1,2,3-Benzenetriol, 1,2,3-triacetate, also known as triacetyl-1,2,3-benzenetriol, is an organic compound characterized by its structure, which includes a benzene ring substituted with three hydroxyl groups and three acetate groups. This compound is a derivative of benzenetriol, where the hydroxyl groups are acetylated, enhancing its solubility in organic solvents and altering its reactivity. It typically appears as a colorless to pale yellow liquid or solid, depending on its form and purity. The presence of multiple functional groups allows for various chemical reactions, making it useful in organic synthesis and as an intermediate in the production of other chemical compounds. Its properties include moderate polarity and potential applications in pharmaceuticals, cosmetics, and as a reagent in chemical research. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if ingested or inhaled. Proper storage and handling protocols are essential to ensure safety in laboratory and industrial settings.

1,2,3-Benzenetriol, 1,2,3-triacetate

525-52-0: 1,2,3-Benzenetriol, 1,2,3-triacetate, 1,2,3-Benzenetriol, triacetate, Acetpyrogall, Benzene-1,2,3-Triol, Benzene-1,2,3-Triyl Triacetate, Lenigallol, NSC 24068, Pyracetol, Pyrogallol Triacetate, Triacetylpyrogallol

Benzene-1,2,3-triyl triacetate

Pyrogallol triacetate is used as an antiasthmatic.

Pyrogallol triacetate

1,2,3-Phenenyl triacetate is a reaction product of 3-hydroxyanthranilic acid and acetyl chloride. It is used as an intermediate for the production of ethyl esters. 1,2,3-Phenenyl triacetate can be used in the manufacture of polymers and pharmaceuticals. 1,2,3-Phenenyl triacetate has been shown to have a viscosity stabilizing effect at low concentrations. The photolytic stability of 1,2,3-phenenyl triacetate is dependent on the concentration of hydroxy groups in the molecule. Hydrolysis by borohydride reduction leads to the formation of 3-phenoxybenzoic acid. This product has been shown to have carcinogenic activity in animal tissues.

CAS 525-52-0: 1,2,3-Benzenetriol, 1,2,3-triacetate

Benzene-1,2,3-triyl triacetate

Ref: IN-DA003DAQ

Pyrogallol triacetate

Ref: TM-T20678

1,2,3-Phenenyl triacetate

Ref: 3D-FP70552