Chemistry:3-Methylphenethylamine
From HandWiki
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| Names | |
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| Preferred IUPAC name
2-(3-Methylphenyl)ethan-1-amine | |
| Other names
2-(3-Methylphenyl)ethanamine
3-Methylbenzeneethanamine 2-(m-Tolyl)ethan-1-amine | |
| Identifiers | |
3D model (JSmol)
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| ChEMBL | |
| ChemSpider | |
PubChem CID
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| UNII | |
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| Properties | |
| C9H13N | |
| Molar mass | 135.20622 |
| Appearance | clear liquid at room temp. |
| Density | 1.0±0.1 g/cm3 |
| Boiling point | 110 °C (230 °F; 383 K) / 20 mmHg 240.9519 °C / 760 mmHg Experimental[1] |
| Hazards | |
| Main hazards | Corrossive |
| Flash point | 90.5 ± 6.3 °C (194.9 ± 11.3 °F; 363.6 ± 6.3 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
3-Methylphenethylamine (3MPEA) is an organic compound with the chemical formula of C
9H
13N. 3MPEA is a human trace amine associated receptor 1 (TAAR1) agonist,[2] a property which it shares with its monomethylated phenethylamine isomers, such as amphetamine (α-methylphenethylamine), β-methylphenethylamine, and N-methylphenethylamine (a trace amine).[2]
Very little data, even on toxicity, is available about its effects on humans other than that it is corrosive and activates the human TAAR1 receptor.[1]
References
- ↑ 1.0 1.1 "2-(3-Methylphenyl)ethanamine". Chemspider. http://www.chemspider.com/Chemical-Structure.362941.html.
- ↑ 2.0 2.1 "Pharmacologic characterization of the cloned human trace amine-associated receptor1 (TAAR1) and evidence for species differences with the rat TAAR1". The Journal of Pharmacology and Experimental Therapeutics 320 (1): 475–85. January 2007. doi:10.1124/jpet.106.112532. PMID 17038507. "Several series of substituted phenylethylamines were investigated for activity at the human TAAR1 (Table 2). A surprising finding was the potency of phenylethylamines with substituents at the phenyl C2 position relative to their respective C4-substituted congeners. In each case, except for the hydroxyl substituent, the C2-substituted compound had 8- to 27-fold higher potency than the C4-substituted compound. The C3-substituted compound in each homologous series was typically 2- to 5-fold less potent than the 2-substituted compound, except for the hydroxyl substituent. The most potent of the 2-substituted phenylethylamines was 2-chloro-β-PEA, followed by 2-fluoro-β-PEA, 2-bromo-β-PEA, 2-methoxy-β-PEA, 2-methyl-β-PEA, and then 2-hydroxy-β-PEA.
The effect of β-carbon substitution on the phenylethylamine side chain was also investigated (Table 3). A β-methyl substituent was well tolerated compared with β-PEA. In fact, S-(−)-β-methyl-β-PEA was as potent as β-PEA at human TAAR1. β-Hydroxyl substitution was, however, not tolerated compared with β-PEA. In both cases of β-substitution, enantiomeric selectivity was demonstrated.
In contrast to a methyl substitution on the β-carbon, an α-methyl substitution reduced potency by ~10-fold for d-amphetamine and 16-fold for l-amphetamine relative to β-PEA (Table 4). N-Methyl substitution was fairly well tolerated; however, N,N-dimethyl substitution was not.".
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