Lithium bis(trimethylsilyl)amide

20% in Tetrahydrofuran, MKSeal

Reagent Code: #88727
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 -108°C
Boiling Point 65°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 effective in deprotonating weakly acidic protons, making it valuable in the generation of carbanions for reactions such as aldol condensations, alkylations, and enolate formations. Its sterically hindered structure minimizes unwanted side reactions, ensuring high selectivity in complex transformations. Additionally, it serves as a key reagent in the synthesis of silicon-containing compounds and in the preparation of organometallic intermediates. Its role in polymerization processes, especially for anionic polymerization of certain monomers, is also noteworthy. Furthermore, it is utilized in the production of pharmaceuticals, agrochemicals, and advanced materials, highlighting its versatility in industrial and research applications.

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Test Parameter Specification
Appearance Clear or slightly hazy, pale yellow to yellow to brown liquid
Assay 18.0-22.0
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5L
10-20 days ฿24,990.00
inventory 500ml
10-20 days ฿4,800.00

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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 effective in deprotonating weakly acidic protons, making it valuable in the generation of carbanions for reactions such as aldol condensations, alkylations, and enolate formations. Its sterically hindered structure minimizes unwanted side reactions, ensuring high selectivity in complex transformations. Additionally, it serves as a key reagent in the synthesis of silicon-containing c

Lithium bis(trimethylsilyl)amide is widely used as a strong, non-nucleophilic base in organic synthesis. It is particularly effective in deprotonating weakly acidic protons, making it valuable in the generation of carbanions for reactions such as aldol condensations, alkylations, and enolate formations. Its sterically hindered structure minimizes unwanted side reactions, ensuring high selectivity in complex transformations. Additionally, it serves as a key reagent in the synthesis of silicon-containing compounds and in the preparation of organometallic intermediates. Its role in polymerization processes, especially for anionic polymerization of certain monomers, is also noteworthy. Furthermore, it is utilized in the production of pharmaceuticals, agrochemicals, and advanced materials, highlighting its versatility in industrial and research applications.

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