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About This Item
Empirical Formula (Hill Notation):
C11H12N2O5
CAS Number:
Molecular Weight:
252.22
MDL number:
UNSPSC Code:
12352208
NACRES:
NA.22
Assay:
95%
Form:
powder
Quality Level
assay
95%
form
powder
manufacturer/tradename
(BCN-001)
mp
206 °C
storage temp.
−20°C
SMILES string
OC[C@@H]1[C@@H](O)C[C@H](N2C(NC(C(C#C)=C2)=O)=O)O1
InChI
1S/C11H12N2O5/c1-2-6-4-13(11(17)12-10(6)16)9-3-7(15)8(5-14)18-9/h1,4,7-9,14-15H,3,5H2,(H,12,16,17)/t7-,8+,9+/m0/s1
InChI key
CDEURGJCGCHYFH-DJLDLDEBSA-N
General description
5-Ethynyl-2′-deoxyuridine (EdU) is a thymidine analogue that can be incorporated into cellular DNA for cell proliferation studies. The incorporated nucleoside analogue can be detected by a copper-catalyzed click reaction with a fluorescent azide.
Application
5-Ethynyl-2′-deoxyuridine (EdU) is used for:
For a listing of the Baseclick kits see: Baseclick kits
- Labeling newly synthesized DNA during replication
- Cell proliferating assay studies
- Cell cycle analysis
For a listing of the Baseclick kits see: Baseclick kits
signalword
Danger
hcodes
Hazard Classifications
Muta. 1B - Repr. 2
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Synthesis, susceptibility to enzymatic phosphorylation, cytotoxicity and in vitro antiviral activity of lipophilic pyrimidine nucleoside/carborane conjugates.
Bialek-Pietras M, et al.
Journal of Organometallic Chemistry, 865, 166-172 (2018)
Click chemistry as a reliable method for the high-density postsynthetic functionalization of alkyne-modified DNA.
Gierlich J, et al.
Organic Letters, 8(17), 3639-3642 (2006)
Site-directed spin-labeling of nucleic acids by click chemistry: detection of abasic sites in duplex DNA by EPR spectroscopy.
Jakobsen A, et al.
Journal of the American Chemical Society, 132(30), 10424-10428 (2010)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 900584-500MG | 04061833250372 |
| 900584-50MG | 04061833250389 |
