
Coumarin 525 | CAS 87331-47-3
| Catalog Number | A17-0115 |
| Category | Laser Dyes |
| Molecular Formula | C22H18N2O3 |
| Molecular Weight | 358.397 |
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Product Introduction
High-intensity fluorescent dye used in spectroscopy and photonic materials. Delivers clear emission for high-sensitivity optical detection.
Chemical Information
Application
Computed Properties
Patents
Chemical Information
| Synonyms | 10-(2-benzoxazolyl)-2,3,6,7-tetrahydro-1H,5H,11H-[1]benzopyrano[6,7,8-ij]quinolizin-11-one |
| IUPAC Name | 5-(1,3-benzoxazol-2-yl)-3-oxa-13-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1,5,7,9(17)-tetraen-4-one |
| SMILES | C1CC2=C3C(=C4C(=C2)C=C(C(=O)O4)C5=NC6=CC=CC=C6O5)CCCN3C1 |
| InChI | InChI=1S/C22H18N2O3/c25-22-16(21-23-17-7-1-2-8-18(17)26-21)12-14-11-13-5-3-9-24-10-4-6-15(19(13)24)20(14)27-22/h1-2,7-8,11-12H,3-6,9-10H2 |
| InChIKey | XYFLALJXCJWBPG-UHFFFAOYSA-N |
Application
Coumarin 525 is a coumarin-based fluorescent dye used as a bright, compact fluorophore for fluorescence labeling workflows. Its strong emission in the visible range and compatibility with common labeling chemistries make it a practical choice for constructing fluorescent conjugates for microscopy and quantitative fluorescence assays. Researchers often leverage Coumarin 525 as a reference fluorophore in probe and labeling reagent development where reliable spectral performance and straightforward readout are required.
1. Fluorescence Labeling Probes
Coumarin 525 is widely used to generate fluorescent labeling reagents for biomolecule conjugates, including proteins, peptides, and polymeric carriers used in chemical biology and materials research. In these workflows, the dye's small coumarin scaffold helps maintain conjugate behavior while enabling sensitive fluorescence readout in standard plate readers and fluorescence microscopes. Teams developing fluorescent tracking reagents for binding studies, reagent localization experiments, or labeling controls commonly select Coumarin 525 when a visible-range coumarin signal is preferred over larger fluorophores.
2. Fluorescence Microscopy Tracing
Coumarin 525 supports fluorescence microscopy applications where researchers need clear visualization of labeled targets in fixed samples or model systems. Its emission properties make it useful for multicolor imaging strategies when paired with spectrally separated dyes, and it is commonly incorporated into labeling constructs for cellular and biomaterials imaging experiments. Laboratories using fluorescence imaging for co-localization studies, surface-associated labeling, or reagent distribution mapping rely on Coumarin 525 to provide a consistent fluorescent signal suitable for qualitative and semi-quantitative microscopy.
3. Flow Cytometry Dye Conjugates
Coumarin 525 is used to prepare fluorescence-tagged conjugates for flow cytometry experiments that require a stable, readily detectable emission signal. Researchers incorporate the dye into labeling reagents for analyzing fluorescently labeled biomolecules, affinity reagents, or polymer conjugates in cell-associated or particle-associated formats. In assay development and method optimization, Coumarin 525 can serve as a practical fluorophore for establishing gating strategies and comparing labeling conditions using instrument-compatible fluorescence detection.
4. Fluorescence-Based Bioassays
Coumarin 525 is frequently employed in fluorescence assay development where labeled reagents enable quantitative monitoring of binding, uptake, or reaction-linked readouts. Assay developers use coumarin-labeled conjugates as reporter tags in plate-based formats, including endpoint fluorescence measurements for screening workflows and method qualification experiments. The dye's straightforward fluorescence response supports routine assay readout using standard excitation/emission optics, making Coumarin 525 a common choice for building and troubleshooting fluorescence-based assay reagents.
Computed Properties
| XLogP3 | 4.3 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 1 |
| Exact Mass | 358.13174244 g/mol |
| Monoisotopic Mass | 358.13174244 g/mol |
| Topological Polar Surface Area | 55.6Ų |
| Heavy Atom Count | 27 |
| Formal Charge | 0 |
| Complexity | 650 |
| 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 |
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| US-2021277250-A1 | Aminocoumarin compound, and aminocoumarin compound-containing resin particles | 2017-02-14 |
| US-11434376-B2 | Aminocoumarin compound, and aminocoumarin compound-containing resin particles | 2017-02-14 |
| US-2016202560-A1 | Photo-alignment material and photo-alignment method | 2013-08-14 |
| US-2019086738-A1 | Photo-alignment material and photo-alignment method | 2013-08-14 |
| US-10788715-B2 | Photo-alignment material and photo-alignment method | 2013-08-14 |
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