Lithium bis(trimethylsilyl)amide

1.0 M solution in THF, MKSeal

Reagent Code: #88704
label
Alias Lithium bis(trimethylsilyl)amide; lithium hexamethyldisilazide, lithium bistrimethylsilylamide
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CAS Number 4039-32-1

science Other reagents with same CAS 4039-32-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.33 g/mol
Formula C₆H₁₈LiNSi₂
badge Registry Numbers
EC Number 223-725-6
MDL Number MFCD00008261
thermostat Physical Properties
Melting Point 73°C
Boiling Point 55-56 °C
inventory_2 Storage & Handling
Density 0.891 g/mL at 25 °C
Storage 2~8 ℃

description Product Description

Lithium bis(trimethylsilyl)amide is widely used as a strong, non-nucleophilic base in organic synthesis. It is particularly valuable in deprotonation reactions, where it facilitates the generation of carbanions from weakly acidic compounds. This makes it essential in the preparation of enolates, which are key intermediates in aldol reactions and other carbon-carbon bond-forming processes. Additionally, it is employed in the synthesis of organometallic compounds, where its ability to remove protons without interfering with the metal center is crucial. The chemical is also utilized in the production of specialty chemicals, including pharmaceuticals and agrochemicals, where precise control over reaction conditions is required. Its role in polymerization processes, particularly in anionic polymerization, further highlights its versatility in industrial applications.

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Test Parameter Specification
Appearance Pale yellow to amber liquid
Concentration 1.0 M
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1L
10-20 days ฿6,880.00
inventory 100ml
10-20 days ฿1,670.00
inventory 500ml
10-20 days ฿4,570.00

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Lithium bis(trimethylsilyl)amide
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Lithium bis(trimethylsilyl)amide is widely used as a strong, non-nucleophilic base in organic synthesis. It is particularly valuable in deprotonation reactions, where it facilitates the generation of carbanions from weakly acidic compounds. This makes it essential in the preparation of enolates, which are key intermediates in aldol reactions and other carbon-carbon bond-forming processes. Additionally, it is employed in the synthesis of organometallic compounds, where its ability to remove protons withou

Lithium bis(trimethylsilyl)amide is widely used as a strong, non-nucleophilic base in organic synthesis. It is particularly valuable in deprotonation reactions, where it facilitates the generation of carbanions from weakly acidic compounds. This makes it essential in the preparation of enolates, which are key intermediates in aldol reactions and other carbon-carbon bond-forming processes. Additionally, it is employed in the synthesis of organometallic compounds, where its ability to remove protons without interfering with the metal center is crucial. The chemical is also utilized in the production of specialty chemicals, including pharmaceuticals and agrochemicals, where precise control over reaction conditions is required. Its role in polymerization processes, particularly in anionic polymerization, further highlights its versatility in industrial applications.

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