4-Methylbenzylamine
4-Methylbenzylamine structure
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Common Name | 4-Methylbenzylamine | ||
|---|---|---|---|---|
| CAS Number | 104-84-7 | Molecular Weight | 121.180 | |
| Density | 1.0±0.1 g/cm3 | Boiling Point | 195.0±0.0 °C at 760 mmHg | |
| Molecular Formula | C8H11N | Melting Point | 12-13 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 75.0±0.0 °C | |
| Symbol |
GHS05 |
Signal Word | Danger | |
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New efficient substrates for semicarbazide-sensitive amine oxidase/VAP-1 enzyme: analysis by SARs and computational docking.
J. Med. Chem. 49 , 6197-208, (2006) Structure activity relationships for semicarbazide-sensitive amine oxidase/vascular adhesion protein-1 (SSAO/VAP-1) were studied using a library of arylalkylamine substrates, with the aim of contributing to the discovery of more efficient SSAO substrates. Exp... |
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Systemic absorption of the sunscreens benzophenone-3, octyl-methoxycinnamate, and 3-(4-methyl-benzylidene) camphor after whole-body topical application and reproductive hormone levels in humans.
J. Invest. Dermatol. 123(1) , 57-61, (2004) Recent in vitro and animal studies have reported estrogen-like activity of chemicals used in sunscreen preparations. We investigated whether the three sunscreens benzophenone-3 (BP-3), octyl-methoxycinnamate (OMC), and 3-(4-methylbenzylidene) camphor (4-MBC) ... |
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4-methyl benzylamine stimulates food consumption and counteracts the hypophagic effects of amphetamine acting on brain Shaker-like Kv1.1 channels.
Br. J. Pharmacol. 147(2) , 218-24, (2006) 1.--4-methyl benzylamine (4-MBZ; 28 microg, 231 nmol) elicits a hyperphagic response in starved mice in contrast to the hypophagia induced by the parent compound benzylamine (BZ; 33 microg, 231 nmol) or by amphetamine (AMPH, 2 mug). 2.--In mice starved for on... |
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High-performance liquid chromatographic determination of beta-phenylethylamine in human plasma with fluorescence detection.
Anal. Biochem. 184(1) , 86-9, (1990) A simple and highly sensitive method for the determination of beta-phenylethylamine in human plasma is investigated. The method employs high-performance liquid chromatography with fluorescence detection. beta-Phenylethylamine and p-methylbenzylamine (internal... |