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*For research and further manufacturing use only, not for direct human use.
Structure of 330641-16-2
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This reagent enables efficient amide bond formation under mild conditions, featuring a highly reactive tetrafluoroborate counterion that enhances coupling kinetics. The chlorobenzotriazole group ensures excellent leaving group stability and minimal side reactions, making it ideal for peptide synthesis and functionalization of sensitive substrates.
O-(6-Chlorobenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate serves as a highly effective coupling reagent in peptide and oligonucleotide synthesis, enabling efficient amide bond formation under mild conditions. Its bench-stable solid form facilitates handling, while the tetrafluoroborate counterion enhances solubility and minimizes side reactions. This reagent is widely used for its high reaction efficiency, clean byproduct formation, and compatibility with diverse functional groups in complex molecule assembly.
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GHS Pictogram :
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GHS No : GHS02,GHS07
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Signal Word : Danger
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UN#: 1325
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Class : 4.1
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Packing Group : Ⅱ
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Hazard Statements : H228-H317
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Precautionary Statements : P210-P240-P241-P261-P272-P280-P302+P352-P363-P370+P378-P501
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Lot numbers can be found on the outside label of a product: