Phosphazene base P1-t-Bu

≥97.0% (GC)

Reagent Code: #224862
label
Alias N′-tert-butyl-N,N,N′,N′,N″,N″-hexamethyliminophosphate triamide; tert-butylimino-tris(dimethylamino)n-phosphine
fingerprint
CAS Number 81675-81-2

science Other reagents with same CAS 81675-81-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.32 g/mol
Formula C₁₀H₂₇N₄P
badge Registry Numbers
MDL Number MFCD00145111
thermostat Physical Properties
Boiling Point 175 °C at 760 mmHg
inventory_2 Storage & Handling
Density 0.94 g/mL(Predicted)
Storage Room temperature

description Product Description

Used as a powerful non-ionic base in organic synthesis, particularly in polymer chemistry and catalysis. It facilitates reactions such as Michael additions, aldol condensations, and esterifications by promoting deprotonation without nucleophilic attack. Commonly applied in the synthesis of advanced materials, pharmaceuticals, and fine chemicals due to its high basicity and low nucleophilicity. Also employed in fuel cell technologies as a proton scavenger and in CO2 capture systems for efficient carbon dioxide absorption.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1ml
10-20 days ฿14,000.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Phosphazene base P1-t-Bu
No image available

Used as a powerful non-ionic base in organic synthesis, particularly in polymer chemistry and catalysis. It facilitates reactions such as Michael additions, aldol condensations, and esterifications by promoting deprotonation without nucleophilic attack. Commonly applied in the synthesis of advanced materials, pharmaceuticals, and fine chemicals due to its high basicity and low nucleophilicity. Also employed in fuel cell technologies as a proton scavenger and in CO2 capture systems for efficient carbon di

Used as a powerful non-ionic base in organic synthesis, particularly in polymer chemistry and catalysis. It facilitates reactions such as Michael additions, aldol condensations, and esterifications by promoting deprotonation without nucleophilic attack. Commonly applied in the synthesis of advanced materials, pharmaceuticals, and fine chemicals due to its high basicity and low nucleophilicity. Also employed in fuel cell technologies as a proton scavenger and in CO2 capture systems for efficient carbon dioxide absorption.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...