What is tripropylamine used for?

Tripropylamine was employed as coreactant in sandwich-type electrochemiluminescence biosensor for detection of α-fetoprotein. It was used as extraction agent for the reactive extraction of succinic acid in various alcohol diluents.

Is Tripropylamine soluble in water?

Tripropylamine is a colourless liquid with ammonia-like smell (MW 143.27 g/mol) at 20°C. The substance is soluble in water (444 mg/L at 20°C) and has a LogPow of 0.9.

Is Tripropylamine basic?

Tripropylamine, also known as (N-C3H7)3N or NPR3, belongs to the class of organic compounds known as trialkylamines. Tripropylamine is a very strong basic compound (based on its pKa).

Is Tripropylamine a tertiary amine?

A tertiary amine that is ammonia in which each hydrogen atom is substituted by a propyl group.

Which is the correct formula for Tripropylamine in PubChem?

Tripropylamine is a tertiary amine that is ammonia in which each hydrogen atom is substituted by a propyl group. N, N -dipropylpropan-1-amine Computed by LexiChem 2.6.6 (PubChem release 2019.06.18)

How is Tripropylamine used in the real world?

Tripropylamine is of little commercial value in comparison to dipropylamine and monoisopropylamine (1); however, it has been employed in some specialized uses. Tripropylamine has been used to synthesize wall carbon nanotubes(2), which may result in its release to the environment through various waste streams.

How does Tripropylamine react with ruthenium to produce light?

The resulting TPA radical reacts with oxidized ruthenium, resulting in the excited state of the ruthenium label, which decays with the emission of a photon (620 nm). As the ruthenium label returns to ground state, it is regenerated and available to perform multiple light-generating cycles ( Fig. 9 ).

Where does the reaction between ruthenium and TPA occur?

The reactions occur at the electrode surface inside the measuring cell. As an electrical potential is applied, the ruthenium label is oxidized at the electrode surface; simultaneously, TPA is oxidized to a radical cation that spontaneously loses a proton.