
Cyanine5 NHS ester minimal dye
| Catalog Number | R01-0020 |
| Category | NHS Esters |
| Molecular Formula | C36H42BF4N3O4 |
| Molecular Weight | 667.5 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
Cyanine5 minimal dye for protein labeling, an analog of Cy5® minimal dye. This reagent is specially quantified for the use in 2D proteomics. Each package contains specified amount of NHS ester with quantity variation within 10%.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Synonyms | Cyanine5 NHS ester |
| Purity | NMR 1H, HPLC-MS, functional testing |
| IUPAC Name | (2,5-dioxopyrrolidin-1-yl) 6-[3,3-dimethyl-2-[5-(1,3,3-trimethylindol-1-ium-2-yl)penta-2,4-dienylidene]indol-1-yl]hexanoate;trifluoroborane;fluoride |
| SMILES | B(F)(F)F.CC1(C2=CC=CC=C2[N+](=C1C=CC=CC=C3C(C4=CC=CC=C4N3CCCCCC(=O)ON5C(=O)CCC5=O)(C)C)C)C.[F-] |
| InChI | InChI=1S/C36H42N3O4.BF3.FH/c1-35(2)26-16-11-13-18-28(26)37(5)30(35)20-8-6-9-21-31-36(3,4)27-17-12-14-19-29(27)38(31)25-15-7-10-22-34(42)43-39-32(40)23-24-33(39)41;2-1(3)4;/h6,8-9,11-14,16-21H,7,10,15,22-25H2,1-5H3;;1H/q+1;;/p-1 |
| InChIKey | LWBHPHPQYRCYHI-UHFFFAOYSA-M |
| Appearance | dark blue solid |
Product Specification
| Excitation | 645 |
| Emission | 660 |
| Storage | 12 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
Cyanine5 NHS ester minimal dye is a reactive cyanine dye supplied as an NHS ester for efficient covalent labeling of primary amines on proteins, peptides, and other amine-containing biomolecules. Its long-wavelength fluorescence supports fluorescence microscopy and fluorescence-based readouts where reduced background from shorter-wavelength channels is advantageous. In conjugate and assay development workflows, the NHS ester functionality enables straightforward dye incorporation into research-grade bioconjugates for imaging and quantification.
1. Protein And Antibody Labeling
Cyanine5 NHS ester minimal dye is widely used by protein chemistry and antibody conjugation teams to generate fluorescently labeled antibodies, antibody fragments, and affinity reagents for binding studies and imaging workflows. The NHS ester reacts with lysine residues and N-terminal amines, enabling stable covalent incorporation of the dye into biomolecule conjugates used in fluorescence microscopy and plate-based fluorescence assays. Researchers often choose this dye form when they need a direct labeling reagent that can be carried through downstream experimental steps without relying on noncovalent dye association.
2. Fluorescence Microscopy Tracing
Cyanine5 NHS ester minimal dye supports cellular and molecular fluorescence microscopy applications where long-wavelength emission helps separate the labeled target from cellular autofluorescence and other fluorophores. Imaging groups use labeled proteins, peptides, or other amine-containing probes to visualize binding, uptake, and localization patterns in fixed-cell workflows or in labeled biomaterial contexts. Because the dye is introduced through covalent amine labeling, it is frequently selected for experiments requiring retention of fluorescence signal during washing steps and multi-step staining or sample preparation.
3. Flow Cytometry And Cell Sorting
Cyanine5 NHS ester minimal dye is used in flow cytometry workflows to produce fluorescently labeled biomolecules for staining cells and analyzing fluorescence intensity distributions. Typical users include immunophenotyping and assay development groups that need a robust, covalent dye attachment strategy for conjugates such as labeled antibodies or labeled targeting ligands. The dye's emission in the far-red range aligns with common cytometer channel configurations used for multiplex panels, enabling researchers to track labeled populations and compare staining conditions across experimental replicates.
4. Fluorescence Bioassay Development
Cyanine5 NHS ester minimal dye is also employed in fluorescence assay development to generate labeled reagents used as detection elements in binding assays, immobilized-probe formats, and other fluorescence-based quantification experiments. Assay development teams often incorporate the dye into protein conjugates that serve as fluorescent reporters, enabling readout by standard plate readers and fluorescence imaging systems. Covalent NHS ester labeling provides a practical route to consistent reagent preparation for comparative studies across buffers, washing conditions, and assay formats where noncovalent dye retention would be less reliable.
Computed Properties
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 11 |
| Exact Mass | 667.3204496 g/mol |
| Monoisotopic Mass | 667.3204496 g/mol |
| Topological Polar Surface Area | 69.9Ų |
| Heavy Atom Count | 48 |
| Formal Charge | 0 |
| Complexity | 1200 |
| 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 | 3 |
| Compound Is Canonicalized | Yes |
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