N1,N2-Dimesitylethane-1,2-diamine

97%

Reagent Code: #50234
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CAS Number 134030-21-0

science Other reagents with same CAS 134030-21-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.45 g/mol
Formula C₂₀H₂₈N₂
badge Registry Numbers
MDL Number MFCD16877211
thermostat Physical Properties
Boiling Point 471.5°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.033g/cm3
Storage Room temperature, away from light, stored in an inert gas

description Product Description

Used as a ligand in coordination chemistry to stabilize metal complexes, particularly in catalysis and materials science. Its bulky mesityl groups enhance steric hindrance, making it valuable in asymmetric synthesis and the development of chiral catalysts. Also employed in the synthesis of organic electronic materials due to its electron-donating properties and ability to modify electronic structures.

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Test Parameter Specification
Appearance White to yellow powder or crystals
Purity 96.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿7,820.00
inventory 10g
10-20 days ฿16,180.00
inventory 250mg
10-20 days ฿990.00
inventory 1g
10-20 days ฿3,350.00

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N1,N2-Dimesitylethane-1,2-diamine
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Used as a ligand in coordination chemistry to stabilize metal complexes, particularly in catalysis and materials science. Its bulky mesityl groups enhance steric hindrance, making it valuable in asymmetric synthesis and the development of chiral catalysts. Also employed in the synthesis of organic electronic materials due to its electron-donating properties and ability to modify electronic structures.

Used as a ligand in coordination chemistry to stabilize metal complexes, particularly in catalysis and materials science. Its bulky mesityl groups enhance steric hindrance, making it valuable in asymmetric synthesis and the development of chiral catalysts. Also employed in the synthesis of organic electronic materials due to its electron-donating properties and ability to modify electronic structures.

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