Lithium Aluminum Hydride

We are engaged in offering superb grade of lithium aluminum hydride fine crystalline. This lithium aluminum hydride fine crystalline is highly reactive with water and gaseous hydrogen. Furthermore, it is used in different reactions for reducing carboxylic acids, esters and amides.

Lithium borohydride is an inorganic compound with molecular formula LiBH4. It is also known as Lithium hydroborate and Lithium tetrahydroborate. Lithium borohydride is a stronger reducing agent and is highly soluble in ethers. Furthermore, it is prepared by using metathesis reaction.

• Selective reduction of esters, carboxylic acids, amides, epoxides, ketones and aldehydes in the presence of other functional groups such as nitriles, nitro groups, alkenes and halides. The addition of a stoichiometric amount of methanol increases significantly the reducing power without affecting the selectivity.

Lithium hydride sieved is a chemical compound of lithium and hydrogen. It is also used as a reducing agent and widely demanded for the production of monosilane. Lithium hydride sieved is highly appreciated amongst customers for its high melting point.

• Reducing agent
• High density hydrogen source
• Production of high purity monosilane

Lithium triethylborohydride is extensively used in different industrial applications as a strong reducing agent. It is considered stronger than of lithium aluminum hydride (LAH). Furthermore, our product is basically lithium triethylborohydride, typ. 20 % solution in THF (Typ.1.7M).

• Powerful and selective reducing agent

Lithium-tri-(tert-butoxy)-aluminum hydride is processed by our experts by using superior quality lithium and aluminum. It is basically lithium-tri-(tert-butoxy)-aluminum hydride typ. 30 % solution in THF (Typ. 1.1 M). Our product is known for its solubility in water.

• Reduction of acid chlorides to aldehydes
• Stereoselective reductions of carbocyclic and steroid ketones
• Reduction of aldehydes and ketones, leaving unaffected halogen-, ester- lactone, amide-, nitrile-, nitro- and/or epoxy-groups as well as carbon and carbon multiple bonds