3-(1-(4-Aminobutyl)-1H-1,2,3-triazol-4-yl)aniline trihydrochloride

≥98%

Reagent Code: #137708
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CAS Number 1788044-10-9

science Other reagents with same CAS 1788044-10-9

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scatter_plot Molecular Information
Weight 340.68 g/mol
Formula C₁₂H₂₀Cl₃N₅
badge Registry Numbers
MDL Number MFCD28502706
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in bioconjugation and labeling applications, particularly in click chemistry reactions due to the presence of the triazole ring, which is a product of azide-alkyne cycloaddition. The amine groups enable covalent attachment to biomolecules such as proteins, peptides, and nucleic acids, making it useful in the development of fluorescent probes, diagnostic agents, and targeted drug delivery systems. Its structure supports the construction of complex molecular architectures in medicinal chemistry and chemical biology research. Also employed in the synthesis of functionalized polymers and surface modifications where controlled reactivity and stability are required.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿560.00
inventory 1g
10-20 days ฿1,280.00
inventory 5g
10-20 days ฿4,220.00

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3-(1-(4-Aminobutyl)-1H-1,2,3-triazol-4-yl)aniline trihydrochloride
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Used in bioconjugation and labeling applications, particularly in click chemistry reactions due to the presence of the triazole ring, which is a product of azide-alkyne cycloaddition. The amine groups enable covalent attachment to biomolecules such as proteins, peptides, and nucleic acids, making it useful in the development of fluorescent probes, diagnostic agents, and targeted drug delivery systems. Its structure supports the construction of complex molecular architectures in medicinal chemistry and ch

Used in bioconjugation and labeling applications, particularly in click chemistry reactions due to the presence of the triazole ring, which is a product of azide-alkyne cycloaddition. The amine groups enable covalent attachment to biomolecules such as proteins, peptides, and nucleic acids, making it useful in the development of fluorescent probes, diagnostic agents, and targeted drug delivery systems. Its structure supports the construction of complex molecular architectures in medicinal chemistry and chemical biology research. Also employed in the synthesis of functionalized polymers and surface modifications where controlled reactivity and stability are required.

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