Tetramethylethylenediamine


Tetramethylethylenediamine is a chemical compound with the formula 2NCH2CH2N2. This species is derived from ethylenediamine by replacement of the four amine hydrogens with four methyl groups. It is a colorless liquid, although old samples often appear yellow. Its odor is remarkably similar to that of rotting fish.

As a reagent in organic and inorganic synthesis

TMEDA is widely employed as a ligand for metal ions. It forms stable complexes with many metal halides, e.g. zinc chloride and copper iodide, giving complexes that are soluble in organic solvents. In such complexes, TMEDA serves as a bidentate ligand.
TMEDA has an affinity for lithium ions. When mixed with n-butyllithium, TMEDA's nitrogen atoms coordinate to the lithium, forming a cluster of higher reactivity than the tetramer or hexamer that n-butyllithium normally adopts. BuLi/TMEDA is able to metallate or even doubly metallate many substrates including benzene, furan, thiophene, N-alkylpyrroles, and ferrocene. Many anionic organometallic complexes have been isolated as their + complexes. In such complexes + behaves like a quaternary ammonium salt, such as +.
It is also worth noting that s-BuLi/TMEDA is also a useful combination in organic synthesis. Utilization of this is useful in cases where the n-butyl anion is able to add into the starting material due to its weak nucleophilic nature. TMEDA is still capable of forming a metal complex with Li in this case as mentioned above.

Other uses

TEMED is used with ammonium persulfate to catalyze the polymerization of acrylamide when making polyacrylamide gels, used in gel electrophoresis, for the separation of proteins or nucleic acids. Although the amounts used in this technique may vary from method to method, 0.1–0.2% v/v TEMED is a "traditional" range. TEMED can also be a component of hypergolic propellants.