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151378

Sigma-Aldrich

Bis(4-chlorophenyl) sulfone

98%

Synonym(s):

4,4′-Dichlorodiphenyl sulfone, 4-Chlorophenyl sulfone

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About This Item

Linear Formula:
(ClC6H4)2SO2
CAS Number:
80-07-9
Molecular Weight:
287.16
Beilstein:
2052955
EC Number:
201-247-9
MDL number:
MFCD00000619
UNSPSC Code:
12352100
PubChem Substance ID:
24849123
NACRES:
NA.22

Assay

98%

bp

250 °C/10 mmHg (lit.)

mp

143-146 °C (lit.)

SMILES string

Clc1ccc(cc1)S(=O)(=O)c2ccc(Cl)cc2

InChI

1S/C12H8Cl2O2S/c13-9-1-5-11(6-2-9)17(15,16)12-7-3-10(14)4-8-12/h1-8H

InChI key

GPAPPPVRLPGFEQ-UHFFFAOYSA-N

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Application

Bis(4-chlorophenyl) sulfone was used to study the time trends of bis(4-chlorophenyl) sulfone (BCPS). It was also used in thermoplastic production.

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H319,H411

Hazard Classifications

Aquatic Chronic 2 - Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

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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Nurrahmi Handayani et al.
Membranes, 2(2), 198-213 (2012-01-01)
Immobilization of enzymes is one of the most promising methods in enzyme performance enhancement, including stability, recovery, and reusability. However, investigation of suitable solid support in enzyme immobilization is still a scientific challenge. Polyethersulfone (PES) and aminated PES (PES-NH2) were
[Establishment of the maximum permissible concentration of 4,4-dichlorophenylsulfone in reservoir waters].
G T Pis'ko et al.
Gigiena i sanitariia, (2)(2), 84-85 (1982-02-01)
Fred M Parham et al.
Toxicology and applied pharmacology, 181(3), 153-163 (2002-06-25)
A physiologically based pharmacokinetic model of the absorption, distribution, metabolism, and elimination of p,p'-dichlorodiphenylsulfone (DDS) in male and female rats and mice is presented. Data used in constructing the model come from single-dose intravenous administration of DDS to male Fischer
J M Mathews et al.
Drug metabolism and disposition: the biological fate of chemicals, 24(5), 579-587 (1996-05-01)
p, p'-Dichlorodiphenyl sulfone (DDS) is a lipophilic monomer used extensively in the synthesis of high temperature plastics. Studies of the fate of uniformly labeled [14C]DDS in the rat have established that it is readily absorbed from the gastrointestinal tract, distributed
K Bester et al.
Chemosphere, 45(6-7), 817-826 (2001-11-07)
Nonylphenols and nonylphenol-ethoxylates were detected in the water and sediment samples from the German Bight of the North Sea. Additionally bis (4-chlorophenyl)-sulfone and linear alkylbenzenesulfonates (LAS) were detected in marine waters. Proof of identification is given by comparison of spectral
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