
C7-Indocyanine
| Catalog Number | F02-0040 |
| Category | Other Cyanine |
| Molecular Formula | C31H37N2.I |
| Molecular Weight | 564.55 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
C7-Indocyanine is a pharmaceutical tool widely used in biomedical research. With its near-infrared fluorescence properties, it acts as a vital contrast agent for both in vivo imaging and optical diagnostics. C7-Indocyanine is extensively employed for targeting and visualizing tumors, enabling precise surgical navigation and monitoring, effectively improving the accuracy and outcomes of cancer treatments.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Synonyms | 1-Ethyl-2-(7-(1-ethyl-3,3-dimethylindolin-2-ylidene)hepta-1,3,5-trien-1-yl)-3,3-dimethyl-3H-indol-1-ium iodide; Indotricarbocyanine (C7) dye; (2Z)-1-ethyl-2-[(2E,4E,6E)-7-(1-ethyl-3,3-dimethylindol-1-ium-2-yl)hepta-2,4,6-trienylidene]-3,3-dimethylindole;iodide; 1-Ethyl-2-(7-(1-ethyl-3,3-dimethylindolin-2-ylidene)hepta-1,3,5-trien-1-yl)-3,3-dimethyl-3H-indol-1-iumiodide; 1-ethyl-2-[7-(1-ethyl-3,3-dimethyl-1,3-dihydro-2H-indol-2-ylidene)hepta-1,3,5-trien-1-yl]-3,3-dimethyl-3H-indolium iodide |
| IUPAC Name | (2Z)-1-ethyl-2-[(2E,4E,6E)-7-(1-ethyl-3,3-dimethylindol-1-ium-2-yl)hepta-2,4,6-trienylidene]-3,3-dimethylindole;iodide |
| SMILES | CCN1C2=CC=CC=C2C(C1=CC=CC=CC=CC3=[N+](C4=CC=CC=C4C3(C)C)CC)(C)C.[I-] |
| InChI | InChI=1S/C31H37N2.HI/c1-7-32-26-20-16-14-18-24(26)30(3,4)28(32)22-12-10-9-11-13-23-29-31(5,6)25-19-15-17-21-27(25)33(29)8-2;/h9-23H,7-8H2,1-6H3;1H/q+1;/p-1 |
| InChIKey | MOCQTYXDGSDJGM-UHFFFAOYSA-M |
Product Specification
| Excitation | 743 |
| Emission | 771 |
| 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. |
Application
C7-Indocyanine is a near-infrared indocyanine dye designed for fluorescence labeling and optical tracking in research workflows where reduced background from biological autofluorescence is desirable. Its indocyanine scaffold supports strong fluorescence in the NIR region and is commonly leveraged to prepare fluorescent conjugates for imaging, tracing, and fluorescence-based assays. Researchers typically use C7-Indocyanine as a dye component for constructing NIR fluorescent reagents compatible with common fluorescence imaging instrumentation.
1. NIR Fluorescence Labeling
C7-Indocyanine is used by chemical biology and imaging groups to generate near-infrared fluorescent labeling reagents for proteins, polymers, and other macromolecular targets. In practice, it is incorporated into fluorescent conjugates used for localization and tracking studies where NIR emission helps improve contrast relative to visible fluorophores. Teams preparing labeled biomaterials, probe libraries, or imaging standards often select indocyanine dyes like C7-Indocyanine to match NIR detection channels on benchtop fluorescence imagers and microscopy systems.
2. Fluorescence Imaging Tracing
C7-Indocyanine supports fluorescence imaging and tracer experiments in cell and materials research laboratories that monitor signal distribution over time. Investigators use C7-Indocyanine-based fluorescent constructs to visualize uptake, diffusion, and retention in labeled systems, including labeled nanoparticles, polymer matrices, and surface-modified materials. The NIR emission profile makes it a common choice for optical imaging workflows where light scattering and background from endogenous fluorophores can complicate visible-channel readouts.
3. Fluorescence-Based Bioassays
C7-Indocyanine is applied in fluorescence assay development as a dye reporter for monitoring binding, immobilization, or interaction-driven changes in fluorescence intensity. Assay developers incorporate indocyanine-based labels into conjugate formats used in plate-based or instrument-based fluorescence readouts, including workflows where NIR detection is used to reduce interference from assay components. This makes C7-Indocyanine a practical reagent for building fluorescence reagents for screening and characterization of labeled biomolecular or material interactions.
4. NIR FRET Pair Construction
C7-Indocyanine is also used by fluorescence technology developers to assemble NIR FRET systems by pairing the indocyanine donor with compatible acceptor fluorophores. In these applications, C7-Indocyanine-containing conjugates are positioned within distance-dependent architectures such as labeled biomolecules, polymers, or engineered probe constructs to translate molecular proximity into a fluorescence readout. Researchers developing FRET-based molecular imaging reagents and fluorescence sensing platforms often choose C7-Indocyanine to access NIR excitation/emission channels for reduced background in optical measurements.
Computed Properties
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 6 |
| Exact Mass | 564.20015 g/mol |
| Monoisotopic Mass | 564.20015 g/mol |
| Topological Polar Surface Area | 6.2Ų |
| Heavy Atom Count | 34 |
| Formal Charge | 0 |
| Complexity | 784 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 4 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 2 |
| Compound Is Canonicalized | Yes |
Recommended Services
Recommended Articles
- Hoechst Dyes: Definition, Structure, Mechanism and Applications
- Mastering the Spectrum: A Comprehensive Guide to Cy3 and Cy5 Dyes
- Fluorescent Probes: Definition, Structure, Types and Application
- Fluorescent Dyes: Definition, Mechanism, Types and Application
- Coumarin Dyes: Definition, Structure, Benefits, Synthesis and Uses
- Unlocking the Power of Fluorescence Imaging: A Comprehensive Guide
- Cell Imaging: Definitions, Systems, Protocols, Dyes, and Applications
- Lipid Staining: Definition, Principles, Methods, Dyes, and Uses
- Flow Cytometry: Definition, Principles, Protocols, Dyes, and Uses
- Nucleic Acid Staining: Definition, Principles, Dyes, Procedures, and Uses
Recommended Products
Online Inquiry