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Prostaglandin E1

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Identification
Molecular formula
C20H34O5
CAS number
745-65-3
IUPAC name
7-[5-hydroxy-2-(3-hydroxyoct-1-enyl)-3-oxo-cyclopentyl]hept-5-enoic acid
State
State
At room temperature, prostaglandin E1 is typically a viscous liquid. It is sensitive to light and oxygen, and should be stored accordingly to preserve its stability.
Melting point (Celsius)
-54.00
Melting point (Kelvin)
219.15
Boiling point (Celsius)
215.00
Boiling point (Kelvin)
488.15
General information
Molecular weight
354.49g/mol
Molar mass
354.4880g/mol
Density
1.1214g/cm3
Appearence
Prostaglandin E1 (PGE1) typically appears as a colorless to pale-yellow oily liquid. It may also crystallize under certain conditions, taking on a solid form. In its pure form, it is generally free from visible impurities.
Comment on solubility

Solubility of 7-[5-hydroxy-2-(3-hydroxyoct-1-enyl)-3-oxo-cyclopentyl]hept-5-enoic acid

The solubility of 7-[5-hydroxy-2-(3-hydroxyoct-1-enyl)-3-oxo-cyclopentyl]hept-5-enoic acid, with the chemical formula C20H34O5, is influenced by various factors, primarily its molecular structure and functional groups. This compound features multiple hydroxyl (-OH) groups, which significantly contribute to its solubility characteristics.

Key Aspects of Solubility

  • Polarity: The presence of hydroxyl groups increases the polarity of the molecule, promoting solubility in polar solvents such as water.
  • Hydrogen Bonding: The -OH groups can engage in hydrogen bonding with solvent molecules, enhancing interactions and aiding dissolution.
  • Chain Length: The presence of long hydrocarbon chains affects solubility. While long hydrophobic chains usually decrease solubility in water, the functional groups can offset this effect.

In general, you can expect this compound to exhibit moderate solubility in water due to its complex nature, with some solubility in organic solvents. For practical applications, understanding the solubility behavior can aid in solvent selection for processes such as extraction and formulation.

In conclusion, the solubility of 7-[5-hydroxy-2-(3-hydroxyoct-1-enyl)-3-oxo-cyclopentyl]hept-5-enoic acid illustrates the fascinating interplay of molecular features that affect how substances interact with solvents. As succinctly stated, "The structure determines the solubility!"

Interesting facts

Interesting Facts about 7-[5-hydroxy-2-(3-hydroxyoct-1-enyl)-3-oxo-cyclopentyl]hept-5-enoic acid

This intriguing compound, with its complex structure, presents a fascinating subject for chemists and organic researchers alike. Its unique molecular architecture contributes to its potential applications and physiological effects. Here are some noteworthy aspects:

  • Natural Origins: This compound may have biological significance, potentially being derived from natural processes or organisms.
  • Functional Groups: The presence of multiple functional groups, such as hydroxyl and carbonyl groups, showcases its chemical reactivity and interaction capabilities.
  • Potential Applications: Given its structural features, this compound could be explored for use in pharmaceuticals or as a bioactive compound in health supplements.
  • Research Opportunities: The complexity of its structure opens avenues for extensive research, particularly in fields such as medicinal chemistry and materials science.
  • Isomerism and Stereochemistry: The presence of multiple stereogenic centers increases its complexity, raising questions about its isomeric forms and their respective biological activities.

As stated by renowned chemist Linus Pauling, "The science of chemistry is not a mere collection of facts, but an understanding of the principles that govern the interaction of matter." This compound exemplifies this philosophy, as it challenges researchers to delve into its unique properties and potential implications in various scientific fields.

Ultimately, 7-[5-hydroxy-2-(3-hydroxyoct-1-enyl)-3-oxo-cyclopentyl]hept-5-enoic acid serves not only as a chemical curiosity but also as a reminder of the endless possibilities that lie within the realm of organic chemistry.

Synonyms
Prostaglandin D2?
DTXSID50866052
BCP30264
LIA10529
PGD2;11-Dehydroprostaglandin F2-alpha
DB-050775
9,15-dihydroxy-11-oxoprosta-5,13-dien-1-oic acid