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4,4-Difluoro-8(4'-hydroxyphenyl)-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene | CAS 870992-10-2
| Catalog Number | F01-0051 |
| Category | BODIPY |
| Molecular Formula | C19H19BF2N2O |
| Molecular Weight | 340.181 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
BODIPY dyes are used to generate fluorescent conjugates of proteins, nucleotides, oligonucleotides and dextrans, as well as to prepare fluorescent enzyme substrates, fatty acids, phospholipids, lipopolysaccharides, receptor ligands and polystyrene microspheres.
Chemical Information
Product Specification
Application
Computed Properties
| Synonyms | 4,4-Difluoro-8(4'-hydroxyphenyl)-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene, 98% |
| IUPAC Name | 4-(2,2-difluoro-4,6,10,12-tetramethyl-3-aza-1-azonia-2-boranuidatricyclo[7.3.0.03,7]dodeca-1(12),4,6,8,10-pentaen-8-yl)phenol |
| Canonical SMILES | [B-]1(N2C(=CC(=C2C(=C3[N+]1=C(C=C3C)C)C4=CC=C(C=C4)O)C)C)(F)F |
| InChI | InChI=1S/C19H19BF2N2O/c1-11-9-13(3)23-18(11)17(15-5-7-16(25)8-6-15)19-12(2)10-14(4)24(19)20(23,21)22/h5-10,25H,1-4H3 |
| InChIKey | GWBVEDILOKMRQV-UHFFFAOYSA-N |
| Excitation | 585 |
| Emission | 594 |
| Storage | Store at -20°C |
4,4-Difluoro-8(4’-hydroxyphenyl)-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene, more commonly known as BODIPY, is a versatile fluorescent dye utilized across various domains of scientific research.
Fluorescence Microscopy: The widespread application of BODIPY dyes in fluorescence microscopy stems from their robust fluorescence and exceptional photostability. Scientists leverage these dyes to tag cellular structures, proteins, and nucleic acids, generating striking and intricate images of cellular components. This visual representation facilitates the exploration of cell biology and aids in unraveling the intricacies of cellular processes.
Flow Cytometry: Within the realm of flow cytometry, BODIPY-conjugated antibodies play a pivotal role in scrutinizing the expression of cell surface and intracellular molecules. The unparalleled brightness and steadfast fluorescence of BODIPY enable precise quantification and segregation of cells based on specific markers. This methodology is indispensable in fields such as immunology, cancer research, and diagnostics, enabling meticulous analysis and cell sorting.
Environmental Sensing: BODIPY dyes find significant utility in the development of sensors designed to detect environmental pollutants and variations in chemical parameters. These sensors exhibit altered fluorescence in response to specific analytes, rendering them invaluable in monitoring environmental health and safety. With high sensitivity and selectivity towards various ions and molecules, these sensors offer a potent tool for environmental monitoring, providing crucial insights into environmental conditions.
Drug Delivery Systems: At the forefront of drug delivery research, BODIPY-labeled compounds play a fundamental role in investigating drug delivery mechanisms and molecular transport dynamics. Through the observation of BODIPY fluorescence, researchers gain visual insights into the distribution, localization, and release of drugs within biological systems. This profound understanding is pivotal in the design of efficient drug delivery carriers and the optimization of therapeutic outcomes, driving advancements in the realm of drug delivery systems.
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 1 |
| Exact Mass | 340.1558497 g/mol |
| Monoisotopic Mass | 340.1558497 g/mol |
| Topological Polar Surface Area | 28.2Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 649 |
| 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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