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DMT (Dimethyltryptamine)

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Identification
Molecular formula
C14H18N2
CAS number
61-50-7
IUPAC name
N,N-dimethyl-4,4-bis(2-thienyl)but-3-en-2-amine
State
State

At room temperature, DMT is a solid.

Melting point (Celsius)
49.60
Melting point (Kelvin)
322.75
Boiling point (Celsius)
60.00
Boiling point (Kelvin)
333.15
General information
Molecular weight
204.33g/mol
Molar mass
204.3300g/mol
Density
1.0670g/cm3
Appearence

DMT is typically found as a white crystalline powder, but its appearance can vary. It can also be yellow or orange when impure. This compound is usually encountered in powdered form for research and experimental purposes.

Comment on solubility

Solubility of N,N-dimethyl-4,4-bis(2-thienyl)but-3-en-2-amine

N,N-dimethyl-4,4-bis(2-thienyl)but-3-en-2-amine exhibits notable solubility characteristics influenced by its molecular structure. Understanding its solubility is crucial for various applications, especially in organic synthesis and material science. Here are some key points regarding its solubility:

  • Polarity: The presence of amine groups and thienyl rings suggests a balance of polar and nonpolar characteristics, potentially allowing for solubility in both polar and nonpolar solvents.
  • Solvent Interaction: This compound is likely soluble in solvents such as dimethyl sulfoxide (DMSO) and acetonitrile, while exhibiting limited solubility in water due to hydrophobic thienyl groups.
  • Concentration Effects: As with many organic compounds, solubility may increase with higher concentrations of organic solvents, while temperature may also play a role in enhancing solubility.
  • Crystallization: The relative insolubility in polar solvents may lead to crystallization phenomena, which can be utilized in purification processes.

Considering these factors, the solubility properties of N,N-dimethyl-4,4-bis(2-thienyl)but-3-en-2-amine can significantly impact its usability in different environments. Thus, it’s essential to choose the right solvent to optimize its application potential.

Interesting facts

Interesting Facts about N,N-dimethyl-4,4-bis(2-thienyl)but-3-en-2-amine

N,N-dimethyl-4,4-bis(2-thienyl)but-3-en-2-amine is a fascinating compound within the realm of organic chemistry. This compound is notable not only for its unique structure but also for its potential applications in various fields. Here are some intriguing details:

  • Structure and Composition: The compound features a central butenylamine backbone, flanked by two thienyl groups. Thienyl groups are derived from thiophene, a five-membered aromatic ring containing sulfur, which adds interesting electronic properties to the molecule.
  • Electronics: The presence of the thienyl moieties contributes to the electronic delocalization within the molecule, making it a candidate for use in organic semiconductors and photovoltaic devices.
  • Potential Applications: Due to its distinctive properties, this compound may find its way into areas such as:
    • Organic electronics
    • Fluorescent materials
    • Photocatalysts
  • Biological Interest: Some derivatives of similar compounds exhibit biological activity. Investigating N,N-dimethyl-4,4-bis(2-thienyl)but-3-en-2-amine could lead to discoveries in medicinal chemistry.
  • Synthetic Pathways: The synthesis of this compound can offer insights into advanced synthetic techniques, showcasing the use of catalysis and strategic functionalization of starting materials.

As a compound with a rich structural framework, N,N-dimethyl-4,4-bis(2-thienyl)but-3-en-2-amine continues to inspire research and innovation in synthetic and applied chemistry. Scientists are constantly exploring its properties and potential applications, making it a compelling subject of study.

Synonyms
Dimethylthiambutene
Dimethibutin
Ohton
Dimetiltiambuteno
Aminobutene
Kobaton
Takaton
Dimetiltiambutene
Dimethylthiambutenum
3-Dimethylamino-1,1-di-(2'-thienyl)-1-butene
N,N,1-Trimethyl-3,3-di-2-thienylallylamine
3-Dimethylamino-1,1-bis(2-thienyl)-1-butene
Dimetiltiambutene [DCIT]
N,N,1-Trimethyl-3,3-di(2-thienyl)-2-propenylamine
Dimetiltiambuteno [INN-Spanish]
Acscn-9619
Dimethylthiambutenum [INN-Latin]
NIH-4542
Dimethylthiambutene [INN:BAN:DCF]
338C48
UNII-915D88LM9O
Allylamine, N,N,1-trimethyl-3,3-di-2-thienyl-
BRN 0084891
IDS-ND-014
3-Buten-2-amine, N,N-dimethyl-4,4-di-2-thienyl-
CHEBI:59781
915D88LM9O
N,N-Dimethyl-4,4-di-2-thienyl-3-buten-2-amine
N,N-Dimethyl-4,4-di(2-thienyl)-3-buten-2-amine
N,N-dimethyl-4,4-di(thiophen-2-yl)but-3-en-2-amine
ALLYLAMINE, 3,3-DI-2-THIENYL-N,N,1-TRIMETHYL-
N,N-Dimethyl-(1,1-bis(2-thienyl)-1-buten-3-yl)amin
DIMETHYLTHIAMBUTENE [MI]
DIMETHYLTHIAMBUTENE [INN]
DTXSID50862115
4-19-00-04147 (Beilstein Handbook Reference)
Dimethylthiambutene (INN)
3-Dimethylamino-1,1-di-(2'-thienyl)but-1-ene
Dimetiltiambuteno (INN-Spanish)
Dimethylthiambutenum (INN-Latin)
DTXCID20810926
3-Buten-2-amine, N,N-dimethyl-4,4-di-2-thienyl-(9CI)
canbgvxybpolrr-uhfffaoysa-n
524-84-5
NIH4542
DEA No. 9619
Dimethylthiambuten
SCHEMBL25544
CHEMBL2106265
HY-U00164
CS-7219
DB01444
but-1-ene, 3-dimethylamino-1,1-dithienyl-
3-Dimethylamino-1,1-di(2-thienyl)- buten-1
D12665
Q5277350
[4,4-bis(thiophen-2-yl)but-3-en-2-yl]dimethylamine
N,N-Dimethyl-4,4-di(2-thienyl)-3-buten-2-amine #