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Identification
Molecular formula
C10H16O7
CAS number
13700-33-3
IUPAC name
4-[(2,4-dihydroxy-3,3-dimethyl-butanoyl)amino]-3-hydroxy-butanoic acid
State
State

At room temperature, it is typically a solid.

Melting point (Celsius)
127.00
Melting point (Kelvin)
400.00
Boiling point (Celsius)
398.00
Boiling point (Kelvin)
671.00
General information
Molecular weight
234.24g/mol
Molar mass
234.2420g/mol
Density
1.1744g/cm3
Appearence

The pure compound is a crystalline solid.

Comment on solubility

Solubility of 4-[(2,4-dihydroxy-3,3-dimethyl-butanoyl)amino]-3-hydroxy-butanoic acid

The solubility of 4-[(2,4-dihydroxy-3,3-dimethyl-butanoyl)amino]-3-hydroxy-butanoic acid can be influenced by its unique molecular structure and functional groups. Here are some key points regarding its solubility:

  • Hydrophilic Functional Groups: The presence of multiple hydroxy (-OH) groups typically increases the solubility in water, as these groups can form strong hydrogen bonds with water molecules.
  • Overall Polarity: The compound's overall polarity affects its solubility; highly polar compounds generally have better solubility in polar solvents.
  • Concentration Dependence: As with many organic compounds, solubility can vary significantly with concentration; lower concentrations may dissolve more easily.
  • pH Influence: The acidic and basic nature of functional groups can also change solubility depending on the pH of the solution.

Due to these factors, it can be anticipated that 4-[(2,4-dihydroxy-3,3-dimethyl-butanoyl)amino]-3-hydroxy-butanoic acid is likely to display moderate solubility in water, making it suitable for various applications where an aqueous medium is preferable. It is essential to consider these aspects when evaluating its use in biological or chemical processes.

Interesting facts

Interesting Facts About 4-[(2,4-Dihydroxy-3,3-dimethyl-butanoyl)amino]-3-hydroxy-butanoic Acid

This compound, often referred to in shortened terms in scientific discussions, is noteworthy for its intriguing structure and potential applications in various fields. Here are some compelling points:

  • Biochemical Interest: This compound is a derivative of amino acids, showing connections to metabolic pathways and biological processes. Its dual hydroxy groups enhance its reactivity and contribute to diverse biochemical functions.
  • Potential Therapeutic Uses: Due to its unique structure, scientists are investigating the potential of this compound in pharmaceutical applications, particularly in the synthesis of novel drugs aimed at treating metabolic disorders.
  • Structural Complexity: The incorporation of both hydroxyl groups and an amino function within its structure means this compound may engage in hydrogen bonding, which can influence solubility and interaction with other biomolecules.
  • Natural Product Analog: The presence of a branched alkyl group suggests a natural product relationship; indeed, many compounds with similar features can be found in plant extracts, leading to research in natural product chemistry.

This compound exemplifies the fascinating intersection of organic chemistry and biochemistry. By exploring its characteristics, researchers can unravel intricate mechanisms essential for advancements in health science. As one scholar aptly stated, "Understanding complex compounds often reveals nature's hidden secrets," and this compound is a perfect case in point.

Synonyms
beta-Oxy-hopa
beta-Hydroxyhomopantothenic acid
4-(2,4-Dihydroxy-3,3-dimethylbutyramido)-3-hydroxybutyric acid
1977-35-1
Butanoic acid, 4-((2,4-dihydroxy-3,3-dimethyl-1-oxobutyl)amino)-3-hydroxy-
BUTYRIC ACID, 4-(2,4-DIHYDROXY-3,3-DIMETHYLBUTYRAMIDO)-3-HYDROXY-
DTXSID20941542
3-Hydroxy-4-[(1,2,4-trihydroxy-3,3-dimethylbutylidene)amino]butanoic acid