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2-Amino-3-hexanol

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Identification
Molecular formula
C6H15NO
CAS number
1192-41-4
IUPAC name
2-aminohexan-3-ol
State
State

At room temperature, 2-Amino-3-hexanol is a liquid. It is hygroscopic, meaning it can absorb moisture from the environment.

Melting point (Celsius)
12.00
Melting point (Kelvin)
285.15
Boiling point (Celsius)
190.00
Boiling point (Kelvin)
463.15
General information
Molecular weight
117.19g/mol
Molar mass
117.1940g/mol
Density
0.8787g/cm3
Appearence

2-Amino-3-hexanol typically appears as a colorless to pale yellow liquid. It has a characteristic amine and alcohol odor, typical of amino alcohols.

Comment on solubility

Solubility of 2-aminohexan-3-ol

2-aminohexan-3-ol, a compound featuring a hydroxyl group and an amine, exhibits interesting solubility characteristics that can be attributed to its functional groups. Here are some key points regarding its solubility:

  • Polarity: The presence of the hydroxyl group (-OH) makes 2-aminohexan-3-ol a polar molecule, allowing it to interact favorably with polar solvents.
  • Solvent Interaction: It is soluble in water due to hydrogen bonding capabilities, which can be described as "like dissolves like." This means that polar compounds tend to dissolve well in polar solvents such as water.
  • Hydrophobic Chain: The hexane backbone provides nonpolar characteristics to the molecule, which may limit its solubility in nonpolar organic solvents.
  • Temperature Dependence: As with many organic compounds, solubility can be affected by temperature; generally, higher temperatures increase the solubility of solids in liquids.
  • Practical Applications: Its solubility properties make it useful in various fields, such as pharmaceuticals, where solubility is a crucial factor for bioavailability.

Overall, the solubility of 2-aminohexan-3-ol highlights the complex interplay between its polar and nonpolar characteristics, illustrating the significance of functional groups in determining solubility behavior.

Interesting facts

Interesting Facts about 2-Aminohexan-3-ol

2-Aminohexan-3-ol is a fascinating compound with a range of applications in both organic synthesis and biochemistry. Here are some interesting aspects of this compound:

  • Versatile Building Block: This compound acts as a versatile building block in organic synthesis. It can be used to create various derivatives that are important in pharmaceutical research.
  • Biochemical Significance: In biochemistry, 2-aminohexan-3-ol may participate in metabolic processes, making it an interesting subject for studies related to amino acid metabolism and synthesis.
  • Chirality: The presence of an amino group and a hydroxyl group in its structure provides chirality, which gives rise to different enantiomers. This chirality can lead to varied biological activities, especially in drug development.
  • Preparation Methods: Several synthetic methods can yield 2-aminohexan-3-ol, such as the reduction of corresponding keto compounds or the hydroamination of alkenes, showcasing the richness of organic chemistry techniques.
  • Potential Applications: Due to its unique structure, this compound has potential applications in the synthesis of agrochemicals and biologically active compounds, highlighting its relevance in environmental and health sciences.

In summary, 2-aminohexan-3-ol exemplifies the intricate relationship between structure and function in chemistry. Its versatility in applications makes it a compound of interest for chemists and researchers alike, allowing for continuous exploration in both synthetic and applied chemistry.

Synonyms
2-Amino-3-hexanol
USAF CS-2
13325-11-6
3-HEXANOL, 2-AMINO-
2-aminohexan-3-ol
NSC 17699
NSC17699
WLN: ZY1&YQ3
SCHEMBL2100071
SCHEMBL27674365
DTXSID70928020
NSC-17699
AKOS006340329
DS-012920