Phosphazene base P1-t-Bu-tris(tetramethylene)

≥97.0% (NT)

Reagent Code: #76862
label
Alias (tert-butylimino)tris(pyrrolidine)phosphine
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CAS Number 161118-67-8

science Other reagents with same CAS 161118-67-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 312.43 g/mol
Formula C₁₆H₃₃N₄P
badge Registry Numbers
MDL Number MFCD00214188
thermostat Physical Properties
Melting Point −24 °C
Boiling Point 119-122 °C0.1 mm Hg
inventory_2 Storage & Handling
Density 1.022 g/mL at 20 °C
Storage 2~8°C

description Product Description

Used as a strong, non-nucleophilic base in organic synthesis, particularly for deprotonation reactions where a less reactive base is required. It is effective in the preparation of sensitive intermediates, such as in the synthesis of pharmaceuticals and fine chemicals. The base is also employed in polymerization processes, especially for ring-opening polymerization of cyclic esters and carbonates, leading to the production of biodegradable polymers. Its steric bulk helps in minimizing side reactions, making it a valuable tool in complex organic transformations. Additionally, it is utilized in the development of advanced materials, including catalysts and specialty polymers, due to its stability and reactivity under various conditions.

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Test Parameter Specification
Purity 97-100%
Appearance Colorless to dark yellow and colorless to dark brown-yellow liquid

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Size Availability Unit Price Quantity
inventory 1ml
10-20 days ฿9,320.00

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Phosphazene base P1-t-Bu-tris(tetramethylene)
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Used as a strong, non-nucleophilic base in organic synthesis, particularly for deprotonation reactions where a less reactive base is required. It is effective in the preparation of sensitive intermediates, such as in the synthesis of pharmaceuticals and fine chemicals. The base is also employed in polymerization processes, especially for ring-opening polymerization of cyclic esters and carbonates, leading to the production of biodegradable polymers. Its steric bulk helps in minimizing side reactions, mak

Used as a strong, non-nucleophilic base in organic synthesis, particularly for deprotonation reactions where a less reactive base is required. It is effective in the preparation of sensitive intermediates, such as in the synthesis of pharmaceuticals and fine chemicals. The base is also employed in polymerization processes, especially for ring-opening polymerization of cyclic esters and carbonates, leading to the production of biodegradable polymers. Its steric bulk helps in minimizing side reactions, making it a valuable tool in complex organic transformations. Additionally, it is utilized in the development of advanced materials, including catalysts and specialty polymers, due to its stability and reactivity under various conditions.

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