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Glen research/C8-TIPS-Alkyne-dC-CE Phosphoramidite/1kit/10-1541-95E

Technical Documents
Intellectual Property
Dilution/Coupling Data

Technical Documents

Safety Data Sheet

Glen Report 22.11: Simple Oligonucleotide Modification using Click Chemistry

Glen Report 22.12: The copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC)

Glen Report 23.13: New Products – Click Chemistry Update

Glen Report 24.26: Advances in copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC): Introducing Oligo-Click Kits

Glen Report 28.21: Versatile Applications of the Copper(I)-Catalyzed Click Chemistry


The copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) reaction between azides and alkynes to form 1,2,3-triazoles, as reported1 by Sharpless, was found to be so exquisitely regioselective and efficient at even the most mild conditions that Sharpless coined the term ‘Click Chemistry" to describe it.The use of this method for DNA modification has been somewhat delayed by the fact that copper ions damage DNA, typically yielding strand breaks.2 As these problems have now been overcome by the use of copper(I)-stabilizing ligands (e.g., tris(benzyltriazolylmethyl)amine, TBTA3), Carell et al. and Seela et al. discovered that the CuAAC reaction can be used to functionalize alkyne-modified DNA nucleobases with extremely high efficiency.4 Oligonucleotides bearing a single nucleosidic alkyne group can be prepared usinga C8-Alkyne-dC or dT-CE Phosphoramidite.Purified oligonucleotides are usually modified with 2-5 equivalents of the corresponding marker-azide (e.g., fluorescent-dye azides). After the addition of precomplexed Cu(I), complete conversion to the labelled oligo is observed in a time span between 30 min and 4 hours. After a simple precipitation step, labelled oligonucleotides can be recovered in near quantitative yields. Using a combination of C8-Alkyne, C8-TIPS-Alkyne and C8-TMS-Alkyne, it is possible to label oligonucleotides in up to three separate click reactions. The alkyne groups on the last two monomers are protected, respectively, with triisopropylsilyl (TIPS) and trimethylsilyl (TMS) protecting groups.5,6The first click reaction on solid phase on a C8-Alkyne yields the singly modified oligonucleotide with full retention of the TIPS and/or TMS protecting group.For double click, a C8-TIPS-Alkyne is used as the second nucleoside and the TIPS protecting group is cleaved with tetrabutylammonium fluoride (TBAF) without causing any damage to the DNA.The second click reaction in solution yields the doubly modified oligonucleotide in excellent yield. For the introduction of three different labels, all three nucleosides are introduced into oligonucleotides. The first click reaction is performed directly on the resin. The singly modified oligonucleotide is subsequently cleaved from the support with concomitant cleavage of the TMS group and retention of the TIPS protecting group. The second click reaction is performed in solution. Precipitation of the doubly modified oligonucleotide, cleavage of the TIPS group with TBAF, and a subsequent third click reaction in solution furnishes the desired triply modified oligonucleotide in excellent overall yield.



  • Coupling: 3 minute coupling time recommended.
  • Deprotection: Ammonium hydroxide for 2 hours at 55°C or as required by nucleobases. Note: Deprotection in AMA (50:50 Ammonium hydroxide/MethylAmine) may result in about 5% N4-methyl-dC side product at the modification site.|TIPS removal: After deprotection, dry down oligo and take up in 0.5 mL DMF.Add 0.1 mL TBAF. Vortex and keep at 45°C for 15 minutes.Quench with 0.5 mL 2 M TEAA and desalt on Glen Gel-Pak™ column or equivalent.
DiluentAnhydrous Acetonitrile
StorageFreezer storage, -10 to -30�C, dry
Stability1-2 days

Intellectual Property

baseclick GmbH has been granted the following patents (1-3) besides its further patent applications (4-5). |1. WO  2006/117161  (New  labelling  strategies  for  the  sensitive detection of analytes)|2. WO 2008/952775 (Click chemistry for the production of reporter molecules)|3. WO 2010/115957 (Click Chemistry on heterogeneous catalysts)|4. PCT/EP 2013/064610 (Anandamide-modified nucleic molecules)|5. PCT/EP 2015/056007 (Self-assembly of DNA Origami: a diagnostic tool)|baseclick GmbH holds a worldwide exclusive license for granted patent application|WO 03/101972 (Copper-catalysed ligation of azides and acetylenes  for  the  nucleic  acid field) in the area of diagnostics and research. As Glen Research and baseclick are partners, Glen Research is now able to help in sublicensing this outstanding technology.

Dilution/Coupling Data

The table below show pack size data and, for solutions, dilution and approximate coupling based on normal priming procedures.

ABI 392/394

Catalog #Pack SizeGrams/Pack0.1M Dil. (mL)Approximate Number of Additions
10-1541-020.25 g.25grams2.2862.6737.623.517.0912.533.13
10-1541-90100 µmol.109grams120127.55.4541
10-1541-9550 µmol.055grams0.53.3321.250.910.670.17


Catalog #Pack SizeGrams/PackDilution (mL)Approximate Number of Additions
10-1541-020.25 g.25grams3.410.0761.838.6328.093.86
10-1541-90100 µmol.109grams1.50.0723.614.7510.731.48
10-1541-9550 µmol.055grams0.750.078.65.383.910.54