Skip to main content

5-Methyltryptamine

ADVERTISEMENT
Identification
Molecular formula
C11H14N2
CAS number
38953-23-4
IUPAC name
2-(5-methyl-1H-indol-3-yl)ethanamine
State
State

Solid: At room temperature, 5-Methyltryptamine is a solid compound. It is commonly found and handled as a crystalline powder.

Melting point (Celsius)
122.00
Melting point (Kelvin)
395.15
Boiling point (Celsius)
298.00
Boiling point (Kelvin)
571.15
General information
Molecular weight
174.24g/mol
Molar mass
174.2420g/mol
Density
1.2300g/cm3
Appearence

5-Methyltryptamine is typically a white to off-white crystalline powder. It may also appear as small crystalline chunks depending on the form and purity of the sample. The compound is odorless and has a bitter taste.

Comment on solubility

Solubility of 2-(5-methyl-1H-indol-3-yl)ethanamine

The solubility of 2-(5-methyl-1H-indol-3-yl)ethanamine can be characterized by several important factors that influence its ability to dissolve in various solvents.

Key Points on Solubility:

  • Polarity: The presence of an amino group (–NH2) contributes to increased polarity, suggesting potential for good solubility in polar solvents.
  • Hydrogen Bonding: This compound can engage in hydrogen bonding, enhancing its solubility in water and alcohols.
  • Solvent Compatibility: It is likely to be soluble in organic solvents such as methanol and dimethyl sulfoxide (DMSO), while it may exhibit limited solubility in non-polar solvents.
  • Temperature Effects: As with many organic compounds, solubility may increase with temperature, making it easier to dissolve in higher-temperature solutions.

As a general observation, further empirical testing is advised to determine exact solubility limits in various solvent systems. Exploring solubility can greatly inform its applications, particularly in fields such as pharmaceuticals and organic synthesis.

Interesting facts

Exploring 2-(5-methyl-1H-indol-3-yl)ethanamine

2-(5-methyl-1H-indol-3-yl)ethanamine, a fascinating compound, is often associated with the broader category of indole derivatives. Here are some intriguing facts about this compound:

  • Natural Origins: Indole and its derivatives are commonly found in various natural sources, including plants and animals. They play vital roles in biological processes and are integral to the production of vital biomolecules.
  • Pharmacological Potential: Compounds related to 2-(5-methyl-1H-indol-3-yl)ethanamine have gained attention in medicinal chemistry. They possess properties that make them candidates for therapeutic agents in treating depression, anxiety, and other neuropsychiatric disorders.
  • Chemical Reactivity: This compound features an indole structure, which is known for its versatile reactivity. It can undergo a variety of reactions, leading to the synthesis of a vast array of derivative compounds.
  • Research Interest: The study of indole derivatives, including 2-(5-methyl-1H-indol-3-yl)ethanamine, is an exciting frontier in the field of organic chemistry. Researchers delve into its properties and behaviors, aiming to unlock new applications in various fields such as pharmacology and materials science.
  • Addition to the Indole Family: Indole compounds have a rich diversity of structural variants, and 2-(5-methyl-1H-indol-3-yl)ethanamine exemplifies how modifications to the indole nucleus can significantly influence chemical properties and biological activity.

In summary, 2-(5-methyl-1H-indol-3-yl)ethanamine serves as a prime example of how simple modifications in chemical structures can lead to profound implications in both natural and synthetic realms, enhancing our understanding of chemistry and its applications in life sciences.

Synonyms
5-Methyltryptamine
1821-47-2
2-(5-methyl-1H-indol-3-yl)ethanamine
5-Methyl-3-(aminoethyl)indole
1H-Indole-3-ethanamine, 5-methyl-
2-(5-methyl-1H-indol-3-yl)ethan-1-amine
INDOLE, 3-(AMINOETHYL)-5-METHYL-
CHEMBL331241
1H-Indole-3-ethanamine, 5-methyl
2-(5-Methyl-1H-indol-3-yl)-ethylamine
2-(5-methyl-1~{H}-indol-3-yl)ethanamine
NSC 90805
5-metyltryptamine
1H-Indole-3-ethanamine,5-methyl-
Tryptamine, 5-methyl
5-methylpydidin-2-ol
Maybridge3_000089
5-Methyl-tryptamine, 10
Oprea1_689228
CBDivE_014095
SCHEMBL1129793
DTXSID10171250
CHEBI:125675
HMS1431E01
ALBB-018681
NSC90805
BBL022747
BDBM50073691
NSC-90805
PDSP1_000762
PDSP1_001118
PDSP2_000750
PDSP2_001102
STK352130
AKOS000546310
SDCCGMLS-0065817.P001
IDI1_011476
2-(5-Methyl-1H-indol-3-yl)ethylamine
NCGC00332134-01
PD093943
2-(5-Methyl-1H-indol-3-yl)ethylamine #
DB-004001
D87934
EN300-223449
AB01326088-02
AE-848/01581059
L001229
BRD-K93859331-001-01-0
Q27216286
CVW