1,1'-(butane-1,4-diyl)bis(3-(2-(2-(2-aminoethoxy)ethoxy)ethyl)urea)
98%
- Product Code: 38717
CAS:
1571103-88-2
| Molecular Weight: | 436.55 g./mol | Molecular Formula: | C₁₈H₄₀N₆O₆ |
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| Density: | Storage Condition: | 2-8℃ |
Product Description:
This chemical is primarily used in the development of advanced materials and biomedical applications due to its unique structure and functional groups. It serves as a key component in the synthesis of dendrimers and polymers, which are utilized in drug delivery systems to enhance the solubility, stability, and targeted release of therapeutic agents. Its ability to form hydrogen bonds and interact with biological molecules makes it suitable for creating biocompatible coatings and hydrogels, which are applied in tissue engineering and wound healing. Additionally, it is employed in the fabrication of sensors and diagnostic tools, where its amine and ether groups facilitate the binding and detection of specific analytes. Its versatility also extends to industrial applications, such as the modification of surfaces to improve adhesion and corrosion resistance in coatings and composites.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,167.00 |
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| 0.250 | 10-20 days | ฿6,948.00 |
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| 1.000 | 10-20 days | ฿13,896.00 |
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1,1'-(butane-1,4-diyl)bis(3-(2-(2-(2-aminoethoxy)ethoxy)ethyl)urea)
This chemical is primarily used in the development of advanced materials and biomedical applications due to its unique structure and functional groups. It serves as a key component in the synthesis of dendrimers and polymers, which are utilized in drug delivery systems to enhance the solubility, stability, and targeted release of therapeutic agents. Its ability to form hydrogen bonds and interact with biological molecules makes it suitable for creating biocompatible coatings and hydrogels, which are applied in tissue engineering and wound healing. Additionally, it is employed in the fabrication of sensors and diagnostic tools, where its amine and ether groups facilitate the binding and detection of specific analytes. Its versatility also extends to industrial applications, such as the modification of surfaces to improve adhesion and corrosion resistance in coatings and composites.
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