28520-00-5

Usage

Uses

Used in Chemical Synthesis:
2,4,5,6-tetrachlorobenzene-1,3-diol is used as an intermediate in chemical synthesis for the production of various organic compounds, leveraging its reactive functional groups and structural properties.
Used in Dye and Pigment Production:
In the dye and pigment industry, 2,4,5,6-tetrachlorobenzene-1,3-diol is used as a precursor for the synthesis of dyes and pigments, contributing to the color intensity and stability of these products.
Used as a Laboratory Reagent:
2,4,5,6-tetrachlorobenzene-1,3-diol serves as a laboratory reagent in various analytical and synthetic procedures, providing a means to explore its chemical properties and reactivity in controlled settings.

Upstream product

• 82361-26-0 hexachloro-4-cyclohexene-1,3-dione 
• 64-19-7 acetic acid 
• 861782-42-5 2-(2,3,4,4,6,6-hexachloro-1-hydroxy-5-oxo-cyclohex-2-enecarbonyl)-benzoic acid 
• 1897-45-6 chlorothalonil 

Downstream Products

• 69158-26-5 2,4,5,6-tetrachlororesorcinol diacetate 

Relevant academic research and scientific papers

Synthesis of Mn-doped TiO2 by novel route and photocatalytic mineralization/intermediate studies of organic pollutants

The doping of TiO2 particles with various manganese (Mn) concentrations (0.25–1.0%) were synthesized using simple sol–gel and modified sol–gel technique. The characteristics of synthesized particles were found employing standard analytical techniques such as X-ray diffraction, scanning electron microscopy and UV–Vis spectroscopy. The photocatalytic activity of the synthesized particles was compared by investigating the mineralization of two selected organic pollutants like ketoprofen and chlorothalonil. The photocatalysts which were produced by improved sol–gel technique show the lower value of band gap energy and small size crystallite and, hence, exhibit better photocatalytic activity. The outcomes also designate that the concentration of dopant Mn 0.75% indicated the highest photocatalytic activity than other concentrations of dopant in the mineralization of both the compounds. The mineralization kinetics of both compounds was studied under various situations like reaction pH and catalyst dosage. The mineralization rates were highly affected by all the above parameters. An effort has also been performed to highlight the intermediates produced during the photooxidation of both the compounds using the GC–MS analysis method. Both compounds show the production of several intermediates. A possible pathway for the production of different products has been suggested.

Properties of chlorinated dihydroxybenzenes - components of pulp bleaching effluents

Gas chromatography and mass spectrometry data are given for the chlorodihydroxybenzenes which are components of wood pulp bleaching effluents and biologically-treated effluents, and are proposed intermediates in the chlorination of humic acids. The chlorohydroxybenzenes include the nine chlorocatechols, the six chlorohydroquinones and the seven known chlororesorcinols. The 22 chlorinated compounds were generally well separated on a phenyl methyl silicone column with the exception of three dichloro compounds. The chloro compounds with the same level of chlorine substitution were not able to be distinguished on the basis of their electron impact mass spectra.