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Triethylenetetramine (TETA and trien), also known as trientine when used medically, is an organic compound with the formula [CH 2 NHCH 2 CH 2 NH 2] 2. The pure free base is a colorless oily liquid, but, like many amines , older samples assume a yellowish color due to impurities resulting from air oxidation .
Diethylenetriamine (abbreviated Dien or DETA) and also known as 2,2’-Iminodi(ethylamine) [2]) is an organic compound with the formula HN(CH 2 CH 2 NH 2) 2.This colourless hygroscopic liquid is soluble in water and polar organic solvents, but not simple hydrocarbons.
1.80 [16] 1.26: battery, Fluoride-ion [citation needed] 1.7: 2.8: battery, Hydrogen closed cycle H fuel cell [17] 1.62: Hydrazine decomposition (as monopropellant) 1.6: 1.6: Ammonium nitrate decomposition (as monopropellant) 1.4: 2.5: Thermal Energy Capacity of Molten Salt: 1 [citation needed] 98% [18] Molecular spring approximate [citation ...
Here are links to possibly useful sources of information about Triethylenetetramine. PubMed provides review articles from the past five years (limit to free review articles ) The TRIP database provides clinical publications about evidence-based medicine .
Tris(2-aminoethyl)amine is the organic compound with the formula N(CH 2 CH 2 NH 2) 3.This colourless liquid is soluble in water and is highly basic, consisting of a tertiary amine center and three pendant primary amine groups.
In organic chemistry, amine value is a measure of the nitrogen content of an organic molecule. [1] Specifically, it is usually used to measure the amine content of amine functional compounds. [ 2 ] It may be defined as the number of milligrams of potassium hydroxide (KOH) equivalent to one gram of epoxy hardener resin.
PMDTA is used to modify the reactivity of organolithium compounds, which deaggregate in the presence of Lewis bases to enhance their reactivity. [3] Commonly, the ditertiary amine TMEDA is used in these applications; it binds to the lithium center as a bidentate ligand.
These include ethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, other higher homologues and aminoethyl piperazine. [ 2 ] [ 3 ] AEP is also manufactured by reacting ethylenediamine or ethanolamine / ammonia mixtures over a catalyst .