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Lithium bis(trifluoromethanesulphonyl)imide

Short Description:

salt;Bis(trifluoromethane)sulfonimidelithiumsalt,99.95%metalsbasis;Lithiumbis(trifluoromethylsulfonyl)imide,98+%;Lithiumbis(trifluoromethanesulphonyl)imide99%;


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Synonyms:

bis(Trifluoromethanesulphonyl)imide, lithium salt;Bis(trifluoromethane)sulfonimide lithium salt, 99.95% metals basis;Lithium bis(trifluoromethylsulfonyl)imide, 98+%;Lithium bis(trifluoromethanesulphonyl)imide 99%;Lithiumbis(trifluoromethanesulphonyl)imide99%;1,1,1-Trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfon amide lithium salt;Bis(trifluoromethylsulfonyl)amine lithium salt, Lithium bistrifluoromethanesulfonimidate;BIS(TRIFLUOROMETHYLSULFONYL)AMINE LITHIUM SALT

CAS:90076-65-6

MF: C2F6LiNO4S2

MW:287.09

EINECS: 415-300-0

Chemical Properties

Melting point :234-238 °C(lit.)

density :1,334 g/cm3

Fp: >100°C (>212°F)

solubility : H2O: 10 mg/mL, clear, colorless

form :Hygroscopic Powder

color :White

Specific Gravity:1.334

Water Solubility :Soluble in water.

Sensitive:Moisture Sensitive

Introduction: White crystal or powder, can be used as the organic electrolyte lithium salt of lithium ion battery, with high electrochemical stability and conductivity.

Uses: It can be used to prepare electrolytes for lithium batteries and new rare earth Lewis acid catalysts; it is used to prepare chiral imidazolium salts through the anion replacement reaction of corresponding trifluoromethanesulfonates. This product is an important fluorine-containing organic ion compound, which is used in secondary lithium batteries and supercapacitors. As well as clean energy devices such as aluminum electrolytic capacitors, high-performance non-aqueous electrolyte materials, and new high-efficiency catalysts, all have important industrial application value.

Uses: Lithium battery electrolyte: 1. Lithium battery 2. Ionic liquid 3. Antistatic 4. Medicine (this use is less)

Uses: used to prepare electrolytes for lithium batteries and new rare earth Lewis acid catalysts; used to prepare chiral imidazolium salts through the anion replacement reaction of corresponding trifluoromethanesulfonates.


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