| Bioactivity | Tetradecyltrimethylammonium bromide, an organic building block, is a cationic surfactant with asymmetrical structure[1][2]. |
| Invitro | Tetradecyltrimethylammonium bromide (TTAB; TTABr) is increasingly used in capillary electrophoresis as a surface active aid in the separation of acid derived anionic species. It has been observed that Tetradecyltrimethylammonium bromide requires a minimum concentration of approximately 0.4mM for best results. This value has been chosen because it is close to its critical micelle concentration (CMC), and it has been projected that this concentration is required for “hemimicelles” to be formed on the inner wall of the capillary[3]. |
| Name | Tetradecyltrimethylammonium bromide |
| CAS | 1119-97-7 |
| Formula | C17H38BrN |
| Molar Mass | 336.39 |
| Appearance | Solid |
| Transport | Room temperature in continental US; may vary elsewhere. |
| Storage | 4°C, sealed storage, away from moisture and light *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light) |
| Reference | [1]. Dopierala K, et al. The effect of molecular structure on the surface properties of selected quaternary ammonium salts. J Colloid Interface Sci. 2008;321(1):220-226. [2]. N. Gorski, et al. Mixtures of Nonionic and Ionic Surfactants. The Effect of Counterion Binding in Mixtures of Tetradecyldimethylamine Oxide and Tetradecyltrimethylammonium Bromide. Langmuir 1994, 10, 8, 2594-2603. [3]. Cocke DL, et al. The surface properties of tetradecyltrimethylammonium bromide observed by capillary electrophoresis. J Chromatogr Sci. 2002;40(4):187-190. |