Sodium bis(trimethylsilyl)amide

95%

Reagent Code: #232973
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. Commonly employed in the preparation of enolates, organometallic reagents, and in lithiation reactions when combined with lithium salts. It is especially useful in the synthesis of pharmaceuticals and fine chemicals where high reactivity and selectivity are required. Its solubility in nonpolar solvents makes it ideal for use in aprotic environments. Also applied in the generation of anions in polymerization initiators and in the modification of silicon surfaces in semiconductor processing.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,210.00
inventory 5g
10-20 days ฿3,300.00

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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. Commonly employed in the preparation of enolates, organometallic reagents, and in lithiation reactions when combined with lithium salts. It is especially useful in the synthesis of pharmaceuticals and fine chemicals where high reactivity and selectivity are required. Its solubility in nonpolar solvents makes it ideal for use in aprotic environments. Also applie

Widely used as a strong non-nucleophilic base in organic synthesis, it facilitates deprotonation of weakly acidic protons in sensitive compounds. Commonly employed in the preparation of enolates, organometallic reagents, and in lithiation reactions when combined with lithium salts. It is especially useful in the synthesis of pharmaceuticals and fine chemicals where high reactivity and selectivity are required. Its solubility in nonpolar solvents makes it ideal for use in aprotic environments. Also applied in the generation of anions in polymerization initiators and in the modification of silicon surfaces in semiconductor processing.

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