(1S,2S)-1,2-Bis(2-hydroxyphenyl)-1,2-ethanediamine

95%

Reagent Code: #113866
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CAS Number 119386-71-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.29 g/mol
Formula C₁₄H₁₆N₂O₂
badge Registry Numbers
MDL Number MFCD09751761
thermostat Physical Properties
Melting Point 157-162 °C
Boiling Point 457.9±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.294±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of coordination chemistry, where it serves as a versatile ligand for the formation of metal complexes. Its structure, featuring two hydroxyl groups and two amine groups, allows it to chelate metal ions effectively, making it valuable in catalytic processes. It is often employed in asymmetric synthesis, particularly in reactions where chiral induction is required, such as the production of enantiomerically pure pharmaceuticals. Additionally, its ability to bind metals makes it useful in the development of sensors for detecting metal ions in various environmental and biological samples. The compound’s stability and chelating properties also contribute to its application in materials science, where it is used to design functional materials with specific optical or magnetic properties.

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Test Parameter Specification
Appearance White To Light Yellow And Light Beige To Beige Powder Or Crystals Or Solid Or Chunks
Purity (%) 94.5-100%
Optical Rotation (C=0.2%; Chloroform) -70.0 to -60.0 Degree Celsius
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,680.00
inventory 1g
10-20 days ฿8,980.00
(1S,2S)-1,2-Bis(2-hydroxyphenyl)-1,2-ethanediamine
This compound is primarily utilized in the field of coordination chemistry, where it serves as a versatile ligand for the formation of metal complexes. Its structure, featuring two hydroxyl groups and two amine groups, allows it to chelate metal ions effectively, making it valuable in catalytic processes. It is often employed in asymmetric synthesis, particularly in reactions where chiral induction is required, such as the production of enantiomerically pure pharmaceuticals. Additionally, its ability to bind metals makes it useful in the development of sensors for detecting metal ions in various environmental and biological samples. The compound’s stability and chelating properties also contribute to its application in materials science, where it is used to design functional materials with specific optical or magnetic properties.
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