Lithium tri-tert-butoxyaluminum hydride

1.0 M solution in THF, MkSeal

Reagent Code: #88719
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CAS Number 17476-04-9

science Other reagents with same CAS 17476-04-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.27 g/mol
Formula C₁₂H₂₈AlLiO₃
badge Registry Numbers
EC Number 241-490-8
MDL Number MFCD00011532
thermostat Physical Properties
Melting Point 300-319 °C (dec.)(lit.)
inventory_2 Storage & Handling
Density 0.942 g/mL at 25 °C
Storage 2~8°C, dry

description Product Description

Used primarily as a selective reducing agent in organic synthesis, it is particularly effective for reducing esters to alcohols without affecting other functional groups like nitriles or amides. Its sterically hindered structure allows for controlled reactivity, making it useful in complex molecule transformations. Commonly applied in the synthesis of pharmaceuticals and fine chemicals where precise reduction is critical. It is also employed in the reduction of ketones and aldehydes to their corresponding alcohols, offering high yields and selectivity.

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Test Parameter Specification
Concentration 0.95-1.2
Appearance Colorless or slightly turbid liquid

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Size Availability Unit Price Quantity
inventory 100ml
10-20 days ฿7,670.00
inventory 500ml
10-20 days ฿23,260.00

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Lithium tri-tert-butoxyaluminum hydride
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Used primarily as a selective reducing agent in organic synthesis, it is particularly effective for reducing esters to alcohols without affecting other functional groups like nitriles or amides. Its sterically hindered structure allows for controlled reactivity, making it useful in complex molecule transformations. Commonly applied in the synthesis of pharmaceuticals and fine chemicals where precise reduction is critical. It is also employed in the reduction of ketones and aldehydes to their correspondin

Used primarily as a selective reducing agent in organic synthesis, it is particularly effective for reducing esters to alcohols without affecting other functional groups like nitriles or amides. Its sterically hindered structure allows for controlled reactivity, making it useful in complex molecule transformations. Commonly applied in the synthesis of pharmaceuticals and fine chemicals where precise reduction is critical. It is also employed in the reduction of ketones and aldehydes to their corresponding alcohols, offering high yields and selectivity.

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