
BDP R6G alkyne | CAS 2006345-31-7
| Catalog Number | R02-0017 |
| Category | Alkynes |
| Molecular Formula | C21H18N3BF2O |
| Molecular Weight | 377.2 |
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Product Introduction
BDP R6G is a bright and photostable dye whose absorption and emission spectra are similar to R6G (rhodamine 6G). Unlike R6G that is a xanthene dye, BDP R6G belongs to the borondipyrromethene class. This is a terminal alkyne for copper-catalyzed Click chemistry.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Synonyms | BDPR6Galkyne; N-propargyl-3-(3-(4,4-Difluoro-5-phenyl-3a,4a-diaza-4-bora-s-indacen-3-yl)propionamide; 3-(2,2-difluoro-12-phenyl-3-aza-1-azonia-2-boranuidatricyclo[7.3.0.03,7]dodeca-1(12),4,6,8,10-pentaen-4-yl)-N-prop-2-ynylpropanamide |
| Purity | NMR 1H, HPLC-MS (95%) |
| IUPAC Name | 3-(2,2-difluoro-12-phenyl-3-aza-1-azonia-2-boranuidatricyclo[7.3.0.03,7]dodeca-1(12),4,6,8,10-pentaen-4-yl)-N-prop-2-ynylpropanamide |
| SMILES | [B-]1(N2C(=CC=C2CCC(=O)NCC#C)C=C3[N+]1=C(C=C3)C4=CC=CC=C4)(F)F |
| InChI | InChI=1S/C21H18BF2N3O/c1-2-14-25-21(28)13-11-17-8-9-18-15-19-10-12-20(16-6-4-3-5-7-16)27(19)22(23,24)26(17)18/h1,3-10,12,15H,11,13-14H2,(H,25,28) |
| InChIKey | FYYXFSSDBMYMQI-UHFFFAOYSA-N |
| Solubility | good in DMF, DMSO, DCM |
| Appearance | yellow to brown solid |
Product Specification
| Fluorescence Quantum Yield | 0.96 |
| Excitation | 530 |
| Emission | 548 |
| 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
BDP R6G alkyne is an alkyne-functionalized BODIPY-based fluorescent dye designed for click chemistry labeling workflows where a reactive handle is required for bioconjugation or material modification. Its bright visible fluorescence supports direct visualization and quantitative fluorescence readouts after incorporation into biomolecules, linkers, or surfaces. The alkyne functionality enables downstream attachment via copper-catalyzed azide-alkyne cycloaddition (CuAAC) to generate fluorescent conjugates for microscopy and assay development.
1. Biomolecule Labeling
BDP R6G alkyne is used as a fluorescent labeling building block for preparing azide-functional biomolecule conjugates, including proteins, peptides, and other amine- or azide-derivatized targets used in chemical biology. Researchers incorporate the dye into click-ready constructs to track binding, distribution, and reaction outcomes in fluorescence imaging experiments, where the dye's strong emission supports sensitive visualization of labeled species. This reagent format is especially common in workflows that require modular assembly of fluorescent conjugates from separately prepared azide and alkyne components.
2. Fluorescent Probe Construction
BDP R6G alkyne serves as a convenient fluorophore component for constructing fluorescence-based probes and labeling reagents used in assay development. By clicking the alkyne dye onto azide-bearing scaffolds, researchers generate fluorescent reporters for studying biomolecular interactions, reagent localization, and labeling efficiency in plate-based or cuvette-based fluorescence measurements. The resulting conjugates are frequently used in method development for fluorescent tagging strategies where a robust, visible-emitting dye is needed as a readout label.
3. Surface And Material Functionalization
BDP R6G alkyne is applied for fluorescent surface modification of polymers, hydrogels, and biomaterials that are engineered with azide groups. In materials research and biomaterials science, the dye is incorporated via click coupling to create spatially trackable coatings or bulk-labeled matrices used for imaging, material characterization, and fluorescence-based compatibility studies. This approach is also used to generate fluorescently tagged nanoparticles or surface-bound labeling layers for microscopy workflows that require stable covalent attachment rather than passive dye adsorption.
4. Imaging And Quantification Studies
BDP R6G alkyne is used as a fluorescent imaging label in microscopy workflows where quantitative fluorescence intensity is used to compare labeled samples, monitor labeling uniformity, or visualize conjugate localization. After click conjugation to azide-bearing targets, the dye-containing constructs provide a direct fluorescence signal for imaging experiments using standard fluorescence microscope configurations matched to visible excitation/emission. Researchers also use these labeled conjugates in comparative fluorescence assays to evaluate relative labeling outcomes across experimental conditions.
Computed Properties
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 5 |
| Exact Mass | 377.1510987 g/mol |
| Monoisotopic Mass | 377.1510987 g/mol |
| Topological Polar Surface Area | 37Ų |
| Heavy Atom Count | 28 |
| Formal Charge | 0 |
| Complexity | 789 |
| 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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