Interesting facts
Interesting Facts about 3-(Carboxymethyl)-3-hydroxy-pentanedioic Acid
3-(Carboxymethyl)-3-hydroxy-pentanedioic acid, also known as citric acid or citric acid derivative, is a fascinating compound that plays a crucial role in both nature and industry. Here are some noteworthy points about this compound:
- Biological Significance: It is an important intermediate in the citric acid cycle, a fundamental metabolic pathway that occurs in all aerobic organisms. This cycle is vital for energy production in cells.
- Natural Presence: Found naturally in citrus fruits, this compound contributes to their characteristic sour taste and is widely used as a flavoring agent in food and beverages.
- Chelation Properties: The ability of 3-(carboxymethyl)-3-hydroxy-pentanedioic acid to bind metal ions allows it to be utilized as a chelating agent in various chemical applications, including the formulation of cleaning products and in metal extraction processes.
- pH Regulation: This compound is often used in food preservation due to its ability to act as a natural preservative and pH stabilizer, enhancing the shelf life of products.
- Versatile Applications: Beyond food, it finds uses in pharmaceuticals, cosmetics, and even in the production of biodegradable plastics, demonstrating its versatility as a compound.
In summary, 3-(carboxymethyl)-3-hydroxy-pentanedioic acid is more than just a molecule; it is a bridge between chemistry and everyday life, connecting metabolic processes with industrial applications. Its diverse roles illustrate the fascinating interplay between organic chemistry and biological systems.
Synonyms
3-(carboxymethyl)-3-hydroxypentanedioic acid
115996-74-2
SCHEMBL880688
CHEMBL1178248
CHEBI:174024
EN300-188559
Solubility of 3-(Carboxymethyl)-3-hydroxy-pentanedioic acid
3-(Carboxymethyl)-3-hydroxy-pentanedioic acid, often referred to as a derivative of malic acid, displays notable solubility characteristics that are important to understand in various applications. Its structure, featuring multiple carboxyl groups, significantly influences its interaction with solvents.
Key Solubility Traits:
To summarize, the solubility of 3-(carboxymethyl)-3-hydroxy-pentanedioic acid is characterized by high water solubility owing to its polar functional groups, and can vary with both pH and temperature conditions. Understanding these solubility dynamics is essential for optimizing its use in biochemical applications and various chemical syntheses.