Cyanine7 DBCO
Cat. # | Quantity | Price | Lead time | Buy this product |
---|---|---|---|---|
A50F0 | 1 mg | $125 | in stock | |
B50F0 | 5 mg | $260 | in stock | |
C50F0 | 10 mg | $325 | in stock | |
D50F0 | 25 mg |
$510
|
in stock | |
E50F0 | 50 mg |
$895
|
in stock | |
F50F0 | 100 mg |
$1490
|
in stock |
Cyanine7 DBCO is a NIR fluorescent dye with cycloalkyne moiety for the conjugation with azides by means of copper-free, strain-promoted alkyne-azide cycloaddition (SPAAC).
Azodibenzocyclooctyne (DBCO or ADIBO) fragment is a stable but active cycloalkyne that reacts very rapidly with azides.
Absorption and emission spectra of Cyanine7 fluorophore

Customers also purchased with this product
sulfo-Cyanine7 tetrazine
Near infrared, water soluble dye methyltetrazine for the conjugation with strained cycloalkenes in TCO ligation reaction.AMCA azide
Azide derivative of AMCA fluorescent dye for сlick сhemistry. AMCA is one of the brightest blue fluorescent dyes with large Stoke's shift and high resistance to photobleaching.TAMRA azide, 5-isomer
Azide derivative of TAMRA fluorescent dye for сlick chemistry.General properties
Appearance: | dark green solid |
Mass spec M+ increment: | 849.5 |
Molecular weight: | 885.62 |
CAS number: | 2692677-77-1 |
Molecular formula: | C58H65N4ClO2 |
Solubility: | good in DMF, DMSO, DCM |
Quality control: | NMR 1H, HPLC-MS (95%) |
Storage conditions: | Storage: 12 months after receival at -20°C in the dark. Transportation: at room temperature for up to 3 weeks. Avoid prolonged exposure to light. Desiccate. |
MSDS: | Download |
Product specifications |
Spectral properties
Excitation/absorption maximum, nm: | 750 |
ε, L⋅mol−1⋅cm−1: | 199000 |
Emission maximum, nm: | 773 |
Fluorescence quantum yield: | 0.3 |
Product citations
- Park, J. S.; Lim, Y. G.; Park, K. Novel Bidentate β-Glutamic Acid-Based Bone-Targeting Agents for in Vivo Bone Imaging. Journal of Industrial and Engineering Chemistry, 2022, 110, 471–478. doi: 10.1016/j.jiec.2022.03.021
- Jäger, E.; Humajová, J.; Dölen, Y.; Kučka, J.; Jäger, A.; Konefał, R.; Pankrác, J.; Pavlova, E.; Heizer, T.; Šefc, L.; Hrubý, M.; Figdor, C. G.; Verdoes, M. Enhanced Antitumor Efficacy through an “AND Gate” Reactive Oxygen-Species-Dependent PH-Responsive Nanomedicine Approach. Advanced Healthcare Materials, 2021, 10(13), 2100304. doi: 10.1002/adhm.202100304
- Islam, M.R.; Nguy, C.; Pandit, S.; Lyon, L.A. Design and Synthesis of Core–Shell Microgels with One‐Step Clickable Crosslinked Cores and Ultralow Crosslinked Shells. Macromolecular Chemistry and Physics, 2020, 221(19), 2000156. doi: 10.1002/macp.202000156
- Alberg, I.; Kramer, S.; Schinnerer, M.; Hu, Q.; Seidl, C.; Leps, C.; Drude, N.; Möckel, D.; Rijcken, C.; Lammers, T.; Diken, M.; Maskos, M.; Morsbach, S.; Landfester, K.; Tenzer, S.; Barz, M.; Zentel, R. Polymeric Nanoparticles with Neglectable Protein Corona. Small, 2020, 16(18), 1907574. doi: 10.1002/smll.201907574
Short link - lumiprobe.com/sh/p/3F
The count of items is incorrect.
