Sodium bis(trimethylsilyl)amide

98%

Reagent Code: #234397
label
Alias Sodium bis(trimethylsilyl)amino; sodium bisilylamino, sodium hexamethyldisilylamino, sodium hexamethyldisilylamino
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CAS Number 1070-89-9

science Other reagents with same CAS 1070-89-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 183.37 g/mol
Formula C₆H₁₈NNaSi₂
badge Registry Numbers
EC Number 213-983-8
MDL Number MFCD00009835
thermostat Physical Properties
Melting Point 171-175 °C(lit.)
inventory_2 Storage & Handling
Storage 2-8°C, dry, inert gas

description Product Description

Widely used as a strong non-nucleophilic base in organic synthesis, it facilitates deprotonation of weakly acidic protons in sensitive compounds. It is particularly effective in the preparation of enolates, phosphazenes, and other reactive intermediates. Commonly employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials due to its high reactivity and selectivity under anhydrous conditions. Also used in the generation of carbanions and in metalation reactions where a bulky base is required to avoid nucleophilic attack. Its solubility in nonpolar solvents makes it suitable for low-temperature reactions in aprotic media.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,800.00
inventory 5g
10-20 days ฿7,300.00
inventory 25g
10-20 days ฿36,200.00

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Sodium bis(trimethylsilyl)amide
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Widely used as a strong non-nucleophilic base in organic synthesis, it facilitates deprotonation of weakly acidic protons in sensitive compounds. It is particularly effective in the preparation of enolates, phosphazenes, and other reactive intermediates. Commonly employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials due to its high reactivity and selectivity under anhydrous conditions. Also used in the generation of carbanions and in metalation reactions where a bulky base i

Widely used as a strong non-nucleophilic base in organic synthesis, it facilitates deprotonation of weakly acidic protons in sensitive compounds. It is particularly effective in the preparation of enolates, phosphazenes, and other reactive intermediates. Commonly employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials due to its high reactivity and selectivity under anhydrous conditions. Also used in the generation of carbanions and in metalation reactions where a bulky base is required to avoid nucleophilic attack. Its solubility in nonpolar solvents makes it suitable for low-temperature reactions in aprotic media.

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