
R6G alkyne, 6-isomer
| Catalog Number | R02-0029 |
| Category | Alkynes |
| Molecular Formula | C30H29N3O4 |
| Molecular Weight | 495.57 |
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Product Introduction
Rhodamine 6G (R6G) is a xanthene dye of rhodamine series. Compared to fluorescein, its emission is shifted to red. It is also much more photostable. The fluorophore has a high quantum yield. This R6G product contains a terminal alkyne moiety for the conjugation with azides in the presence of copper (I) catalyst.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Purity | NMR 1H, HPLC-MS (95%) |
| IUPAC Name | 2-[3-(ethylamino)-6-ethylimino-2,7-dimethylxanthen-9-yl]-4-(prop-2-ynylcarbamoyl)benzoic acid |
| SMILES | CCNC1=CC2=C(C=C1C)C(=C3C=C(C(=NCC)C=C3O2)C)C4=C(C=CC(=C4)C(=O)NCC#C)C(=O)O |
| InChI | InChI=1S/C30H29N3O4/c1-6-11-33-29(34)19-9-10-20(30(35)36)21(14-19)28-22-12-17(4)24(31-7-2)15-26(22)37-27-16-25(32-8-3)18(5)13-23(27)28/h1,9-10,12-16,31H,7-8,11H2,2-5H3,(H,33,34)(H,35,36) |
| InChIKey | QQIQIYOOKKWTRU-UHFFFAOYSA-N |
| Solubility | good in DMF, DMSO, alcohols |
| Appearance | dark colored solid |
Product Specification
| ε, L⋅mol-1⋅cm-1 | 116000 |
| Fluorescence Quantum Yield | 0.95 |
| Excitation | 518 |
| Emission | 542 |
| 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
R6G alkyne, 6-isomer is a rhodamine-based fluorescent dye bearing an alkyne handle, enabling copper-catalyzed azide-alkyne cycloaddition (CuAAC) for fluorescent labeling and probe construction. Its bright visible emission is widely leveraged in fluorescence microscopy and flow cytometry workflows where covalent attachment to biomolecules, polymers, or surfaces is required. The alkyne functionality supports downstream conjugate assembly for chemical biology, materials staining, and imaging reagent development.
1. Clickable Fluorescent Labeling
R6G alkyne, 6-isomer is used as a clickable rhodamine labeling reagent for covalent attachment to azide-functional biomolecules and affinity reagents. Researchers incorporate it into labeling strategies for proteins, peptides, and other macromolecules to generate stable fluorescent conjugates for visualization and quantitative fluorescence readouts. The alkyne handle supports modular conjugate design, allowing fluorescent tagging to be introduced late in a workflow without changing the core targeting chemistry of an azide-bearing partner.
2. Fluorescence Microscopy Tracing
R6G alkyne, 6-isomer serves as a practical fluorescence imaging tag for microscopy-based localization studies where rhodamine emission provides strong signal in standard visible-light imaging setups. In chemical biology and biomaterials research, it is commonly used to label surfaces, hydrogels, and polymeric scaffolds via click chemistry, enabling spatial tracking of labeled components during cell culture experiments or material characterization. Covalent attachment helps maintain signal during washing steps typical of staining and imaging protocols.
3. Flow Cytometry Conjugate Preparation
R6G alkyne, 6-isomer is employed to prepare fluorescent conjugates for flow cytometry and fluorescence-based cell analysis, particularly when a robust covalent dye attachment is preferred over passive adsorption. By clicking the alkyne dye onto azide-functional targeting reagents or labeling handles, researchers generate cell-associated fluorescent constructs suitable for gating and population-level quantification. This workflow is frequently used in assay development and reagent optimization for fluorescence readouts in suspension assays.
4. Fluorescent Probe Construction
R6G alkyne, 6-isomer is also used as a fluorophore building block in fluorescent probe development, where the alkyne group enables attachment to probe scaffolds, linkers, and reporter architectures. Teams developing molecular imaging reagents and fluorescence-based assay components use it to create modular dye conjugates that can be paired with recognition elements introduced through azide-functional chemistries. The result is a versatile rhodamine reporter suitable for constructing multicomponent fluorescent tools for biochemical and materials studies.
Computed Properties
| XLogP3 | 3.8 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 7 |
| Exact Mass | 495.21580641 g/mol |
| Monoisotopic Mass | 495.21580641 g/mol |
| Topological Polar Surface Area | 100Ų |
| Heavy Atom Count | 37 |
| Formal Charge | 0 |
| Complexity | 1090 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
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