
Coumarin 498 | CAS 87331-48-4
| Catalog Number | A17-0116 |
| Category | Laser Dyes |
| Molecular Formula | C16H17NO4S |
| Molecular Weight | 319.375 |
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Product Introduction
Efficient fluorescent coumarin dye with broad excitation range. Ideal for multiphoton microscopy and photophysical research.
Chemical Information
Application
Computed Properties
Chemical Information
| Synonyms | 2,3,6,7-tetrahydro-10-(methylsulfonyl)-1H,5H,11H-[1]benzopyrano[6,7,8-ij]quinolizin-11-one |
| IUPAC Name | 5-methylsulfonyl-3-oxa-13-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1,5,7,9(17)-tetraen-4-one |
| SMILES | CS(=O)(=O)C1=CC2=CC3=C4C(=C2OC1=O)CCCN4CCC3 |
| InChI | InChI=1S/C16H17NO4S/c1-22(19,20)13-9-11-8-10-4-2-6-17-7-3-5-12(14(10)17)15(11)21-16(13)18/h8-9H,2-7H2,1H3 |
| InChIKey | DPJWIXMOCGJKDG-UHFFFAOYSA-N |
Application
Coumarin 498 is a coumarin-based fluorescent dye used as a bright, environment-sensitive label for fluorescence microscopy and fluorescence-based assay development. Its strong emission in the visible range makes it a practical reporter for tracking labeled biomolecules, polymers, and surfaces in research workflows where optical readout and staining contrast are required. Because coumarin dyes are widely incorporated into labeling strategies through reactive handles or as part of conjugates, Coumarin 498 is frequently selected for constructing fluorescent conjugates and calibration standards for optical instrumentation.
1. Fluorescence Microscopy Labeling
Coumarin 498 is frequently employed in fluorescence microscopy workflows to visualize labeled biomolecules and polymeric materials with coumarin-compatible excitation and emission. Researchers use Coumarin 498 conjugates to track adsorption, diffusion, and localization in fixed-cell or material imaging studies, including labeling of proteins, peptides, and other macromolecules that have been functionalized to carry the dye. In microscopy setups, the dye's bright emission supports clear signal generation for qualitative imaging and for quantitative fluorescence readouts when imaging parameters are kept consistent across samples.
2. Fluorescence Bioassay Tracers
Coumarin 498 is used as a fluorescent tracer in fluorescence-based bioassay development, where dye-tagged reagents enable monitoring of binding, transport, or incorporation into assay components. In many laboratory settings, Coumarin 498 labeling is incorporated into conjugate libraries for screening assay formats that rely on optical intensity changes or endpoint fluorescence measurements. The dye is also commonly selected for preparing fluorescence standards and reference reagents that support assay normalization across plates, cuvettes, or automated readers.
3. Protein And Biomolecule Conjugates
Coumarin 498 is a go-to coumarin fluorophore for constructing fluorescent protein and biomolecule conjugates used in chemical biology and biomaterials research. Teams working on labeling workflows apply Coumarin 498 to generate fluorescent conjugates for tracking reagent uptake, immobilization, or surface association in experimental systems such as functionalized coatings and biomaterial interfaces. When coupled to biomolecule scaffolds, Coumarin 498 enables optical tracking of conjugate distribution and stability during experimental handling, washing, and incubation steps.
4. Polymer And Surface Functionalization
Coumarin 498 is widely used to introduce fluorescent reporting into polymers and engineered surfaces for materials characterization and process monitoring. In biomaterials and surface science workflows, Coumarin 498-containing materials help researchers visualize coating uniformity, track film formation, and monitor surface-bound species in fluorescence microscopy and imaging systems. The dye's role as a stable fluorescent reporter supports routine comparative studies where consistent labeling and optical readout are needed to evaluate material batches, surface treatments, or functionalization conditions.
Computed Properties
| XLogP3 | 2.3 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 1 |
| Exact Mass | 319.08782920 g/mol |
| Monoisotopic Mass | 319.08782920 g/mol |
| Topological Polar Surface Area | 72.1Ų |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 621 |
| 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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