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Diethyltryptamine

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Identification
Molecular formula
C14H20N2
CAS number
61-50-7
IUPAC name
N,N-diethyl-2-(2-methyl-1H-indol-3-yl)ethanamine
State
State

At room temperature, Diethyltryptamine is typically a solid, presenting as crystalline formations.

Melting point (Celsius)
34.00
Melting point (Kelvin)
307.15
Boiling point (Celsius)
160.00
Boiling point (Kelvin)
433.15
General information
Molecular weight
218.33g/mol
Molar mass
218.3300g/mol
Density
0.9390g/cm3
Appearence

Diethyltryptamine typically appears as a crystalline solid, often manifesting in a white to off-white color. These crystals can be seen as fine, powdery substances or more granular forms depending on their state of refinement.

Comment on solubility

Solubility of N,N-diethyl-2-(2-methyl-1H-indol-3-yl)ethanamine

N,N-diethyl-2-(2-methyl-1H-indol-3-yl)ethanamine, often known as a compound of interest in various fields, exhibits specific solubility characteristics that are crucial for its applications. The solubility of this compound can be influenced by several factors, including:

  • Polarity: As an amine, it possesses a degree of polarity that can affect solubility in polar solvents.
  • Hydrogen Bonding: Its ability to participate in hydrogen bonding enhances solubility in alcohols and water.
  • Alkyl Chains: The presence of ethyl groups may increase solubility in organic solvents while decreasing water solubility.

Generally, amines like N,N-diethyl-2-(2-methyl-1H-indol-3-yl)ethanamine tend to be more soluble in:

  1. Polar solvents, such as water and alcohols.
  2. Organic solvents, such as chloroform, depending on the structure.

In practice, one might find that this compound is soluble in a variety of solvents, making it versatile for different experimental conditions. However, the exact solubility should always be quantified experimentally, as it may vary with temperature and concentration. Understanding the solubility profile of this compound is vital for its utilization in biochemical applications and material science.

Interesting facts

Interesting Facts About N,N-Diethyl-2-(2-methyl-1H-indol-3-yl)ethanamine

N,N-diethyl-2-(2-methyl-1H-indol-3-yl)ethanamine, often referred to as a compound of interest in various fields, highlights the fascinating versatility of organic chemistry. Here are some engaging aspects of this compound:

  • Unique Structure: The compound features an indole ring, which is a fundamental structure in many biologically active compounds and pharmaceuticals. This ring system contributes to its diverse chemical properties and interactions.
  • Potential Biological Activity: Compounds like this one, due to their structural components, may exhibit neuropharmacological effects, making them of interest in the study of neurotransmitter systems. Research indicates that indole derivatives can influence serotonin receptors, which are crucial for mood regulation.
  • Synthetic Approaches: The synthesis of N,N-diethyl-2-(2-methyl-1H-indol-3-yl)ethanamine can involve various methods, showcasing the beauty of organic synthesis. Chemists often explore innovative reactions that can lead to such complex molecules from simpler reactants.
  • Applications in Research: This compound is not only important for its potential medicinal properties but also serves as a valuable tool in chemical research. By studying its interactions and reactions, chemists can gain insights into reaction mechanisms and molecular behavior.

In summary, N,N-diethyl-2-(2-methyl-1H-indol-3-yl)ethanamine epitomizes the rich tapestry of organic compounds that bridges the gap between chemistry and biology. Its unique structural attributes and potential applications emphasize the ongoing exploration and excitement within the field of chemistry.

Synonyms
2-ME-DET
BRN 0166959
INDOLE, 3-(2-(DIETHYLAMINO)ETHYL)-2-METHYL-
SSF4F77CV3
3-(2-(Diethylamino)ethyl)-2-methylindole
N,N-Diethyl-2-methyl-1H-indole-3-ethanamine
DTXSID30181174
5-22-10-00158 (Beilstein Handbook Reference)
DIETHYL(2-(2-METHYL-1H-INDOL-3-YL)ETHYL)AMINE
RefChem:197821
DTXCID40103665
26628-88-6
UNII-SSF4F77CV3
SCHEMBL20970934
SCHEMBL29536604
Q4596894