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Medchemexpress LLC 1-Piperidinyloxy, 4-azido-2,2,6,6-tetramethyl- | 63697-61-0 | C9H17N4O | 25 MG
SDP

Catalog No. 5000374274
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N3-TEMPO is a click chemistry reagent containing an azide group. It can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups, and ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups. Click chemistry is utilized in many research fields due to its high yield, high specificity, and simplicity, and has great potential for use in binding between nucleic acids, lipids, proteins, and other molecules.

  • Contains an azide group
  • Undergoes copper-catalyzed azide-alkyne cycloaddition with alkyne groups
  • Undergoes ring strain-promoted alkyne-azide cycloaddition with DBCO or BCN groups
  • Utilized for high yield, high specificity, and simplicity in click chemistry
  • Potential for binding between nucleic acids, lipids, proteins, and other molecules

Catalog No. 50-003-74274 Supplier Medchemexpress LLC Supplier No. 25MGHY151847
May include imposed supplier surcharges.
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N3-TEMPO is a click chemistry reagent containing an azide group. It can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups, and ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups. Click chemistry is utilized in many research fields due to its high yield, high specificity, and simplicity, and has great potential for use in binding between nucleic acids, lipids, proteins, and other molecules.

  • Contains an azide group
  • Undergoes copper-catalyzed azide-alkyne cycloaddition with alkyne groups
  • Undergoes ring strain-promoted alkyne-azide cycloaddition with DBCO or BCN groups
  • Utilized for high yield, high specificity, and simplicity in click chemistry
  • Potential for binding between nucleic acids, lipids, proteins, and other molecules

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