
Cyanine7.5 tetrazine
| Catalog Number | R08-0010 |
| Category | Tetrazines |
| Molecular Formula | C55H58N7BF4O |
| Molecular Weight | 919.9 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
Cyanine7.5 tetrazine for tetrazine ligation contains a near infrared fluorophore suitable for in vivo imaging.Absorption and emission spectra of Cyanine7.5 are similar to ICG (indocyanine green), but Cyanine7.5 is significantly brighter.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Purity | NMR 1H, HPLC-MS (95%) |
| IUPAC Name | 6-[1,1-dimethyl-2-[2-[3-[2-(1,1,3-trimethylbenzo[e]indol-3-ium-2-yl)ethenyl]cyclohex-2-en-1-ylidene]ethylidene]benzo[e]indol-3-yl]-N-[[4-(6-methyl-1,2,4,5-tetrazin-3-yl)phenyl]methyl]hexanamide;trifluoroborane;fluoride |
| SMILES | B(F)(F)F.CC1=NN=C(N=N1)C2=CC=C(C=C2)CNC(=O)CCCCCN3C4=C(C5=CC=CC=C5C=C4)C(C3=CC=C6CCCC(=C6)C=CC7=[N+](C8=C(C7(C)C)C9=CC=CC=C9C=C8)C)(C)C.[F-] |
| InChI | InChI=1S/C55H57N7O.BF3.FH/c1-37-57-59-53(60-58-37)43-26-22-40(23-27-43)36-56-50(63)21-8-7-13-34-62-47-31-29-42-18-10-12-20-45(42)52(47)55(4,5)49(62)33-25-39-16-14-15-38(35-39)24-32-48-54(2,3)51-44-19-11-9-17-41(44)28-30-46(51)61(48)6;2-1(3)4;/h9-12,17-20,22-33,35H,7-8,13-16,21,34,36H2,1-6H3;;1H |
| InChIKey | TYBJGGWWXYOTON-UHFFFAOYSA-N |
| Solubility | good in DMF, DMSO, dichloromethane |
| Appearance | dark colored solid |
Product Specification
| ε, L⋅mol-1⋅cm-1 | 223000 |
| Excitation | 788 |
| Emission | 808 |
| 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. Desiccate. |
Application
Cyanine7.5 tetrazine is a tetrazine-functionalized cyanine dye designed for fast, bioorthogonal click chemistry workflows. Its extended conjugated polymethine framework supports far-red fluorescence, while the tetrazine handle enables reaction with strained trans-cyclooctenes (TCO) to generate a fluorescently labeled conjugate in situ. This combination makes it useful for constructing fluorescence imaging reagents, labeling biomolecules, and building targeted probes where rapid conjugation is advantageous.
1. Bioorthogonal Biomolecule Labeling
Cyanine7.5 tetrazine is used by chemical biology and imaging groups to label proteins, peptides, and other biomolecules that have been pre-functionalized with TCO groups. In practical workflows, researchers prepare TCO-bearing targeting ligands or biomolecule carriers (for example, affinity reagents, enzyme substrates, or scaffold proteins) and then add Cyanine7.5 tetrazine to generate fluorescent conjugates for downstream microscopy and fluorescence-based readouts. The far-red cyanine emission supports low-background imaging in complex mixtures, and the tetrazine click handle is particularly valued for rapid labeling steps that can be performed under bioconjugation-compatible conditions.
2. In Vivo-Style Imaging Probe Construction
Cyanine7.5 tetrazine is frequently employed in molecular imaging reagent development where fast fluorophore installation is required to minimize handling time and streamline probe assembly. Teams building imaging probes often use a modular strategy: a targeting component is first equipped with a TCO moiety, and Cyanine7.5 tetrazine is then used as the fluorescent reporter to produce the final conjugate immediately before imaging experiments. This approach supports iterative probe optimization in fluorescence microscopy and whole-sample fluorescence workflows, including studies that require consistent labeling across multiple samples or timepoints.
3. Fluorescent Surface and Material Functionalization
Cyanine7.5 tetrazine is also applied in biomaterials and surface chemistry workflows to introduce far-red fluorescence onto TCO-functionalized materials. Researchers use it to create fluorescently traceable coatings, labeled hydrogels, and engineered interfaces by reacting the tetrazine dye with TCO groups presented on polymer backbones, nanoparticles, or material surfaces. The resulting fluorescent materials are used for imaging-guided material characterization, tracking of biomaterial-associated components, and assay development where surface-associated fluorescence provides a convenient readout.
4. Targeted Probe Panel Development
Cyanine7.5 tetrazine supports fluorescence probe development efforts that require rapid generation of multiple labeled conjugates from a shared set of TCO-bearing precursors. In assay development and imaging method development, laboratories often prepare a panel of differently targeted or differently sized TCO constructs and then label each with the same Cyanine7.5 tetrazine reporter to standardize the fluorescent channel. This modular labeling strategy helps teams compare targeting formats while keeping the fluorophore identity consistent, which is useful when building multiplexed experimental designs or when optimizing imaging conditions across probe variants.
Computed Properties
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 12 |
| Exact Mass | 919.4732023 g/mol |
| Monoisotopic Mass | 919.4732023 g/mol |
| Topological Polar Surface Area | 86.9Ų |
| Heavy Atom Count | 68 |
| Formal Charge | 0 |
| Complexity | 1760 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 3 |
| Covalently-Bonded Unit Count | 3 |
| Compound Is Canonicalized | Yes |
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