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Boron, [3-ethyl-5-[1-(4-ethyl-3,5-dimethyl-2H-pyrrol-2-ylidene-κN)ethyl]-4-methyl-1H-pyrrole-2-carboxal-

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Boron, [3-ethyl-5-[1-(4-ethyl-3,5-dimethyl-2H-pyrrol-2-ylidene-κN)ethyl]-4-methyl-1H-pyrrole-2-carboxal-

Boron, [3-ethyl-5-[1-(4-ethyl-3,5-dimethyl-2H-pyrrol-2-ylidene-κN)ethyl]-4-methyl-1H-pyrrole-2-carboxal- | CAS 162844-74-8

Catalog Number	F01-0088
Category	BODIPY
Molecular Formula	C18H23BF2N2O
Molecular Weight	332.201

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* Please be kindly noted products are not for therapeutic use. We do not sell to patients.

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Product Introduction

A BODIPY-related fluorescent dye used for spectroscopy and optical device calibration. Buy fluorescent labeling reagents online for precise emission control.

Product Specification
Application

Excitation	649
Emission	667
Storage	Store at -20°C

Boron, [3-ethyl-5-[1-(4-ethyl-3,5-dimethyl-2H-pyrrol-2-ylidene-κN)ethyl]-4-methyl-1H-pyrrole-2-carboxal, is a boron-dipyrromethene (BODIPY) derivative known for its extended conjugation and unique photophysical properties. The molecule features a boron center integrated into a dipyrromethene framework, further modified with ethyl and methyl substitutions. These structural elements enhance its fluorescence quantum yield, chemical stability, and absorption/emission tunability, making it an ideal fluorescent compound for diverse scientific and technological applications.

This compound is extensively employed in fluorescence imaging and spectroscopy. Its high fluorescence intensity and narrow emission spectra allow for precise visualization of biological structures, processes, and molecular interactions. It is especially valuable in live-cell imaging and fluorescence resonance energy transfer (FRET) experiments for studying protein-protein interactions.

In chemical sensing, this BODIPY derivative acts as a sensitive fluorescent probe for detecting ions, pH changes, and small molecules. Its conjugated structure and boron atom provide exceptional selectivity and sensitivity, making it a reliable tool for environmental monitoring and biomedical diagnostics.

The compound is also utilized in photodynamic therapy (PDT). Upon activation by light, it generates reactive oxygen species (ROS), making it a powerful photosensitizer for applications in cancer treatment and antimicrobial therapies. Its tunable photophysical properties further enable precise control over therapeutic interventions.

In material science, this BODIPY derivative is a key component in optoelectronic devices, including organic photovoltaics and light-emitting diodes (OLEDs). Its strong light absorption and emission properties contribute to efficient energy transfer, enhancing the performance of next-generation energy conversion and display technologies.