Interesting facts
Interesting Facts About 2-(1,2-Dicarboxyethoxy)butanedioic Acid
2-(1,2-Dicarboxyethoxy)butanedioic acid, commonly known in biochemical contexts for its functional groups and unique structure, comes from the family of dicarboxylic acids. Its importance spans across various fields, including pharmaceuticals and materials science. Here are some notable insights:
- Versatile Building Block: This compound serves as a critical building block in organic synthesis, facilitating the creation of more complex molecules.
- Biological Relevance: Its structure suggests possible roles in biochemical pathways, making it a compound of interest for enzyme interactions and metabolic studies.
- Polymer Chemistry: Scientists often explore this acid's capacity to form polymers, leading to materials with varied physical properties and potential applications in coatings and plastics.
- Acidity: The presence of multiple carboxylic acid groups contributes to its acidic behavior, which can be leveraged in acid-base reactions in various synthetic contexts.
- Hydrophilic Nature: Given its functional groups, the compound is likely to exhibit hydrophilic characteristics, making it suitable for various solvation processes in chemical reactions.
As you can see, 2-(1,2-dicarboxyethoxy)butanedioic acid is more than just a compound; it's a key player that opens doors to innovative solutions and research opportunities in chemistry. The intricate design of its molecular structure invites further exploration into its practical applications and theoretical implications. "In the realm of science, every molecule has a story to tell!"
Synonyms
Butanedioic acid, 2,2'-oxybis-
DTXSID00884382
DTXCID601023825
7408-18-6
oxydisuccinic acid
Butanedioic acid,2,2'-oxybis-
Malomalic ether
2,2'-Oxydisuccinic acid
UNII-2V675X30VA
EINECS 231-015-2
2-(1,4-dihydroxy-1,4-dioxobutan-2-yl)oxybutanedioic acid
SCHEMBL30293
CFPOJWPDQWJEMO-UHFFFAOYSA-N
2V675X30VA
NS00047180
Solubility of 2-(1,2-dicarboxyethoxy)butanedioic acid
2-(1,2-dicarboxyethoxy)butanedioic acid, a compound featuring dual carboxylic acid functional groups, exhibits interesting solubility characteristics that are noteworthy:
It is essential to consider that while its solubility in aqueous solutions is significant, pH levels can influence protonation states, thereby affecting overall solubility. As carboxyl groups can lose protons in alkaline conditions, the compound's overall charge and interaction with solvents may be modified.
In sum, 2-(1,2-dicarboxyethoxy)butanedioic acid boasts commendable solubility in water and a variety of polar solvents, making it a valuable candidate for numerous applications in both research and industry.