N-Methylbenzylamine structure 
             | 
        Common Name | N-Methylbenzylamine | ||
|---|---|---|---|---|
| CAS Number | 103-67-3 | Molecular Weight | 121.180 | |
| Density | 0.9±0.1 g/cm3 | Boiling Point | 180.5±0.0 °C at 760 mmHg | |
| Molecular Formula | C8H11N | Melting Point | -24 °C | |
| MSDS | Chinese USA | Flash Point | 77.8±0.0 °C | |
| Symbol | 
             
            
             
            
            GHS05, GHS08  | 
        Signal Word | Danger | |
            Use of N-MethylbenzylamineN-methylbenzylamine is a member of phenylmethylamines. N-methylbenzylamine can be found in carrot, which makes N-methylbenzylamine a potential biomarker for the consumption of these food products[1].  | 
    
| Name | N-Methylbenzylamine | 
|---|---|
| Synonym | More Synonyms | 
| Description | N-methylbenzylamine is a member of phenylmethylamines. N-methylbenzylamine can be found in carrot, which makes N-methylbenzylamine a potential biomarker for the consumption of these food products[1]. | 
|---|---|
| Related Catalog | 
| Density | 0.9±0.1 g/cm3 | 
|---|---|
| Boiling Point | 180.5±0.0 °C at 760 mmHg | 
| Melting Point | -24 °C | 
| Molecular Formula | C8H11N | 
| Molecular Weight | 121.180 | 
| Flash Point | 77.8±0.0 °C | 
| Exact Mass | 121.089149 | 
| PSA | 12.03000 | 
| LogP | 1.52 | 
| Vapour Pressure | 0.9±0.3 mmHg at 25°C | 
| Index of Refraction | 1.513 | 
| Stability | Stable, but may be air sensitive through reaction with carbon dioxide. Combustible. Incompatible with strong oxidizing agents, acids, acid chlorides, acid anhydrides, carbon dioxide. | 
| Water Solubility | 65 g/L (20 ºC) | 
| Symbol | 
                                    
                                     
                                    
                                     
                                    
                                    GHS05, GHS08  | 
                            
|---|---|
| Signal Word | Danger | 
| Hazard Statements | H314-H317-H334 | 
| Precautionary Statements | P261-P280-P305 + P351 + P338-P310 | 
| Personal Protective Equipment | Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter | 
| Hazard Codes | C:Corrosive | 
| Risk Phrases | R22;R34 | 
| Safety Phrases | S23-S26-S36/37/39-S45 | 
| RIDADR | UN 2735 8/PG 2 | 
| WGK Germany | 1 | 
| Packaging Group | III | 
| Hazard Class | 8 | 
| HS Code | 29214980 | 
| Precursor 9 | |
|---|---|
| DownStream 10 | |
| HS Code | 2921499090 | 
|---|---|
| Summary | 2921499090 other aromatic monoamines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0% | 
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                                    Superparamagnetic core-shells anchored onto graphene oxide grafted with phenylethyl amine as a nano-adsorbent for extraction and enrichment of organophosphorus pesticides from fruit, vegetable and water samples.
                                    
                                    
                                     J. Chromatogr. A. 1406 , 48-58, (2015) A novel adsorbent composed of silica coated magnetic microparticles (Fe3O4@SiO2) and graphene oxide (GO) functionalized with phenylethyl amine (PEA) was synthesized and characterized using Fourier tra...  | 
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                                    New procedure of selected biogenic amines determination in wine samples by HPLC.
                                    
                                    
                                     Anal. Chim. Acta 834 , 58-66, (2014) A new procedure for determination of biogenic amines (BA): histamine, phenethylamine, tyramine and tryptamine, based on the derivatization reaction with 2-chloro-1,3-dinitro-5-(trifluoromethyl)-benzen...  | 
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                                    Structural analysis of dopamine- and amphetamine-induced depolarization currents in the human dopamine transporter.
                                    
                                    
                                     ACS Chem. Neurosci. 6(4) , 551-8, (2015) Amphetamine (AMPH) induces depolarizing currents through the human dopamine transporter (hDAT). Recently we discovered that the S(+) enantiomer of AMPH induces a current through hDAT that persists lon...  | 
                                
| BENZYLAMINE, N-METHYL | 
| Benzenemethanamine, N-methyl- | 
| N-Mehtylbenzylamine | 
| N-Methy-N-benzylamine | 
| N-Methylbenzylamine | 
| N-benzyl-N-methyl-amine | 
| N-Benzylmethylamine | 
| EINECS 203-133-4 | 
| N-Methylbenzylamin | 
| N-methylbenzenemethanamine | 
| N-Methyl-1-phenylmethanamine | 
| BENZYL METHYLAMINE | 
| methylbenzylamine | 
| N-methyl-benzylamine | 
| NMBA | 
| Benzylmethylamine | 
| omega-Methylaminotoluene | 
| MFCD00008289 | 
| N-benzyl-N-methylamine | 
| N-Methyl Benylamine | 
| ω-Methylaminotoluene |