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Bimatoprost

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Identification
Molecular formula
C25H37NO4
CAS number
155206-00-1
IUPAC name
7-[3-(3-hydroxyoct-1-enyl)norpinan-2-yl]hept-5-enoic acid
State
State

At room temperature, Bimatoprost is typically in an oily liquid state.

Melting point (Celsius)
62.00
Melting point (Kelvin)
335.15
Boiling point (Celsius)
658.60
Boiling point (Kelvin)
931.75
General information
Molecular weight
415.57g/mol
Molar mass
415.5710g/mol
Density
1.0360g/cm3
Appearence

Bimatoprost appears as a colorless to slightly yellow oily liquid. It is often encountered in formulations for ophthalmic solutions, which are clear and colorless.

Comment on solubility

Solubility of 7-[3-(3-hydroxyoct-1-enyl)norpinan-2-yl]hept-5-enoic acid

The solubility of 7-[3-(3-hydroxyoct-1-enyl)norpinan-2-yl]hept-5-enoic acid (C25H37NO4) can be quite intriguing due to its complex structure. This compound contains a hydrophobic region, primarily contributed by its long hydrocarbon chains, and a polar functional group, the carboxylic acid. Here are key points to consider regarding its solubility:

  • Hydrophilicity vs. Hydrophobicity: The presence of the carboxylic acid group enhances its solubility in polar solvents, such as water, but the long hydrocarbon chain may resist solvation in the same medium.
  • Solvent Compatibility: This compound is likely to exhibit better solubility in organic solvents like ethyl acetate and dichloromethane than in aqueous solutions.
  • Temperature Dependence: As with many organic compounds, solubility can increase with temperature, making it an important factor during the dissolution process.

In summary, the solubility of 7-[3-(3-hydroxyoct-1-enyl)norpinan-2-yl]hept-5-enoic acid is governed by a balance between its polar and nonpolar components, affecting its interactions with various solvents. Understanding these interactions is crucial in applications such as formulation chemistry and drug delivery systems.

Interesting facts

Exploring 7-[3-(3-hydroxyoct-1-enyl)norpinan-2-yl]hept-5-enoic Acid

This compound, tentatively recognized in the field of organic chemistry, contains a series of intricate structural features that give it a unique profile among organic acids. One of its notable aspects is its combination of both an acid and a norbornane-like structure, which contributes to its distinctive reactivity and potential biological activities.

Key Features:

  • Versatile Structure: The presence of a norbinane framework suggests interesting conformational possibilities that can significantly influence its chemical behavior.
  • Hydroxyl Group: The 3-hydroxyoct-1-enyl moiety may contribute to hydrogen bonding capabilities, making this compound potentially water-soluble and reactive in various chemical environments.
  • Potential Applications: Various compounds of this type have been explored for applications ranging from pharmaceuticals to agrochemicals, owing to their biological activity.

Moreover, the stereochemistry of this compound can be pivotal. As noted by chemists, “The spatial arrangement of atoms in these organic compounds can create a diverse array of functions.” Understanding its three-dimensional structure could uncover new pathways for synthetic pathways or biological interactions.

Current Research Directions:

  • Investigating the compound's metabolic pathways and biological effects in living organisms.
  • Exploring its potential as a precursor in organic synthesis.
  • Understanding its role in complex natural product synthesis.

With ongoing studies surrounding this compound, researchers remain intrigued by its potential implications in various scientific fields. The journey of unraveling its properties and applications is undoubtedly an exciting venture for chemists and researchers alike!

Synonyms
74034-56-3
7-[3-(3-Hydroxyoct-1-enyl)-2-bicyclo[3.1.1]heptanyl]hept-5-enoic acid