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Tyramine

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Identification
Molecular formula
C8H11NO
CAS number
51-67-2
IUPAC name
4-(2-aminoethyl)-3-phenyl-phenol
State
State

At room temperature, tyramine is a solid.

Melting point (Celsius)
164.00
Melting point (Kelvin)
437.00
Boiling point (Celsius)
179.00
Boiling point (Kelvin)
452.00
General information
Molecular weight
137.18g/mol
Molar mass
137.1800g/mol
Density
1.0700g/cm3
Appearence

Tyramine is a white crystalline solid that can appear as a powder. It is often encountered in its hydrochloride or other salt forms, which may affect its color and solubility.

Comment on solubility

Solubility of 4-(2-aminoethyl)-3-phenyl-phenol

4-(2-aminoethyl)-3-phenyl-phenol, also known as 4-aminoethyl-3-phenylphenol, exhibits varying solubility characteristics that are pertinent to its applications in various fields. Its solubility can be influenced by a combination of factors, including:

  • Polarity: This compound possesses both hydrophilic and hydrophobic elements due to the amino group and phenyl rings, respectively, indicating that it has a moderate tendency to dissolve in polar and non-polar solvents.
  • pH Level: The solubility may increase in aqueous solutions at varying pH levels, particularly under acidic conditions where protonation of the amino group occurs, making it more soluble.
  • Temperature: Like many organic compounds, increased temperature may enhance solubility due to higher kinetic energy, allowing for greater interaction with the solvent.
  • Concentration: At higher concentrations, solubility limits can be reached, leading to precipitation in certain solvents.

In summary, the solubility of 4-(2-aminoethyl)-3-phenyl-phenol can be described as:

  1. Soluble in organic solvents such as ethanol and acetone.
  2. Partially soluble in water, especially under acidic conditions.
  3. Influenced by temperature and solvent nature.

Understanding these solubility characteristics is essential for researchers and practitioners who seek to utilize this compound effectively in their methodologies.

Interesting facts

Interesting Facts about 4-(2-aminoethyl)-3-phenyl-phenol

4-(2-aminoethyl)-3-phenyl-phenol, also known as a derivative of phenolic compounds, presents a fascinating case in the world of organic chemistry. This compound features a phenolic core, which is a common structural motif found in many biologically active molecules. Here are some noteworthy aspects:

  • Biological Relevance: Phenolic compounds are often recognized for their roles in natural products and pharmaceuticals. They exhibit various biological activities, including antimicrobial and antioxidant properties.
  • Aminoethyl Group: The presence of the aminoethyl substituent suggests that this compound may participate in a range of biochemical interactions, making it an interesting candidate for drug design.
  • Potential Applications: Due to its unique structure, 4-(2-aminoethyl)-3-phenyl-phenol could be studied for applications in fields such as materials science, medicinal chemistry, and even in the synthesis of novel polymers.
  • Research Opportunities: This compound can serve as a model for investigating the reactivity of amines with phenols, leading to insights into synthetic methods or mechanisms of action in biological systems.

As we continue to explore the multifaceted world of organic compounds, 4-(2-aminoethyl)-3-phenyl-phenol serves as a reminder of the intricate connections between structure and function in chemistry.