Cyanine7 amine

Cat. # Quantity Price Lead time
150C0 1 mg $125 in stock
250C0 5 mg $260 in stock
450C0 25 mg $510 in stock
550C0 50 mg $895 in stock
650C0 100 mg $1490 in stock
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Near-infrared dye with free amine group for the conjugation with activated esters and other reactive molecules.

Cyanine7 is a near-infrared dye, an analog of Cy7® which is especially suitable for live organism imaging, and demanding low-background applications.

Cyanine7 absorbance and emission spectra

Cyanine7 absorbance and emission spectra

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BDP® 558/568 DBCO

BDP 558/568 DBCO is a bright and photostable dye with emission in the yellow spectrum range. It contains a cyclooctyne substituting group (i.e. DBCO), which can react with various azides in Click Chemistry reactions.

Cyanine7 DBCO

NIR fluorescent dye functionalized with cyclooctyne moiety for copper free click chemistry conjugation with azides.
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Azide-PEG4-amine

PEG4 amine azide is a bifunctional linker with amine and azide functional groups. It is based on a tetraethyleneglycol core. The length of the PEG4 linker is 1.4 nm.

General properties

Appearance: green powder
Molecular weight: 719.87
CAS number: 1650635-41-8, 1650559-73-1 [Cl-]
Molecular formula: C43H60Cl2N4O
Solubility: soluble in water (72 mM = 51 g/L), well soluble in DMSO, DMF, alcohols
Quality control: NMR 1H, HPLC-MS (95%)
Storage conditions: Storage: 24 months after receival at -20°C in the dark. Transportation: at room temperature for up to 3 weeks. Avoid prolonged exposure to light.
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
CF260: 0.022
CF280: 0.029

Product citations

  1. Smirnov, A.N.; Shevchuk, A.I.; Volkova, A.V.; Kalganov, V.D.; Solovyeva, E.V. Gold-silica plasmonic nanobones with tunable size and optical bimodality for bioimaging. Colloids and surfaces. A, Physicochemical and engineering aspects, 2024, 684, 133115. doi: 10.1016/j.colsurfa.2023.133115
  2. Ayala-Orozco, C.; Li, G.; Li, B.; Vardanyan, V.; Kolomeisky, A. B.; Tour, J. M. How to Build Plasmon-Driven Molecular Jackhammers That Disassemble Cell Membranes and Cytoskeletons in Cancer. Advanced Materials, 2024, 36(14), 2309910. doi: 10.1002/adma.202309910
  3. Pytlíková, S.; Pechar, M.; Chytil, P.; Studenovský, M.; Pola, R.; Kotrchová, L.; Konefał, R.; Čtveráčková, L.; Laga, R.; Pankrác, J.; Gao, S.; Jiang, B.; Yang, K.; Fang, J.; Filipová, M.; Etrych, T. Highly hydrophilic methacrylamide-based copolymers as precursors for polymeric nanomedicines containing anthracyclines. European Polymer Journal, 2024, 205, 112756. doi: 10.1016/j.eurpolymj.2024.112756
  4. Ayala-Orozco, C.; Galvez-Aranda, D.; Corona, A.; Seminario, J. M.; Rangel, R.; Myers, J. N.; Tour, J. M. Molecular Jackhammers Eradicate Cancer Cells by Vibronic-Driven Action. Nature Chemistry, 2023. doi: 10.1038/s41557-023-01383-y
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