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Merck

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:
80-09-1
Molecular Weight:
250.27
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
24846593
EC Number:
201-250-5
Beilstein/REAXYS Number:
2052954
MDL number:
MFCD00002350

Key Documents

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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

200

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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.

pictograms

Health hazard
GHS08

signalword

Danger

hcodes

H360FD

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

80-09-1

CAS No.

80-09-1

CAS No.

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Certificates of Analysis (COA)

Lot/Batch Number
WXBD2812V
MKCJ3019
MKCL2824
MKCF0795
MKCB4700

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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
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.
Chunyang Liao et al.
Environmental science & technology, 46(12), 6860-6866 (2012-05-25)
As concern regarding the toxic effects of bisphenol A (BPA) grows, BPA in many consumer products is gradually being replaced with compounds such as bisphenol S (BPS). Nevertheless, data on the occurrence of BPS in human specimens are limited. In
Chunyang Liao et al.
Environmental science & technology, 46(12), 6515-6522 (2012-05-18)
As the evidence of the toxic effects of bisphenol A (BPA) grows, its application in commercial products is gradually being replaced with other related compounds, such as bisphenol S (BPS). Nevertheless, very little is known about the occurrence of BPS
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
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