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Albuterol

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Identification
Molecular formula
C11H17NO
CAS number
18559-94-9
IUPAC name
1-(tert-butylamino)-4-phenyl-butan-2-ol
State
State

The compound is typically a solid at room temperature, often found in powder form.

Melting point (Celsius)
158.50
Melting point (Kelvin)
431.65
Boiling point (Celsius)
197.00
Boiling point (Kelvin)
470.15
General information
Molecular weight
239.36g/mol
Molar mass
239.3640g/mol
Density
1.0500g/cm3
Appearence

Albuterol typically appears as a white or off-white crystalline powder. It may also be found in a more amorphous solid form depending on its preparation and storage conditions.

Comment on solubility

Solubility of 1-(tert-butylamino)-4-phenyl-butan-2-ol

1-(tert-butylamino)-4-phenyl-butan-2-ol, a compound with interesting chemical properties, exhibits unique solubility characteristics that are influenced by its structural components. Here are some key points regarding its solubility:

  • Polarity: The presence of the tert-butylamino group suggests a degree of polarity, as the nitrogen atom can engage in hydrogen bonding.
  • Hydrophobicity: The phenyl group contributes to hydrophobic characteristics, potentially limiting solubility in polar solvents.
  • Solvent Interaction: It is likely to have improved solubility in organic solvents such as ethanol or methanol, while demonstrating limited solubility in water due to its hydrophobic regions.
  • Temperature Dependence: Solubility may increase with temperature, as is common with many organic compounds.

In summary, while 1-(tert-butylamino)-4-phenyl-butan-2-ol may show moderate solubility in certain organic solvents, its complex structure suggests that careful consideration is needed when predicting behavior in various environments. Ultimately, the balance between polar and non-polar characteristics creates a fascinating interplay that directly affects its solubility.

Interesting facts

Interesting Facts about 1-(tert-butylamino)-4-phenyl-butan-2-ol

1-(tert-butylamino)-4-phenyl-butan-2-ol is a fascinating organic compound that bridges the world of synthetic chemistry and pharmacology. Here are some notable aspects of this compound:

  • Structure and Functional Groups: This compound contains a tert-butylamino group, which is known for its ability to increase lipophilicity, potentially enhancing membrane permeability in biological systems.
  • Optical Activity: Due to its chiral center, 1-(tert-butylamino)-4-phenyl-butan-2-ol can exist as enantiomers, which are mirror images of each other. This property is crucial as different enantiomers can have vastly different biological activities.
  • Potential Therapeutic Applications: Compounds with structure-activity relationships similar to 1-(tert-butylamino)-4-phenyl-butan-2-ol have been studied for their potential in treating various neurological disorders due to their ability to interact with neurotransmitters.
  • Versatility in Synthesis: The synthetic routes leading to this compound can also yield a variety of other related compounds, making it a valuable building block in medicinal chemistry and organic synthesis.
  • Research Interest: Ongoing studies may reveal novel uses for this compound, especially in drug design, highlighting the ever-evolving nature of organic compounds in scientific research.

This compound exemplifies the intricate relationship between molecular structure and biological function, making it an intriguing subject for both chemists and pharmacologists.

Synonyms
AKOS012177769