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Lithium aluminium hydride for sale

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Lithium aluminium hydride for saleLithium aluminium hydride, commonly abbreviated to LAH or known as LithAl, is an inorganic compound with the chemical formula LiAlH4. It was discovered by Finholt, Bond and Schlesinger in 1947. This compound is used as a reducing agent in organic synthesis, especially for the reduction of esters, carboxylic acids, and amides. The solid is dangerously reactive toward water, releasing gaseous hydrogen (H2). Some related derivatives have been discussed for the hydrogen storage.LAH is a white solid, but commercial samples are usually gray due to contamination. This material can be purified by recrystallization from diethyl ether. Large-scale purifications employ a Soxhlet extractor. Commonly, the impure gray material is used in synthesis, since the impurities are innocuous and can be easily separated from the organic products. The pure powdered material is pyrophoric, but not its large crystals. Some commercial materials contain mineral oil to inhibit reactions with atmospheric moisture, but more commonly it is packed in moisture-proof plastic sacks. LAH is soluble in many etheral solutions. However, it may spontaneously decompose due to the presence of catalytic impurities, though, it appears to be more stable in tetrahydrofuran (THF). Thus, THF is preferred over, e.g., diethyl ether, despite the lower solubility Lithium aluminium hydride is widely used in organic chemistry as a reducing agent. It is more powerful than the related reagent sodium borohydride due to the weaker Al-H bond compared to the B-H bond. Often as a solution in diethyl ether and followed by an acid work-up, it will convert esters, carboxylic acids, aldehydes, and ketones into the corresponding alcohols (see: carbonyl reduction). Similarly, it converts amide, nitro, nitrile, imine, oxime, and azide compounds into the amines (see: amide reduction). It reduces quaternary ammonium cations into the corresponding tertiary amines. Reactivity can be tuned by replacing hydride groups by alkoxy groups. Despite handling problems associated with its reactivity, it is even used at the small-industrial scale, although for large-scale reductions, the related reagent sodium bis(2-methoxyethoxy)aluminium hydride is more commonly used. LAH is most commonly used for the reduction of esters and carboxylic acids to primary alcohols; prior to the advent of LiAlH4, this was a difficult conversion involving sodium metal in boiling ethanol (the Bouveault-Blanc reduction). Aldehydes and ketones can also be reduced to alcohols by LAH, but this is usually done using milder reagents such as NaBH4; α,β-unsaturated ketones are reduced to allylic alcohols. When epoxides are reduced using LAH, the reagent attacks the less hindered end of the epoxide, usually producing a secondary or tertiary alcohol. Epoxycyclohexanes are reduced to give axial alcohols preferentially. Partial reduction of acid chlorides to give the corresponding aldehyde product cannot proceed via LAH, since the latter reduces all the way to the primary alcohol. Instead, the milder lithium aluminium tri(t-butoxy)hydride must be used, which reacts significantly faster with the acid chloride than with the aldehyde. For example, when isovaleric acid is treated with thionyl chloride to give isovaleroyl chloride, it can then be reduced via lithium aluminium tri(t-butoxy)hydride to give isovaleraldehyde in 65% yield. Using LAH, amines can be prepared by the reduction of amides, oximes, nitriles, nitro compounds or alkyl azides. Lithium aluminium hydride also reduces alkyl halides to alkanes, although this reaction is rarely employed. Alkyl iodides react the fastest, followed by alkyl bromides and then alkyl chlorides. Primary halides are the most reactive followed by secondary halides. Tertiary halides react only in certain cases. Lithium aluminium hydride does not reduce simple alkenes, arenes, and alkynes are only reduced if an alcohol group is nearby.LiAlH4 contains 10.6 wt% hydrogen thereby making LAH a potential hydrogen storage medium for future fuel cell powered vehicles. The high hydrogen content, as well as the discovery of reversible hydrogen storage in Ti-doped NaAlH4, have sparked renewed research into LiAlH4 during the last decade. A substantial research effort has been devoted to accelerating the decomposition kinetics by catalytic doping and by ball milling. In order to take advantage of the total hydrogen capacity, the intermediate compound LiHmust be dehydrogenated as well. Due to its high thermodynamic stability this requires temperatures in excess of 400 °C which is not considered feasible for transportation purposes. Accepting LiH + Al as the final product, the hydrogen storage capacity is reduced to 7.96 wt%. Another problem related to hydrogen storage is the recycling back to LiAlH4 which, due to its relatively low stability, requires an extremely high hydrogen pressure in excess of 10000 bar. Cycling only reaction R2, that is using Li3AlH6 as starting material, would store 5.6 wt% hydrogen in a single step (vs. two steps for NaAlH4 which stores about the same amount of hydrogen). However, attempts on this have not been successful so far.  Read more:Lithium aluminium hydride for sale

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