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Tris[(1-benzyl-1H-1,2,3-triazol-4-yl)methyl]amine (TBTA), 100 mg, 100 mg

From  baseclick
≥95 %, baseclick Grade
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TBTA
Empirical formula C30H30N10
Molar mass (M) 530,63 g/mol
Melting point (mp) 143 °C
Storage temp. -20 °C
Transport temp. cooled
WGK 1
CAS No. 510758-28-8

"baseclick-grade" ligand in high quality for optimal yield in organic solution
If you want to perform click reactions in organic media using e.g. CuBr as catalytic source, TBTA is the right ligand to use. It speeds-up the reactions plus maintaining the Cu(I) oxidation state of the copper source to protect your biomolecules from damage and degradation.

€160.20/Pack Qty. 

excl. VAT. | 100 mg per Pack Qty.

Art. No. 7814.4

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Tris[(1-benzyl-1H-1,2,3-triazol-4-yl)methyl]amine (TBTA)
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Art. No. Pack Qty. Pack. Packaging Price Quantity
7814.1 5 mg plastic 5 mg

€33.25

7814.2 10 mg plastic 10 mg

€51.50

7814.4 100 mg plastic 100 mg

€160.20

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Downloads / MSDS

General information

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.


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.


Certificates of Analysis

You can search for and download your certificate of analysis for the selected product here. Please provide your batch number.
The following analysis certificates have been found:

Type analysis

Appearancewhite to off-white powder
Assay (H-NMR)≥95 %