Propargyl benzenesulfonate

Propargyl benzenesulfonate
Product Name Propargyl benzenesulfonate
CAS No.: 6165-75-9
Catalog No.: CFN90093
Molecular Formula: C9H8O3S
Molecular Weight: 196.22 g/mol
Purity: >=98%
Type of Compound: Miscellaneous
Physical Desc.: Cryst.
Source:
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Price:
Propargyl benzenesulfonate improves the SEI formation process.
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Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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    214th ECS Meeting, Abstract #1204, © The Electrochemical Society
    Propargyl Benzenesulfonate – A Triple-Bonded Electrolyte Additive for Electrolytes in Lithium Ion Batteries.[Reference: WebLink]

    METHODS AND RESULTS:
    We focused on a triple-bonded compound, Propargyl benzenesulfonate (S1), which influences the SEI formation process in ethylene carbonate, diethylene carbonate (EC/DEC)- and propylene carbonate (PC)- based electrolytes. In contrast to many other additives Propargyl benzenesulfonate decomposes in a potential range of 1200 mV to 1400 mV against Li/Li+. This fact is very meaningful because S1 provides SEI formation before we reach the edge of the potential window of carbonate based electrolytes. K. Abe et al. already investigated a compound called propargyl methanesulfonate. By the substitution of the methyl-group for a phenyl-group we found a compound which is commercially available and in the comparison cheaper. Propargyl benzenesulfonate was surveyed by cyclovoltammetry, constant current cycling and in situ Fourier transform infrared (FTIR) spectroscopy in a specially developed IR cell.
    CONCLUSIONS:
    It was concluded that Propargyl benzenesulfonate improves the SEI formation process. By the obtained IR data a possible reaction mechanism of Propargyl benzenesulfonate in the electrolyte was investigated.
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