N-(4-(6-Methyl-1,2,4,5-tetrazin-3-yl)benzyl)-4,7,10,13,16-pentaoxanonadec-18-ynamide
98%
- Product Code: 109021
CAS:
2322322-23-4
| Molecular Weight: | 487.55 g./mol | Molecular Formula: | C₂₄H₃₃N₅O₆ |
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| EC Number: | MDL Number: | MFCD31811434 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in bioorthogonal chemistry, particularly in the field of bioconjugation and labeling of biomolecules. Its tetrazine group enables rapid and selective reactions with dienophiles, such as trans-cyclooctenes or norbornenes, through the inverse electron-demand Diels-Alder (IEDDA) reaction. This makes it highly effective for labeling proteins, nucleic acids, or other biomolecules in live cells or complex biological systems without interfering with native biochemical processes. The polyether chain enhances water solubility, making it suitable for use in aqueous environments, while the alkyne group allows for further functionalization via click chemistry. Its applications include imaging, drug delivery, and the study of molecular interactions in real-time.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | £408.94 |
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| 0.100 | 10-20 days | £1,045.24 |
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N-(4-(6-Methyl-1,2,4,5-tetrazin-3-yl)benzyl)-4,7,10,13,16-pentaoxanonadec-18-ynamide
This chemical is primarily utilized in bioorthogonal chemistry, particularly in the field of bioconjugation and labeling of biomolecules. Its tetrazine group enables rapid and selective reactions with dienophiles, such as trans-cyclooctenes or norbornenes, through the inverse electron-demand Diels-Alder (IEDDA) reaction. This makes it highly effective for labeling proteins, nucleic acids, or other biomolecules in live cells or complex biological systems without interfering with native biochemical processes. The polyether chain enhances water solubility, making it suitable for use in aqueous environments, while the alkyne group allows for further functionalization via click chemistry. Its applications include imaging, drug delivery, and the study of molecular interactions in real-time.
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