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In mice this disinfectant was found to cause infertility and birth defects when combined with Alkyl (60% C14, 25% C12, 15% C16) dimethyl benzyl ammonium chloride (ADBAC). [ 5 ] [ 6 ] These studies contradict the older toxicology data set on quaternary ammonia compounds which was reviewed by the U.S. Environmental Protection Agency (U.S. EPA ...
Dimethyldioctadecylammonium chloride (also commonly distearyl dimethyl ammonium chloride or distearyldimonium chloride) is an organic compound classified as quaternary ammonium salt. The nitrogen center substituted with two methyl groups and two stearyl groups.
Dimethyldioctadecylammonium bromide (also dioctadecyldimethylammonium bromide or DODAB) is a double-chained quaternary ammonium surfactant that forms unilamellar vesicles (ULVs) in water. Among various preparation methods, the ‘‘hot-water” method offers a simple procedure to prepare DODAB cationic vesicles by simply dissolving the DODAB ...
Polydiallyldimethylammonium chloride (shortened polyDADMAC or polyDDA), also commonly polyquaternium-6, is a homopolymer of diallyldimethylammonium chloride (DADMAC). The molecular weight of polyDADMAC is typically in the range of hundreds of thousands of grams per mole, and even up to a million for some products.
The most significant use for DMAEA is the quaternization with alkylating agents (for example chloromethane, dimethyl sulfate or benzyl chloride) to the quaternary ammonium salt. [9] Quaternisierung von Dimethylaminoethylacrylat. The most important compound is the reaction product with methyl chloride, trimethylammonium ethyl acrylate chloride. [10]
The chemical reactions of dimethylacetamide are typical of N,N-disubstituted amides. Hydrolysis of the acyl-N bond occurs in the presence of acids: . CH 3 CON(CH 3) 2 + H 2 O + HCl → CH 3 COOH + (CH 3) 2 NH 2 + Cl −
Dimethylaluminium chloride is an organoaluminium compound with the chemical formula [(CH 3) 2 AlCl] 2. It behaves similarly to diethylaluminium chloride but is more expensive. Hence, it is less commonly used. [2] Like other organoaluminium chlorides, dimethylaluminium chloride is a Lewis acid.
Electrophilic methylating agents like dimethyl sulfate attack the amine to give the quaternary ammonium salt: [8] C 6 H 5 N(CH 3) 2 +(CH 3 O) 2 SO 2 → C 6 H 5 N(CH 3) 3 CH 3 OSO 3. Diethylaniline and dimethylaniline are both used as acid-absorbing bases.