N-Methylphenethylamine hydrochloride

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N-Methylphenethylamine hydrochloride manufacturers

N-Methylphenethylamine hydrochloride Basic information
Product Name:N-Methylphenethylamine hydrochloride
Synonyms:Methyl(2-phenylethyl)amine hydrochloride;N-methyl-2-phenylethanamine hydrochloride;N-Methyl-2-phenylethanamine hydrochloride (1:1);N-Methyl-2-phenylethylamine Hydrochloride (N-Methyl-PEA HCl) 1.0 mg/ml in Methanol (as free base);N-Methyl-2-phenylethylamine Hydrochloride (N-Methyl-PEA HCl);N-Methylphenethylamine hydrochloride
CAS:4104-43-2
MF:C9H14ClN
MW:0
EINECS:
Product Categories:
Mol File:4104-43-2.mol
N-Methylphenethylamine hydrochloride Structure
N-Methylphenethylamine hydrochloride Chemical Properties
Melting point 164.1-164.9 °C
solubility DMF: 30 mg/ml
DMSO: 30 mg/ml
Ethanol: 30 mg/mlPBS (pH 7.2): 10 mg/ml
Safety Information
MSDS Information
N-Methylphenethylamine hydrochloride Usage And Synthesis
UsesN-Methylphenethylamine (NMPEA) hydrochloride is a potent TAAR1 agonist. N-Methylphenethylamine hydrochloride also is a trace amine neuromodulator[1].
References[1] Khan MZ, et al. The emerging roles of human trace amines and human trace amine-associated receptors (hTAARs) in central nervous system. Biomed Pharmacother. 2016 Oct;83:439-449. DOI:10.1016/j.biopha.2016.07.002
[2] Khan MZ, et al. The emerging roles of human trace amines and human trace amine-associated receptors (Khan MZ, et al. The emerging roles of human trace amines and human trace amine-associated receptors (hTAARs) in central nervous system. Biomed Pharmacother. 2016 Oct;83:439-449.hTAARs) in central nervous system. Biomed Pharmacother. 2016 Oct;83:439-449. DOI:10.1016/j.biopha.2016.07.002
[3] BENNIE J. CAMP  Carl M L. The Isolation of N-Methyl beta-Phenylethylamine from Acacia berlandieri*[J]. Journal of the American Pharmaceutical Association (Scientific ed.), 1956, 45 11: Pages 719-721. DOI: 10.1002/jps.3030451104
N-Methylphenethylamine hydrochloride Preparation Products And Raw materials
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