87-87-6
87-87-6
Chemical Structure
Tetrachlorohydroquinone
Synonym(s): TCHQ; Tetrachloroquinol
- CAS No.: 87-87-6
- Formula:C6H2Cl4O2
- Molecular Weight:247.89
IUPAC Name: 2,3,5,6-tetrachlorobenzene-1,4-diol
InChIKey: STOSPPMGXZPHKP-UHFFFAOYSA-N
SMILES: C1(=C(C(=C(C(=C1Cl)O)Cl)Cl)O)Cl
Biological Activity: Tetrachlorohydroquinone (TCHQ) is a metabolite of Pentachlorophenol. Tetrachlorohydroquinone induces reactive oxidant stress (ROS), inhibits apoptosis and induces necrosis in primary mouse splenocytes. Tetrachlorohydroquinone increases DNA lesions and induces oxidative stress in rodents[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Tetrachlorohydroquinone | 98.45% | Tetrachlorohydroquinone (TCHQ) is a metabolite of Pentachlorophenol. Tetrachlorohydroquinone induces reactive oxidant stress (ROS), inhibits apoptosis and induces necrosis in primary mouse splenocytes. Tetrachlorohydroquinone increases DNA lesions and induces oxidative stress in rodents. | ||||||||||||||||||||
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Tetrachlorohydroquinone (Standard) | ≥98% | Tetrachlorohydroquinone (Standard) is the analytical standard of Tetrachlorohydroquinone (HY-W144308). This product is intended for research and analytical applications. Tetrachlorohydroquinone (TCHQ) is a metabolite of Pentachlorophenol. Tetrachlorohydroquinone induces reactive oxidant stress (ROS), inhibits apoptosis and induces necrosis in primary mouse splenocytes. Tetrachlorohydroquinone increases DNA lesions and induces oxidative stress in rodents. | ||||||||||||||||||||
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References
