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Trametenolic acid

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Identification
Molecular formula
C30H50O2
CAS number
84898-46-2
IUPAC name
2-(4-methoxy-2-phenyl-phenyl)ethylammonium;chloride
State
State

Trametenolic acid is typically in a solid state at room temperature, often found in a powder form which is stable under normal conditions.

Melting point (Celsius)
199.00
Melting point (Kelvin)
472.15
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.15
General information
Molecular weight
396.60g/mol
Molar mass
396.5980g/mol
Density
1.3150g/cm3
Appearence

Trametenolic acid typically appears as a white crystalline solid. It is usually odorless and is known for its pure, simple appearance in a dry powder form.

Comment on solubility

Solubility of 2-(4-methoxy-2-phenyl-phenyl)ethylammonium chloride

The compound 2-(4-methoxy-2-phenyl-phenyl)ethylammonium chloride exhibits intriguing solubility characteristics, primarily influenced by its polar and non-polar functional groups. Here are some details regarding its solubility:

  • Solvent Compatibility: This compound is generally more soluble in polar solvents such as water and alcohols due to the presence of the ammonium group, which can form hydrogen bonds.
  • Hydrophilicity: The chloride ion enhances its hydrophilic nature, facilitating dissolution in aqueous environments.
  • Temperature Dependency: Like many chemical compounds, solubility may increase with temperature; thus, heating might improve its solubility in water and organic solvents.
  • Concentration Effects: It is also worth noting that the solubility may vary depending on the concentration of the solution, being potentially less soluble at higher concentrations due to saturation.

Overall, while 2-(4-methoxy-2-phenyl-phenyl)ethylammonium chloride shows a strong tendency for solubility in polar media, the specific conditions and solvent choice play crucial roles in achieving optimal dissolution.

Interesting facts

Interesting Facts about 2-(4-Methoxy-2-phenyl-phenyl)ethylammonium Chloride

This compound, often referred to in scientific discussions for its unique structural features, showcases a fascinating blend of organic chemistry and biological applications. Here are some intriguing elements to note about 2-(4-methoxy-2-phenyl-phenyl)ethylammonium chloride:

  • Structural Complexity: The compound incorporates an ethylammonium moiety, which is notable for its ability to interact with biological membranes, potentially influencing permeability and transport mechanisms.
  • Pharmacological Potential: Due to its ammonium functional group, this compound may participate in various biochemical interactions and could be a candidate for drug development, particularly in fields such as neurology or cardiology.
  • Functional Groups: The presence of a methoxy group adds not only steric hindrance but also electron-donating properties, which may enhance the compound’s reactivity and pharmacological efficacy.
  • Research Applications: Compounds like this one are often subjects of studies in the area of molecular biology, particularly in researching their effects on cell signaling pathways and potential therapeutic roles.
  • Preparation and Synthesis: The synthesis of such complex organic compounds often requires sophisticated methodologies, including multi-step synthesis from simpler precursors, showcasing the ingenuity of modern organic chemistry.

In conclusion, 2-(4-methoxy-2-phenyl-phenyl)ethylammonium chloride not only stands out due to its structural features but also serves as a potential key player in the exploration of new pharmacological avenues. This compound exemplifies the intersection of chemistry and biology, illuminating an exciting path in the realm of scientific research.

Synonyms
2-BIPHENYLETHYLAMINE, 5-METHOXY-, HYDROCHLORIDE
2-(5-Methoxy-2-biphenylyl)ethylamine hydrochloride
13394-80-4