1,10-Phenanthroline-5,6-dione,3,8-dibromo

97%

Reagent Code: #70039
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CAS Number 602331-25-9

science Other reagents with same CAS 602331-25-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 367.98 g/mol
Formula C₁₂H₄Br₂N₂O₂
badge Registry Numbers
MDL Number MFCD09953785
thermostat Physical Properties
Melting Point >300°C
Boiling Point 538.186ºC at 760 mmHg
inventory_2 Storage & Handling
Density 2.069 g/cm3
Storage room temperature

description Product Description

Used primarily as a chelating agent in coordination chemistry, it forms stable complexes with metal ions, aiding in the study of metal-ligand interactions. It is also employed in analytical chemistry for the detection and quantification of metal ions due to its distinct color change upon complexation. In materials science, it serves as a precursor for the synthesis of organic semiconductors and conductive polymers. Additionally, it finds use in biochemical research as a redox-active compound for studying electron transfer processes in biological systems. Its applications extend to catalysis, where it acts as a ligand in various catalytic reactions, enhancing efficiency and selectivity.

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Test Parameter Specification
Appearance Light yellow to yellow solid
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,000.00
inventory 250mg
10-20 days ฿1,710.00

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1,10-Phenanthroline-5,6-dione,3,8-dibromo
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Used primarily as a chelating agent in coordination chemistry, it forms stable complexes with metal ions, aiding in the study of metal-ligand interactions. It is also employed in analytical chemistry for the detection and quantification of metal ions due to its distinct color change upon complexation. In materials science, it serves as a precursor for the synthesis of organic semiconductors and conductive polymers. Additionally, it finds use in biochemical research as a redox-active compound for studying

Used primarily as a chelating agent in coordination chemistry, it forms stable complexes with metal ions, aiding in the study of metal-ligand interactions. It is also employed in analytical chemistry for the detection and quantification of metal ions due to its distinct color change upon complexation. In materials science, it serves as a precursor for the synthesis of organic semiconductors and conductive polymers. Additionally, it finds use in biochemical research as a redox-active compound for studying electron transfer processes in biological systems. Its applications extend to catalysis, where it acts as a ligand in various catalytic reactions, enhancing efficiency and selectivity.

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