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103039

Sigma-Aldrich

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
Beilstein:
2052954
EC Number:
201-250-5
MDL number:
MFCD00002350
UNSPSC Code:
12162002
PubChem Substance ID:
24846593
NACRES:
NA.23

Assay

98%

form

solid

mp

245-250 °C (lit.)

SMILES string

Oc1ccc(cc1)S(=O)(=O)c2ccc(O)cc2

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

InChI key

VPWNQTHUCYMVMZ-UHFFFAOYSA-N

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Pictograms

Health hazard
GHS08

Signal Word

Danger

Hazard Statements

H360FD

Hazard Classifications

Repr. 1B

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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René Viñas et al.
Environmental health perspectives, 121(3), 352-358 (2013-03-06)
Bisphenol A (BPA) is a well-known endocrine disruptor that imperfectly mimics the effects of physiologic estrogens via membrane-bound estrogen receptors (mERα, mERβ, and GPER/GPR30), thereby initiating nongenomic signaling. Bisphenol S (BPS) is an alternative to BPA in plastic consumer products
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
C Simoneau et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 28(12), 1763-1768 (2011-10-13)
This work presents two analytical methods developed for measuring three components of polyethersulphone (PES) and applying them to the migration testing of 30 baby bottles made of PES. The study also provides migration results under the same conditions for bisphenol
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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