
sulfo-Cyanine7.5 maleimide
| Catalog Number | F03-0021 |
| Category | sulfo-Cyanine7.5 |
| Molecular Formula | C51H51N4K3O15S4 |
| Molecular Weight | 1205.52 |
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Product Introduction
sulfo-Cyanine7.5 is a near infrared fluorophore with absorption and emission ranges around 800 nm. Its spectral properties allow for the efficient leveraging of tissue NIR transparency window. The fluorophore is available as different reactive forms, this one is maleimide for the labeling of SH groups of proteins and peptides. The sulfo-version is highly hydrophilic.Such labeled biomolecules are useful in biodistribution studies and visualization in intact organisms.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Synonyms | Sulfo-Cyanine7.5 |
| Purity | NMR 1H, HPLC-MS (95%) |
| IUPAC Name | tripotassium;3-[6-[2-(2,5-dioxopyrrol-1-yl)ethylamino]-6-oxohexyl]-1,1-dimethyl-2-[2-[3-[2-(1,1,3-trimethyl-6,8-disulfonatobenzo[e]indol-3-ium-2-yl)ethenyl]cyclohex-2-en-1-ylidene]ethylidene]benzo[e]indole-6,8-disulfonate |
| SMILES | CC1(C(=[N+](C2=C1C3=C(C=C2)C(=CC(=C3)S(=O)(=O)[O-])S(=O)(=O)[O-])C)C=CC4=CC(=CC=C5C(C6=C(N5CCCCCC(=O)NCCN7C(=O)C=CC7=O)C=CC8=C6C=C(C=C8S(=O)(=O)[O-])S(=O)(=O)[O-])(C)C)CCC4)C.[K+].[K+].[K+] |
| InChI | InChI=1S/C51H54N4O15S4.3K/c1-50(2)43(53(5)39-17-15-35-37(48(39)50)27-33(71(59,60)61)29-41(35)73(65,66)67)19-13-31-10-9-11-32(26-31)14-20-44-51(3,4)49-38-28-34(72(62,63)64)30-42(74(68,69)70)36(38)16-18-40(49)54(44)24-8-6-7-12-45(56)52-23-25-55-46(57)21-22-47(55)58;;;/h13-22,26-30H,6-12,23-25H2,1-5H3,(H4-,52,56,59,60,61,62,63,64,65,66,67,68,69,70);;;/q;3*+1/p-3 |
| InChIKey | LPYYYGPYGCVNAA-UHFFFAOYSA-K |
| Solubility | good in water, DMF, DMSO |
| 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
Sulfo-Cyanine7.5 maleimide is a water-soluble, thiol-reactive cyanine dye designed for fast, covalent labeling of biomolecules through maleimide-cysteine/thiol coupling. Its near-infrared fluorescence is commonly leveraged for low-background imaging and fluorescence-based tracking in aqueous biological workflows, including conjugate preparation for microscopy and assay development.
1. Protein And Peptide Labeling
Sulfo-Cyanine7.5 maleimide is frequently used by bioconjugation groups to generate fluorescent protein and peptide conjugates for fluorescence imaging and quantitative assays. Researchers typically label accessible cysteine residues on purified proteins, antibody fragments, enzymes, or synthetic peptides to create NIR fluorescent tracers for binding studies, reagent characterization, and downstream assay readouts. The sulfonated dye improves handling in aqueous buffers, supporting workflows where conjugates must remain soluble during labeling, purification, and assay incubation.
2. Antibody Conjugate Imaging
Sulfo-Cyanine7.5 maleimide supports fluorescent antibody conjugate development for microscopy and flow-based characterization of labeled binding reagents. In research settings, it is used to attach cyanine7.5 fluorophores to thiol-bearing antibody formats (for example, after controlled reduction to expose cysteines), enabling visualization of antigen-binding reagents and comparative studies of labeling density across antibody lots. The maleimide handle provides a practical route to produce NIR imaging reagents that are compatible with common fluorescence imaging platforms used for binding validation and reagent screening.
3. Cell Surface Thiol Labeling
Sulfo-Cyanine7.5 maleimide is used in cellular imaging workflows where thiol-reactive labeling is employed to tag cell-surface or membrane-associated biomolecules containing accessible cysteine residues. Laboratories often apply the reagent to generate fluorescent cell-associated tracers for microscopy-based localization studies and for monitoring relative labeling patterns across experimental conditions. The dye's near-infrared emission helps reduce interference from autofluorescence in many biological samples, which is advantageous when imaging in complex media or when background suppression is important.
4. NIR Fluorescent Tracer Conjugates
Sulfo-Cyanine7.5 maleimide is also used to prepare NIR fluorescent tracer conjugates for materials and biomolecule tracking studies, including fluorescent labeling of thiol-functionalized linkers, polymers, and biomaterial components. Researchers incorporate the dye into conjugates that are subsequently used to follow transport, distribution, or association in fluorescence imaging experiments, or to create labeled reagents for assay development. The maleimide functionality enables straightforward attachment to thiol-containing building blocks, supporting modular construction of fluorescent tracer systems used across chemical biology and biomaterials research.
Computed Properties
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 16 |
| Rotatable Bond Count | 15 |
| Exact Mass | 1204.1144961 g/mol |
| Monoisotopic Mass | 1204.1144961 g/mol |
| Topological Polar Surface Area | 335Ų |
| Heavy Atom Count | 77 |
| Formal Charge | 0 |
| Complexity | 2890 |
| 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 | 4 |
| Compound Is Canonicalized | Yes |
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