amino acids and derivatives. Here are some captivating aspects of this compound:

  • Dietary Relevance: As an amino acid derivative, it implies potential roles in various biochemical pathways, possibly influencing nutritional or metabolic processes in organisms.
  • Structure and Function: The compound features a sophisticated structure, which includes an enedione moiety. This structural aspect could be integral in biochemical reactions, particularly in enzyme catalysis and metabolic pathways.
  • Potential Therapeutic Applications: Research into amino acid derivatives often uncovers their roles in pharmaceutical chemistry. This compound could offer insights into new drug development, particularly in conditions driven by metabolic dysfunctions.
  • Natural Occurrence: While synthetic pathways are explored, there is potential for this compound to naturally occur in specific plants or organisms, which could lead to discoveries in ecology and bioactive compounds.
  • Research Interest: This compound's complexity garners the interest of researchers looking to unravel the relationships between structure and biological activity, making it a worthwhile subject of study in advanced organic and medicinal chemistry.

As noted in one scientific exploration, "The intersection of amino acid derivatives and their functional implications offers a vast landscape for discovery," emphasizing the importance of such compounds in broadening our understanding of biochemistry.
The potential applications and the structural features of 2-amino-3-(3-oxoprop-1-enyl)but-2-enedioic acid create rich opportunities for further research and exploration in the chemical sciences.

Synonyms
2-Amino-3-(3-oxo-1-propen-1-yl)-2-butenedioic acid
SCHEMBL188166
DTXSID10274255
1-amino-4-formyl-1,3-butadiene-1,2-dicarboxylic acid