| |||
Names | |||
---|---|---|---|
Preferred IUPAC name
N,N-Dimethyl-1-phenylmethanamine | |||
Other names
N,N-Dimethylbenzenemethanamine, N,N-Dimethylbenzylamine, N-Benzyldimethylamine, Dimethylbenzylamine, Benzyl-N,N-dimethylamine, N-(Phenylmethyl)dimethylamine, BDMA, Sumine 2015, Benzenemethanamine, Dabco B-16, Araldite accelerator 062, N,N-Dimethyl(phenyl)methanamine, DMBA[1]
| |||
Identifiers | |||
3D model (JSmol)
|
|||
ChEMBL | |||
ChemSpider | |||
ECHA InfoCard | 100.002.863 | ||
EC Number |
| ||
PubChem CID
|
|||
RTECS number |
| ||
UNII | |||
UN number | 2619 | ||
CompTox Dashboard (EPA)
|
|||
| |||
| |||
Properties | |||
C9H13N | |||
Molar mass | 135.210 g·mol−1 | ||
Appearance | colourless liquid | ||
Density | 0.91 g/cm3 at 20 °C | ||
Melting point | −75 °C (−103 °F; 198 K) | ||
Boiling point | 180 to 183 °C (356 to 361 °F; 453 to 456 K) | ||
1.2 g/100mL | |||
Hazards | |||
GHS labelling: | |||
Danger | |||
H226, H302, H312, H314, H332, H412 | |||
P210, P233, P240, P241, P242, P243, P260, P261, P264, P270, P271, P273, P280, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P312, P304+P340, P305+P351+P338, P310, P312, P321, P322, P330, P363, P370+P378, P403+P235, P405, P501 | |||
NFPA 704 (fire diamond) | |||
Flash point | 55 °C (131 °F; 328 K) | ||
410 °C (770 °F; 683 K) | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
Dimethylbenzylamine is the organic compound with the formula C6H5CH2N(CH3)2. The molecule consists of a benzyl group, C6H5CH2, attached to a dimethylamino functional group. It is a colorless liquid. It is used as a catalyst for the formation of polyurethane foams and epoxy resins.