
3-Bodipy-propanoic Acid Ethyl Ester | CAS 1418610-53-3
| Catalog Number | F01-0033 |
| Category | BODIPY |
| Molecular Formula | C16H19BF2N2O2 |
| Molecular Weight | 320.15 |
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Product Introduction
3-Bodipy-propanoic Acid Ethyl Ester is a significant and indispensable biomedical compound that finds extensive application in fluorescent staining and cellular imaging, thereby facilitating meticulous studies in the field. Its versatile utility encompasses the monitoring of cell metabolism, scrutinizing lipid oxidation, and evaluating mitochondrial function. Moreover, it serves as a potent visual aid in drug metabolism visualization, cancer cell research, and neurodegenerative disease investigations.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Purity | 98% |
| IUPAC Name | ethyl 3-(2,2-difluoro-10,12-dimethyl-1-aza-3-azonia-2-boranuidatricyclo[7.3.0.03,7]dodeca-3,5,7,9,11-pentaen-4-yl)propanoate |
| SMILES | [B-]1(N2C(=CC(=C2C=C3[N+]1=C(C=C3)CCC(=O)OCC)C)C)(F)F |
| InChI | InChI=1S/C16H19BF2N2O2/c1-4-23-16(22)8-7-13-5-6-14-10-15-11(2)9-12(3)20(15)17(18,19)21(13)14/h5-6,9-10H,4,7-8H2,1-3H3 |
| InChIKey | UEGDIEANOMZZBH-UHFFFAOYSA-N |
Product Specification
| 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
3-Bodipy-propanoic Acid Ethyl Ester is a BODIPY-based fluorescent dye ester designed for fluorescence labeling workflows where a hydrophobic, cell-compatible precursor is advantageous before conversion to the corresponding carboxylic acid form. Its strong visible-light absorption and emission make it useful for fluorescence microscopy and imaging assays, while the propanoate ester functionality supports downstream conjugation or incorporation into labeling strategies that rely on carboxylate handles. Researchers often use this dye to generate fluorescent conjugates for tracking, localization, and quantitative fluorescence readouts in chemical biology and biomaterials studies.
1. Fluorescence Microscopy Labeling
3-Bodipy-propanoic Acid Ethyl Ester is used as a fluorescent labeling reagent for cellular imaging experiments, including membrane-associated and general uptake studies where BODIPY brightness supports clear visualization under standard fluorescence microscope configurations. Lab groups commonly incorporate the dye into staining or labeling protocols to track distribution patterns in fixed or prepared samples, and the resulting BODIPY signal is well-suited for multi-color imaging workflows when spectral overlap is managed by appropriate filter sets. Because the dye contains a masked carboxylate motif, it is also selected when subsequent conjugation steps or immobilization strategies are planned after initial staining.
2. Fluorescent Conjugate Preparation
3-Bodipy-propanoic Acid Ethyl Ester serves as a convenient precursor for building BODIPY-labeled probes and conjugates used in fluorescence-based assays and molecular imaging reagent development. Researchers use it to introduce a BODIPY fluorophore into biomolecule- or polymer-containing constructs where a carboxylate handle is required for coupling to amines, surfaces, or other functional materials. This makes the dye relevant to workflows such as fluorescent tagging of peptides, labeling of labeling scaffolds for binding studies, and preparation of fluorescent standards used to calibrate imaging or plate-reader measurements.
3. Fluorescence-Based Tracing Studies
3-Bodipy-propanoic Acid Ethyl Ester is applied in tracer experiments that rely on stable, quantifiable fluorescence to follow distribution, transport, or incorporation into labeled materials. In chemical biology and biomaterials research, investigators use BODIPY fluorescence to monitor how labeled components partition within complex systems, including polymer matrices, nanoparticle formulations, and surface-modified materials used for imaging and characterization. The dye's compact BODIPY core and bright emission are particularly useful when researchers need consistent signal for comparative studies across samples or time points, such as uptake/retention measurements and material localization mapping by fluorescence readout.
Computed Properties
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 5 |
| Exact Mass | 320.1507643 g/mol |
| Monoisotopic Mass | 320.1507643 g/mol |
| Topological Polar Surface Area | 34.2Ų |
| Heavy Atom Count | 23 |
| Formal Charge | 0 |
| Complexity | 615 |
| 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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