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N,N-Dimethyl-1-naphthylpropylamine

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Identification
Molecular formula
C15H21N
CAS number
1029-84-7
IUPAC name
N,N-dimethyl-3-(1-naphthyl)propan-1-amine
State
State

At room temperature, N,N-Dimethyl-1-naphthylpropylamine is in a liquid state. It remains stable and does not solidify unless it is cooled below -22°C, making it suitable for various applications in its liquid form.

Melting point (Celsius)
-22.00
Melting point (Kelvin)
251.15
Boiling point (Celsius)
290.00
Boiling point (Kelvin)
563.15
General information
Molecular weight
213.33g/mol
Molar mass
213.3290g/mol
Density
1.0300g/cm3
Appearence

N,N-Dimethyl-1-naphthylpropylamine typically appears as a colorless to pale yellow liquid. This compound is often synthesized in laboratories and tends to have an oily texture. It may exhibit a slight aromatic odor that is characteristic of amine compounds.

Comment on solubility

Solubility of N,N-Dimethyl-3-(1-naphthyl)propan-1-amine

The solubility of N,N-dimethyl-3-(1-naphthyl)propan-1-amine is notable due to its unique chemical structure, which influences its interactions with solvents.

Factors Influencing Solubility

  • Polarity: The compound contains both hydrophobic (naphthyl group) and hydrophilic (amine functional group) components, which can lead to varied solubility behavior.
  • Solvent Compatibility: It tends to be more soluble in organic solvents like ethanol, acetone, and chloroform due to its non-polar characteristics.
  • Temperature: Solubility can increase with temperature, making it more soluble in warm solutions compared to cold ones.

In summary, while N,N-dimethyl-3-(1-naphthyl)propan-1-amine has good solubility in organic solvents, its overall solubility might be limited in polar solvents like water. Therefore, understanding the implications of polarity and solvent choice is essential for practical applications.

Interesting facts

Interesting Facts About N,N-Dimethyl-3-(1-naphthyl)propan-1-amine

N,N-Dimethyl-3-(1-naphthyl)propan-1-amine, commonly referred to as a stimulant compound, belongs to a class of chemicals known for their influence on the central nervous system. This compound has so much to offer in terms of its unique structure and biological applications. Here are some captivating details:

  • Chemical Structure: The molecule is characterized by its branched amine structure, which plays a crucial role in its pharmacological activity.
  • Stimulant Properties: This compound has been studied for its effects similar to amphetamines, making it of interest in the fields of pharmacology and drug discovery.
  • Selective Activity: N,N-Dimethyl-3-(1-naphthyl)propan-1-amine showcases a selective affinity for certain receptor sites, influencing neurotransmitter release and uptake.
  • Research Applications: It is primarily explored in the context of neuroscience, where it aids in understanding mechanisms of addiction and cognitive enhancement.
  • Potential Therapeutics: Due to its stimulant properties, there are ongoing discussions regarding its potential therapeutic uses in treating conditions like ADHD and narcolepsy.

Despite its potential, it is important to approach this compound with caution, given the implications of its stimulant effects. As with many chemicals in the realm of pharmacology, further research is essential to uncover its full potential and ensure its safe application. As scientists continue to explore compounds like N,N-dimethyl-3-(1-naphthyl)propan-1-amine, we unravel the intricate relationships between chemical structure and biological function.

Synonyms
1-Naphthalenepropanamine, N,N-dimethyl-
DTXSID10275025
25913-62-6
RefChem:232311
DTXCID30226473
SCHEMBL4006370
SCHEMBL10390339
(N,N-dimethylamino)propyl naphthalene