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| Product | Description | |
|---|---|---|
| Lithium Aluminum Hydride | Lithium Aluminum Hydride. Group: Biochemicals. Alternative Names: Tetrahydro-d4-Aluminate(1-) Lithium; Aluminum Lithium Hydride; Aluminum Lithium Hydride; Aluminum Lithium Hydride AlLiH4; Lithium Aluminum Hydride (LiAlH4); Lithium Tetrahydro-aluminate; Lithium Tetrahydroaluminate(1-); LAH. Grades: Highly Purified. CAS No. 16853-85-3. Pack Sizes: 5g. Molecular Formula: AlH4Li, Molecular Weight: 37.95. US Biological Life Sciences. |  Worldwide |
| Lithium aluminum silicate | Heterocyclic Organic Compound. Alternative Names: Aluminosilicicacidlithiumsalt; Lithiumaluminiumsilicate; silicicacid(h2sio3), aluminumlithiumsalt(2:1:1); ALPHA-SPODUMENE; LITHIUM ALUMINUM SILICATE;aluminium lithium silicate;SILICICACID, LITHIUMALUMINIUMSALT. CAS No. 12068-40-5. Molecular formula: AlLiO6Si2. Mole weight: 306.26. Purity: 0.96. IUPACName: aluminum lithium dioxido(oxo)silane. Canonical SMILES: [Li+]. [O-][Si](=O)[O-]. [O-][Si](=O)[O-]. [Al+3]. Density: g/cm³. ECNumber: 235-098-6. Catalog: ACM12068405. |  |
| Aluminum-lithium | Heterocyclic Organic Compound. CAS No. 12042-37-4. Catalog: ACM12042374. | |
| Lithium-aluminum alloy | Lithium-aluminum alloy. Group: Electrode materials lithium-ion batteries. CAS No. 87871-87-2. |  |
| Lithium Nickel Cobalt Aluminum Oxide | Lithium Nickel Cobalt Aluminum Oxide (NCA) is a highly thermally stable cathode material used lithium-ion batteries. Doping the lithium nickel cobalt oxide with aluminum both stabilizes its thermal and charge transfer resistance. Group: Battery materials. Alternative Names: Lithium nickel cobalt aluminium oxide, LiNi0.8Co0.15Al0.05O2, NCA, Li(NCA)O2, Lithium nickel cobalt aluminum dioxide, Lithium nickel cobalt oxide, doped with aluminum, lithium mixed metal oxide, Aluminum doped Lithium nickel cobalt oxide (LNCO), LiNiCoAlO2, CAS 207803-51-8, 177997-13-6. CAS No. 193214-24-3. Molecular formula: 183.54(LiNiCoAlO2); variesbycomposition. Mole weight: LiNiCoAlO2. >98%. | |
| Lithium Nickel Cobalt Aluminum Oxide | Lithium Nickel Cobalt Aluminum Oxide (NCA) is a highly thermally stable cathode material used lithium-ion batteries. Doping the lithium nickel cobalt oxide with aluminum both stabilizes its thermal and charge transfer resistance. Group: Cathode materials. Alternative Names: Lithium nickel cobalt aluminium oxide, LiNi0.8Co0.15Al0.05O2, NCA, Li(NCA)O2, Lithium nickel cobalt aluminum dioxide, Lithium nickel cobalt oxide, doped with aluminum, lithium mixed metal oxide, Aluminum doped Lithium nickel cobalt oxide (LNCO), LiNiCoAlO2, CAS 207803-51-8, 177997-13-6. CAS No. 193214-24-3. Molecular formula: LiNiCoAlO2. Mole weight: 183.54(LiNiCoAlO2); variesbycomposition. Appearance: black powder. Purity: >98%. Catalog: ACM193214243-1. | |
| Silicic acid,aluminum lithium salt | Heterocyclic Organic Compound. CAS No. 12253-68-8. Catalog: ACM12253688. | |
| 1,6-Hexanediol | 1,6-Hexanediol is a saturated straight-chain diol, colorless liquid at room temperature, soluble in water. Industrially, 1,6-hexanediol can be synthesized by hydrogenation of adipic acid or its esters. It is usually prepared in the laboratory by the reduction of adipic acid with lithium aluminum hydride. Uses: 1,6-hexanediol can be used for a variety of s such as: a structure-directing agent for the synthesis of zsm-5 zeolite a solvent for titanium tetraisopropoxide to form titanium oxide (tio2) nanocrystals a phase change material in combination with lauric acid for thermal energy storage s. Group: 3d printing materials monomers. Alternative Names: Hexamethylene glycol. CAS No. 629-11-8. Pack Sizes: Packaging 50 g in poly bottle. Product ID: hexane-1,6-diol. Molecular formula: 118.17. Mole weight: HO(CH2)6OH. OCCCCCCO. 1S/C6H14O2/c7-5-3-1-2-4-6-8/h7-8H, 1-6H2. XXMIOPMDWAUFGU-UHFFFAOYSA-N. ≥ 97%. | |
| 1,6-Hexanediol | 1,6-Hexanediol is a saturated straight-chain diol, colorless liquid at room temperature, soluble in water. Industrially, 1,6-hexanediol can be synthesized by hydrogenation of adipic acid or its esters. It is usually prepared in the laboratory by the reduction of adipic acid with lithium aluminum hydride. Uses: 1,6-hexanediol can be used for a variety of s such as: a structure-directing agent for the synthesis of zsm-5 zeolite a solvent for titanium tetraisopropoxide to form titanium oxide (tio2) nanocrystals a phase change material in combination with lauric acid for thermal energy storage s. Group: Diol monomers. Alternative Names: 1,6-Dihydroxyhexane; Hexamethylene Glycol; 1,6-Hexylene Glycol. CAS No. 629-11-8. Molecular formula: C6H14O2. Mole weight: 118.18 g/mol. Appearance: White to Almost White Powder to Lump. Purity: 97.0%(GC). IUPACName: hexane-1,6-diol. Canonical SMILES: OCCCCCCO. Density: 0.96. ECNumber: 211-074-0. Catalog: ACM-MO-629118. | |
| 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. | |
| Diethylamine | Diethylamine, can be used for the preparation of alkali metal diethylamides, generated with n-BuLi or NaH, have been used for the cleavage of ethers. Also, in combination with Lithium aluminum hydride, generates lithium tris (diethylamino)aluminum hydride, which is a useful selective reducing agent. Group: Biochemicals. Grades: Highly Purified. CAS No. 109-89-7. Pack Sizes: 50ml, 100ml. Molecular Formula: C4H11N. US Biological Life Sciences. | Worldwide |
| DO3A tert-Butyl ester | DOTA tert-Butyl ester is a benxyl derivative of the cyclic tosamide; can be nitrated directly; is more convenient to incorporate the nitro group after deprotection lithium aluminum hydride. Synonyms: Tri-tert-butyl 1,4,7,10-tetraazacyclododecane-1,4,7-triacetate; DO3A-t-Bu-ester; 1,4,7,10-Tetraazacyclododecane-1,4,7-triacetic Acid Tri-tert-butyl Ester. Grades: >98%. CAS No. 122555-91-3. Molecular formula: C26H50N4O6. Mole weight: 514.70. |  |
| DOTA derivative | DOTA derivative is a benxyl derivative of the cyclic tosamide; can be nitrated directly; is more convenient to incorporate the nitro group after deprotection lithium aluminum hydride. Synonyms: DOTA derivative. Grades: >98%. CAS No. 153777-70-9. Molecular formula: C43H50N4O8S4. Mole weight: 879.14. | |
| Lithium aluminate | DryPowder. Group: Metal & ceramic materials. Alternative Names: ALUMINUM LITHIUM OXIDE;LITHIUM ALUMINUM OXIDE;LITHIUM ALUMINATE;LITHIUM METAALUMINATE;Aluminate (AlO21-), lithium;Aluminate (AlO21-), lithium;aluminate(alo21-), lithium;LiAlO2. CAS No. 12003-67-7. Molecular formula: AlLiO2;AlLiO2. Mole weight: 65.9g/mol. Purity: N/A. IUPACName: lithium;oxido(oxo)alumane. Canonical SMILES: [Li+].[O-][Al]=O. ECNumber: 234-434-9. Catalog: ACM12003677. | |
| Lithium aluminate | DryPowder. Group: Phosphors - phosphor materials. Alternative Names: ALUMINUM LITHIUM OXIDE; LITHIUM ALUMINUM OXIDE; LITHIUM ALUMINATE; LITHIUM METAALUMINATE; Aluminate (AlO21-), lithium; Aluminate (AlO21-), lithium; aluminate(alo21-),lithium; LiAlO2. CAS No. 12003-67-7. Product ID: lithium; oxido(oxo)alumane. Molecular formula: 65.9g/mol. Mole weight: AlLiO2;AlLiO2. [Li+].[O-][Al]=O. InChI=1S/Al.Li.2O/q;+1;;-1. YQNQTEBHHUSESQ-UHFFFAOYSA-N. | |
| Lithium Aluminium Deuteride | . Uses: Could be used in various analytical organic chemistry studies related to single-electron-transfer pathway or mechanisms of reactions involving transition metals. Synonyms: Aluminate(1-)-d4, tetrahydro-, lithium (1:1); Lithium Aluminum Hydride-d4; LAH-d4. Grades: ≥95%; 98% atom D. CAS No. 14128-54-2. Molecular formula: AlD4Li. Mole weight: 41.99. | |
| Myristyl Alcohol | Myristyl alcohol occurs as a white crystalline solid with a waxy odor. Also reported as opaque leaflets or crystals from ethanol. Synonyms: Alcohol miristilo; Dytol R-52; Lanette Wax KS; Lorol C14-95; Loxanol V; myristic alcohol; Nacol 14-95; Nacol 14-98; 1- tetradecanol; n-tetradecanol-1; n-tetradecyl alcohol; tetradecyl alcohol; Unihydag WAX-14. CAS No. 112-72-1. Product ID: PE-0606. Molecular formula: C14H30O. Mole weight: 214.4. Category: Emollient; Emulsion Stabilizer; Oleaginous vehicle; Surfactant; Thickening Agents; Viscosity-controlling Agents. Product Keywords: Surfactant Excipients; Stabilizers; PE-0606; Myristyl Alcohol; Emollient; Emulsion Stabilizer; Oleaginous vehicle; Surfactant; Thickening Agents; Viscosity-controlling Agents; C14H30O; 112-72-1. UNII: V42034O9PU. Chemical Name: Tetradecan-1-ol. Grade: Pharmceutical Excipients. Stability and Storage Conditions: The bulk material should be stored in a well-closed container in a cool, dry place. Source and Preparation: Myristyl alcohol is found in spermaceti wax and sperm oil, and may be synthesized by sodium reduction of fatty acid esters or the reduction of fatty acids by lithium aluminum hydride. It can also be formed from acetaldehyde and dimethylamine. Applications: Myristyl alcohol is used in oral, parenteral, and topical pharmaceutical formulations. It has been evaluated as a penetration enhancer in melatonin transdermal patches in rats.MyristÂ… |  |
| Ti3C2 MXene load aluminum | This product is a new current collector with MXene coating evenly coated on the surface of aluminum foil. This product utilizes the excellent conductive properties and two-dimensional layered structure of MXene to form an ultra-thin coating with excellent conductive properties (thickness less than 1um) on the surface of the current collector, which can significantly reduce the interface resistance and improve the adhesion of active materials. Uses: Its comprehensive performance is better than that of coated aluminum foil modified with ordinary carbon black and graphite, and it can replace traditional aluminum foil and corroded aluminum foil and be widely used in lithium-ion batteries and supercapacitors. Group: Mxenes materials. | |
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