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N-methylbenzylamine

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Identification
Molecular formula
C8H11N
CAS number
103-67-3
IUPAC name
N-methyl-1-phenyl-methanamine
State
State

At room temperature, N-methylbenzylamine is a liquid.

Melting point (Celsius)
-55.00
Melting point (Kelvin)
218.15
Boiling point (Celsius)
180.70
Boiling point (Kelvin)
453.85
General information
Molecular weight
135.21g/mol
Molar mass
135.2110g/mol
Density
0.9300g/cm3
Appearence

N-Methylbenzylamine is a colorless liquid that can sometimes appear slightly yellow. It is typically clear and has a characteristic amine odor.

Comment on solubility

Solubility of N-methyl-1-phenyl-methanamine

N-methyl-1-phenyl-methanamine, also known as N-methyl-α-phenylethylamine, presents unique solubility characteristics that are noteworthy for both chemists and industrial applications.

The solubility of this compound is influenced by several factors:

  • Polarity: Being a primary amine, N-methyl-1-phenyl-methanamine possesses a polar amine group that often enhances its solubility in polar solvents.
  • Solvent Type: It is more soluble in organic solvents such as ethanol and acetone, while its solubility in water is significantly lower due to the hydrocarbon phenyl group.
  • Temperature: Like many organic compounds, solubility can increase with temperature, allowing for greater dissolution in both polar and non-polar solvents.

It is critical to note that the overall solubility can still be challenging to predict without experimental data, as the effects of intermolecular interactions can vary widely. As chemists often say, "the solution to solubility is often in the solvent choice."

In summary, while N-methyl-1-phenyl-methanamine shows good solubility in certain organic solvents, its solubility in aqueous environments is limited. Understanding these solubility characteristics is vital for effective application and synthesis in laboratory and industrial settings.

Interesting facts

Interesting Facts about N-methyl-1-phenyl-methanamine

N-methyl-1-phenyl-methanamine, commonly known as methamphetamine, is a fascinating compound with a storied history and significant impact on both chemistry and society. Here are some intriguing points to consider:

  • Discovery and Use: This compound was first synthesized in 1893 by the Japanese chemist Nobuhiro Nakagawa. Initially developed as a medication for breathing difficulties, it later found a place in the treatment of attention deficit hyperactivity disorder (ADHD) and obesity.
  • Mechanism of Action: N-methyl-1-phenyl-methanamine acts primarily as a potent central nervous system stimulant. It increases the release of dopamine, leading to heightened alertness, increased energy, and an improved mood, which explains its historical medical use.
  • Illicit Use and Regulation: While it has legitimate medical applications, the compound is widely recognized for its potential for abuse and addiction. This has led to strict regulations in many countries, classifying it as a controlled substance due to its illegal recreational use.
  • Chemical Family: It belongs to the amphetamine family, which includes other notable compounds like amphetamine and dextroamphetamine. All share similar structural characteristics and effects, but N-methyl-1-phenyl-methanamine is particularly potent.
  • Synthesis Techniques: The synthetic pathways to create this compound often involve the reduction of phenylacetone and various alkylation methods. This has made it a topic of interest in organic chemistry labs, particularly for those studying synthetic methodologies.

As noted by researchers, “Understanding the chemistry and effects of compounds like N-methyl-1-phenyl-methanamine not only enlightens us about their potential uses but also underscores the importance of responsibility in chemical practice.” This compound truly encapsulates the dual nature of chemistry, where entities can serve both beneficial and harmful roles in society.

Synonyms
N-METHYLBENZYLAMINE
103-67-3
N-Benzylmethylamine
N-methyl-1-phenylmethanamine
Methylbenzylamine
Benzylmethylamine
Benzyl(methyl)amine
Benzenemethanamine, N-methyl-
Benzylamine, N-methyl-
N-Benzyl-N-methylamine
N-Methy-N-benzylamine
Benzyl-methyl-amine
BENZYLAMINE, N-METHYL
N-methyl-N-benzylamine
methyl benzylamine
N-Methyl(phenyl)methanamine
NSC 8059
MFCD00008289
N-benzyl-methylamine
N-methyl benzylamine
N-methyl-N-(phenylmethyl)amine
N-methylbenzenemethanamine
EINECS 203-133-4
N-methyl-1-phenyl-methanamine
AI3-26793
7KN7F4X49E
DTXSID9048439
EC 203-133-4
NSC-8059
AR1001
methylbezylamine
benzyl methylamine
benzyl-methylamine
NBenzylmethylamine
HNMeBzl
NMethyNbenzylamine
N-benzylmethanamine
benzyl methyl amine
methyl-benzyl amine
N-benzyl methylamine
N-methyl-benzylamine
N-methylbenzyl amine
N-benzyl methyl amine
N-benzyl-methyl amine
N-methyl -benzylamine
N-methyl benzyl amine
N-methyl-benzyl amine
(-)-methylbenzylamine
Methylbenzylamine, N-
omega-Methylaminotoluene
Spectrum_001362
N-benzyl methyl ammonium
Methyl(phenylmethyl)amine
N-benzyl-N-methyl-amine
N-methyl-N-benzyl amine
Spectrum4_001764
Spectrum5_000347
Racemic methylbenzyl amine
N-methyl-benzenemethanamine
Benzenemethanamine, Nmethyl
BENZYLAMINE, NMETHYL
N-(Phenylmethyl)methylamine
N-Benzylmethylamine, 97%
SCHEMBL2271
CHEMBL1338
UNII-7KN7F4X49E
Benzylamine, Nmethyl (8CI)
KBioGR_002247
KBioSS_001842
MLS004773900
Benzylamine, N-methyl-(8CI)
DTXCID9028413
KBio2_001842
KBio2_004410
KBio2_006978
NSC8059
STR02536
STL196319
AKOS000119094
CS-W007426
HY-W007426
SDCCGMLS-0066901.P001
NCGC00166047-01
SMR000112361
M0164
NS00007234
EN300-18191
BRD-K44558320-003-01-7
Q23978278
Z57327124
F2190-0316
InChI=1/C8H11N/c1-9-7-8-5-3-2-4-6-8/h2-6,9H,7H2,1H
203-133-4