2-tert-Butyl-1,1,3,3-tetramethylguanidine

≥97.0% (GC)

Reagent Code: #78381
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CAS Number 29166-72-1

science Other reagents with same CAS 29166-72-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.28 g/mol
Formula C₉H₂₁N₃
badge Registry Numbers
MDL Number MFCD01862972
thermostat Physical Properties
Boiling Point 88-89ºC43 mm Hg
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily used as a strong, non-nucleophilic base in organic synthesis. It facilitates various reactions, such as deprotonation of weakly acidic compounds, enabling the formation of carbanions. Its sterically hindered structure makes it particularly useful in reactions where less basic or nucleophilic reagents might interfere. It is also employed in the synthesis of pharmaceuticals and fine chemicals, where its high basicity and low nucleophilicity are advantageous. Additionally, it serves as a catalyst in polymerization processes, particularly for producing polyurethanes and other polymers. Its stability and efficiency make it a valuable reagent in both industrial and laboratory settings.

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Test Parameter Specification
Purity (GC) 97-100%
Appearance Liquid

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Size Availability Unit Price Quantity
inventory 25ml
10-20 days ฿3,360.00
inventory 5ml
10-20 days ฿800.00
inventory 1ml
10-20 days ฿300.00

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2-tert-Butyl-1,1,3,3-tetramethylguanidine
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This chemical is primarily used as a strong, non-nucleophilic base in organic synthesis. It facilitates various reactions, such as deprotonation of weakly acidic compounds, enabling the formation of carbanions. Its sterically hindered structure makes it particularly useful in reactions where less basic or nucleophilic reagents might interfere. It is also employed in the synthesis of pharmaceuticals and fine chemicals, where its high basicity and low nucleophilicity are advantageous. Additionally, it serv

This chemical is primarily used as a strong, non-nucleophilic base in organic synthesis. It facilitates various reactions, such as deprotonation of weakly acidic compounds, enabling the formation of carbanions. Its sterically hindered structure makes it particularly useful in reactions where less basic or nucleophilic reagents might interfere. It is also employed in the synthesis of pharmaceuticals and fine chemicals, where its high basicity and low nucleophilicity are advantageous. Additionally, it serves as a catalyst in polymerization processes, particularly for producing polyurethanes and other polymers. Its stability and efficiency make it a valuable reagent in both industrial and laboratory settings.

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