Date published: 2025-10-14

1-800-457-3801

SCBT Portrait Logo
Seach Input

Resorcinol (CAS 108-46-3)

0.0(0)
Write a reviewAsk a question

See product citations (1)

Alternate Names:
1,3-benzenediol; m-benzenediol; 1,3-dihydroxybenzene
Application:
Resorcinol is an aromatic alcohol used as a chemical intermediate
CAS Number:
108-46-3
Purity:
≥99%
Molecular Weight:
110.11
Molecular Formula:
C6H6O2
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Resorcinol is a dihydroxybenzene that is extensively used in chemical research due to its distinctive properties as a phenolic compound. It is particularly important in the synthesis of plastics and adhesives, where its ability to form resins is exploited. Resorcinol is also used in the preparation of various fluorescent and colorimetric reagents, which are crucial in analytical chemistry for detecting and quantifying other substances. Its bifunctional nature with two hydroxyl groups makes it a valuable intermediate in organic synthesis, particularly in the creation of pharmaceuticals, UV absorbers, and dyes. In polymer chemistry, resorcinol is employed to enhance the cross-linking density of polymers, improving their mechanical strength and thermal stability, which is vital for producing high-performance materials. Moreover, its role in the development of flame retardants and its use as a stabilizing agent in the production of certain chemical fibers highlight its versatility. In environmental science, resorcinol has been studied for its potential to remove pollutants from water through processes like adsorption and photocatalytic degradation. These diverse applications underline the importance of resorcinol in advancing research across multiple scientific disciplines, providing essential insights into material properties and environmental interactions.


Resorcinol (CAS 108-46-3) References

  1. Cytokine release and cytotoxicity in human keratinocytes and fibroblasts induced by phenols and sodium dodecyl sulfate.  |  Newby, CS., et al. 2000. J Invest Dermatol. 115: 292-8. PMID: 10951249
  2. Determination of major phenolic compounds in water by reversed-phase liquid chromatography after pre-column derivatization with benzoyl chloride.  |  Asan, A. and Isildak, I. 2003. J Chromatogr A. 988: 145-9. PMID: 12647829
  3. Routes and modes of administration of resorcinol and their relationship to potential manifestations of thyroid gland toxicity in animals and man.  |  Welsch, F. 2008. Int J Toxicol. 27: 59-63. PMID: 18293213
  4. Advances in tailoring resorcinol-formaldehyde organic and carbon gels.  |  Elkhatat, AM. and Al-Muhtaseb, SA. 2011. Adv Mater. 23: 2887-903. PMID: 21608048
  5. Comparative cytotoxicity of phenols in vitro.  |  Passi, S., et al. 1987. Biochem J. 245: 537-42. PMID: 2822025
  6. Environmental and occupational exposure to resorcinol in Finland.  |  Porras, SP., et al. 2018. Toxicol Lett. 298: 125-133. PMID: 29596886
  7. Characterization and topical delivery of phenylethyl resorcinol.  |  Zhang, Y., et al. 2019. Int J Cosmet Sci. 41: 479-488. PMID: 31378949
  8. Alkyl-Resorcinol Derivatives as Inhibitors of GDP-Mannose Pyrophosphorylase with Antileishmanial Activities.  |  Levaique, H., et al. 2021. Molecules. 26: PMID: 33799883
  9. Discovery of novel resorcinol biphenyl ether-based macrocyclic small molecules as PD-1/PD-L1 inhibitors with favorable pharmacokinetics for cancer immunotherapy.  |  Yang, Z., et al. 2023. Bioorg Chem. 139: 106740. PMID: 37478546
  10. Anaerobic metabolism of aromatic compounds.  |  Heider, J. and Fuchs, G. 1997. Eur J Biochem. 243: 577-96. PMID: 9057820

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Resorcinol, 100 g

sc-203371
100 g
$56.00

Resorcinol, 500 g

sc-203371A
500 g
$205.00

Resorcinol, 25 g

sc-203371B
25 g
$30.00