
sulfo-Cyanine5 hydrazide | CAS 2055138-61-7
| Catalog Number | F03-0041 |
| Category | sulfo-Cyanine5 |
| Molecular Formula | C32H40N4O7S2 |
| Molecular Weight | 656.83 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
sulfo-Cyanine5 is a sulfated derivative of Cyanine5 dye.
Chemical Information
Product Specification
Application
Chemical Information
| IUPAC Name | (2Z)-1-(6-hydrazinyl-6-oxohexyl)-3,3-dimethyl-2-[(2E,4E)-5-(1,3,3-trimethyl-5-sulfoindol-1-ium-2-yl)penta-2,4-dienylidene]indole-5-sulfonate |
| SMILES | CC1(C2=C(C=CC(=C2)S(=O)(=O)O)[N+](=C1C=CC=CC=C3C(C4=C(N3CCCCCC(=O)NN)C=CC(=C4)S(=O)(=O)[O-])(C)C)C)C |
| InChI | InChI=1S/C32H40N4O7S2/c1-31(2)24-20-22(44(38,39)40)15-17-26(24)35(5)28(31)12-8-6-9-13-29-32(3,4)25-21-23(45(41,42)43)16-18-27(25)36(29)19-11-7-10-14-30(37)34-33/h6,8-9,12-13,15-18,20-21H,7,10-11,14,19,33H2,1-5H3,(H2-,34,37,38,39,40,41,42,43) |
| InChIKey | UXHHBJOLTZIDLS-UHFFFAOYSA-N |
| Appearance | dark blue solid |
Product Specification
| Excitation | 646 |
| Emission | 662 |
Application
Sulfo-Cyanine5 hydrazide is a water-soluble cyanine dye hydrazide designed for fluorescence labeling of aldehyde-bearing biomolecules and materials, enabling bright far-red imaging readouts in labeling workflows. The hydrazide functional group reacts with carbonyls to form stable hydrazone linkages, which supports conjugate construction for microscopy, gel-based analysis, and fluorescence-based assay development.
1. Aldehyde Biomolecule Labeling
Sulfo-Cyanine5 hydrazide is used to fluorescently tag aldehyde-functionalized proteins, peptides, and carbohydrate-modified biomolecules in chemical biology and glycoconjugate research. Researchers commonly incorporate it after mild oxidation steps (e.g., converting glycan or carbohydrate motifs to aldehydes) to generate far-red fluorescent conjugates for tracking binding, uptake, and localization in complex biological mixtures. The sulfonate-containing dye structure supports aqueous handling during conjugate preparation and downstream fluorescence readouts, making it a practical reagent for preparing labeled reagents for microscopy and fluorescence assays.
2. Fluorescence Microscopy Tracing
Sulfo-Cyanine5 hydrazide-labeled conjugates are frequently employed as far-red fluorescent tracers to visualize biomolecule distribution in fixed-cell imaging workflows and in microscopy-based studies of labeled targets. In cell biology laboratories, the dye is used to follow the localization of carbonyl-containing biomolecule derivatives, including glycoconjugates and oxidized biomaterials, where far-red emission helps reduce background from cellular autofluorescence. Labeling with this hydrazide is also leveraged for multi-step probe construction, such as generating fluorescent affinity reagents or imaging-compatible conjugates for confocal and widefield fluorescence microscopy.
3. Gel Electrophoresis and Blotting
Sulfo-Cyanine5 hydrazide is applied in fluorescence-based protein analysis workflows where aldehyde-containing samples are labeled prior to electrophoresis or blot imaging. In proteomics and analytical biochemistry, the reagent enables sensitive visualization of labeled proteins and conjugates using far-red fluorescence detection, supporting workflows such as monitoring labeling efficiency, comparing relative labeling across samples, and validating conjugate formation in experimental optimization. Because the dye is water-soluble and attaches through hydrazone formation to carbonyl groups, it is commonly used to generate fluorescent standards and to support quantitative imaging on fluorescence-capable gel documentation systems.
4. Fluorescent Probe Conjugate Building
Sulfo-Cyanine5 hydrazide serves as a dye-building block for constructing fluorescent probe conjugates used in assay and molecular imaging development. Chemical biology groups use the hydrazide to introduce a far-red fluorophore onto aldehyde-functional linkers, affinity reagents, or scaffold molecules, enabling downstream incorporation into larger probe architectures such as labeled binding reagents and imaging-compatible platforms. This approach is particularly useful when a stable carbonyl-reactive handle is needed to attach a cyanine fluorophore to an intermediate containing aldehyde functionality, supporting consistent probe preparation for fluorescence readouts in research assays.
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