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Sodium Adenosine Monophosphate

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Identification
Molecular formula
C10H12N5NaO7P
CAS number
4578-31-8
IUPAC name
sodium;[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl hydrogen phosphate
State
State
Sodium Adenosine Monophosphate is typically found in a solid state at room temperature, appearing as a crystalline powder.
Melting point (Celsius)
197.00
Melting point (Kelvin)
470.00
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.00
General information
Molecular weight
347.22g/mol
Molar mass
347.2210g/mol
Density
2.2200g/cm3
Appearence

Sodium Adenosine Monophosphate (AMP) appears as a white, odorless crystalline powder. It is typically used in biochemical applications.

Comment on solubility

Solubility of Sodium;[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl hydrogen phosphate

The solubility of sodium;[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl hydrogen phosphate can be quite intriguing due to its complex structure. This compound, characterized by the presence of both hydrogen phosphate and an amino-purine base, offers unique solubility behavior depending on several factors:

  • Polarity: The presence of hydroxyl groups enhances the molecule's polarity, typically allowing for better solubility in polar solvents such as water.
  • Salt Formation: As a sodium compound, it is likely to be more soluble in aqueous solutions compared to its non-sodium counterparts, facilitating ionic interactions that can promote solubility.
  • Concentration Effects: Increased concentration can lead to saturation points, where the solubility will reach a limit, potentially forming precipitates.
  • Temperature: Like many chemical compounds, higher temperatures generally increase solubility; however, this can vary based on the specific interactions within the molecule.

In summary, the solubility profile of this compound is primarily influenced by its ionic nature, polarity, and external conditions. Understanding these factors can be essential when considering its applications in biochemical processes or pharmaceutical formulations.

Interesting facts

Interesting Facts about Sodium; [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]methyl hydrogen phosphate

This unique compound, often abbreviated as a nucleoside analog, plays a significant role in biochemistry and pharmaceutical research, primarily due to its structural resemblance to natural nucleosides. Here are some noteworthy points to consider:

  • Structural Complexity: The compound features a complex organic structure characterized by a modified sugar component, which contributes to its biological activity.
  • Biological Relevance: As a nucleoside analog, it can interfere with nucleic acid metabolism, making it a valuable tool in the study of cellular processes, especially those involved in DNA and RNA synthesis.
  • Research Applications: Its potential as an antiviral or anticancer agent is of significant interest in medicinal chemistry. Researchers are exploring its ability to inhibit the replication of certain pathogens.
  • Chemical Properties: The presence of both hydroxyl groups and an amino group suggests that the compound can participate in various chemical reactions, which may enhance its therapeutic potential.
  • Historical Insight: The study of nucleoside analogs has paved the way for developing antiviral medications, highlighting the ongoing importance of compounds like this in modern medicine.

As a chemistry student or science enthusiast, understanding the structure and functions of such compounds contributes to a broader knowledge of biochemistry and pharmacology, illustrating how intricate molecular designs can lead to significant biological outcomes. Indeed, this compound serves as an excellent example of how modifications in chemical structure can lead to enhanced biological activity, showcasing the art and science of medicinal chemistry.