Potassium bis(trimethylsilyl)amide

1.0 M solution in THF, MKSeal

Reagent Code: #87935
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Alias Potassium bis(trimethylsilyl)amide; Potassium hexamethyldisilazide
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CAS Number 40949-94-8

science Other reagents with same CAS 40949-94-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.48 g/mol
Formula C₆H₁₈KNSi₂
badge Registry Numbers
MDL Number MFCD00010330
thermostat Physical Properties
Boiling Point 111 °C
inventory_2 Storage & Handling
Density 0.877 g/mL at 25 °C
Storage 2~8 ℃

description Product Description

Used as a strong, non-nucleophilic base in organic synthesis, particularly in deprotonation reactions to generate carbanions. It is effective in the preparation of enolates from carbonyl compounds, which are key intermediates in aldol reactions. Additionally, it is employed in the synthesis of organosilicon compounds and as a reagent in the production of pharmaceuticals and fine chemicals. Its steric bulk makes it suitable for selective deprotonation in complex molecules.

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Test Parameter Specification
Purity (Titration with HClO4) 0.95m - 1.1m
Appearance colorless to brown liquid

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1L
10-20 days ฿13,680.00
inventory 100ml
10-20 days ฿2,780.00
inventory 500ml
10-20 days ฿8,480.00

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Potassium bis(trimethylsilyl)amide
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Used as a strong, non-nucleophilic base in organic synthesis, particularly in deprotonation reactions to generate carbanions. It is effective in the preparation of enolates from carbonyl compounds, which are key intermediates in aldol reactions. Additionally, it is employed in the synthesis of organosilicon compounds and as a reagent in the production of pharmaceuticals and fine chemicals. Its steric bulk makes it suitable for selective deprotonation in complex molecules.
Used as a strong, non-nucleophilic base in organic synthesis, particularly in deprotonation reactions to generate carbanions. It is effective in the preparation of enolates from carbonyl compounds, which are key intermediates in aldol reactions. Additionally, it is employed in the synthesis of organosilicon compounds and as a reagent in the production of pharmaceuticals and fine chemicals. Its steric bulk makes it suitable for selective deprotonation in complex molecules.
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