Diazirine-labelled compound | Solubility of Things

Identification

Molecular formula

C₁₇H₂₁N₇NaO₇

CAS number

.5569-09-9

IUPAC name

sodium;5-[3-[[2-[(4-amino-4-carboxy-butanoyl)amino]-5-(3H-diazirin-3-yl)-5-oxo-pentanoyl]amino]diazirin-3-yl]-5-oxo-pentanoate

State

In its standard state, the compound is typically a solid.

Melting point (Celsius)

128.50

Melting point (Kelvin)

401.65

Boiling point (Celsius)

310.20

Boiling point (Kelvin)

583.35

General information

Molecular weight

450.49g/mol

Molar mass

450.4860g/mol

Density

1.3500g/cm³

Appearence

The compound typically appears as an off-white crystalline powder. The compound's structure contains diazirine moieties which are often used as photoreactive crosslinkers, making it useful for biochemical and analytical applications.

Comment on solubility

Solubility of Sodium 5-[3-[[2-[(4-amino-4-carboxy-butanoyl)amino]-5-(3H-diazirin-3-yl)-5-oxo-pentanoyl]amino]diazirin-3-yl]-5-oxo-pentanoate

The solubility of sodium 5-[3-[[2-[(4-amino-4-carboxy-butanoyl)amino]-5-(3H-diazirin-3-yl)-5-oxo-pentanoyl]amino]diazirin-3-yl]-5-oxo-pentanoate can be quite complex due to its elaborate structure. Generally, the solubility of such compounds can be influenced by several factors:

Ionization: Being a sodium salt, this compound is likely to exhibit enhanced solubility in aqueous solutions due to the presence of sodium ions that stabilize the ionic interactions.
Functional Groups: The presence of amino and carboxyl groups suggests potential hydrogen bonding and dipole interactions, which can significantly increase solubility in polar solvents.
Structure: The intricate structure featuring diazirine rings may impact its solubility characteristics, potentially limiting solubility in non-polar solvents.
pH Dependence: The solubility may vary with changes in pH, particularly due to the carboxylic acid group; elevated pH could lead to deprotonation, enhancing solubility.

In conclusion, while the detailed solubility profile would require empirical testing under controlled conditions, it is reasonable to anticipate that sodium 5-[3-[[2-[(4-amino-4-carboxy-butanoyl)amino]-5-(3H-diazirin-3-yl)-5-oxo-pentanoyl]amino]diazirin-3-yl]-5-oxo-pentanoate will display a trend of higher solubility in polar solvents like water, especially at an optimal pH level.

Interesting facts

Interesting Facts about Sodium;5-[3-[[2-[(4-amino-4-carboxy-butanoyl)amino]-5-(3H-diazirin-3-yl)-5-oxo-pentanoyl]amino]diazirin-3-yl]-5-oxo-pentanoate

This compound, commonly referred to in studies involving bioactive molecules, showcases some fascinating characteristics worth exploring. Here are some key points that highlight its significance:

Bioactivity: The presence of diazirin groups adds luminescent properties to the compound, making it pivotal in photoreactive studies where the interaction of biological systems with light is essential.
Amino Acid Structure: The structure includes multiple amino groups, which makes it an interesting candidate for studying protein interactions and biochemical pathways.
Application in Research: Due to its unique structure, this compound is often utilized in medicinal chemistry to investigate mechanisms of action for drug delivery systems.
Potential Therapeutic Uses: The compound’s components hint at potential applications in designing drugs that target specific biological pathways, particularly in cancer research.
Complex Composition: The synthesis of this compound is intricate, highlighting the challenges and artistry involved in organic synthesis – a testament to modern chemical engineering.

As a researcher or chemistry student, exploring sodium;5-[3-[[2-[(4-amino-4-carboxy-butanoyl)amino]-5-(3H-diazirin-3-yl)-5-oxo-pentanoyl]amino]diazirin-3-yl]-5-oxo-pentanoate provides invaluable insight into the integration of chemistry, biology, and materials science. Its multi-faceted applications not only emphasize the importance of interdisciplinary studies but also pave the way for innovative solutions in medicine and technology.