(1S,2S)-1,2-Bis(2-hydroxyphenyl)-1,2-ethanediamine
95%
- Product Code: 113866
CAS:
119386-71-9
| Molecular Weight: | 244.29 g./mol | Molecular Formula: | C₁₄H₁₆N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09751761 | |
| Melting Point: | 157-162 °C | Boiling Point: | 457.9±40.0 °C(Predicted) |
| Density: | 1.294±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C |
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.
Product Specification:
| Test | 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 -60.0 Degree Celsius |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,680.00 |
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| 1.000 | 10-20 days | ฿8,980.00 |
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(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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