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| Product | Description | |
|---|---|---|
| Lithium perchlorate | 25g Pack Size. Group: Inorganic Chemicals, Salts. Formula: ClLiO4. CAS No. 7791-3-9. Prepack ID 11397179-25g. Molecular Weight 106.39. See USA prepack pricing. |  |
| Lithium perchlorate | Lithium perchlorate. Group: Biochemicals. Grades: Highly Purified. CAS No. 7791-3-9. Pack Sizes: 250g, 500g, 1kg, 2kg, 5kg. US Biological Life Sciences. |  Worldwide |
| Lithium perchlorate 99+.9% | Lithium perchlorate 99+.9%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100g, 250g, 1Kg, 5Kg. US Biological Life Sciences. | Worldwide |
| Lithium perchlorate trihydrate | Lithium perchlorate trihydrate. Group: Biochemicals. Grades: Highly Purified. CAS No. 13453-78-6. Pack Sizes: 50g, 100g, 250g, 500g, 1Kg. Molecular Formula: ClLiO4ยท3H2O. US Biological Life Sciences. | Worldwide |
| Lithium perchlorate trihydrate, 63.0-68.0% ACS | Lithium perchlorate trihydrate, 63.0-68.0% ACS. Group: Biochemicals. Grades: ACS Grade. CAS No. 13453-78-6. Pack Sizes: 100g, 250g, 1Kg, 2.5Kg, 5Kg. US Biological Life Sciences. | Worldwide |
| 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. | |
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