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*For research and further manufacturing use only, not for direct human use.
Structure of 51444-31-6
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This triazolyl ethylamine integrates a reactive 1H-1,2,4-triazole moiety with a primary amine handle, enabling efficient conjugation in bioconjugation workflows. The electron-rich triazole facilitates robust coupling under mild conditions, while the terminal amine supports derivatization or immobilization. Bench-stable and moisture-tolerant, it streamlines synthesis of functionalized probes and molecular scaffolds.
2-(1H-1,2,4-Triazol-1-yl)ethan-1-amine serves as a versatile building block in medicinal chemistry, enabling the construction of triazole-containing scaffolds through standard coupling reactions. Its primary amine functionality facilitates derivatization, while the 1,2,4-triazole ring imparts metabolic stability and hydrogen-bonding capacity. The compound exhibits good bench stability and compatibility with common functional groups, simplifying purification and integration into multi-step syntheses.
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H318-H335
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Precautionary Statements : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P310-P312-P330-P332+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: