103039
4,4′-Sulfonyldiphenol
98%
Synonym(s):
4-Hydroxyphenyl sulfone, Bis(4-hydroxyphenyl) sulfone, Bisphenol S
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About This Item
Linear Formula:
O2S(C6H4OH)2
CAS Number:
Molecular Weight:
250.27
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
201-250-5
Beilstein/REAXYS Number:
2052954
MDL number:
Product Name
4,4′-Sulfonyldiphenol, 98%
InChI key
VPWNQTHUCYMVMZ-UHFFFAOYSA-N
InChI
1S/C12H10O4S/c13-9-1-5-11(6-2-9)17(15,16)12-7-3-10(14)4-8-12/h1-8,13-14H
SMILES string
Oc1ccc(cc1)S(=O)(=O)c2ccc(O)cc2
assay
98%
form
solid
mp
245-250 °C (lit.)
Quality Level
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Application
4,4′-Sulfonyldiphenol can be used:
- As a monomer to synthesize fibrous poly(arylene ether ketone)s with excellent water affinity, thermal stability and film forming capability. This can be utilized to fabricate Proton exchange membranes for electrodialysis, fuel cells and flow batteries.
- As a precursor to prepare polyphosphazene-based contrast agents for magnetic resonance imaging (MRI) and computed tomography (CT). It enhances the thermal stability, chemical resistance and allows easy functionalization of contrast agents.
- As a monomer to prepare poly (cyclotriphosphazene-co-4,4-sulfonyldiphenol) (PZS) coating for separators, in lithium-ion battery. The coated separators show sufficient enhancement of liquid electrolyte wettability and ionic conductivity, resulting in better cycle performance.
General description
4,4′-Sulfonyldiphenol also known as Bisphenol S(BPS) is a monomer characterized by its sulfone group (-SO2-) linking two phenolic rings. Its unique chemical structure imparts high thermal stability, chemical resistance, and tensile strength. It is often used as a monomer or additive in the synthesis of high-performance polymers, particularly polyethersulfones (PES) and polyphenylsulfones (PPSU). It is widely used in the field of polymer synthesis, medical devices, and dental composites.
signalword
Danger
hcodes
Hazard Classifications
Repr. 1B
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Erica Danzl et al.
International journal of environmental research and public health, 6(4), 1472-1484 (2009-05-15)
A group of compounds structurally similar to bis(4-hydroxyphenyl)propane (bisphenol A, BPA) are called bisphenols (BPs), and some of them can partially replace BPA in industrial applications. The production and consumption of BPs other than BPA, especially those of bis(4-hydroxyphenyl)methane (bisphenol
Elise Grignard et al.
Toxicology in vitro : an international journal published in association with BIBRA, 26(5), 727-731 (2012-04-18)
In 2011, the European Commission has restricted the use of Bisphenol A in plastic infant feeding bottles. In a response to this restriction, Bisphenol S is now often used as a component of plastic substitutes for the production of babybottles.
Imèn Khmiri et al.
Environment international, 138, 105644-105644 (2020-03-18)
The measurement of bisphenol-S (BPS) and its glucurono-conjugate (BPSG) in urine may be used for the biomonitoring of exposure in populations. However, this requires a thorough knowledge of their toxicokinetics. The time courses of BPS and BPSG were assessed in
Jeremy Gingrich et al.
Archives of toxicology, 92(5), 1861-1876 (2018-03-20)
Exposure to bisphenolic chemicals during pregnancy occurs in > 90% of pregnancies. Bisphenolic compounds can cross the placental barrier reaching fetal circulation. However, the effects of emerging bisphenolic compounds, such as bisphenol S (BPS), on placental function remain untested. The aim
José-Manuel Molina-Molina et al.
Toxicology and applied pharmacology, 272(1), 127-136 (2013-05-30)
Bisphenols are a group of chemicals structurally similar to bisphenol-A (BPA) in current use as the primary raw material in the production of polycarbonate and epoxy resins. Some bisphenols are intended to replace BPA in several industrial applications. This is
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