Date published: 2025-11-30

1-800-457-3801

SCBT Portrait Logo
Seach Input

4,4′-Ethylidenebisphenol (CAS 2081-08-5)

0.0(0)
Write a reviewAsk a question

See product citations (1)

Alternate Names:
1,1-Bis(4-hydroxyphenyl)ethane
CAS Number:
2081-08-5
Molecular Weight:
214.26
Molecular Formula:
C14H14O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

4,4′-Ethylidenebisphenol is a vital organic compound with extensive use across various industrial applications. It exists as a white crystalline solid and features a high solubility in water, alcohol, and other organic solvents. The compound′s structure includes two phenol groups linked by an ethane bridge, earning it its label as a bisphenol. Its many uses span from the synthesis of polymers to functioning as a reagent in organic synthesis. Additionally, it serves as a stabilizer in various applications. 4,4′-Ethylidenebisphenol is routinely utilized in scientific research, particularly in the synthesis of polymers like polycarbonates and polyurethanes, where it acts as a monomer. Moreover, it is incorporated in the production process of paints, adhesives, and an array of other coatings. The precise mechanism of action of 4,4′-Ethylidenebisphenol remains unclear. However, it is understood that 4,4′-Ethylidenebisphenol can form robust hydrogen bonds with other molecules, which may stabilize the molecule and boost its catalytic abilities. Additionally, 4,4′-Ethylidenebisphenol can form complexes with other molecules, potentially increasing its reactivity.


4,4′-Ethylidenebisphenol (CAS 2081-08-5) References

  1. Measurement of estrogenic activity of chemicals for the development of new dental polymers.  |  Hashimoto, Y., et al. 2001. Toxicol In Vitro. 15: 421-5. PMID: 11566573
  2. Photodegradation mechanism for bisphenol A at the TiO2/H2O interfaces.  |  Watanabe, N., et al. 2003. Chemosphere. 52: 851-9. PMID: 12757786
  3. Suppression of CINNAMOYL-CoA REDUCTASE increases the level of monolignol ferulates incorporated into maize lignins.  |  Smith, RA., et al. 2017. Biotechnol Biofuels. 10: 109. PMID: 28469705
  4. Binding modes of environmental endocrine disruptors to human serum albumin: insights from STD-NMR, ITC, spectroscopic and molecular docking studies.  |  Yang, H., et al. 2017. Sci Rep. 7: 11126. PMID: 28894220
  5. Overexpression of the Sorghum bicolor SbCCoAOMT alters cell wall associated hydroxycinnamoyl groups.  |  Tetreault, HM., et al. 2018. PLoS One. 13: e0204153. PMID: 30289910
  6. Acetyl Groups in Typha capensis: Fate of Acetates during Organosolv and Ionosolv Pulping.  |  Audu, IG., et al. 2018. Polymers (Basel). 10: PMID: 30966652
  7. Overcoming cellulose recalcitrance in woody biomass for the lignin-first biorefinery.  |  Yang, H., et al. 2019. Biotechnol Biofuels. 12: 171. PMID: 31297159
  8. Endocrine disruption: Molecular interactions of environmental bisphenol contaminants with thyroid hormone receptor and thyroxine-binding globulin.  |  Beg, MA. and Sheikh, IA. 2020. Toxicol Ind Health. 36: 322-335. PMID: 32496146
  9. A rapid thioacidolysis method for biomass lignin composition and tricin analysis.  |  Chen, F., et al. 2021. Biotechnol Biofuels. 14: 18. PMID: 33430954
  10. Fenton-like chain reactions by coupling nanoscale tungsten powders and peroxydisulfate: Performance and mechanistic insights.  |  Cheng, F., et al. 2021. J Hazard Mater. 413: 125304. PMID: 33626474
  11. Estrogenic activity of lignin-derivable alternatives to bisphenol A assessed via molecular docking simulations.  |  Amitrano, A., et al. 2021. RSC Adv. 11: 22149-22158. PMID: 35480830
  12. USAEME-GC/MS Method for Easy and Sensitive Determination of Nine Bisphenol Analogues in Water and Wastewater.  |  Kiejza, D., et al. 2022. Molecules. 27: PMID: 35956929
  13. Electrospun Polycrown Ether Composite Nanofibers as an Adsorbent for On-Line Solid Phase Extraction of Eight Bisphenols from Drinking Water Samples with Column-Switching Prior to High Performance Liquid Chromatography.  |  Xu, T., et al. 2022. Polymers (Basel). 14: PMID: 36365764

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4,4′-Ethylidenebisphenol, 25 g

sc-486607
25 g
$107.00