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Prostaglandin E2

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Identification
Molecular formula
C20H32O5
CAS number
363-24-6
IUPAC name
7-[3-hydroxy-2-(4-hydroxy-4-methyl-oct-1-enyl)-5-oxo-cyclopentyl]heptanoic acid
State
State

Prostaglandin E2 is typically in a liquid state at room temperature due to its relatively low melting point. It is an oily compound.

Melting point (Celsius)
-132.00
Melting point (Kelvin)
141.15
Boiling point (Celsius)
500.00
Boiling point (Kelvin)
773.15
General information
Molecular weight
352.47g/mol
Molar mass
352.4660g/mol
Density
1.0900g/cm3
Appearence

Prostaglandin E2 is typically a colorless to pale yellow viscous liquid or oil. It is sensitive to light and air.

Comment on solubility

Solubility of 7-[3-hydroxy-2-(4-hydroxy-4-methyl-oct-1-enyl)-5-oxo-cyclopentyl]heptanoic acid (C20H32O5)

The solubility of 7-[3-hydroxy-2-(4-hydroxy-4-methyl-oct-1-enyl)-5-oxo-cyclopentyl]heptanoic acid plays a critical role in determining its biological activity and potential applications. Understanding its solubility can provide insight into its use in various formulations. Here are some key points to consider:

  • Apolar Characteristics: Its large organic structure may lead to limited solubility in water. Compounds with significant hydrophobic regions generally exhibit reduced solubility in polar solvents.
  • Possible Solvents: While predominantly insoluble in water, it might find better solubility in organic solvents such as ethanol, methanol, or dimethyl sulfoxide (DMSO).
  • Influence of Functional Groups: The presence of hydroxyl groups can enhance solubility in polar environments, potentially increasing solubility when forming hydrogen bonds with solvent molecules.
  • Temperature Effects: Solubility may improve with increasing temperature, which can provide beneficial solubility characteristics for practical applications.

In summary, while C20H32O5 may demonstrate limited aqueous solubility, factors such as solvent choice, temperature, and functional group interactions can significantly influence its overall solubility profile.

Interesting facts

Interesting Facts about 7-[3-hydroxy-2-(4-hydroxy-4-methyl-oct-1-enyl)-5-oxo-cyclopentyl]heptanoic acid

This intriguing compound, known as 7-[3-hydroxy-2-(4-hydroxy-4-methyl-oct-1-enyl)-5-oxo-cyclopentyl]heptanoic acid, showcases the fascinating complexity of organic chemistry. Here are some notable aspects:

  • Natural Source: This compound is derived from natural sources and is a part of the diverse family of biologically active molecules.
  • Cyclopentane Structure: The presence of a cyclopentyl group in its structure contributes to its unique properties, including potential interactions with biological systems.
  • Functional Groups: The compound is rich in functional groups, such as hydroxyl and keto groups, making it versatile in chemical reactions.
  • Biological Potential: Due to its unique structure, this compound may exhibit various biological activities, including anti-inflammatory or antioxidant effects, making it a subject of interest in pharmaceutical research.

Researchers are continually exploring the mechanisms through which such compounds exert their effects, guided by the notion that "the greater the structural complexity, the richer the potential for unique biological interactions."
In summary, 7-[3-hydroxy-2-(4-hydroxy-4-methyl-oct-1-enyl)-5-oxo-cyclopentyl]heptanoic acid epitomizes the intersection of organic chemistry and biological research, highlighting the importance of structure in determining function.

Synonyms
(+/-)-15-DEOXY-[16RS]-16-HYDROXY-16-METHYLPROSTAGLANDIN E1
7-[3-hydroxy-2-(4-hydroxy-4-methyloct-1-en-1-yl)-5-oxocyclopentyl]heptanoic acid
Prost-13-en-1-oic acid, 11,16-dihydroxy-16-methyl-9-oxo-, (11alpha,13E )-(+-)-
BCP32053
IM181087
Misoprostol Impurity 13 (mixture of diastereomers)