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| Product | Description | |
|---|---|---|
| Lithium trifluoromethanesulfonate | 25g Pack Size. Group: Building Blocks, Fluorinated Products, Inorganic Chemicals, Salts. Formula: CF3 LiO3S. CAS No. 33454-82-9. Prepack ID 56978926-25g. Molecular Weight 156.01. See USA prepack pricing. |  |
| Lithium Trifluoromethanesulfonate | Lithium Trifluoromethanesulfonate. Group: Electrolyteslithium-ion batteriesbattery materials. Alternative Names: Lithium triflate. CAS No. 33454-82-9. Product ID: Lithium; trifluoromethanesulfonate. Molecular formula: 156. Mole weight: CF3LiO3S. [Li+].C(F)(F)(F)S(=O)(=O)[O-]. InChI=1S/CHF3O3S.Li/c2-1(3, 4)8(5, 6)7;/h(H, 5, 6, 7);/q;+1/p-1. MCVFFRWZNYZUIJ-UHFFFAOYSA-M. 99%+. |  |
| Trifluoromethanesulfonate lithium | Trifluoromethanesulfonate (lithium) is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Triflate lithium; Trifluoromethylsulfonate lithium; Trifluoromethanesulphonic acid lithium. CAS No. 33454-82-9. Pack Sizes: 25 g. Product ID: HY-21170B. |  |
| 1-Butyl-3-methylimidazolium trifluoromethanesulfonate | 1-Butyl-3-methylimidazolium trifluoromethanesulfonate is an aprotic neutral ionic liquid. It can be used as an alternative to lithium perchlorate-diethyl ether mixture in the Diels-Alder reaction. Uses: Metal plating, electropolishing, metal reprocessing, phase transfer media, batteries fuel cells, nanomaterials, industrial solvents, nuclear fuel red waste, enzymatic catalysis, lubricants heat transfer and solar energy conversion. Alternative Names: BMIMOtf. CAS No. 174899-66-2. Molecular formula: C9H15F3N2O3S. Mole weight: 288.29. Appearance: Colorless to Yellow to Green clear liquid. Purity: >98.0%(N). IUPACName: 1-butyl-3-methylimidazol-3-ium;trifluoromethanesulfonate. Canonical SMILES: CCCCN1C=C[N+](=C1)C. C(F)(F)(F)S(=O)(=O)[O-]. Density: 1.2951. Catalog: ACM174899662. |  |
| 1-Butyl-3-methylimidazolium trifluoromethanesulfonate | 1-Butyl-3-methylimidazolium trifluoromethanesulfonate is an aprotic neutral ionic liquid. It can be used as an alternative to lithium perchlorate-diethyl ether mixture in the Diels-Alder reaction. Uses: Metal plating, electropolishing, metal reprocessing, phase transfer media, batteries fuel cells, nanomaterials, industrial solvents, nuclear fuel red waste, enzymatic catalysis, lubricants heat transfer and solar energy conversion. Group: Electrolytesbattery materials. Alternative Names: BMIMOtf. CAS No. 174899-66-2. Product ID: 1-butyl-3-methylimidazol-3-ium; trifluoromethanesulfonate. Molecular formula: 288.29. Mole weight: C9H15F3N2O3S. CCCCN1C=C[N+](=C1)C. C(F)(F)(F)S(=O)(=O)[O-]. 1S/C8H15N2. CHF3O3S/c1-3-4-5-10-7-6-9(2)8-10; 2-1(3, 4)8(5, 6)7/h6-8H, 3-5H2, 1-2H3; (H, 5, 6, 7)/q+1; /p-1. FRZPYEHDSAQGAS-UHFFFAOYSA-M. >98.0%(N). | |
| Aluminum trifluoromethanesulfonate | Friedel-Crafts Reactions. Aluminum trifluoromethanesulfonate has been used for the Friedel-Crafts alkylation reaction of toluene with isopropyl and tert-butyl chlorides (eq 1), and for theacylationof Benzene andtoluenewithacetylandbenzoylchlo- rides in low to moderate yields. Intramolecular Friedel-Crafts acylation of an aromatic compound with Meldrum's acid has also been reported using catalytic amounts of Al(OTf) 3. Acylation of 2-methoxynaphthalene with acetic anhydride has been reported using Al(OTf) 3 and lithium perchlorate as an additive to afford the corresponding 6-acetylated adduct in 83% yield. Effective acylation of arenes with carboxylic acids has also been disclosed using polystyrene-supported Al(OTf)3. Group: Organic aluminium. Alternative Names: Aluminum triflate. CAS No. 74974-61-1. Molecular formula: C3AlF9O9S3. Mole weight: 474.2. Appearance: Powder. Purity: 0.99. IUPACName: aluminum;trifluoromethanesulfonate. Canonical SMILES: C(F)(F)(F)S(=O)(=O)[O-]. C(F)(F)(F)S(=O)(=O)[O-]. C(F)(F)(F)S(=O)(=O)[O-]. [Al+3]. Catalog: ACM74974611-1. | |
| Lithium triflate | Lithium triflate. Group: other electronic materials. CAS No. 33454-82-9. Product ID: lithium; trifluoromethanesulfonate. Molecular formula: 156g/mol. Mole weight: CF3LiO3S. [Li+].C(F)(F)(F)S(=O)(=O)[O-]. InChI=1S/CHF3O3S.Li/c2-1(3, 4)8(5, 6)7;/h(H, 5, 6, 7);/q;+1/p-1. MCVFFRWZNYZUIJ-UHFFFAOYSA-M. | |
| 1,3-Diethoxyimidazolium hexafluorophosphate | 1,3-Diethoxyimidazolium hexafluorophosphate can be prepared by reacting 1-hydroxyimidazole-3-oxide with diethyl sulfate and subsequently with ammonium hexafluorophosphate. It may be used in the preparation of 1,3-diethoxyimidazolium bis(trifluoromethanesulfonyl)imide via ion metathesis with lithium bis(trifluoromethanesulfonyl)imide. Group: Electrolytes. Alternative Names: (OEt)2Im-PF6. CAS No. 951020-87-4. Product ID: 1,3-diethoxyimidazol-1-ium; hexafluorophosphate. Molecular formula: 302.14999999999998. Mole weight: C7H13F6N2O2P. CCON1C=C[N+](=C1)OCC. F[P-](F)(F)(F)(F)F. 1S/C7H13N2O2. F6P/c1-3-10-8-5-6-9(7-8)11-4-2; 1-7(2, 3, 4, 5)6/h5-7H, 3-4H2, 1-2H3; /q+1; -1. OCMLXXOSZWGVIL-UHFFFAOYSA-N. ≥97%(H-NMR). | |
| 1-Allyl-3-methylimidazolium Bis(trifluoromethanesulfonyl)imide | 1-Allyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide is an ionic liquid which can be used to prepare AMIMTFSI-propylene carbonate based electrolyte, with potential application in lithium-ion batteries. It also finds application in alkanes/alkenes separation process. Group: Battery materials. Alternative Names: AMIMTFSI. CAS No. 655249-87-9. Product ID: bis(trifluoromethylsulfonyl)azanide; 1-methyl-3-prop-2-enylimidazol-1-ium. Molecular formula: 403.31. Mole weight: C9H11F6N3O4S2. C[N+]1=CN (C=C1)CC=C. C (F) (F) (F)S (=O) (=O)[N-]S (=O) (=O)C (F) (F)F. 1S/C7H11N2. C2F6NO4S2/c1-3-4-9-6-5-8(2)7-9; 3-1(4, 5)14(10, 11)9-15(12, 13)2(6, 7)8/h3, 5-7H, 1, 4H2, 2H3; /q+1; -1. DHMWATGUEVQTIY-UHFFFAOYSA-N. >98.0%(HPLC). | |
| 1-Butyl-2,3-dimethylimidazolium Bis(trifluoromethanesulfonyl)imide | Ionic liquids (ILs) are molten salts with melting points lower than 100 °C. They usually consist of pair of organic cation and anion. ILs exhibit unique properties such as non-volatility, high thermal stability, and high ionic conductivity and find applications as electrolytes in lithium/sodium ion batteries and dye-sensitized solar cells. Group: Battery materials electronic materials. CAS No. 350493-08-2. Product ID: bis(trifluoromethylsulfonyl)azanide; 1-butyl-2,3-dimethylimidazol-3-ium. Molecular formula: 433.38. Mole weight: C11H17F6N3O4S2. CCCCN1C=C[N+] (=C1C)C. C (F) (F) (F)S (=O) (=O)[N-]S (=O) (=O)C (F) (F)F. InChI=1S/C9H17N2. C2F6NO4S2/c1-4-5-6-11-8-7-10 (3)9 (11)2; 3-1 (4, 5)14 (10, 11)9-15 (12, 13)2 (6, 7)8/h7-8H, 4-6H2, 1-3H3; /q+1; -1. UCCKRVYTJPMHRO-UHFFFAOYSA-N. >98.0%(T). | |
| Lithium bis(trifluoromethanesulfonyl)imide | PelletsLargeCrystals. Group: Battery materials. Alternative Names: lithium; bis(trifluoromethylsulfonyl)azanide. CAS No. 90076-65-6. Product ID: lithium; bis(trifluoromethylsulfonyl)azanide. Molecular formula: 287.09. Mole weight: C2F6LiNO4S2. [Li+]. C (F) (F) (F)S (=O) (=O)[N-]S (=O) (=O)C (F) (F)F. InChI=1S/C2F6NO4S2.Li/c3-1(4, 5)14(10, 11)9-15(12, 13)2(6, 7)8;/q-1;+1. QSZMZKBZAYQGRS-UHFFFAOYSA-N. 98%. | |
| Lithium bis(trifluoromethanesulfonyl)imide | PelletsLargeCrystals. Group: Lithium electrolytes. Alternative Names: lithium; bis(trifluoromethylsulfonyl)azanide. CAS No. 90076-65-6. Molecular formula: C2F6LiNO4S2. Mole weight: 287.09. Appearance: White hygroscopic powder. Purity: 0.98. IUPACName: lithium; bis(trifluoromethylsulfonyl)azanide. Canonical SMILES: [Li+]. C (F) (F) (F)S (=O) (=O)[N-]S (=O) (=O)C (F) (F)F. Catalog: ACM90076656-2. | |
| Lithium (fluorosulfonyl) (trifluoromethanesulfonyl)imide | Lithium (fluorosulfonyl) (trifluoromethanesulfonyl)imide. Group: Electrolytesbattery materials. Alternative Names: Lithium; fluorosulfonyl (trifluoromethylsulfonyl)azanide. CAS No. 192998-62-2. Product ID: lithium; fluorosulfonyl (trifluoromethylsulfonyl)azanide. Molecular formula: 237.07. Mole weight: CF4LiNO4S2. [Li+]. C(F)(F)(F)S(=O)(=O)[N-]S(=O)(=O)F. InChI=1S/CF4NO4S2.Li/c2-1(3, 4)11(7, 8)6-12(5, 9)10;/q-1;+1. ZIRAMZRKLHPLPK-UHFFFAOYSA-N. 95%+. | |
| Tributylmethylammonium Bis(trifluoromethanesulfonyl)imide | Tributylmethylammonium bis(trifluoromethylsulfonyl)imide is a class of electrolytic materials that can be used in the fabrication of lithium-ion batteries. Lithium-ion batteries consist of anode, cathode, and electrolyte with a charge-discharge cycle. These materials enable the formation of greener and sustainable batteries for electrical energy storage. Group: Battery materials. Alternative Names: Tributylmethylammonium Bis(trifluoromethanesulfonyl)imide, 405514-94-5, DSSTox_CID_27881, DSSTox_RID_82634, DSSTox_GSID_47905, CTK8B3621, Tox21_200582, ANW-42830, AKOS005762829, NCGC00248746-01, NCGC00258136-01, CAS-405514-94-5, Tributylmethylammonium bis(trifluoromethylsulfonyl)imde. CAS No. 405514-94-5. Product ID: bis(trifluoromethylsulfonyl)azanide; tributyl(methyl)azanium. Molecular formula: 480.53. Mole weight: C15H30F6N2O4S2. CCCC[N+] (C) (CCCC)CCCC. C (F) (F) (F)S (=O) (=O)[N-]S (=O) (=O)C (F) (F)F. InChI=1S/C13H30N. C2F6NO4S2/c1-5-8-11-14(4, 12-9-6-2)13-10-7-3; 3-1(4, 5)14(10, 11)9-15(12, 13)2(6, 7)8/h5-13H2, 1-4H3; /q+1; -1. XALVHDZWUBSWES-UHFFFAOYSA-N. >98.0%(T). | |
| Tributylmethylammonium Bis(trifluoromethanesulfonyl)imide | Tributylmethylammonium bis(trifluoromethylsulfonyl)imide is a class of electrolytic materials that can be used in the fabrication of lithium-ion batteries. Lithium-ion batteries consist of anode, cathode, and electrolyte with a charge-discharge cycle. These materials enable the formation of greener and sustainable batteries for electrical energy storage. Group: Heterocyclic organic compound. Alternative Names: Tributylmethylammonium Bis(trifluoromethanesulfonyl)imide, 405514-94-5, DSSTox_CID_27881, DSSTox_RID_82634, DSSTox_GSID_47905, CTK8B3621, Tox21_200582, ANW-42830, AKOS005762829, NCGC00248746-01, NCGC00258136-01, CAS-405514-94-5, Tributylmethylammonium bis(trifluoromethylsulfonyl)imde. CAS No. 405514-94-5. Molecular formula: C15H30F6N2O4S2. Mole weight: 480.53. Appearance: Colorless to Light orange to Yellow clear liquid. Purity: >98.0%(T). IUPACName: bis(trifluoromethylsulfonyl)azanide; tributyl(methyl)azanium. Canonical SMILES: CCCC[N+] (C) (CCCC)CCCC. C (F) (F) (F)S (=O) (=O)[N-]S (=O) (=O)C (F) (F)F. Catalog: ACM405514945. | |
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