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L-Ascorbic acid

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Identification
Molecular formula
C6H8O6
CAS number
50-81-7
IUPAC name
(2R)-2-[(1S)-1,2-dihydroxyethyl]-4,5-dihydroxy-furan-3-one
State
State

At room temperature, L-Ascorbic acid is typically found in a solid state as a crystalline powder.

Melting point (Celsius)
190.00
Melting point (Kelvin)
463.15
Boiling point (Celsius)
553.00
Boiling point (Kelvin)
826.15
General information
Molecular weight
176.12g/mol
Molar mass
176.1240g/mol
Density
1.6940g/cm3
Appearence

L-Ascorbic acid, commonly known as vitamin C, appears as a white to very pale yellow crystalline powder or granules. It is generally odorless but may have a slightly acidic taste.

Comment on solubility

Solubility of (2R)-2-[(1S)-1,2-dihydroxyethyl]-4,5-dihydroxy-furan-3-one (C6H8O6)

The compound (2R)-2-[(1S)-1,2-dihydroxyethyl]-4,5-dihydroxy-furan-3-one, with its chemical formula C6H8O6, presents a fascinating profile in terms of solubility. Understanding its solubility is crucial for applications in both pharmaceuticals and food sciences. Here are some key points regarding its solubility:

  • Polar Nature: The presence of multiple hydroxyl (-OH) groups greatly enhances its polar character, promoting solubility in polar solvents such as water.
  • Hydrogen Bonding: This compound can form extensive hydrogen bonds, which is a significant factor that facilitates its dissolution in aqueous solutions.
  • Temperature Dependence: As with many organic compounds, temperature can impact solubility, commonly increasing at higher temperatures for most solid solutes.
  • pH Influence: The solubility may also vary with pH, as deprotonation of hydroxyl groups could lead to increased solubility in alkaline conditions.

To summarize, one can assert that (2R)-2-[(1S)-1,2-dihydroxyethyl]-4,5-dihydroxy-furan-3-one is likely soluble in water owing to its numerous hydroxyl groups, and its solubility characteristics make it suitable for various applications in solution-based reactions.

Interesting facts

Interesting Facts about (2R)-2-[(1S)-1,2-Dihydroxyethyl]-4,5-Dihydroxy-Furan-3-One

(2R)-2-[(1S)-1,2-Dihydroxyethyl]-4,5-dihydroxy-furan-3-one, commonly referred to in scientific literature by its systematic name, is a fascinating compound that belongs to the category of furanoids. Known for its unique structure and functional groups, this compound boasts several intriguing characteristics:

  • Natural Sources: This compound is often found in various biological systems, where it plays a role in the biosynthesis of important metabolites.
  • Chirality: It exhibits chirality due to the presence of asymmetric carbon atoms, which means it can exist in different enantiomeric forms. This characteristic can significantly influence biological activity and reactivity.
  • Potential Applications: Compounds like this are of interest in pharmaceutical chemistry due to their potential biological activities, including antioxidant and anti-inflammatory properties.
  • Versatile Building Block: Its furan backbone allows for chemical modifications, making it a valuable building block for the synthesis of more complex organic compounds.
  • Research Significance: Ongoing studies explore the roles of such compounds in metabolic pathways and their possible therapeutic implications, paving the way for innovative drug design.

As scientists continue to explore compounds like (2R)-2-[(1S)-1,2-Dihydroxyethyl]-4,5-Dihydroxy-Furan-3-One, it becomes increasingly clear that their multifaceted nature holds promises for the development of novel therapeutic agents. Remember, in the world of chemistry, it’s not just about the compound itself; it's about how it interacts with the environment and biological systems.