Cyanine7 NHS ester

Cat. # Quantity Price Lead time
15020 1 mg $110.00 in stock
25020 5 mg $210.00 in stock
45020 25 mg $410.00 in stock
55020 50 mg $695.00 in stock
65020 100 mg $1190.00 in stock

Amine reactive Cyanine7, near infrared fluorescent dye, an improved analog of Cy7®.

NIR fluorophores can be used to take advantage of near infrared window of biological tissues - increased transparency of tissues in this spectral region allows to carry out in vivo imaging.

This reagent can be utilized to produce Cyanine7-labeled biomolecules for subsequent use in various in vivo research, and drug design related experiments.

The structure of Cyanine7 features rigidized design of central polymethyne chain. This molecular reinforcement allows to increase quantum yield by 20% compared with parent structure, increasing fluorescence brightness.

This reagent requires organic co-solvent for the labeling (please see Recommended Protocols section below). Water-soluble Cyanine7 NHS ester is also available, and recommended for protein NIR labeling.

Cy7 absorbance and emission spectra

Cy7 absorbance and emission spectra

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General properties

Appearance: dark green solid
Molecular weight: 733.64
CAS number: 2408482-09-5
Molecular formula: C41H48N3BF4O4
IUPAC name: 1‐{6‐[(2,5‐dioxopyrrolidin‐1‐yl)oxy]‐6‐oxohexyl}‐ 3,3‐dimethyl‐2‐[(E)‐2‐[(3E)‐3‐{2‐[(2E)‐1,3,3‐ trimethyl‐2,3‐dihydro‐1H‐indol‐2‐ ylidene]ethylidene}cyclohex‐1‐en‐1‐yl]ethenyl]‐3H‐ indol‐1‐ium tetrafluoroborate
Solubility: soluble in organic solvents (DMSO, DMF, dichloromethane), low solubility in water
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
CF260: 0.022
CF280: 0.029

Product citations

  1. Yu, J.-H.; Steinberg, I.; Davis, R.M.; Malkovskiy, A.V.; Zlitni, A.; Chung, D.T.; Curet, L.D.; D’Souza, A.L.; Jung, K.o.; Chang, E.; Campbell, J.; Frostig, H.; Park, S.-m.; Pratx, G.; Gambhir, S.S. Noninvasive and Highly Multiplexed Five-Color Tumor Imaging of Near-Infrared Resonant Surface-Enhanced Raman Nanoparticles In Vivo. ChemRxiv, preprint. doi: 10.26434/chemrxiv.13232246.v1
  2. Poreba, M.; Groborz, K.; Rut, W.; Pore, M.; Snipas, S.J.; Vizovisek, M.; Turk, B.; Kuhn, P.; Drag, M.; Salvesen, G.S. The Activome: multiplexed probing of activity of proteolytic enzymes using mass cytometry-compatible activity-based probes (TOF-probes). bioRxiv, preprint. doi: 10.1101/775627
  3. Bagheri, M.; Fens, M.H.; Kleijn, T.G.; Capomaccio, R.B.; Mehn, D.; Krawczyk, P.M.; Scutigliani, E.M.; Gurinov, A.; Baldus, M.; van Kronenburg, N.C.H.; Kok, R.J.; Heger, M.; van Nostrum, C.F.; Hennink, W.E. In Vitro and In Vivo Studies on HPMA-Based Polymeric Micelles Loaded with Curcumin. Molecular Pharmaceutics, 2021, 18(3), 1247–1263. doi: 10.1021/acs.molpharmaceut.0c01114
  4. Yang, Y.; Zhang, Q.; Zhang, J.; Chen, A.; Chen, Y.; Li, S.; Ye, M.; Xuan, X.; Li, X.; He, H.; Wu, J. Natural pollen extract for photothermal therapy. Materials & Design, 2021, 202, 109573. doi: 10.1016/j.matdes.2021.109573
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