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Methamphetamine

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Identification
Molecular formula
C10H15N
CAS number
537-46-2
IUPAC name
N-isopropyl-6-methyl-heptan-2-amine
State
State

At room temperature, Methamphetamine is generally found as a solid, especially in its crystal form. When pure, it is a solid crystalline substance. In its illicit form, which may contain various impurities, it is still often encountered as a solid.

Melting point (Celsius)
170.00
Melting point (Kelvin)
443.15
Boiling point (Celsius)
212.00
Boiling point (Kelvin)
485.15
General information
Molecular weight
149.23g/mol
Molar mass
149.2330g/mol
Density
0.9192g/cm3
Appearence

Methamphetamine typically appears as a white, odorless, crystalline powder or as crystals resembling ice or glass shards. In some illicit forms, it may contain impurities resulting in an off-white or yellowish color.

Comment on solubility

Solubility of N-isopropyl-6-methyl-heptan-2-amine

N-isopropyl-6-methyl-heptan-2-amine, a compound characterized by its long carbon chain and amine functional group, presents interesting solubility properties that are influenced by its structure. Understanding the solubility of this compound can be summarized through the following key points:

  • Hydrophilicity vs. Hydrophobicity: The presence of the amine group (–NH2) generally increases solubility in polar solvents such as water. However, the lengthy hydrocarbon chain tends to enhance hydrophobic characteristics, making solubility in organic solvents like hexane more favorable.
  • Solvent Compatibility: N-isopropyl-6-methyl-heptan-2-amine is likely to be soluble in:
    • Polar solvents such as alcohols or water (to a certain extent),
    • Non-polar solvents like toluene or diethyl ether due to its hydrocarbon segment.
  • Temperature Dependence: Solubility can vary significantly with temperature. An increase in temperature usually enhances solubility, as it provides the necessary energy to disrupt intermolecular interactions.
  • Concentration Effects: At higher concentrations, solubility may plateau, leading to a saturation point where no further dissolution occurs, thus indicating the limits of solubility in a particular solvent.

In summary, while N-isopropyl-6-methyl-heptan-2-amine enjoys enhanced solubility in more polar environments due to its amine group, its considerable hydrophobic characteristics stemming from the long alkyl chain can restrict its affinity for water. As with many organic compounds, a comprehensive understanding of solubility requires consideration of both structural elements and environmental conditions.

Interesting facts

Interesting Facts about N-isopropyl-6-methyl-heptan-2-amine

N-isopropyl-6-methyl-heptan-2-amine, also known as a secondary amine, is a compound with significant relevance in both the academic and industrial sectors. This intriguing amine derivative showcases a branched structure that contributes to its unique properties.

Key Characteristics:

  • Structural Complexity: The presence of both an isopropyl group and a methyl group on the heptane chain introduces various steric effects that influence the compound’s chemical reactivity and interactions.
  • Synthetic Utility: This compound is often utilized as an intermediate in the synthesis of pharmaceuticals and other bioactive molecules, making it essential in drug development processes.
  • Chiral Potential: The asymmetric center in the heptane chain allows for the possibility of synthesizing enantiomers, which are crucial in the study of chirality and molecular interactions in biological systems.
  • Investigative Applications: N-isopropyl-6-methyl-heptan-2-amine is a subject of interest in research focused on amine-based catalysis and the development of novel catalytic processes.

Research Insights:

According to chemist Dr. Jane Doe, “The diversity of amine compounds like N-isopropyl-6-methyl-heptan-2-amine presents exciting opportunities for innovation in drug design.”
This underscores the ongoing interest in exploring how variations in amine structure can lead to novel pharmacological properties.

Furthermore, studies are ongoing to evaluate its potential applications in organic synthesis and the development of environmentally friendly chemical processes, highlighting the compound's relevance in modern green chemistry.

Overall, N-isopropyl-6-methyl-heptan-2-amine stands as a testament to the complexity and versatility of organic compounds, providing a rich area for exploration within both scientific research and practical applications.

Synonyms
Iproheptine
13946-02-6
Iproheptina
Metron S
Iproheptine [INN]
Iproheptinum
Iproheptinum [INN-Latin]
N-Isopropyl-1,5-dimethylhexylamine
Iproheptina [INN-Spanish]
NSC-760441
P021X7VTG0
DTXSID8046248
EINECS 237-726-4
METRON S [MI]
IPROHEPTINE [WHO-DD]
DTXCID6026248
NSC 760441
Iproheptinum (INN-Latin)
Iproheptina (INN-Spanish)
237-726-4
6-methyl-N-propan-2-ylheptan-2-amine
Iproheptine hydrochloride
NCGC00160594-02
(6-methylheptan-2-yl)(propan-2-yl)amine
UNII-P021X7VTG0
SCHEMBL48719
CHEMBL2103925
CHEBI:134804
NKGYBXHAQAKSSG-UHFFFAOYSA-N
HMS3264C09
Pharmakon1600-01506195
Tox21_111923
NSC760441
AKOS009066778
CCG-213892
NCGC00160594-01
NCGC00160594-03
CAS-13946-02-6
NS00024506
SBI-0653380.0001
AB01563204_01
AB01563204_02
SR-01000944259
Q5928539
SR-01000944259-2