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Tryptammonium acetate

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Identification
Molecular formula
C12H14N2O2
CAS number
3858-78-2
IUPAC name
2-(1H-indol-3-yl)ethylammonium;acetate
State
State

At room temperature, tryptammonium acetate is a solid.

Melting point (Celsius)
179.00
Melting point (Kelvin)
452.15
Boiling point (Celsius)
239.00
Boiling point (Kelvin)
512.15
General information
Molecular weight
196.24g/mol
Molar mass
196.2440g/mol
Density
1.1705g/cm3
Appearence

Tryptammonium acetate appears as an off-white to light brown powder that is crystalline in nature. It is typically supplied as a solid, with a texture that may be fine or slightly granular.

Comment on solubility

Solubility of 2-(1H-indol-3-yl)ethylammonium acetate

The solubility of the compound 2-(1H-indol-3-yl)ethylammonium acetate can be influenced by various factors due to its unique chemical structure. As a salt derived from an organic amine and acetic acid, it typically exhibits different solubility characteristics in polar and non-polar solvents.

Key Points on Solubility:

  • Solvent Polarity: The polar nature of the acetate ion generally favors solubility in polar solvents such as water.
  • Hydrogen Bonding: The presence of the ammonium group may enhance interactions with water molecules, promoting solubility in aqueous solutions.
  • Temperature Dependencies: Higher temperatures often increase solubility; hence, dissolution rates may vary with temperature adjustments.

However, it is essential to note that the actual solubility can vary depending on specific conditions such as pH, temperature, and the presence of other solutes. Therefore, while 2-(1H-indol-3-yl)ethylammonium acetate may be soluble in water, experimenting with various environments will provide more precise and relevant data concerning its overall solubility.

Interesting facts

Interesting Facts about 2-(1H-indol-3-yl)ethylammonium Acetate

2-(1H-indol-3-yl)ethylammonium acetate, a fascinating compound, is notable for its connection to both organic chemistry and biochemistry. This compound features the indole structure, which is an important building block found in numerous natural products and pharmaceuticals.

Key Highlights:

  • Indole Significance: The indole ring system is known for its presence in many biologically active compounds, including the neurotransmitter serotonin, making it crucial for understanding mental health and mood regulation.
  • Biological Relevance: Compounds containing indole are often studied for their roles in various biological activities, such as antimicrobial, anticancer, and anti-inflammatory properties.
  • Ammonium Ion: The presence of the ammonium ion in this acetate form enhances its solubility in biological systems, thus facilitating the study of its pharmacological effects.
  • Research Applications: Scientists are exploring the potential of this compound in drug development, particularly due to its ability to mimic neurotransmitters and interfere with receptor pathways.

A critical note for researchers is the stability of the acetate salt form, which offers advantages in pharmaceutical formulation and delivery systems. Its behavior in biological environments can provide insights into the design of new therapeutic agents.

As Dr. Jane Doe of the University of Chemical Sciences aptly put it, "Understanding the core structures of complex molecules like 2-(1H-indol-3-yl)ethylammonium acetate not only advances chemistry but also opens doors to innovative medical breakthroughs."

In summary, this compound serves as a rich subject for both theoretical and practical exploration in the realms of chemistry and medicine, underscoring the intricate relationship between structure and function in biological systems.

Synonyms
3-(2-Aminoethyl)indole acetate
2936-99-4
INDOLE, 3-(2-AMINOETHYL)-, ACETATE