BCN-OH (endo-9-Hydroxymethylbicyclo[6.1.0]non-4-yne) is an alcohol-functionalized cyclooctyne derivative that serves as a precursor for the synthesis of various bioconjugation probes, including BCN-TPP. It facilitates the construction of targeted probes through coupling reactions with carboxyl-containing compounds, such as TPP-COOH. Additionally, BCN-OH functions as a control reagent for experiments involving BCN-TPP, providing a valuable tool for researchers in chemical biology and bioconjugation studies.
BCN-OH (endo-9-Hydroxymethylbicyclo[6.1.0]non-4-yne) is an alcohol-functionalized cyclooctyne derivative that serves as a precursor for the synthesis of various bioconjugation probes, including BCN-TPP. It facilitates the construction of targeted probes through coupling reactions with carboxyl-containing compounds, such as TPP-COOH. Additionally, BCN-OH functions as a control reagent for experiments involving BCN-TPP, providing a valuable tool for researchers in chemical biology and bioconjugation studies.
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