![Boron, [4-[(3,5-dimethyl-1H-pyrrol-2-yl-κN)(3,5-dimethyl-2H-pyrrol-2-ylidene-κN)methyl]-2-nitrophenolato]difluoro-, (T-4)-](https://resource.bocsci.com/structure/1181844-40-5.gif)
Boron, [4-[(3,5-dimethyl-1H-pyrrol-2-yl-κN)(3,5-dimethyl-2H-pyrrol-2-ylidene-κN)methyl]-2-nitrophenolato]difluoro-, (T-4)- | CAS 1181844-40-5
Catalog Number | F01-0061 |
Category | BODIPY |
Molecular Formula | C19H18BF2N3O3 |
Molecular Weight | 385.178 |
* 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.
Product Specification
Application
Excitation | 649 |
Emission | 667 |
Storage | Store at -20°C |
Boron [4-[(3,5-dimethyl-1H-pyrrol-2-yl-κN)(3,5-dimethyl-2H-pyrrol-2-ylidene-κN)methyl]-2-nitrophenolato]difluoro- (T-4)- is a chemical compound with unique properties, often applicable in various scientific and industrial fields.
Optoelectronic Devices: This boron complex is investigated for use in optoelectronic devices due to its unique electronic properties. Its stability and fluorescence make it suitable for organic light-emitting diodes (OLEDs) and other display technologies. This application provides a pathway for developing more efficient and cost-effective light-producing devices.
Photodynamic Therapy (PDT): This compound can play a role in photodynamic therapy for cancer treatment. It acts as a photosensitizer, which, upon activation by light, produces reactive oxygen species that destroy cancer cells. This approach is minimally invasive and can be tailored for targeting specific tumor sites.
Chemical Sensors: The compound is used in developing chemical sensors due to its ability to bind selectively and produce a detectable signal. These sensors are valuable in detecting pollutants, ions, and small organic compounds in environmental and clinical settings. Its use enhances sensitivity and selectivity, crucial for accurate monitoring and diagnostics.
Fluorescent Probes: As a fluorescent compound, it can be used in biological imaging and tracking applications. Its tunable emission properties allow for specific labeling of biological molecules, facilitating the study of cellular processes and protein interactions. This application is important in advancing our understanding of molecular biology and disease pathology.
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