Weight | 135.21 g/mol |
---|---|
Formula | C9H13N |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 3 |
N-Methylphenethylamine (589-08-2)
N-methylphenethylamine hydrochloride · N-methylphenylethylamine · N-methyl-beta-phenethylamine
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- Sigma-Aldrich - N-Methylphenethylamine74.50 - 734.00 USD
- Fisher Scientific - Search for N-Methylphenethylamine
- TCI - N-Methylphenethylamine82.00 - 246.00 USD
- Characterization of N-methylphenylethylamine and N-methylphenylethanolamine as substrates for type A and type B monoamine oxidase (Biochemical Pharmacology, 1980)
- Synthesis, identification, and acute toxicity of alpha-benzylphenethylamine and alpha-benzyl-N-methylphenethylamine. Contaminants in clandestine preparation of amphetamine and methamphetamine. (Journal - Association of Official Analytical Chemists, 1985)
- Copper(II) complexes of methamphetamine and N-methylphenethylamine (Journal of Inorganic and Nuclear Chemistry, 1976)
- (-Benzyl-N-Methylphenethylamine (BNMPA), an Impurity of Illicit Methamphetamine Synthesis: I. Physical Characterization and GC-MS Analysis of BNMPA and Anticipated Metabolites in Urine (Journal of Analytical Toxicology, 1995)
- -Benzyl-N-methylphenethylamine (BNMPA), an impurity of illicit methamphetamine synthesis: pharmacological evaluation and interaction with methamphetamine (Drug and Alcohol Dependence, 1995)
- -Benzyl-N-methylphenethylamine (BNMPA), an impurity of illicit methamphetamine synthesis. II: Metabolism and urinary excretion (human) (Journal of Analytical Toxicology, 1995)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - N-methylphenethylamine hydrochloride
- N-methylphenylethylamine
- N-methyl-beta-phenethylamine
- N-methylphenethylamine sodium
- N-methylphenethylamine, conjugate acid
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SMILESCNCCC1=CC=CC=C1
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InChIKeySASNBVQSOZSTPD-UHFFFAOYSA-N
- Pubchem - N-Methylphenethylamine
- Wikipedia - N-methylphenethylamine
N-Methylphenethylamine (NMPEA) is a naturally occurring trace amine neuromodulator in humans that is derived from the trace amine, phenethylamine (PEA). It has been detected in human urine (<1g over 24hours) and is produced by phenylethanolamine N-methyltransferase with phenethylamine as a substrate. PEA and NMPEA are both alkaloids that are found in a number of different plant species as well.
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