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LiTFSI

CAS No.
90076-65-6
Chemical Name:
LiTFSI
Synonyms
LITFSI;LITHIUM BIS(TRIFLUOROMETHANESULFONYL)IMIDE;LITHIUM BIS(TRIFLUOROMETHANESULFONIMIDE);LithiuM bis;BISTRIFLUOROMETHANESULFONIMIDE LITHIUM SALT;LiTFSA;lithiuM bis((trifluoroMethyl)sulfonyl)aMide;LiN(SO2CF3)2;LITHIUM BIS(TRIFLUOROMETHANESULFONYL)AMIDE;bis(Trifluoromethanesulphonyl)imide, lithium salt
CBNumber:
CB6311504
Molecular Formula:
C2HF6NO4S2.Li
Molecular Weight:
288.1
MDL Number:
MFCD00210017
MOL File:
90076-65-6.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-07-31 17:49:05
Product description Number Pack Size Price
Bis(trifluoromethane)sulfonimide lithium salt 449504 250G $1410
Bis(trifluoromethane)sulfonimide lithium salt puriss., ≥99.0% (19F-NMR) 15224 10G $103
Bis(trifluoromethane)sulfonimide lithium salt puriss., ≥99.0% (19F-NMR) 15224 50G $269
Lithium Bis(trifluoromethanesulfonyl)imide >98.0%(T) B2542 25g $87
Lithium Bis(trifluoromethanesulfonyl)imide B2542 5G $26
More product size

LiTFSI Properties

Melting point 234-238 °C(lit.)
Density 1,334 g/cm3
vapor pressure 0Pa at 25℃
Flash point >100°C (>212°F)
storage temp. Inert atmosphere,Room Temperature
solubility H2O: 10 mg/mL, clear, colorless
form Hygroscopic Powder
color White
Specific Gravity 1.334
Water Solubility Soluble in water.
Sensitive Moisture Sensitive
BRN 6625414
InChI 1S/C2F6NO4S2.Li/c3-1(4,5)14(10,11)9-15(12,13)2(6,7)8;/q-1;+1
InChIKey QSZMZKBZAYQGRS-UHFFFAOYSA-N
SMILES [Li]N(S(=O)(=O)C(F)(F)F)S(=O)(=O)C(F)(F)F
LogP -1.46
CAS DataBase Reference 90076-65-6(CAS DataBase Reference)
FDA UNII 9Y730392A5
EPA Substance Registry System Methanesulfonamide, 1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]-, lithium salt (90076-65-6)
Boiling point 234-238°C (lit.)
UNSPSC Code 12352302
NACRES NA.23

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)Skull and Crossbones (GHS06)Health Hazard (GHS08)
GHS05,GHS06,GHS08
Signal word  Danger
Hazard statements  H301+H311-H314-H373-H412
Precautionary statements  P260-P273-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338
target organs Nervous system
PPE Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  T,C
Risk Statements  24/25-34-52/53-48/22
Safety Statements  22-26-36/37/39-45-61
RIDADR  UN 2923 8/PG 2
WGK Germany  2
Hazard Note  Harmful/Corrosive/Moisture Sensitive
TSCA  TSCA listed
HazardClass  8
PackingGroup  II
HS Code  29309090
Storage Class 6.1B - Non-combustible acute toxic Cat. 1 and 2
very toxic hazardous materials
Hazard Classifications Acute Tox. 3 Dermal
Acute Tox. 3 Oral
Aquatic Chronic 3
Eye Dam. 1
Skin Corr. 1B
STOT RE 2 Oral
REACH Registrations Active
Limited Quantities 1 Kg (2.2 lbs) (solid)
Excepted Quantities Max Inner Pack (30g or 30ml) and Max Outer Pack (500g or 500ml)
NFPA 704
1
3 0

LiTFSI price More Price(68)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 449504 Bis(trifluoromethane)sulfonimide lithium salt 90076-65-6 250G $1410 2026-04-30 Buy
Sigma-Aldrich 15224 Bis(trifluoromethane)sulfonimide lithium salt puriss., ≥99.0% (19F-NMR) 90076-65-6 10G $103 2026-04-30 Buy
Sigma-Aldrich 15224 Bis(trifluoromethane)sulfonimide lithium salt puriss., ≥99.0% (19F-NMR) 90076-65-6 50G $269 2026-04-30 Buy
TCI Chemical B2542 Lithium Bis(trifluoromethanesulfonyl)imide >98.0%(T) 90076-65-6 25g $87 2026-04-30 Buy
TCI Chemical B2542 Lithium Bis(trifluoromethanesulfonyl)imide 90076-65-6 5G $26 2021-12-16 Buy
Product number Packaging Price Buy
449504 250G $1410 Buy
15224 10G $103 Buy
15224 50G $269 Buy
B2542 25g $87 Buy
B2542 5G $26 Buy

LiTFSI Chemical Properties,Uses,Production

Description

Lithium bis(trifluoromethylsulphonyl)imide (LiTFSI) is normally used as a p-dopant to enhance the conductivity and hole mobility of the Spiro-OMeTAD for perovskite solar cells. It is believed that The function of LiTFSI in PSCs is similar to that in solid-state dye-sensitised solar cells.

Chemical Properties

White hygroscopic powder

Uses

Lithium bis(trifluoromethylsulfonyl)imide is used in the preparation of chiral imidazolium salt through an anion metathesis of the corresponding triflate organic electrolyte-based lithium batteries. It finds application in the preparation of rare-earth Lewis acid catalysts. It is also useful in primary and secondary lithium cells using organic liquid electrolytes and polymer batteries.

General Description

Bis(trifluoromethane)sulfonimide lithium salt is a synthetic reagent.

Flammability and Explosibility

Non flammable

Battery Materials

The non-isothermal kinetics of poly (ε-caprolactone) (PCL):lithium bis(trifluoromethanesulfonyl) imide (LiTFSI) and PEO:LiTFSI systems were explored, leading to the identification of different behaviors of effective crystal growth rate dependencies with temperature for PEO:LiTFSI (linear) and PCL:LiTFSI (exponential). Comparative study of these two SPE systems enabled the advancement of understanding on the role of LiTFSI in the crystallization process for both poly (ether) and poly (ester) based solid polymer electrolytes[1].

Synthesis

5.91 g of anhydrous lithium fluoride and N-butyl-bistrifluoromethylsulfonimide 51.26 g. Add to 250 g of isopropyl acetate and reflux for 10 hours. It was filtered after being cooled to room temperature, and the filtrate was concentrated to dryness under reduced pressure.200 g of dichloromethane was added dropwise, and the mixture was stirred at 20 ° C for 2 hours and then filtered. Wash with dichloromethane. The filter cake was dried at 80 ° C to obtain 39.57 g of Lithium bis(trifluoromethanesulphonyl)imide. The yield is 90.7%.
Lithium bis(trifluoromethanesulphonyl)imide

Properties and Applications

Lithium bis(trifluoromethanesulphonyl)imide (LiTFSI) is a hydrophilic organic salt with many uses in electric and electronic systems. Its bis(trifluoromethane)sulfonimide anion, often called bistriflimide, is helpful in coordinating weakly with cations. LiTFSI's other important property is its extremely high solubility in water: 21 molal or ≈6 kg/L of solution. LiTFSI is safer than the formerly used salt, lithium hexafluorophosphate (LiPF6). To improve the cells' ability to transport electrical charges, researchers are doped with a combination of LiTFSI and a semiconductor called Spiro-OMeTAD1; however, this process is extremely slow. Taylor and his fellow researchers solved the problem by bubbling carbon dioxide into a solution of spiro-OMeTAD and LiTFSI while irradiating the mixture with ultraviolet light. They then cast a film from the solution onto the perovskite light absorber. The process can be completed in ≈1 minute, compared with the older, hours-long doping procedure.

Toxics Screening Level

There are two Initial Threshold Screening Levels (ITSLs) for lithium bis(trifluoromethane sulfonyl)imide (LiTFMSI) (CAS No. 90076-65-6): Acute ITSL: 40 μg/m3 with a 24-hr. averaging time, and Chronic ITSL: 1 μg/m3 with an annual averaging time

References

[1] Perodeau, T., Vargas, J. A., Dollé, M., & Laventure, A. (2026). Exploring the impact of LiTFSI on solid polymer electrolytes crystallization behavior. Polymer, 352, Article 129839. https://doi.org/10.1016/j.polymer.2026.129839

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Related articles

Related Questions

Ask a question
Q:How to dehydrate LiTFSI?Alex - Jun 9,2026
A:LiTFSI is highly hygroscopic. To dehydrate it you need to dry it in a vacuum oven at 80 °C to 140 °C for a minimum of 12 hours. This process is necessary if you use LiTFSI for battery applications.
Q:Besides batteries, what other emerging applications does ?Lithium bis(trifluoromethanesulphonyl)imide have?wed - May 26,2026
A:Lithium bis(trifluoromethanesulphonyl)imide, commonly abbreviated as LiTFSI, is a high‑performance organic lithium salt with excellent thermal stability, hydrolysis resistance and high ionic conductivity, widely known as a key electrolyte material for advanced lithium‑ion and solid‑state batteries. Beyond its dominant role in battery systems, it has gained growing attention in multiple emerging fields. It can serve as a high‑efficiency Lewis acid catalyst in organic synthesis and fine chemical manufacturing to facilitate complex reactions. It is also applied in ionic liquids and deep eutectic solvents for supercapacitors, providing stable electrochemical performance for energy‑storage devices. In addition, LiTFSI is explored in biomedical fields as a non‑coordinating electrolyte material for implantable devices and drug‑delivery systems, thanks to its chemically inert anionic structure.

View Lastest Price from LiTFSI manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Lithium bis(trifluoromethanesulphonyl)imide pictures 2026-08-29 Lithium bis(trifluoromethanesulphonyl)imide
90076-65-6
0.99 RongNa Biotechnology Co.,Ltd
Lithium bis(trifluoromethanesulphonyl)imide pictures 2026-08-29 Lithium bis(trifluoromethanesulphonyl)imide
90076-65-6
1KG 98%min 30tons/month WUHAN FORTUNA CHEMICAL CO., LTD
Lithium bis(trifluoromethanesulphonyl)imide pictures 2026-08-28 Lithium bis(trifluoromethanesulphonyl)imide
90076-65-6
1kg/bag ≥98% 50 T/Month Hebei Qujie Technology Co., Ltd.
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 BIS(TRIFLUOROMETHANESULFONYL)IMIDE LITHIUM SALT LITHIUM TRIFLUOROMETHANESULFONIMIDE LITHIUM BISTRIFLUOROMETHANESULFONIMIDATE LITHIUM BIS(TRIFLUOROMETHANESULPHONYL)IMIDE Lithium bis(trifluoromethanesulfonimide),99% Lithium bis(trifluoromethansulfon)imide 1,1,1-trifluoro-n-[(trifluoromethyl)sulfonyl]-methanesulfonamidlithiumsalt Bis[(trifluoromethyl)sulfonyl]imide lithium salt Lithium bis(trifluoromethanesulphonyl)imide (LiTFSI) ithium Bis(trifL Bistrifluoromethanesulfonimide lithium salt (LiTFSi) JACS-90076-65-6 Methanesulfonamide, 1,1,1-trifluoro-N-[ (trifluoromethyl)sulfonyl]-, lithium salt (1:1) LiTFSI(Lithiumbis(trifluoromethanesulfonyl)imide) Bistrifluoromethanesulfonimide lithium Lithium bis(trifluoromethanesulphonyl)imide Factory Bis(trifluoromethylsulfonyl)amine lithium salt Factory Lithium bis(trifluoromethanesulphonyl)imide COA Lithium bis(trifluoromethanesulfonyl)imide ,98.5% Bis(trifluoromethane)sulfonimide lithium salt,Bis(trifluoromethylsulfonyl)amine lithium salt, Lithium bistrifluoromethanesulfonimidate LithiuM bis(trifluor bistrifluoroMethanesulfoniMidate LithiuM-bis(frifluoroMethanesulfonyl)iMlde Lithium bis(trifluoromethanesulfonyl)imide ,98% LiNTF2(LiTFSI) Bis(trifluoroMethane)sulfoniMide lithiuM salt 99.95% trace Metals basis Bis(trifluoroMethane)sulfoniMide lithiuM salt puriss., >=99.0% (19F-NMR) Trifluoromethanesulfonimide Lithium Salt, TFSILi Bis(trifluoromethane)sulfonimide lithium salt≥ 99.95% Lithium Triflimide Lithium Bis(trifluoromethane)sulfonimide lithium salt N-LITHIOTRIFLUOROMETHANESULFONIMIDE lithiumbis(trifluoromethylsulfonyl)imide Methanesulfonamide,1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]-,lithiumsalt Lithium Bis(trifluoromethanesulfonyl)imide > Lithium bis(trifluoromethanesulphonyl)imide>98% Li[(CF3SO2)2N]LiTFSI bis trifluoromethane sulfonyl amine lithium LiTFSA LiTFSi/Lithium bis(trifluoromethanesulphonyl)imide Lithiumbis(trifluoromethanesulph LiN(SO2CF3)2 Bis(trifluoromethane)sulphonimide lithium salt, 99.95% Lithium triflimide, 99%+ Bis(trifluoromethane)sulphonimide lithium salt Lithium bis[(trifluoromethyl)sulfonyl]azanide Bis[(trifluoromethyl)sulfonyl]imide lithium Lithium difluoromethane sulfonamide lithium salt 1,1,1-trifluoro-N-(trifluoromethylsulfonyl)methanesulfonamide Bis(trifluoromethane)sulfonimide lithium salt (HQ-115), 2 μg/mL in Methanol Bis(perfluoromethanesulfonyl)imide lithium Lithium bis(trifluoromethanesulphonyl)imide (LiTFSI salt)