Skip to main content

Adenosine

ADVERTISEMENT
Identification
Molecular formula
C10H13N5O4
CAS number
58-61-7
IUPAC name
4-(6-aminopurin-9-yl)-2,3-dihydroxy-butanoic acid
State
State
Adenosine is solid at room temperature.
Melting point (Celsius)
234.00
Melting point (Kelvin)
507.15
Boiling point (Celsius)
215.60
Boiling point (Kelvin)
488.75
General information
Molecular weight
267.24g/mol
Molar mass
267.2410g/mol
Density
2.0800g/cm3
Appearence

Adenosine appears as a white crystalline solid or powder. It is often found in its anhydrous or hydrated form and can be slightly soluble in water.

Comment on solubility

Solubility of 4-(6-aminopurin-9-yl)-2,3-dihydroxy-butanoic acid

The solubility of the compound 4-(6-aminopurin-9-yl)-2,3-dihydroxy-butanoic acid, with the chemical formula C10H13N5O4, is influenced by various factors. Here are some important points to consider:

  • Polarity: This compound contains multiple hydroxyl (–OH) groups and an amine (–NH2) group, indicating it is likely to be polar and, thus, soluble in polar solvents like water.
  • Hydrogen bonding: The presence of both hydroxyl and amino groups suggests the compound can engage in hydrogen bonding, enhancing its solubility in polar environments.
  • pH dependence: The carboxylic acid functional group may lead to ionic forms at higher pH levels, which can further increase solubility in water, making it especially soluble in neutral to basic conditions.
  • Solvent interactions: While it is expected to dissolve well in water, its solubility might vary in organic solvents depending on their polarity.

In summary, the solubility characteristics of 4-(6-aminopurin-9-yl)-2,3-dihydroxy-butanoic acid can be categorized as follows:

  1. Highly soluble in water due to hydrogen bonding and polar nature.
  2. Moderately soluble in certain organic solvents where polar characteristics align.
  3. Solubility affected by pH, particularly for its carboxylic acid group.

Understanding these solubility aspects is essential for practical applications in biochemical contexts and therapeutic implementations.

Interesting facts

4-(6-Aminopurin-9-yl)-2,3-dihydroxy-butanoic acid

This compound, a modified amino acid derivative, is notable for its intriguing biological roles and potential therapeutic applications. It is fundamentally linked to the nitrogenous base structure of purines, which are essential components of nucleic acids like DNA and RNA. Here are some fascinating insights:

  • Biological Importance: The purine base structure a characteristic of this compound suggests potential involvement in cellular metabolism and signaling pathways.
  • Structural Diversity: The presence of both amino and hydroxyl groups enhances its reactivity and versatility in biochemical reactions, making it an interesting subject of study in organic chemistry.
  • Therapeutic Potential: Compounds of this nature have been investigated for their roles in antiviral and anticancer therapies, as they can potentially inhibit the replication of harmful pathogens and cancer cells.
  • Analytical Techniques: Scientists often utilize sophisticated techniques such as NMR (Nuclear Magnetic Resonance) and mass spectrometry to elucidate the structure and behavior of compounds like this one.

As a chemistry student, exploring such compounds opens windows to understanding the intricate interplay between chemistry and biology. The pathway from bench research to potential clinical applications is filled with challenges and exciting discoveries, making the study of such molecular constructs a thrilling endeavor for budding scientists.

In the words of a famous scientist, "Research is what I'm doing when I don't know what I'm doing." Let this compound inspire you!

Synonyms
D-erythro-Eritadenine
Lentysine;Lentinacin
6-amino-alpha,beta-dihydroxy-9H-purine-9-butanoic acid
4-(6-aminopurin-9-yl)-2,3-dihydroxybutanoic acid
4-(6-amino-9H-purin-9-yl)-2,3-dihydroxybutanoic acid
CHEBI:179057