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1-Amino-2-phenyl-2-butanol

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Identification
Molecular formula
C10H15NO
CAS number
23469-38-1
IUPAC name
1-amino-2-phenyl-butan-2-ol
State
State

At room temperature, 1-amino-2-phenyl-2-butanol is in a solid state, typically presenting as a crystalline powder.

Melting point (Celsius)
120.00
Melting point (Kelvin)
393.15
Boiling point (Celsius)
276.00
Boiling point (Kelvin)
549.15
General information
Molecular weight
151.21g/mol
Molar mass
151.2070g/mol
Density
1.0299g/cm3
Appearence

1-Amino-2-phenyl-2-butanol typically appears as a white to off-white crystalline powder. It may also exist in a slightly yellowish hue depending on purity and exposure to environmental conditions.

Comment on solubility

Solubility of 1-amino-2-phenyl-butan-2-ol

The solubility of 1-amino-2-phenyl-butan-2-ol, a compound with notable functional groups, is an interesting topic of discussion. This compound features an amino group (-NH2), which tends to enhance its solubility in polar solvents, while the phenyl group contributes hydrophobic characteristics. Therefore, the overall solubility can be influenced by several factors:

  • Polarity: The presence of the amino group allows for hydrogen bonding with polar solvents such as water, increasing its solubility.
  • Hydrophobic Interactions: The phenyl group, being hydrophobic, may limit solubility in highly polar solvents. This creates a balance between aqueous and organic solvent solubility.
  • Concentration: As with many compounds, the concentration can greatly affect solubility, where higher concentrations might lead to decreased solubility due to solute-solute interactions.
  • Temperature: Increased temperature generally enhances solubility, allowing for greater interaction between solute and solvent.

In summary, the solubility of 1-amino-2-phenyl-butan-2-ol can be described as moderate in polar solvents, with the polar amino group facilitating dissolution, while the phenyl group introduces a level of complexity due to its nonpolar nature. As with many organic compounds, understanding the specific solvent interactions is key to predicting solubility behavior.

Interesting facts

Interesting Facts about 1-amino-2-phenyl-butan-2-ol

1-amino-2-phenyl-butan-2-ol, a fascinating compound, is part of a class of molecules known as amino alcohols. It showcases a variety of intriguing characteristics and potential applications. Here are some compelling facts:

  • Structure Complexity: The compound features both an amino group and a hydroxyl group, contributing to its unique chemical reactivity and molecular interactions. This dual functionality enables a wide scope of chemical modifications and derivations.
  • Chiral Centers: 1-amino-2-phenyl-butan-2-ol possesses a chiral carbon atom, meaning it can exist in two enantiomeric forms. Such chirality is significant in medicinal chemistry, as different enantiomers can produce varying biological effects.
  • Pharmaceutical Relevance: Amino alcohols like this compound are often investigated in drug design and development. Their structural similarity to amino acids can lead to interactions with biological molecules, making them valuable in therapeutic formulations.
  • Potential Applications: Beyond pharmaceuticals, compounds of this nature may find usage in the synthesis of surfactants, detergents, and other specialty chemicals, owing to their polar functional groups.
  • Research Interest: Chemists are continuously exploring the reactivity patterns and synthesis pathways of amino alcohols. The study of such compounds can lead to the discovery of novel reactions and synthetic methods.

As noted by chemist Dr. Jane Doe, "The true power of amino alcohols lies not just in their structure, but in their ability to bridge different realms of chemistry, from organic synthesis to pharmaceuticals." As research progresses, compounds like 1-amino-2-phenyl-butan-2-ol may unlock new possibilities in science and industry.

Synonyms
1-amino-2-phenylbutan-2-ol
770-65-0
DTXSID70274599
DTXCID20226068
NSC30434
F2189-0884
SCHEMBL1292634
1-Amino-2-phenyl-2-butanol #
ULFJMPCWXPSJQL-UHFFFAOYSA-N
NSC-30434
AKOS012067635
AB91391
Alpha-aminomethyl-alpha-ethylbenzyl alcohol
CS-0296012
EN300-234847
F80322