
Cyanine3 hydrazide
| Catalog Number | R05-0007 |
| Category | Hydrazides |
| Molecular Formula | C30H40Cl2N4O |
| Molecular Weight | 543.57 |
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Product Introduction
Cyanine3 hydrazide is a carbonyl-reactive dye, an analog of Cy3® hydrazide. This reagent allows to label various carbonyl-containing molecules such as antibodies and other glycoproteins after periodate oxidation, proteins which have undergone oxidative stress or deamination, or reducing saccarides. Cyanine3 is compatible with a number of fluorescent instruments.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Purity | NMR 1H and HPLC-MS (95%) |
| IUPAC Name | [6-[3,3-dimethyl-2-[3-(1,3,3-trimethylindol-1-ium-2-yl)prop-2-enylidene]indol-1-yl]hexanoylamino]azanium;dichloride |
| SMILES | CC1(C2=CC=CC=C2[N+](=C1C=CC=C3C(C4=CC=CC=C4N3CCCCCC(=O)N[NH3+])(C)C)C)C.[Cl-].[Cl-] |
| InChI | InChI=1S/C30H38N4O.2ClH/c1-29(2)22-14-8-10-16-24(22)33(5)26(29)18-13-19-27-30(3,4)23-15-9-11-17-25(23)34(27)21-12-6-7-20-28(35)32-31;;/h8-11,13-19H,6-7,12,20-21,31H2,1-5H3;2*1H |
| InChIKey | KTNWWVFMUUKQDD-UHFFFAOYSA-N |
| Solubility | moderate solubility in water, good in polar organic solvents (DMF, DMSO, alcohols) |
| Appearance | red powder |
Product Specification
| ε, L⋅mol-1⋅cm-1 | 150000 |
| Fluorescence Quantum Yield | 0.31 |
| Excitation | 555 |
| Emission | 570 |
| 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
Cyanine3 hydrazide is a fluorescent hydrazide reagent designed for conjugation workflows that rely on click-compatible coupling strategies in chemical biology and imaging. As a Cy3-based dye, it provides bright red-orange emission and is commonly used to label biomolecules, polymers, and surfaces for microscopy, tracking, and assay development. Its hydrazide functionality enables incorporation into hydrazone-forming labeling schemes and downstream conjugate construction for fluorescence-based research tools.
1. Fluorescent Biomolecule Labeling
Cyanine3 hydrazide is widely used to generate Cy3-labeled biomolecules for cell biology and biochemical assays where sensitive fluorescence readouts are required. Researchers employ it to tag proteins, peptides, and other functional ligands that will be visualized by fluorescence microscopy, flow cytometry–style workflows, or fluorescence-based binding/interaction studies. The Cy3 scaffold is particularly valued for imaging compatibility in multi-color experiments, where red-orange emission helps separate labeled targets from background autofluorescence and other fluorophores.
2. Hydrazone-Based Probe Conjugation
Cyanine3 hydrazide is commonly incorporated into hydrazone-forming labeling strategies to build fluorescent probes from carbonyl-containing handles on biomolecules and materials. This usage pattern appears frequently in molecular imaging reagent development and in platform studies that require modular attachment of a dye to an existing targeting or recognition component. By leveraging the hydrazide reactive motif, teams can prepare conjugates suitable for tracking reaction progress, monitoring biomolecular localization, or producing fluorescent standards for assay calibration.
3. Live-Cell Imaging Reagent Development
Cyanine3 hydrazide is used in the development of fluorescent imaging reagents and labeling kits for cellular studies, where dye conjugates enable visualization of uptake, trafficking, and compartmentalization of tagged components. In typical workflows, the reagent is converted into Cy3-containing conjugates that can be introduced into experimental systems to generate spatial and temporal fluorescence signals. Its widespread adoption in imaging-focused laboratories is driven by the practical balance of brightness, spectral positioning, and compatibility with common fluorescence microscope filter sets.
4. Fluorescent Surface and Material Tagging
Cyanine3 hydrazide is also applied to label polymeric materials, biomaterial surfaces, and diagnostic reagent supports for fluorescence-based characterization. Researchers use Cy3 hydrazide-derived labeling to quantify surface functionalization, visualize coating uniformity, and track immobilized components during material processing or assay development. This application is common in biomaterials science and molecular diagnostics R&D, where robust fluorescent tagging supports method optimization, quality control of functional layers, and readout development for platform assays.
Computed Properties
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 8 |
| Exact Mass | 542.2579173 g/mol |
| Monoisotopic Mass | 542.2579173 g/mol |
| Topological Polar Surface Area | 63Ų |
| Heavy Atom Count | 37 |
| Formal Charge | 0 |
| Complexity | 868 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 2 |
| Covalently-Bonded Unit Count | 3 |
| Compound Is Canonicalized | Yes |
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