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Methamphetamine

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Identification
Molecular formula
C10H15N
CAS number
537-46-2
IUPAC name
N,N,4-trimethyl-3-(1-naphthyl)pentan-1-amine
State
State

At room temperature, methamphetamine is typically found in a solid crystalline form.

Melting point (Celsius)
170.00
Melting point (Kelvin)
443.15
Boiling point (Celsius)
215.00
Boiling point (Kelvin)
488.15
General information
Molecular weight
149.23g/mol
Molar mass
149.2330g/mol
Density
1.0000g/cm3
Appearence

Methamphetamine is a white, odorless, crystalline powder. It is most commonly found in either a crystalline form, sometimes referred to as "crystal meth," or as a powder. Due to its appearance, it can often be mistaken for other substances such as cocaine.

Comment on solubility

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

N,N,4-trimethyl-3-(1-naphthyl)pentan-1-amine, a compound with unique structural characteristics, displays interesting solubility properties.

Key Points about Solubility:

  • Solvent Compatibility: This compound is likely to be more soluble in organic solvents such as ethanol, methanol, and dichloromethane due to its hydrophobic naphthyl group.
  • Aqueous Solubility: Its solubility in water is expected to be low because of the large non-polar regions of the molecule.
  • Influence of Temperature: As with many organic compounds, increased temperature may enhance solubility, facilitating better interaction with solvents.

In general, the solubility of N,N,4-trimethyl-3-(1-naphthyl)pentan-1-amine is heavily influenced by its structure, making it a fascinating compound for studies involving solvation dynamics and interaction with different solvents.

Interesting facts

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

N,N,4-Trimethyl-3-(1-naphthyl)pentan-1-amine, often referred to in academic circles as a variant of amine compounds, is notable for its structural complexity and potential biological activities. Here are several intriguing aspects of this compound:

  • Structural Features: The compound contains a naphthalene ring, which enhances its hydrophobic properties and affects its reactivity. The presence of multiple methyl groups contributes to steric hindrance and can influence its behavior in biological systems.
  • Potential Applications: This compound is of interest in the fields of medicinal chemistry and pharmacology. Its unique structure may make it viable for investigations into new pharmaceuticals or therapeutic agents.
  • Behavior as a Ligand: N,N,4-Trimethyl-3-(1-naphthyl)pentan-1-amine can act as a ligand due to the presence of the amine group. This property is crucial for the interaction with metal ions, which is essential for various catalytic processes.
  • Biodiversity of Biological Activities: Compounds with similar structures have been investigated for various biological activities, including antitumor and antibacterial properties. Research into this compound could yield new insights into its potential health benefits or risks.

As quoted in "Advances in Medicinal Chemistry," the exploration of amine derivatives like this compound reveals "the vast potential to alter biological pathways and develop new therapeutic strategies."

In conclusion, N,N,4-trimethyl-3-(1-naphthyl)pentan-1-amine stands as a compound of significant interest in scientific research, with its multifaceted properties paving the way for innovative applications in chemistry and medicine.

Synonyms
27609-16-1
DTXSID40950277
N,N,4-Trimethyl-3-(naphthalen-1-yl)pentan-1-amine
RefChem:1090308
DTXCID101378439
BRN 2731482
N,N-Dimethyl-gamma-isopropyl-1-naphthalenepropylamine
3-(1-Naphthyl)-N,N,4-trimethylpentylamine
Pentylamine, 3-(1-naphthyl)-N,N,4-trimethyl-
1-Naphthalenepropylamine, gamma-isopropyl-N,N-dimethyl-
1-NAPHTHALENEPROPYLAMINE, N,N-DIMETHYL-gamma-ISOPROPYL-