Lithium Aluminium Hydride

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USD 150.00 / 1 Kilogram

100 Kilogram (MOQ)

Business Type Manufacturer, Exporter, Supplier
Packaging Size 20-30 Kg, 10-20 Kg
Grade Standard Reagent Grade
Purity 99.9%
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Preferred Buyer From

Location Worldwide ( Except India, Tanzania, United Republic of)

Product Details

Application
Industrial
Form
Lumps
Color
Grey
Country of Origin
Tanzania
Payment Terms
D/A, D/P, T/T

Lithium aluminum hydride (LiAlH₄) is a white, odorless, inorganic solid that's used as a reducing agent in organic synthesis. It's also known as LAH. 

  • Properties Molar mass: 37.95 g/mol, Density: 917 kg/m³, and Melting point: 150 °C.
  • Safety 
  • Highly reactive and pyrophoric
  • Can cause violent fires
  • Reacts violently with water, acids, and oxygenated compounds
  • Can ignite in moist air or because of friction or static sparks
  • Highly corrosive to eyes, skin, and mucous membranes
  • Handling
  • Researchers should be trained on the proper use of LiAlH 
  • Laboratories should have written SOPs for the proper use of LiAlH 
  • Extreme caution is used when handling LiAlH 
  • It is never left out on the bench for any extended period 
  • Systematic
  • namelithium tetrahydridoaluminate
  • AbbreviationsLAH
  • Traditional namesLithium tetrahydridoaluminate, lithium aluminum hydride, lithium aluminum hydride, lithium alanate
  • Chemical formulaLiAlH4​
  • Statewhite crystals
  • Molar mass37.95 g/mol
  • Density0.917 g/cm³
  • T. divers.150 °C
  • Enthalpy of formation-107 kJ/mol
  • Solubility in diethyl ether25 g/100 ml
  • Solubility in THF15 g/100 ml
  • Crystal structuremonoclinic
  • Reg. CAS number16853-85-3
  • PubChem28112
  • EINECS Reg. No.240-877-9
  • SMILES [show]
  • EC Reg. No.240-877-9
  • RTECSBD0100000
  • ChemSpider26150
  • Data are given for standard conditions (25 °C, 100 kPa), unless otherwise stated.

Lithium aluminum hydride  ( lithium alanate ) is an inorganic compound, a complex mixed hydride of lithium and aluminum with the formula Li[AlH 4 ], white crystals. A strong reducing agent used in organic synthesis. More powerful than other commonly used agents, such as sodium borohydride, due to the weaker Al-H bonds compared to B-H. Reduces esters, carboxylic acids and ketones to alcohols, nitro compounds to amines.

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