|Preferred IUPAC name
3D model (JSmol)
CompTox Dashboard (EPA)
|Molar mass||31.058 g·mol−1|
|Density||656.2 kg m−3 (at 25 °C)|
|Melting point||−93.10 °C; −135.58 °F; 180.05 K|
|Boiling point||−6.6 to −6.0 °C; 20.0 to 21.1 °F; 266.5 to 267.1 K|
|1080 g.L−1 (at 20 °C)|
|Vapor pressure||186.10 kPa (at 20 °C)|
|1.4 mmol Pa−1 kg−1|
|Viscosity||230 μPa s (at 0 °C)|
Std enthalpy of
|−23.5 kJ mol−1|
|Safety data sheet||emdchemicals.com|
|GHS signal word||DANGER|
|H220, H315, H318, H332, H335|
|P210, P261, P280, P305+351+338, P410+403|
|Flash point||−10 °C; 14 °F; 263 K (liquid, gas is extremely flammable)|
|430 °C (806 °F; 703 K)|
|Lethal dose or concentration (LD, LC):|
LD50 (median dose)
|100 mg kg−1 (oral, rat)|
LC50 (median concentration)
|1860 ppm (mouse, 2 hr)|
|US health exposure limits (NIOSH):|
|TWA 10 ppm (12 mg/m3)|
|TWA 10 ppm (12 mg/m3)|
IDLH (Immediate danger)
|ethylamine, dimethylamine, trimethylamine|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Methylamine is an organic compound with a formula of CH3NH2. This colorless gas is a derivative of ammonia, but with one hydrogen atom being replaced by a methyl group. It is the simplest primary amine. It is sold as a solution in methanol, ethanol, tetrahydrofuran, or water, or as the anhydrous gas in pressurized metal containers. Industrially, methylamine is transported in its anhydrous form in pressurized railcars and tank trailers. It has a strong odor similar to fish. Methylamine is used as a building block for the synthesis of many other commercially available compounds.
Methylamine is prepared commercially by the reaction of ammonia with methanol in the presence of an aluminosilicate catalyst. Dimethylamine and trimethylamine are co-produced; the reaction kinetics and reactant ratios determine the ratio of the three products. The product most favored by the reaction kinetics is trimethylamine.
In this way, an estimated 115,000 tons were produced in 2005.
Methylamine was first prepared in 1849 by Charles-Adolphe Wurtz via the hydrolysis of methyl isocyanate and related compounds. An example of this process includes the use of the Hofmann rearrangement, to yield methylamine from acetamide and bromine gas.
The colorless hydrochloride salt can be converted to an amine by the addition of a strong base, such as sodium hydroxide (NaOH):
Methylamine is a good nucleophile as it is an unhindered amine. As an amine it is considered a weak base. Its use in organic chemistry is pervasive. Some reactions involving simple reagents include: with phosgene to methyl isocyanate, with carbon disulfide and sodium hydroxide to the sodium methyldithiocarbamate, with chloroform and base to methyl isocyanide and with ethylene oxide to methylethanolamines. Liquid methylamine has solvent properties analogous to those of liquid ammonia.
Representative commercially significant chemicals produced from methylamine include the pharmaceuticals ephedrine and theophylline, the pesticides carbofuran, carbaryl, and metham sodium, and the solvents N-methylformamide and N-methylpyrrolidone. The preparation of some surfactants and photographic developers require methylamine as a building block.
The Occupational Safety and Health Administration (OSHA) and National Institute for Occupational Safety and Health (NIOSH) have set occupational exposure limits at 10 ppm or 12 mg/m3 over an eight-hour time-weighted average.
...an unhindered amine such as methylamine