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730882

Sigma-Aldrich

Disodium bis(4-chloro-3-sulfophenyl)sulfone

greener alternative

97%

Synonym(s):

Disodium 4,4′-dichloro-3,3′-sulfodiphenyl sulfone

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About This Item

Empirical Formula (Hill Notation):
C12H6Cl2Na2O8S3
CAS Number:
Molecular Weight:
491.25
MDL number:
UNSPSC Code:
26111700
PubChem Substance ID:
NACRES:
NA.23

Assay

97%

form

crystals

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Design for Energy Efficiency
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sustainability

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mp

>300 °C

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SMILES string

[Na+].[Na+].[O-]S(=O)(=O)c1cc(ccc1Cl)S(=O)(=O)c2ccc(Cl)c(c2)S([O-])(=O)=O

InChI

1S/C12H8Cl2O8S3.2Na/c13-9-3-1-7(5-11(9)24(17,18)19)23(15,16)8-2-4-10(14)12(6-8)25(20,21)22;;/h1-6H,(H,17,18,19)(H,20,21,22);;/q;2*+1/p-2

InChI key

KKEBUZUONXHUNE-UHFFFAOYSA-L

General description

Disodium bis(4-chloro-3-sulfophenyl)sulfone (SDCDPS) is a hydrophilic sulfonic monomer, which can be synthesized by electrophilic aromatic substitution by sulfonating the 4,4′-dichlorodiphenyl sulfone (DCDPS) monomer.
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Application

SDCDPS can be used in the formation of a sulfonated membrane for the fabrication of proton exchange membrane fuel cells. It can also be used in the synthesis of a stable solid acid catalyst for esterification.

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Eye Dam. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Sulfonated polyethersulfone directly synthesized through sulfonic monomer as a new stable solid acid catalyst for esterification
Wang Z, et al.
Catalysis Communications, 27, 164-168 (2012)

Articles

Advances in the electrochemical conversion of water to and from hydrogen and oxygen have principally been achieved through the development of new materials and by understanding the mechanisms of the degradation of proton exchange membrane fuel cells (PEMFC) during operation.

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