151378
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:
Molecular Weight:
287.16
Beilstein/REAXYS Number:
2052955
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
assay
98%
bp
250 °C/10 mmHg (lit.)
mp
143-146 °C (lit.)
functional group
chloro
sulfone
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.
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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[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)
[Plasma levels of DDS in leprosy patients admitted in the National Sanatorium Oshima Seisho-en].
E Kubo et al.
Nihon Rai Gakkai zasshi, 52(1), 29-34 (1983-01-01)
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
Christina Larsson et al.
Environmental science & technology, 38(19), 4950-4955 (2004-10-28)
PCB methyl sulfones (MeSO2-PCBs) are lipophilic PCB metabolites of which five of the environmentally relevant meta/para pairs are chiral (i.e., exist as atropisomeric pairs). Methylsulfonyl-DDE (MeSO2-DDE) is a DDE metabolite, while bis(4-chlorophenyl) sulfone (BCPS) is a commercial monomer used for
[Late sequelae of the action of diphenyl derivatives].
T F Byshovets et al.
Gigiena i sanitariia, (4)(4), 19-20 (1983-04-01)
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