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Methamphetamine

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Identification
Molecular formula
C12H19NO
CAS number
69610-10-6
IUPAC name
2-(methylamino)-3-phenyl-pentan-3-ol
State
State

Under standard conditions, 2-(methylamino)-3-phenyl-pentan-3-ol is in a solid state at room temperature.

Melting point (Celsius)
145.00
Melting point (Kelvin)
418.15
Boiling point (Celsius)
297.50
Boiling point (Kelvin)
570.65
General information
Molecular weight
193.29g/mol
Molar mass
193.2850g/mol
Density
1.0040g/cm3
Appearence

2-(Methylamino)-3-phenyl-pentan-3-ol typically appears as a white crystalline solid.

Comment on solubility

Solubility of 2-(methylamino)-3-phenyl-pentan-3-ol

The solubility of 2-(methylamino)-3-phenyl-pentan-3-ol is influenced by several factors including its molecular structure, functional groups, and environmental conditions. This compound possesses both hydrophilic and hydrophobic characteristics due to the presence of the hydroxyl group (-OH) and the methylamino group (-NH2), as well as the phenyl group attached to the pentan-3-ol chain.

Key points to consider regarding its solubility include:

  • Polarity: The hydroxyl and amino groups contribute to the compound's polarity, which generally increases its solubility in polar solvents such as water.
  • Hydrogen Bonding: The ability to form hydrogen bonds with water molecules can enhance solubility, making 2-(methylamino)-3-phenyl-pentan-3-ol more soluble in aqueous solutions.
  • Hydrophobic Interactions: The phenyl group can lead to hydrophobic interactions, potentially decreasing solubility in non-polar solvents.
  • Temperature Dependence: Solubility may also vary with temperature; typically, higher temperatures increase solubility.

Thus, while 2-(methylamino)-3-phenyl-pentan-3-ol is likely more soluble in polar solvents, the presence of its hydrophobic character may limit solubility in non-polar environments. Overall, the compound's solubility profile can be quite complex, making it a fascinating subject for further exploration in various solvent systems.

Interesting facts

Interesting Facts about 2-(methylamino)-3-phenyl-pentan-3-ol

2-(methylamino)-3-phenyl-pentan-3-ol, often simply referred to as a complex amine, has interesting characteristics that highlight its significance in various fields, particularly in medicinal chemistry and organic synthesis.

Key Highlights:

  • Functional Group Diversity: This compound features a unique combination of an alcohol group and an amine group, making it versatile for various chemical reactions.
  • Biological Relevance: Compounds similar to 2-(methylamino)-3-phenyl-pentan-3-ol often serve as important intermediates in drug development, potentially aiding in the modification of bioactive molecules.
  • Synthetic Applications: The presence of both an amino and an alcohol functional group can allow chemists to perform reactions like alkylation and acylation, expanding its utility in synthetic organic chemistry.
  • Chiral Center: The structure of this compound includes a chiral center, making it possible to produce enantiomers which can exhibit different biological activities.

The complexity of this molecule makes it a fascinating subject of study, as scientists explore its potential applications in therapeutic areas. As the renowned chemist "The ability to manipulate such diverse functional groups lies at the heart of organic synthesis", and this compound exemplifies that capability well.

Hence, 2-(methylamino)-3-phenyl-pentan-3-ol is more than just a compound; it is a bridge connecting the realms of synthetic methodology and biological application, symbolizing the intersection of chemistry and medicine.