Hexadecyldimethylamine is Liquid/Solid
Barlene(R) tertiary amines are used as chemical intermediates for the manufacture of quaternary ammonium compounds, amine oxide and betaine surfactants
N,N-Dimethylhexadecylamine may be employed in the following studies:
- As pore size mediator for the synthesis of monodispersed mesoporous silica nanoparticles.
- As swelling agent in the fabrication of colloidal mesoporous silica nanoparticles of a tunable mesopore size.
- Preparation of 1,4-bis(N-hexadecyl-N,N-dimethylammonium)butane dibromide, Gemini surfactant.
Hexadecyldimethylamine is a clear yellow colored liquid with a fishlike odor. Insoluble in water and less dense than water. Hence floats on water. Contact may irritate skin, eyes and mucous membranes. May be toxic by ingestion, inhalation or skin absorption. Used to make other chemicals.
Hexadecyldimethylamine neutralizes acids in exothermic reactions to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen may be generated in combination with strong reducing agents, such as hydrides.
TOXIC; inhalation, ingestion or skin contact with material may cause severe injury or death. Contact with molten substance may cause severe burns to skin and eyes. Avoid any skin contact. Effects of contact or inhalation may be delayed. Fire may produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.
Combustible material: may burn but does not ignite readily. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form.
In a 250 mL four-necked flask equipped with mechanical stirring, 24.1 g of cetylamine and 100 mL of anhydrous ethanol were added, and the temperature was controlled to be below 20C. 20.9 g of 88% formic acid and 24.3 g of
37% formaldehyde, closed the reaction system with a balloon, heated to reflux the reaction for 10 hours, cooled down and sampled, and the reaction was completely detected by TLC. To the reaction solution add 30% liquid alkali neutralization to pH 10, add toluene extraction, toluene layer combined and washed, desolvation, distillation under reduced pressure to obtain colorless transparent liquid 16.8g, yield 62%, content 95.0%.
