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(2S,4S)-H-L-Pro(4-N3)-OH (hydrochloride) functions as a reagent in click chemistry. This form of chemistry is celebrated for its potential applications in the conjugation of nucleic acids, lipids, proteins, and other molecules, owing to its high yield, specificity, and simplicity. The compound features an Azide group that can undergo copper-catalyzed azide-alkyne cycloaddition reactions (CuAAC) with molecules containing Alkyne groups. Additionally, it can participate in strain-promoted azide-alkyne cycloaddition reactions (SPAAC) with molecules that possess DBCO or BCN groups.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | (2S,4S)-H-L-Pro(4-N3)-OH (hydrochloride) functions as a reagent in click chemistry. This form of chemistry is celebrated for its potential applications in the conjugation of nucleic acids, lipids, proteins, and other molecules, owing to its high yield, specificity, and simplicity. The compound features an Azide group that can undergo copper-catalyzed azide-alkyne cycloaddition reactions (CuAAC) with molecules containing Alkyne groups. Additionally, it can participate in strain-promoted azide-alkyne cycloaddition reactions (SPAAC) with molecules that possess DBCO or BCN groups. |
| Formula | C5H9ClN4O2 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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