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Dimethylamine is an organic compound with the formula (CH 3) 2 NH. This secondary amine is a colorless, flammable gas with an ammonia-like odor. Dimethylamine is commonly encountered commercially as a solution in water at concentrations up to around 40%. An estimated 270,000 tons were produced in 2005. [5]
Myristamine oxide is an amine oxide based zwitterionic surfactant with a C 14 (tetradecyl) alkyl tail. It is used as a foam stabilizer and hair conditioning agent in some shampoos and conditioners.
The ultimate products of its hydrolysis is titanium dioxide and dimethylamine: Ti(NMe 2) 4 + 2 H 2 O → TiO 2 + 4 HNMe 2. In a related reaction, the compound undergoes exchange with other amines, evolving dimethylamine. TMAT has been used in metalorganic chemical vapor deposition (MOCVD). [citation needed]
Dimethylethanolamine (DMAE or DMEA) is an organic compound with the formula (CH 3) 2 NCH 2 CH 2 OH. It is bifunctional, containing both a tertiary amine and primary alcohol functional groups. It is a colorless viscous liquid. It is used in skin care products for improving skin tone and also taken orally as a nootropic.
Generic aminal. In organic chemistry, an aminal or aminoacetal is a functional group or type of organic compound that has two amine groups attached to the same carbon atom: −C(NR 2)(NR 2)−.
N-Methylmethanimine or N‐methyl methylenimine is a reactive molecular substance containing a methyl group attached to an imine.It can be written as CH 3 N=CH 2.On a timescale of minutes it self reacts to form the trimer trimethyl 1,3,5-triazinane.
1,8-Bis(dimethylamino)naphthalene is an organic compound with the formula C 10 H 6 (NMe 2) 2 (Me = methyl). It is classified as a peri-naphthalene, i.e. a 1,8-disubstituted derivative of naphthalene. Owing to its unusual structure, it exhibits exceptional basicity.
Bis(dimethylamino)methane is the organic compound with the formula [(CH 3) 2 N] 2 CH 2. It is classified as an aminal as well as a ditertiary amine, in fact the simplest. It is a colorless liquid that is widely available. It is prepared by the reaction of dimethylamine and formaldehyde: [1] 2 (CH 3) 2 NH + CH 2 O → [(CH 3) 2 N] 2 CH 2 + H 2 O