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Scopolamine hydrobromide

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Identification
Molecular formula
C17H23NO4Br
CAS number
114-49-8
IUPAC name
[(3S)-6-methoxy-8,8-dimethyl-8-azoniabicyclo[3.2.1]octan-3-yl] 3,4-dimethoxybenzoate;bromide
State
State

At room temperature, Scopolamine hydrobromide is typically a solid. It is readily soluble in water and ethanol.

Melting point (Celsius)
165.00
Melting point (Kelvin)
438.15
Boiling point (Celsius)
260.00
Boiling point (Kelvin)
533.15
General information
Molecular weight
438.30g/mol
Molar mass
438.3030g/mol
Density
1.4000g/cm3
Appearence

Scopolamine hydrobromide appears as a white crystalline powder. It is hygroscopic in nature, which means it can absorb moisture from the air.

Comment on solubility

Solubility of [(3S)-6-methoxy-8,8-dimethyl-8-azoniabicyclo[3.2.1]octan-3-yl] 3,4-dimethoxybenzoate; bromide

The solubility of the compound [(3S)-6-methoxy-8,8-dimethyl-8-azoniabicyclo[3.2.1]octan-3-yl] 3,4-dimethoxybenzoate; bromide can be influenced by several factors, including its ionic nature and structural properties.

Key points regarding its solubility include:

  • Ionic Compounds: As an ammonium ion compound, its bromide salt suggests high solubility in polar solvents such as water due to ion-dipole interactions.
  • Organic Solvents: The presence of methoxy groups may enhance solubility in organic solvents, making it more soluble in ethanol or methanol.
  • Temperature Dependance: Like many compounds, solubility can increase with temperature, which may allow for better dissolution in various media.

In conclusion, while ionic characteristics suggest a general trend of increased solubility in polar environments, the compound's specific solubility behavior will require empirical testing in various solvents to confirm predictions.

Interesting facts

Exploring [(3S)-6-methoxy-8,8-dimethyl-8-azoniabicyclo[3.2.1]octan-3-yl] 3,4-dimethoxybenzoate; bromide

This intriguing compound, distinguished by its complex structure, belongs to a fascinating class of chemicals known as quaternary ammonium salts. Here are some noteworthy aspects:

  • Stereochemistry: The (3S) notation indicates a specific chiral configuration, which is essential in the field of pharmaceuticals. Stereochemistry plays a crucial role in how compounds interact biologically, influencing their efficacy and safety.
  • Diversity of Applications: Compounds with structures like this one often serve multiple roles, including:
    • Pharmacological agents, particularly in the realm of neuromuscular blocking.
    • Antimicrobial agents, due to their ability to disrupt cell membranes.
    • Research tools in various biochemical studies.
  • Functional Groups: Its structure features impressive functional groups, such as:
    • Methoxy groups that enhance lipophilicity.
    • Aromatic benzene derivatives, often critical for biological activity.
  • Significance of Quaternization: The quaternization process, which introduces the positively charged nitrogen atom, is key in enhancing the solubility and reactivity of organic compounds, making them more usable in medicinal chemistry.

As chemistry students or enthusiasts, it’s essential to delve deeper into these structures. Not only do they challenge our understanding of molecular interactions, but they also invite us to consider the real-world implications and potential innovations arising from their synthesis and application. Remember, “Every molecule tells a story,” making compounds like this one critical in our quest for knowledge and discovery in the chemical sciences!