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Fructose 1,6-bisphosphate

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Identification
Molecular formula
C6H14O12P2
CAS number
488-69-7
IUPAC name
(2,3-dihydroxy-4-oxo-5-phosphonooxy-pentyl) dihydrogen phosphate
State
State
At room temperature, fructose 1,6-bisphosphate is a solid. It is stable under normal conditions, although it should be kept in a dry and cool environment to prevent decomposition and degradation.
Melting point (Celsius)
228.00
Melting point (Kelvin)
501.15
Boiling point (Celsius)
-1.00
Boiling point (Kelvin)
272.15
General information
Molecular weight
340.13g/mol
Molar mass
340.1260g/mol
Density
1.8000g/cm3
Appearence

Fructose 1,6-bisphosphate typically appears as a colorless or white crystalline powder. It is highly soluble in water and slightly soluble in alcohol, showing typical behavior of a carbohydrate phosphate ester.

Comment on solubility

Solubility of (2,3-Dihydroxy-4-oxo-5-phosphonooxy-pentyl) Dihydrogen Phosphate (C6H14O12P2)

The solubility of (2,3-dihydroxy-4-oxo-5-phosphonooxy-pentyl) dihydrogen phosphate is influenced by its structural features, namely its multiple hydroxyl and phosphate groups. These functional groups can enhance solubility in polar solvents, particularly water. Here are some notable points regarding its solubility:

  • Hydrophilicity: The presence of hydroxyl (–OH) and phosphate (–PO42−) groups promotes hydrogen bonding with water molecules, leading to increased solubility.
  • Polar Nature: Since this compound is polar, it is more likely to dissolve well in polar solvents, such as water, making it easily soluble in aqueous solutions.
  • Applications: High solubility in physiological conditions can facilitate its use in biochemical applications, particularly in metabolic processes.

In conclusion, the overall solubility of (2,3-dihydroxy-4-oxo-5-phosphonooxy-pentyl) dihydrogen phosphate is expected to be quite favorable in polar environments, aiding in its bioavailability and potential interactive processes in various media.

Interesting facts

Interesting Facts about (2,3-dihydroxy-4-oxo-5-phosphonooxy-pentyl) dihydrogen phosphate

(2,3-dihydroxy-4-oxo-5-phosphonooxy-pentyl) dihydrogen phosphate, often abbreviated in academic circles, stands out as a fascinating compound within the field of biochemistry, particularly due to its role in cellular processes. Here are some engaging insights about this compound:

  • Biological Significance: As a phosphonated compound, it plays a crucial role in cellular signaling pathways, impacting processes such as energy metabolism and signal transduction.
  • Enzymatic Interactions: This compound can act as a substrate or inhibitor for various enzymes, which makes it a key player in biochemical reactions and offers insights into metabolic control mechanisms.
  • Phosphorylation: The presence of phosphate groups contributes to its ability to mimic natural substrates in phosphorylation reactions, an important process in the regulation of protein functions.
  • Potential Applications: Researchers are exploring its potential in drug development, especially as a part of therapies targeting metabolic disorders or cancer, given its influence on key biological pathways.

In conclusion, the study of (2,3-dihydroxy-4-oxo-5-phosphonooxy-pentyl) dihydrogen phosphate not only deepens our understanding of biochemical systems but also opens avenues for innovative medical research and applications. As scientists and students delve into its properties and functions, the implications for health and disease continue to make this compound a subject of great interest.

Synonyms
1,5-di-o-phosphonopent-2-ulose
DTXSID50274299
(2,3-dihydroxy-4-oxo-5-phosphonooxypentyl) dihydrogen phosphate
ribulose-1,5-bisphosphat
Ribulose 1,5 bisphosphate
SCHEMBL19717630
DTXCID80225779
CHEBI:189434
ZAA21800
D-Ribulose 1,5-bisphosphate sodium hydrate