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Oxaloacetic acid

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Identification
Molecular formula
C4H4O5
CAS number
328-42-7
IUPAC name
2-oxopropanedioic acid
State
State

At room temperature, oxaloacetic acid is typically found in a solid crystalline form.

Melting point (Celsius)
162.00
Melting point (Kelvin)
435.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
132.07g/mol
Molar mass
132.0720g/mol
Density
1.6630g/cm3
Appearence

Oxaloacetic acid typically appears as a colorless crystalline solid.

Comment on solubility

Solubility of 2-oxopropanedioic acid

2-oxopropanedioic acid, commonly known as pyruvic acid, exhibits notable solubility characteristics that are critical for its applications in various fields. This compound is a versatile organic acid with the formula C3H4O3, known for its ability to dissolve in both water and organic solvents.

Key Points about Solubility:

  • Water Solubility: 2-oxopropanedioic acid is highly soluble in water due to its polar nature. The presence of carboxylic acid groups allows for hydrogen bonding with water molecules, facilitating effective dissolution.
  • Solvent Compatibility: This compound also dissolves well in organic solvents, making it versatile for use in diverse reactions and applications.
  • pH Influence: The solubility of pyruvic acid can be affected by the pH of the solution; it is more soluble at lower pH levels where it exists predominantly in its protonated form.

To emphasize, the solubility of 2-oxopropanedioic acid in water makes it an essential compound in biochemical processes, where it plays a role in metabolic pathways.

Interesting facts

Interesting Facts about 2-Oxopropanedioic Acid

2-Oxopropanedioic acid, commonly known as malonic acid, is a fascinating compound that plays a significant role in various chemical and biological processes. Here are some intriguing insights about this versatile molecule:

  • Biochemical Significance: 2-Oxopropanedioic acid is a pivotal intermediate in the citric acid cycle, an essential pathway for energy production in living organisms. It contributes to the metabolism of carbohydrates, fats, and proteins.
  • Synthesis of Derivatives: This compound serves as a precursor for the synthesis of numerous bioactive compounds, including drugs and agricultural chemicals. The ability to easily modify its structure makes it a valuable building block in organic synthesis.
  • Flavor Enhancer: Interestingly, malonic acid is also utilized as a food additive, providing a tart flavor in various products. It enhances the taste profile of certain foods and beverages.
  • Historical Context: Named in the 19th century, malonic acid earned its name from the Latin word malum, meaning apple, as it was first isolated from apple juice. This reflects the compound's connection to natural sources.
  • Research Applications: Ongoing studies highlight its potential therapeutic applications, particularly in the fields of cancer research and metabolic disorders. The compound’s properties are being explored for innovative treatment strategies.
  • Versatile Reactions: Malonic acid participates in several chemical reactions, such as the malonic ester synthesis, which enables the formation of various carbon skeletons in organic chemistry. This reaction is essential for synthesizing larger, more complex molecules.

Overall, 2-oxopropanedioic acid stands as a prime example of a compound that bridges the gap between chemistry and biology, showcasing its multifaceted applications and significance in science.

Synonyms
MESOXALIC ACID
Ketomalonic acid
Oxomalonic acid
2-Oxomalonic acid
473-90-5
2-oxopropanedioic acid
Oxopropanedioic acid
2-Oxomalonsaeure
CCRIS 1453
Propanedioic acid, oxo-
EINECS 207-473-4
BRN 1754123
Mesoxalic acid, 8CI
UNII-62R514HE48
62R514HE48
MESOXALIC ACID [MI]
DTXSID3021649
CHEBI:30842
3-03-00-01355 (Beilstein Handbook Reference)
ketomalonate
alpha-ketomalonate
a-ketomalonic acid
a-KETOMALONate
DTXCID101649
Propanedioic acid, oxo-(9CI)
207-473-4
Mesoxalate
ALPHA-KETOMALONIC ACID
Propanedioic acid, oxo- (9CI)
Ketomalonic acid; Mesoxalate
SCHEMBL28953
AKOS006282599
DB03589
DB-352625
HY-114634
CS-0063624
NS00022212
C00830
Q2823289
F8881-6998