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Alprostadil

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Identification
Molecular formula
C20H34O5
CAS number
745-65-3
IUPAC name
6-[(2R)-2-oct-1-ynylcyclopentoxy]hexanoic acid
State
State

At room temperature, Alprostadil is in a solid state as it is generally provided or utilized in its crystalline form.

Melting point (Celsius)
116.00
Melting point (Kelvin)
389.15
Boiling point (Celsius)
289.00
Boiling point (Kelvin)
562.15
General information
Molecular weight
354.49g/mol
Molar mass
354.4930g/mol
Density
1.0500g/cm3
Appearence

Alprostadil is typically provided as a white to off-white crystalline powder that is odorless. It is soluble in alcohol and practically insoluble in water.

Comment on solubility

Solubility of 6-[(2R)-2-oct-1-ynylcyclopentoxy]hexanoic acid

The solubility of 6-[(2R)-2-oct-1-ynylcyclopentoxy]hexanoic acid is influenced by its unique structure, which includes a hydrophobic alkyl chain and a polar carboxylic acid group. Here are some key points regarding its solubility:

  • Polar vs. non-polar: The compound has both polar and non-polar characteristics, suggesting that it might exhibit variable solubility in different solvents.
  • Aqueous solubility: The presence of the carboxylic acid group typically enhances solubility in water, particularly at lower concentrations, as it can form hydrogen bonds.
  • Organic solvents: Given its hydrophobic regions, 6-[(2R)-2-oct-1-ynylcyclopentoxy]hexanoic acid may be more soluble in organic solvents such as ethanol, acetone, or chloroform.
  • Temperature effects: Solubility can also change with temperature; as temperature increases, solubility in both water and organic solvents typically increases.

In conclusion, while this compound shows potential for solubility in water due to its acid functional group, it may also exhibit significant solubility in organic solvents owing to its non-polar characteristics. As with many chemical compounds, solubility ultimately depends on the specific conditions and solvent used.

Interesting facts

Interesting Facts about 6-[(2R)-2-oct-1-ynylcyclopentoxy]hexanoic acid

6-[(2R)-2-oct-1-ynylcyclopentoxy]hexanoic acid is a fascinating compound that showcases the intricate relationship between organic chemistry and biochemistry. Here are some intriguing aspects of this compound:

  • Structural Complexity: This compound is notable for its unique structure, which features both an octynyl group and a cyclopentoxy moiety. The interplay between these different functional groups contributes to its chemical reactivity and potential applications.
  • Synthetic Potential: The presence of an alkyne (the oct-1-ynyl part) allows for diverse synthetic manipulation, making it a valuable building block in organic synthesis. Scientists often harness such compounds to create more complex molecules through various reactions like cross-coupling and cycloaddition.
  • Biological Relevance: Compounds with similar structural features often exhibit interesting biological activities. Investigating the potential bioactivity of 6-[(2R)-2-oct-1-ynylcyclopentoxy]hexanoic acid might reveal novel pharmacological properties that could be harnessed for therapeutic purposes.
  • Applications in Material Science: Due to its unique chemical properties, this compound may find applications in the field of material science, particularly in the creation of advanced polymers or other new materials that leverage its structural features.
  • Configuration Matters: The (2R) configuration indicates specific stereochemistry that can significantly influence the properties and reactivity of the compound. Understanding chirality is crucial in areas such as drug design, where the efficacy of a compound can depend heavily on its stereochemical configuration.

In summary, 6-[(2R)-2-oct-1-ynylcyclopentoxy]hexanoic acid exemplifies the intersection of structural complexity and functional potential in organic compounds. As researchers continue to explore its properties and applications, it may pave the way for advancements in various scientific fields.

Synonyms
27166-04-7
(1S-trans)-6-((2-(1-Octynyl)cyclopentyl)oxy)hexanoic acid
6-[(2R)-2-oct-1-ynylcyclopentyl]oxyhexanoic acid
HEXANOIC ACID, 6-((2-(1-OCTYNYL)CYCLOPENTYL)OXY)-, (1S-trans)-