
Cyanine7.5 azide
| Catalog Number | F02-0020 |
| Category | Cyanine7.5 |
| Molecular Formula | C48H55ClN6O |
| Molecular Weight | 767.44 |
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Product Introduction
Cyanine7.5 is a NIR dye with long-wave infrared fluorescence. This derivative is azide for Click Chemistry.Can be used for the construction of various labeled biomolecules containing Cyanine7.5, near infrared fluorescent dye, and an improved analog of Cy7.5®. These conjugates can take advantage of NIR tissue transparency when used for in vivo imaging. This fluorophore is also useful for other fluorescent applications, especially requiring low fluorescent background.Azide is available as DMSO solution, ready for general Click Chemistry labeling protocol, or in solid form for custom labeling applications.
Chemical Information
Product Specification
Application
Computed Properties
Patents
Chemical Information
| Purity | NMR 1H, HPLC-MS (95%) |
| IUPAC Name | N-(3-azidopropyl)-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]hexanamide;chloride |
| SMILES | CC1(C(=[N+](C2=C1C3=CC=CC=C3C=C2)C)C=CC4=CC(=CC=C5C(C6=C(N5CCCCCC(=O)NCCCN=[N+]=[N-])C=CC7=CC=CC=C76)(C)C)CCC4)C.[Cl-] |
| InChI | InChI=1S/C48H54N6O.ClH/c1-47(2)42(53(5)40-26-24-36-17-8-10-19-38(36)45(40)47)28-22-34-15-13-16-35(33-34)23-29-43-48(3,4)46-39-20-11-9-18-37(39)25-27-41(46)54(43)32-12-6-7-21-44(55)50-30-14-31-51-52-49;/h8-11,17-20,22-29,33H,6-7,12-16,21,30-32H2,1-5H3;1H |
| InChIKey | FPZSVKZEBJWZOE-UHFFFAOYSA-N |
| Solubility | soluble in organic solvents (DMSO, DMF, dichloromethane), low solubility in water |
| Appearance | green powder / solution |
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 azide is a cyanine-family near-infrared fluorescent dye equipped with an azide functional group for bioorthogonal click chemistry labeling. In conjugation workflows, the azide enables rapid attachment to alkyne-bearing biomolecules, linkers, and surfaces, producing fluorescent conjugates for imaging and quantitative fluorescence readouts. Its far-red spectral character supports low-background visualization in microscopy and fluorescence-based assays where red/NIR channels are preferred.
1. Biomolecule Labeling
Cyanine7.5 azide is used to generate fluorescently labeled proteins, peptides, and other biomolecules via azide-alkyne click conjugation with alkyne-tagged targets or labeling scaffolds. Researchers employ the resulting Cyanine7.5 conjugates in fluorescence imaging and binding studies where near-infrared detection helps separate signal from autofluorescence. This reagent format is also common in chemical biology workflows that require modular dye installation onto sensitive biomolecules while maintaining compatibility with downstream purification and assay handling.
2. Fluorescence Imaging Probes
Cyanine7.5 azide serves as a dye-building block for constructing imaging probes and multicomponent fluorescent reagents, including conjugates used in cellular and molecular microscopy experiments. By clicking the azide dye onto alkyne-functional probe backbones, investigators can tune labeling density and probe architecture while keeping the fluorescent reporter constant. The far-red emission profile is particularly useful for imaging configurations that collect red/NIR channels to improve contrast in complex biological samples.
3. Surface And Material Functionalization
Cyanine7.5 azide is applied in biomaterials and surface engineering to create fluorescently trackable coatings, nanoparticles, and polymer-modified materials through click attachment to alkyne-functional surfaces or carriers. Teams in materials science and industrial research use these Cyanine7.5-labeled materials to monitor surface coverage, track material localization, and support fluorescence-based characterization of engineered interfaces. The azide handle enables straightforward incorporation of the dye into functional materials without requiring dye redesign for each platform.
4. Fluorescence-Based Bioassays
Cyanine7.5 azide is used to prepare fluorescent conjugates for plate-based and cuvette-based fluorescence assays, including labeling reagents for binding assays and reporter conjugates in assay development. After click conjugation to alkyne-bearing assay components, the resulting near-infrared dye conjugates provide a consistent fluorescent reporter for signal readout on standard fluorescence instrumentation with appropriate far-red excitation/emission settings. This approach is frequently chosen when a modular labeling strategy is needed to standardize reagent performance across multiple assay formats.
Computed Properties
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 13 |
| Exact Mass | 766.4125881 g/mol |
| Monoisotopic Mass | 766.4125881 g/mol |
| Topological Polar Surface Area | 49.7Ų |
| Heavy Atom Count | 56 |
| Formal Charge | 0 |
| Complexity | 1590 |
| 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 | 2 |
| Compound Is Canonicalized | Yes |
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| US-2014283896-A1 | Transparent Energy-Harvesting Devices | 2013-03-21 |
| WO-2015143038-A1 | Transparent energy-harvesting devices | 2013-03-21 |
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