Lithium amide

95%

Reagent Code: #88737
label
Alias lithium amide
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CAS Number 7782-89-0

science Other reagents with same CAS 7782-89-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 22.96 g/mol
Formula LiNH₂
badge Registry Numbers
MDL Number MFCD00011093
thermostat Physical Properties
Melting Point 373 °C
Boiling Point 430 °C
inventory_2 Storage & Handling
Density 1.178 g/mL
Storage room temperature

description Product Description

Lithium amide is widely used as a strong base in organic synthesis, particularly in deprotonation reactions to generate carbanions. It is employed in the preparation of lithium enolates from carbonyl compounds, which are key intermediates in aldol reactions and other carbon-carbon bond-forming processes. In the pharmaceutical industry, it plays a crucial role in the synthesis of complex molecules, including active pharmaceutical ingredients (APIs). Additionally, it is utilized in the production of specialty chemicals, such as polymers and agrochemicals, where precise control over reactivity is essential. Its ability to act as a nucleophile also makes it valuable in the synthesis of organometallic compounds.

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Test Parameter Specification
Purity (Titration by NaOH) 94-106%
Appearance White to off-white powder

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 100g
10-20 days ฿7,340.00
inventory 5g
10-20 days ฿880.00
inventory 25g
10-20 days ฿2,300.00

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Lithium amide
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Lithium amide is widely used as a strong base in organic synthesis, particularly in deprotonation reactions to generate carbanions. It is employed in the preparation of lithium enolates from carbonyl compounds, which are key intermediates in aldol reactions and other carbon-carbon bond-forming processes. In the pharmaceutical industry, it plays a crucial role in the synthesis of complex molecules, including active pharmaceutical ingredients (APIs). Additionally, it is utilized in the production of specia

Lithium amide is widely used as a strong base in organic synthesis, particularly in deprotonation reactions to generate carbanions. It is employed in the preparation of lithium enolates from carbonyl compounds, which are key intermediates in aldol reactions and other carbon-carbon bond-forming processes. In the pharmaceutical industry, it plays a crucial role in the synthesis of complex molecules, including active pharmaceutical ingredients (APIs). Additionally, it is utilized in the production of specialty chemicals, such as polymers and agrochemicals, where precise control over reactivity is essential. Its ability to act as a nucleophile also makes it valuable in the synthesis of organometallic compounds.

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