1-(3,4-Dimethoxyphenyl)methanamine
1-(3,4-Dimethoxyphenyl)methanamine structure
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Common Name | 1-(3,4-Dimethoxyphenyl)methanamine | ||
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| CAS Number | 5763-61-1 | Molecular Weight | 167.205 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 291.1±0.0 °C at 760 mmHg | |
| Molecular Formula | C9H13NO2 | Melting Point | N/A | |
| MSDS | USA | Flash Point | 122.1±30.4 °C | |
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Spectrofluorimetric determination of 5-hydroxyindoles with benzylamine or 3,4-dimethoxybenzylamine as a selective fluorogenic reagent.
Analyst 116(3) , 301-4, (1991) A spectrofluorimetric method has been developed for the sensitive and selective determination of 5-hydroxyindoles; the method is based on the reaction of 5-hydroxyindoles in a weakly alkaline solution (pH 9.0) with aromatic methylamines in the presence of pot... |
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3,4-Dimethoxybenzylamine as a sensitive pre-column fluorescence derivatization reagent for the determination of serotonin in human platelet-poor plasma.
J. Chromatogr. B. Biomed. Sci. Appl. 692(1) , 31-6, (1997) 3,4-Dimethoxybenzylamine is shown to be a highly sensitive pre-column fluorescence derivatization reagent for the determination of serotonin in plasma by high-performance liquid chromatography. The reagent reacts selectively with 5-hydroxyindoles including se... |
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Capsaicin and its analogs induce ion channels in planar lipid bilayers.
Neuroreport 6(16) , 2134-6, (1995) The irritating, pungent compound, capsaicin (10-20 microM), induces the formation of non-selective ion channels with a wide variety of conductances in protein-free lipid bilayers form from a mixture of zwitterionic phospholipids. The channel-forming activity ... |