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Methamphetamine (Naphthyl Analog)

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Identification
Molecular formula
C19H29N
CAS number
223121-13-3
IUPAC name
N-ethyl-N,4-dimethyl-3-(1-naphthyl)pentan-1-amine
State
State
The compound is in a liquid state at room temperature.
Melting point (Celsius)
-45.00
Melting point (Kelvin)
228.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
253.45g/mol
Molar mass
253.3910g/mol
Density
1.0069g/cm3
Appearence

The compound appears as a colorless to pale yellow liquid. It possesses an aromatic odor and is typically transparent. Its viscosity is similar to that of common organic liquids.

Comment on solubility

Solubility of N-ethyl-N,4-dimethyl-3-(1-naphthyl)pentan-1-amine

N-ethyl-N,4-dimethyl-3-(1-naphthyl)pentan-1-amine, a compound with a complex structure, demonstrates interesting solubility characteristics that are influenced by various factors. Its solubility is primarily affected by:

  • Polarity: The presence of the naphthyl group, combined with the alkyl functional groups, contributes to its overall hydrophobic nature, potentially leading to lower solubility in water.
  • Temperature: As is common with many organic compounds, solubility may increase with temperature, providing insights into the thermal stability of the compound.
  • Solvent choice: N-ethyl-N,4-dimethyl-3-(1-naphthyl)pentan-1-amine is expected to be more soluble in non-polar organic solvents compared to polar solvents. Solvents like ethanol or chloroform could enhance solubility due to similar polarities.

Overall, the solubility behavior can be summarized as follows:

  1. Moderate to low solubility in water
  2. Higher solubility in organic solvents
  3. Temperature-dependent solubility characteristics

Understanding the solubility of this compound is essential for applications where it may be used, particularly in pharmaceutical contexts where proper solvent systems are critical for effective formulation and delivery.

Interesting facts

Interesting Facts about N-ethyl-N,4-dimethyl-3-(1-naphthyl)pentan-1-amine

N-ethyl-N,4-dimethyl-3-(1-naphthyl)pentan-1-amine, commonly known in the scientific community as a research chemical, has gained attention for its intriguing properties and potential applications. Here are some notable facts about this compound:

  • Reductive Amination: The synthesis of N-ethyl-N,4-dimethyl-3-(1-naphthyl)pentan-1-amine often involves the technique of reductive amination, which is a crucial reaction in organic chemistry. This process allows for the introduction of amine groups into organic frameworks, making it a valuable method for synthesizing various nitrogen-containing compounds.
  • Pharmacological Interest: Research surrounding this compound has highlighted its potential for pharmacological applications. While its specific effects are still being studied, compounds of similar structure have shown various interactions with neurotransmitter systems, which may lead to novel therapeutic avenues.
  • Structure-Activity Relationship: The distinct structural elements of N-ethyl-N,4-dimethyl-3-(1-naphthyl)pentan-1-amine, such as the naphthyl group and the ethyl substitution, open up discussions regarding its interaction with biological targets. Understanding these relationships is vital in medicinal chemistry and can offer insights into designing more effective drugs.
  • Legal Status: Depending on the jurisdiction, this compound may be classified differently under drug control laws. It is essential for researchers to be aware of the regulatory landscape, as this can influence the feasibility of investigating the compound further.
  • Continued Research: As with many research chemicals, ongoing studies aim to uncover both the beneficial and adverse effects of N-ethyl-N,4-dimethyl-3-(1-naphthyl)pentan-1-amine. Such investigations are essential not only for expanding creditable knowledge but also for ensuring safety in experimental and some potential therapeutic applications.

In conclusion, the exploration of N-ethyl-N,4-dimethyl-3-(1-naphthyl)pentan-1-amine represents a fascinating intersection of organic chemistry and pharmacology. As research continues, the compound may pave the way for new discoveries in both therapeutic applications and synthetic methodologies.
The **scientific curiosity** surrounding compounds like this one drives innovation and the advancement of chemical sciences.

Synonyms
27609-19-4
1-NAPHTHALENEPROPYLAMINE, N-ETHYL-N-METHYL-gamma-ISOPROPYL-
RefChem:1055991
BRN 2732206
N,4-Dimethyl-N-ethyl-3-(1-naphthyl)pentylamine
Pentylamine, N,4-dimethyl-N-ethyl-3-(1-naphthyl)-
N-Ethyl-N-methyl-gamma-isopropyl-1-naphthalenepropylamine
DTXSID00950278
N-Ethyl-N,4-dimethyl-3-(naphthalen-1-yl)pentan-1-amine