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DBCO-C6-Alkyne, 5 mg

Van  baseclick
≥95 %
Icon_Kuehltransport The products marked accordingly are shipped refrigerated in special, sustainable cooling boxes with cooling packs or dry ice.
VE
Verp.
Empirical formula C24H22N2O2
Molar mass (M) 370,45 g/mol
Storage temp. -20 °C
Transport temp. cooled
WGK 1

The heterobifunctional linker DBCO-C6-Alkyne contains an Alkyne and a DBCO moiety which enable the possibility to perform two sequential click reactions in an orthogonal way. Therefore this linker offers a great potential to cross link to azide containg biomolecules by just using high efficient Click Chemistry. There is also the possibility to selectively click the alkyne before the DBCO [1]. Therefore this linker offers great potential for the synthesis of Antibody-drug-conjugates (ADC).
Bifunctional linker

102,15 €/VE 

Excl. btw | 5 mg Per VE

Bestelnr. 259H.1

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Voor dit artikel gelden extra transportkosten.
Vanaf 6 VE 97,04 €/VE
Vanaf 24 VE 91,94 €/VE
DBCO-C6-Alkyne
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Bestelnr. VE Verp. Prijs Hoeveelheid
259H.1 5 mg plastic

102,15 €

259H.2 10 mg plastic

170,95 €

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Downloads / MSDS

Algemene informatie

Click Chemistry

The copper(I)-catalysed azide-alkyne cycloaddition (CuAAC) is the most prominent example of a group of reactions named click reactions. According to Sharpless’ definition, these reactions are characterised by high yields, mild reaction conditions, and by their tolerance of a broad range of functional groups.[1-3] Typically, the reactions require simple or no workup or purification of the product. The most important characteristic of the CuAAC reaction is its unique bioorthogonality as neither azide nor terminal alkyne functional groups are generally present in natural systems.


References:
1 H. C. Kolb, M.G. Finn, K. B. Sharpless, Angew. Chem. Int. Ed. 2001, 40, 2004-2021.
2 C.W. Tornoe, C. Christensen, M. Meldal, J. Org. Chem. 2002, 67, 3057-3064.
3 V. V. Rostovtsev, L. G. Green, V. V. Fokin, K. B. Sharpless, Angew. Chem. 2002, 114, 2708-2711; Angew. Chem. Int. Ed. 2002, 41, 2596-2599.


Click Chemistry

In recent years, click chemistry has become increasingly important and steadily more popular in research and development. The reasons for this are not only the easy handling and the high yields but also the countless application possibilities. Carl ROTH offers you the possibility to purchase the broad portfolio of click reagents, various kits for EdU-based cell proliferation assays and numerous other applications from the well-known brand baseclick. This enables us to offer you a necessary and comprehensive assortment for click chemistry.


Tip:

Consumer Notice:

aqueous media: copper(II) sulfate 7816, sodium ascorbate 7819, THPTA 7822organic solvents (e.g. DMSO): Copper(I) bromide 7813, TBTA 7814 (copper stabilizing ligand)


Reagents for Click Chemistry

Starting from diverse copper catalyst sources, over Cu(I) stabilising ligands to buffer additives and solvents, you will find all necessary reagents in the special ROTI®Click quality to perform your click reactions here.


Linker

Linker

Click chemistry opens the door to introduce polyethylene glycols (PEGs) or other linkers in very sophisticated manner into your sample, which are still active for following reaction by the means of amine, carboxyl, malemide or NHS-functional terminal groups. You can choose between alkyne and azide structured PEGs and linkers which you find in the table below.


Analysecertificaten

Hier kunt u uw analysecertificaat voor het geselecteerde product zoeken en downloaden. Geef een chargenummer op.
De volgende analysecertificaten werden gevonden:

Type analysis

Appearanceslightly grey solid
Purity (HPLC)≥95 %