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5-MeO-DMT

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Identification
Molecular formula
C13H18N2O
CAS number
1019-45-0
IUPAC name
2-(5-methoxy-1H-indol-3-yl)-N,N-dimethyl-ethanamine
State
State

At room temperature, 5-MeO-DMT is typically in a solid state as a powder or crystalline substance. It is not commonly found in a liquid or gaseous form under standard conditions.

Melting point (Celsius)
69.50
Melting point (Kelvin)
342.65
Boiling point (Celsius)
160.00
Boiling point (Kelvin)
433.15
General information
Molecular weight
218.30g/mol
Molar mass
218.3150g/mol
Density
1.1338g/cm3
Appearence

5-MeO-DMT is typically encountered as a white, off-white, or slightly yellow crystalline solid. It may also be found as a powder that is often light in color.

Comment on solubility

Solubility of 2-(5-methoxy-1H-indol-3-yl)-N,N-dimethyl-ethanamine (C13H18N2O)

The solubility characteristics of the compound 2-(5-methoxy-1H-indol-3-yl)-N,N-dimethyl-ethanamine can be quite intriguing due to its molecular structure. This compound contains both hydrophobic and hydrophilic functional groups, which can influence its solubility in various solvents. Here are some key points to consider:

  • Solvent Polarity: The presence of the methoxy group (-OCH3) suggests that the compound may exhibit some degree of solubility in polar solvents such as water or alcohols, while also being capable of dissolving in non-polar solvents due to its bulky indole structure.
  • Hydrophobic Interactions: The indole moiety offers hydrophobic characteristics that might limit solubility in highly polar solvents but can enhance solubility in organic solvents.
  • pH Dependence: The compound’s solubility may be affected by the pH of the solution, as protonation of the amine groups can increase solubility in aqueous environments under acidic conditions.

In summary, while 2-(5-methoxy-1H-indol-3-yl)-N,N-dimethyl-ethanamine may exhibit moderate solubility in polar solvents, it is essential to consider solvent choice and environmental conditions for optimal solubility outcomes.

Interesting facts

Interesting Facts about 2-(5-methoxy-1H-indol-3-yl)-N,N-dimethyl-ethanamine

2-(5-methoxy-1H-indol-3-yl)-N,N-dimethyl-ethanamine, often referred to as a compound with intriguing psychoactive properties, is part of the indole class of structures. Here are some fascinating points about this compound:

  • Psychoactive Potential: This compound is noted for its potential influence on serotonin receptors, which makes it a subject of interest in the study of hallucinogens and therapeutic applications in mental health.
  • Structure-Activity Relationship: The structural components, including the indole and methoxy groups, play critical roles in defining the compound’s biological activity. The interaction with neurotransmitter systems is a key area of research.
  • Natural Sources: Indole derivatives are often found in various plants and fungi, suggesting that compounds similar to this one might have natural analogs that contribute to their psychoactive effects.
  • Safety and Research: While there is ongoing research into the effects of this compound, it’s important to note that many such substances require careful study due to their complex effects on the human brain and potential legal implications.

This compound embodies the intersection of chemistry, pharmacology, and psychology, paving the way for further investigations into its beneficial or harmful effects. As scientists continue to explore compounds like 2-(5-methoxy-1H-indol-3-yl)-N,N-dimethyl-ethanamine, they hope to unlock new avenues for treatment and understanding of mental health conditions.

Synonyms
N,N-Dimethyl-5-methoxytryptamine
5-Methoxy-N,N-dimethyltryptamine
1019-45-0
Methoxybufotenin
O-Methylbufotenine
5-MeO-DMT
MeODMT
5-Methoxydimethyltryptamine
Methylbufotenine
Bufotenine, O-methyl-
3-(2-Dimethylaminoethyl)-5-methoxyindole
2-(5-Methoxy-1H-indol-3-yl)-N,N-dimethylethanamine
Mebufotenin
1H-Indole-3-ethanamine, 5-methoxy-N,N-dimethyl-
CT 4334
5-Methoxy-N,N-dimethyl-1H-indole-3-ethanamine
NSC 88624
EINECS 213-813-2
NSC-88624
5-Methoxy-N,N-dimethyl-1H-indole-3-ethylamine
3-(2-(N,N-Dimethyl)aminoethyl)-5-methoxyindole
BRN 0164771
INDOLE, 3-(2-(N,N-DIMETHYLAMINO)ETHYL)-5-METHOXY-
CHEBI:2086
5-OMe-DMT
X0MKX3GWU9
5-METHOXY-N-DIMETHYLTRYPTAMINE
Indole, 3-(2-(dimethylamino)ethyl)-5-methoxy-
3-[2-(N,N-Dimethylamino)ethyl]-5-methoxy-indole
CHEMBL7257
MLS000069438
DTXSID70144324
Indole, 3-[2-(dimethylamino)ethyl]-5-methoxy-
5-22-12-00027 (Beilstein Handbook Reference)
2-(5-methoxy-1H-indol-3-yl)-N,N-dimethylethan-1-amine
SMR000059066
[2-(5-METHOXY-1H-INDOL-3-YL)-ETHYL]-DIMETHYL-AMINE
3-(2-(N,N-Dimethylamino)ethyl)-5-methoxy-indole
3-(2-(N,N-Dimethylamino)ethyl)-5-methoxyindole
3-[2-(N,N-Dimethylamino)ethyl]-5-methoxyindole
UNII-X0MKX3GWU9
(2-(5-Methoxy-1H-Indol-3-Yl)-Ethyl)-Dimethyl-Amine
Mebufotenina
Mebufotenine
mebufotenin [INN]
5-Methoxy-DMT
Maybridge3_000045
Lopac-M-2381
DMT,5-Me
cid_1832
Lopac0_000724
Oprea1_596468
GTPL145
SCHEMBL132733
2-(5-methoxy-1H-indol-3-yl)-N,N-dimethyl-ethanamine
DTXCID1066815
BDBM30707
HMS1431C01
HMS2235C20
HMS3370M04
N,N-Dimethyl-5-methoxy tryptamine
NSC88624
MFCD00005658
PDSP1_000032
PDSP1_000447
PDSP2_000032
PDSP2_000445
STK368074
AKOS005203483
Bufotenine, 5-Methoxydimethyltryptamine
CCG-204809
DB14010
SDCCGMLS-0003129.P003
IDI1_011432
WLN: T56 BMJ D2N1&1 GO1
NCGC00015654-01
NCGC00015654-02
NCGC00015654-03
NCGC00015654-04
NCGC00015654-05
NCGC00015654-06
NCGC00023288-03
NCGC00023288-04
Indole,N-dimethylamino)ethyl]-5-methoxy-
DB-005455
3-[2-(Dimethylamino)ethyl]-5-methoxyindole
NS00023092
C08309
D-5380
[2-(5-methoxy-1H-indol-3-yl)ethyl]dimethylamine
2-(5-methoxy-1H-indol-3-yl)ethyl-dimethyl-amine
5-methoxyindole 3-(2-(N,N-Dimethylamino)ethyl)
L000724
Q570757
2-(5-methoxy-1H-indol-3-yl)-ethyl-dimethyl-amine
BRD-K34224286-001-07-1
Indole, 3-(2-(dimethylamino)ethyl)-5-methoxy-(8CI)
1H-Indole-3-ethanamine, 5-methoxy-N,N-dimethyl-(9CI)
2-(5-Methoxy-1H-indol-3-yl)-N,N-dimethylethanamine #
3-(2-Dimethylaminoethyl)-5-methoxyindole; 2-(5-methoxy-1H-indol-3-yl)-N,N-dimethylethanamine
YFW