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About This Item
Linear Formula:
ClSO3Si(CH3)3
CAS Number:
Molecular Weight:
188.71
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-425-8
Beilstein/REAXYS Number:
1763675
MDL number:
Assay:
99%
Form:
liquid
InChI key
QWQONZVLXJGXHV-UHFFFAOYSA-N
InChI
1S/C3H9ClO3SSi/c1-9(2,3)7-8(4,5)6/h1-3H3
SMILES string
C[Si](C)(C)OS(Cl)(=O)=O
assay
99%
form
liquid
refractive index
n20/D 1.424 (lit.)
bp
168-169 °C (lit.), 62-64 °C/10 mmHg (lit.)
mp
−26 °C (lit.)
density
1.225 g/mL at 25 °C (lit.)
Quality Level
Related Categories
General description
Trimethylsilyl chlorosulfonate is commonly employed as sulfonating agent.
Application
Trimethylsilyl chlorosulfonate may be used:
- in the sulfonation of small organic molecules
- in the synthesis of sulfonated polysulfone
- as sulfonating agent in the preparation of nano-structured organic-inorganic membranes for proton exchange membrane fuel cells (PEMFC) based on methacrylate and epoxy polymeric structures
- in the preparation of sulfonated polysulfone (sPS)/titanium dioxide (TiO2) composite membranes for use in PEMFCs
- in the preparation of iodosobenzene sulfate, required for the synthesis of cyclic sulfates
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
107.6 °F - closed cup
flash_point_c
42 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Hybrid organic-inorganic nanostructured membranes for high temperature proton exchange membranes fuel cells (PEMFC).
Aparicio M, et al.
Journal of Sol-Gel Science and Technology, 40(2-3), 309-315 (2006)
Preparation and characterization of sulfonated polysulfone/titanium dioxide composite membranes for proton exchange membrane fuel cells.
Devrim Y, et al.
International Journal of Hydrogen Energy, 34(8), 3467-3475 (2009)
Sulfonated polysulfone as promising membranes for polymer electrolyte fuel cells.
Lufrano F, et al.
Journal of Applied Polymer Science, 77(6), 1250-1256 (2000)
Improved simple synthesis of cyclic sulfates from trimethylsilyl chlorosulfonate.
Bassindale AR, et al.
Canadian Journal of Chemistry, 78(11), 1479-1483 (2000)
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