N-(4-(6-Methyl-1,2,4,5-tetrazin-3-yl)benzyl)-4,7,10,13,16-pentaoxanonadec-18-ynamide

98%

Reagent Code: #109021
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CAS Number 2322322-23-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 487.55 g/mol
Formula C₂₄H₃₃N₅O₆
badge Registry Numbers
MDL Number MFCD31811434
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description 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.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿18,081.00
inventory 100mg
10-20 days ฿46,215.00
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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