Skip to Content
Merck
All Photos(3)

Documents

777374

Sigma-Aldrich

DBCO-Cy5

for Copper-free Click Chemistry

Synonym(s):

ADIBO-Cy5, Azadibenzocyclooctyne-Cy5, Dibenzocyclooctyne-Cy5

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C64H86N6O11S3
Molecular Weight:
1211.60
UNSPSC Code:
12171501
PubChem Substance ID:
NACRES:
NA.22

Quality Level

form

solid

reaction suitability

reaction type: click chemistry

storage temp.

−20°C

SMILES string

CC[NH+](CC)CC.O=C(CCNC(CCCCC[N+]1=C(/C=C/C=C/C=C2C(C)(C)C3=CC(S([O-])(=O)=O)=CC=C3N\2CCCS([O-])(=O)=O)C(C)(C)C4=C1C=CC(S([O-])(=O)=O)=C4)=O)N5CC6=C(C=CC=C6)C#CC7=C5C=CC=C7.CC[NH+](CC)CC

InChI

1S/C52H56N4O11S3.2C6H15N/c1-51(2)42-34-40(69(62,63)64)25-27-45(42)54(31-14-6-9-22-49(57)53-30-29-50(58)56-36-39-18-11-10-16-37(39)23-24-38-17-12-13-19-44(38)56)47(51)20-7-5-8-21-48-52(3,4)43-35-41(70(65,66)67)26-28-46(43)55(48)32-15-33-68(59,60)61;2*1-4-7(5-2)6-3/h5,7-8,10-13,16-21,25-28,34-35H,6,9,14-15,22,29-33,36H2,1-4H3,(H3-,53,57,59,60,61,62,63,64,65,66,67);2*4-6H2,1-3H3

InChI key

PNVUJAWSQCGWCT-UHFFFAOYSA-N

Application

This azadibenzocyclooctyne-cyanine dye derivative is a versatile labeling reagent for detection of azide containing molecules or compounds. Cyclooctynes are useful in strain-promoted copper-free azide-alkyne cycloaddition reactions.This dibenzocyclooctyne will react with azide-functionalized compounds or biomolecules without the need for a Cu(I) catalyst to result in a stable triazole linkage.

Solubility : DMSO, DMF
Abs/Em - 646/661 nm
Extinction Coefficient:- 251,000 cm-1M-1
This azadibenzocyclooctyne-cyanine dye derivative is a versatile labeling reagent for detection of azide containing molecules or compounds. Cyclooctynes are useful in strain-promoted copper-free azide-alkyne cycloaddition reactions.This dibenzocyclooctyne will react with azide-functionalized compounds or biomolecules without the need for a Cu(I) catalyst to result in a stable triazole linkage.

Solubility : DMSO, DMF
Abs/Em - 646/661 nm
Extinction Coefficient:- 251,000 cm-1M-1

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Yang Bo et al.
Biomaterials, 238, 119843-119843 (2020-02-18)
The early in vivo diagnosis of infectious disease foci is largely hindered by invasion and concealment of pathogens in host cells, making it difficult for conventional probes to detect and analyze intracellular pathogens. Taking advantage of the excessively produced reactive
Jianan Qiao et al.
Theranostics, 10(12), 5305-5321 (2020-05-07)
Chemo-photothermal synergistic treatment has a high potential to complement traditional cancer therapy and amplify its outcome. Precision in the delivery of these therapeutic agents to tumor cells has been indicated as being key to maximizing their therapeutic effects. Method: We
Edward S X Moh et al.
Analytical biochemistry, 584, 113385-113385 (2019-08-06)
Immunoglobulin M (IgM) type antibodies play a significant role in complement activation, cellular debris clearance and cell quality control, and have the potential to be used as a therapeutic or targeting/delivery antibody. However, this potential has not been explored thoroughly
Kirandeep K Deol et al.
Molecular cell, 80(5), 796-809 (2020-11-07)
The linkage, length, and architecture of ubiquitin (Ub) chains are all important variables in providing tight control over many biological paradigms. There are clear roles for branched architectures in regulating proteasome-mediated degradation, but the proteins that selectively recognize and process
Michael R Wasserman et al.
Cell, 178(3), 600-611 (2019-07-28)
The eukaryotic replicative helicase CMG is a closed ring around double-stranded (ds)DNA at origins yet must transition to single-stranded (ss)DNA for helicase action. CMG must also handle repair intermediates, such as reversed forks that lack ssDNA. Here, using correlative single-molecule

Articles

Copper-free click chemistry is an alternative approach to click chemistry that proceeds at a lower activation barrier and is free of cytotoxic transition metal catalysts.

Drug discovery process by utilizing chemistry reaction of Cu(I)-catalyzed Huisgen 1,3-dipolar cycloaddition of terminal alkynes with organoazides to yield 1,4-disubstituted 1,2,3-triazoles.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service