A triol is a molecule with three alcohol groups.

The triol tautomer, which may have aromatic character, predominates in solution.

An example of triol on benzene is benzenetriol.

The acetonide was removed, giving triol 5.5.

This colorless solid is a triol.

This reaction lacked stereospecificity and the yield of triol 9 with the correct stereochemistry was therefore reduced.

This colorless solid is a triol, that is it contains three hydroxy functional groups.

The ester groups were then reduced by lithium aluminium hydride to a triol in a deprotection step.

Lactone diol 2.1, after selective protection, was reduced with lithium aluminium hydride to give triol 2.4.

Allylic alcohol 29 was oxidized with osmium tetroxide in pyridine to give triol 30.

Finally, the primary alcohol group was protected as a tert-butyldimethylsilyl ether by the corresponding silylchloride and imidazole in triol 15.

Broke up the original insulating material into its constituent tolylene diisocyanate and poly(oxypropylene)triol.

A triol is a chemical compound containing three hydroxyl groups (-OH functional groups), such as glycerol.

The final step in its organic synthesis is reaction of the triol with stannous chloride and hydrochloric acid in diethyl ether.

Reduction of the ketone group with 20 equivalents of Red-Al gave a triol which was immediately converted to carbonate 12 using phosgene.

Triethanolamine, often abbreviated as TEA, is a viscous organic compound that is both a tertiary amine and a triol.

A molecule with two hydroxyl groups is a diol, one with three is a triol, one with four is a tetrol and so on.

The structure and absolute configuration of the triol were determined by nuclear magnetic resonance (NMR) spectroscopy and later confirmed by x-ray crystallography.

The examples shown below are fairly low molecular weight triols based on glycerin (a triol) being reacted with propylene oxide, ethylene oxide or a combination of the two.

This triol, after protection as the 5-membered ring acetonide, was selectively oxidized to the aldehyde using tetrapropylammonium perruthenate (TPAP) and N-methylmorpholine N-oxide.

The first Headmaster was Robert W. Trusdale and first Upper School Principal was Thomas Triol, whose wife Helen taught chemistry and physics.

The primary hydroxyl group in triol 30 (Scheme 4) was protected as a TMS ether allowing activation of the secondary hydroxyl group as a tosylate leaving group.

"Most of our athletes on scholarship enroll the summer before the freshman year for orientation plus work on basic skills in English and math," said Deborah Triol Perry, Miami's dean of enrollments.

It is principally used as a precursor to trimethylolethane (CHC(CHOH)) through a condensation reaction with formaldehyde; this triol is an important intermediate in the production of alkyd resins.