11-Mercaptoundecyl 2-Bromo-2-methylpropanoate
≥95%(LC&T)
- Product Code: 66847
CAS:
404857-69-8
| Molecular Weight: | 353.36 g./mol | Molecular Formula: | C₁₅H₂₉BrO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD32706494 | |
| Melting Point: | Boiling Point: | 391.0±12.0 °C | |
| Density: | 1.151±0.06 g/cm3 | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of surface chemistry and material science for the modification of surfaces, particularly gold and other noble metals. It serves as a key component in the formation of self-assembled monolayers (SAMs), which are used to create highly ordered, functionalized surfaces. These SAMs find applications in biosensors, where they enhance the sensitivity and specificity of detection by providing a stable and well-defined interface for the immobilization of biomolecules such as proteins, DNA, or antibodies. Additionally, it is employed in the development of advanced coatings for electronic devices, where it helps improve adhesion, corrosion resistance, and electrical properties. Its unique structure, combining a thiol group with a bromo-ester moiety, allows for versatile chemical reactions, making it a valuable tool in nanotechnology and organic synthesis.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to Light yellow clear liquid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,260.00 |
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11-Mercaptoundecyl 2-Bromo-2-methylpropanoate
This chemical is primarily utilized in the field of surface chemistry and material science for the modification of surfaces, particularly gold and other noble metals. It serves as a key component in the formation of self-assembled monolayers (SAMs), which are used to create highly ordered, functionalized surfaces. These SAMs find applications in biosensors, where they enhance the sensitivity and specificity of detection by providing a stable and well-defined interface for the immobilization of biomolecules such as proteins, DNA, or antibodies. Additionally, it is employed in the development of advanced coatings for electronic devices, where it helps improve adhesion, corrosion resistance, and electrical properties. Its unique structure, combining a thiol group with a bromo-ester moiety, allows for versatile chemical reactions, making it a valuable tool in nanotechnology and organic synthesis.
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