1,2,4,5-Tetrazine-3,6-dicarboxylic acid

95%

Reagent Code: #244805
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CAS Number 117943-07-4

science Other reagents with same CAS 117943-07-4

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scatter_plot Molecular Information
Weight 170.08 g/mol
Formula C₄H₂N₄O₄
badge Registry Numbers
MDL Number MFCD04000257
inventory_2 Storage & Handling
Storage -20°C, Sealed, Drying, Inert Gas

description Product Description

Used primarily in bioorthogonal chemistry due to its ability to undergo rapid inverse electron-demand Diels-Alder reactions with strained alkenes and alkynes. This makes it valuable in labeling biomolecules in live cells without interfering with natural biochemical processes. Commonly employed in imaging, drug delivery systems, and targeted therapy where selective and fast conjugation is required. Also utilized in materials science for constructing functional polymers and responsive nanomaterials through click chemistry approaches.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,770.00
inventory 1g
10-20 days ฿71,880.00
inventory 250mg
10-20 days ฿20,540.00
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1,2,4,5-Tetrazine-3,6-dicarboxylic acid
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Used primarily in bioorthogonal chemistry due to its ability to undergo rapid inverse electron-demand Diels-Alder reactions with strained alkenes and alkynes. This makes it valuable in labeling biomolecules in live cells without interfering with natural biochemical processes. Commonly employed in imaging, drug delivery systems, and targeted therapy where selective and fast conjugation is required. Also utilized in materials science for constructing functional polymers and responsive nanomaterials through

Used primarily in bioorthogonal chemistry due to its ability to undergo rapid inverse electron-demand Diels-Alder reactions with strained alkenes and alkynes. This makes it valuable in labeling biomolecules in live cells without interfering with natural biochemical processes. Commonly employed in imaging, drug delivery systems, and targeted therapy where selective and fast conjugation is required. Also utilized in materials science for constructing functional polymers and responsive nanomaterials through click chemistry approaches.

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