Cyanine7 amine

Cyanine7 Amines Near infrared (NIR) imaging
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 amine
Cyanine7 amine
Cyanine7 amine
Structure of Cyanine7 amine
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Cyanine7 absorbance and emission spectra

Cyanine7 absorbance and emission spectra

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Cyanine3 amine

Cyanine3 is an fluorophore with free amino group (amino-dye). It can be conjugated with NHS esters, carboxy groups (after activation), and epoxides.

sulfo-Cyanine7 amine

NIR dye amine, sulfonated derivative of Cyanine7 dye, for the modification via enzymatical transamination.

TAMRA NHS ester, 5-isomer

Amine-reactive, activated N-hydroxysuccinimidyl ester of TAMRA dye for the labeling of amine groups of proteins, peptides, and amino-oligonucleotides. Pure 5-isomer.

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. 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
  2. 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
  3. 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
  4. Agnello, L.; Tortorella, S.; d’Argenio, A.; Carbone, C.; Camorani, S.; Locatelli, E.; Auletta, L.; Sorrentino, D.; Fedele, M.; Zannetti, A.; Franchini, M.C.; Cerchia, L. Optimizing cisplatin delivery to triple-negative breast cancer through novel EGFR aptamer-conjugated polymeric nanovectors. Journal of Experimental & Clinical Cancer Research : CR, 2023, 40, 239. doi: 10.1186/s13046-021-02039-w
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Cy® is a trademark of GE Healthcare.
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