2,6-Diiodo-1,3,5,7-tetramethyl-8-phenyl-4,4-difluoroboradiazasindacene | CAS 1083009-44-2

Catalog Number	F01-0075
Category	BODIPY
Molecular Formula	C19H17BF2I2N2
Molecular Weight	575.974

Catalog Number	Size	Price	Quantity
F01-0075	10 mg	$198

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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
QC Data

Synonyms	5,5-Difluoro-2,8-diiodo-1,3,7,9-tetramethyl-10-phenyl-5H-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-4-ium-5-uide
Purity	95%
IUPAC Name	2,2-difluoro-5,11-diiodo-4,6,10,12-tetramethyl-8-phenyl-3-aza-1-azonia-2-boranuidatricyclo[7.3.0.03,7]dodeca-1(12),4,6,8,10-pentaene
Canonical SMILES	[B-]1(N2C(=C(C(=C2C(=C3[N+]1=C(C(=C3C)I)C)C4=CC=CC=C4)C)I)C)(F)F
InChI	InChI=1S/C19H17BF2I2N2/c1-10-16(23)12(3)25-18(10)15(14-8-6-5-7-9-14)19-11(2)17(24)13(4)26(19)20(25,21)22/h5-9H,1-4H3
InChIKey	DLDOADVXWJCBOG-UHFFFAOYSA-N

Excitation	649
Emission	667
Storage	Store at -20°C

2,6-Diiodo-1,3,5,7-tetramethyl-8-phenyl-4,4-difluoroboradiazasindacene, commonly known as a BODIPY dye, is a versatile fluorescent compound extensively utilized in diverse scientific domains.

Fluorescent Imaging: Employed in fluorescent imaging methodologies, the BODIPY dye acts as a crucial tool for labeling and visualizing biological molecules within cellular and tissue settings. With its exceptional fluorescence quantum yield and photostability, it emerges as an ideal choice for conducting prolonged imaging investigations. Researchers leverage its capabilities to monitor molecular dynamics and interactions in real-time, thereby offering profound insights into the intricate workings of cellular processes.

Environmental Sensing: The inherent fluorescent characteristics of 2,6-Diiodo-1,3,5,7-tetramethyl-8-phenyl-4,4-difluoroboradiazasindacene render it invaluable for environmental sensing undertakings. Integrated into sensors, it facilitates the detection of alterations in environmental parameters such as pH, temperature, or the presence of specific ions or gases. This integration leads to the creation of sensitive and precise biosensors for monitoring environmental conditions with enhanced accuracy.

Photodynamic Therapy: Finding application in medical research, this BODIPY dye is being explored for its potential role in photodynamic therapy (PDT), a treatment modality that harnesses light-activated compounds to target and eliminate cancer cells. When illuminated, the compound generates reactive oxygen species that trigger cell damage and apoptosis in malignant tissues.

Solar Energy Harvesting: Within the realm of solar energy, this fluorescent dye is a subject of exploration for its utility in dye-sensitized solar cells (DSSCs). Boasting strong light absorption and emission properties, it contributes to improving the efficiency of light capture and conversion in solar technologies. Researchers are actively investigating strategies to optimize its incorporation into solar panels to elevate overall energy output.

HNMR