Date published: 2025-10-10

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2,5-Dihydroxybenzoquinone (CAS 615-94-1)

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Alternate Names:
2,5-Dihydroxy-1,4-benzoquinone
CAS Number:
615-94-1
Molecular Weight:
140.09
Molecular Formula:
C6H4O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2,5-Dihydroxybenzoquinone, referred to as DHBQ, is a naturally occurring organic compound that has garnered considerable attention in scientific and medical circles due to its potential applications. Its versatility makes it highly sought-after in both research and industry. This remarkable compound has been the subject of numerous investigations across a wide range of scientific and medical fields. One of its key attributes lies in its ability to function as an antioxidant, safeguarding cells by neutralizing harmful free radicals. Furthermore, 2,5-Dihydroxybenzoquinone′s potential to serve as a fundamental building block for synthesizing various other compounds, including polymers and materials, adds to its value. In the realm of electrochemistry, 2,5-Dihydroxybenzoquinone has been the focus of interest as a redox-active compound, demonstrating its capacity to donate or accept electrons during specific reactions. Although the precise mechanism of its actions remains an ongoing area of exploration, the significance of 2,5-Dihydroxybenzoquinone as an antioxidant and a versatile reagent for compound synthesis has not escaped scientific scrutiny. In summary, 2,5-Dihydroxybenzoquinone (DHBQ) emerges as a promising organic compound with multifaceted potential, captivating researchers and industries alike in their pursuit of valuable applications across a spectrum of fields.


2,5-Dihydroxybenzoquinone (CAS 615-94-1) References

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  4. Catalytic mechanism of 5-chlorohydroxyhydroquinone dehydrochlorinase from the YCII superfamily of largely unknown function.  |  Hayes, RP., et al. 2013. J Biol Chem. 288: 28447-56. PMID: 23955343
  5. Halogen-bonding in a new family of tris(haloanilato)metallate(III) magnetic molecular building blocks.  |  Atzori, M., et al. 2014. Dalton Trans. 43: 7006-19. PMID: 24626345
  6. Structural basis of interprotein electron transfer in bacterial sulfite oxidation.  |  McGrath, AP., et al. 2015. Elife. 4: e09066. PMID: 26687009
  7. An indirect generation of 1D M(II)-2,5-dihydroxybenzoquinone coordination polymers, their structural rearrangements and generation of materials with a high affinity for H2, CO2 and CH4.  |  Abrahams, BF., et al. 2016. Dalton Trans. 45: 1339-44. PMID: 26733002
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2,5-Dihydroxybenzoquinone, 5 g

sc-275409
5 g
$32.00