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Fructose 1,6-bisphosphate

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Identification
Molecular formula
C3H3O9P2
CAS number
488-69-7
IUPAC name
phosphono 2-hydroxy-3-phosphonooxy-propanoate
State
State

At room temperature, Fructose 1,6-bisphosphate is a solid.

Melting point (Celsius)
120.00
Melting point (Kelvin)
393.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
139.03g/mol
Molar mass
139.0530g/mol
Density
2.2720g/cm3
Appearence

Phosphono 2-hydroxy-3-phosphonooxy-propanoate, more commonly known as Fructose 1,6-bisphosphate, appears as a white crystalline solid.

Comment on solubility

Solubility of Phosphono 2-hydroxy-3-phosphonooxy-propanoate

Phosphono 2-hydroxy-3-phosphonooxy-propanoate (C3H3O9P2) exhibits intriguing solubility characteristics primarily due to its structural components. This compound features multiple functional groups that influence its interaction with solvents.

Key Solubility Factors:

  • Hydrophilicity: The presence of hydroxyl groups (-OH) and phosphonate groups contributes to a high degree of polar character, enhancing solubility in polar solvents like water.
  • pH Dependence: The solubility may vary with pH; at different pH levels, protonation and deprotonation of the functional groups can occur, affecting overall solubility.
  • Temperature: Increasing temperature typically increases solubility for many compounds, and this may apply to phosphono 2-hydroxy-3-phosphonooxy-propanoate, although specific data should be referenced for precise behavior.

Furthermore, to understand the compound's solubility thoroughly, it's important to consider:

  1. Interactions with ions in solution, potentially leading to complex formation.
  2. Overall stability of the molecule in various solvents, which can provide insight into its practical applications.

As a summary, the solubility of C3H3O9P2 is influenced by its polar functional groups, which promote solubility in aqueous environments, while pH and temperature can play critical roles in its overall solubility characteristics.

Interesting facts

Interesting Facts about Phosphono 2-Hydroxy-3-phosphonooxy-propanoate

Phosphono 2-hydroxy-3-phosphonooxy-propanoate, often abbreviated as PHPP, is an intriguing compound that plays a significant role in various biochemical processes. Here are some fascinating aspects of this compound:

  • Biological Importance: PHPP works as a biochemical substrate in metabolic pathways, particularly in the context of glycobiology, where it can influence carbohydrate metabolism.
  • Phosphorylation Reactions: Its structure contains multiple phosphorus groups, making it a prime candidate in phosphate transfer reactions, which are crucial in cellular signaling.
  • Research Applications: Scientists are exploring its potential uses in drug design and development, especially concerning treatments that target metabolic disorders.
  • Environmental Impact: As a phosphonated compound, PHPP is examined for its role in nutrient cycling within ecosystems, particularly in aquatic environments.

Interestingly, this compound exemplifies how a simple molecular alteration can lead to significant physiological effects. As the late biochemist Atkinson once said, "The tiniest change in structure can lead to the grandest consequences." Understanding compounds like PHPP not only enhances our knowledge of biochemistry but also fuels advancements in scientific research across multiple disciplines.

With ongoing studies, PHPP continues to reveal its secrets, marking an exciting frontier in the realm of chemical sciences.

Synonyms
glyceric acid 1,3-biphosphate
1981-49-3
1,3-biphosphoglycerate
phosphono 2-hydroxy-3-phosphonooxypropanoate
1,3-diphosphoglycerate
CHEMBL2074701
CHEBI:89363
2-Hydroxy-3-(phosphonooxy)propanoic phosphoric anhydride
(2-HYDROXY-3-PHOSPHONOOXY-PROPANOYL)OXYPHOSPHONIC ACID
1,3-Bisphosphoglycerate
glycerate 1,3-biphosphate
1,3-Biphosphoglyceric acid
Glyceric acid-1,3-diphosphate
SCHEMBL50423
DTXSID50941636
BDBM50420198
DA-53615
HY-113117
CS-0059615
NS00123173
Q1020557
51E9A779-51C5-419D-AB1E-F16509F75573
Propanoic acid, 2-hydroxy-3-(phosphonooxy)-, 1-anhydride with phosphoric acid