1,3,5,7,8-Pentamethyl-2-formyl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene | CAS 198149-19-8

Catalog Number	F01-0107
Category	BODIPY
Molecular Formula	C15H17BF2N2O
Molecular Weight	290.121

Inquiry

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

Worldwide Delivery
Quality Assurance
24/7 Customer Service

Product Introduction

Aldehyde-functional BODIPY fluorophore ideal for biomolecule conjugation. Provides stable emission for biolabeling and sensing.

Product Specification
Application

Excitation	649
Emission	667
Storage	Store at -20°C

1,3,5,7,8-Pentamethyl-2-formyl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene, commonly known as a BODIPY dye, is a fluorescent compound with diverse applications in scientific research.

Fluorescent Labeling: This BODIPY dye is highly esteemed in bioimaging for its exceptional fluorescence intensity and stability. It is utilized to label proteins, nucleic acids, and other biomolecules, allowing researchers to visually track and observe biological processes within live cells. Its robust brightness and enduring nature make it a prime selection for extended imaging investigations, facilitating in-depth studies.

Cellular Tracking: Serving as a potent instrument for monitoring cell dynamics and dispersion in developmental biology and oncology research, this compound plays a crucial role. By tagging cells with this fluorescent dye, scientists can monitor real-time cell movements, proliferation, and tissue integration. This aids in uncovering intricate cellular behaviors during developmental stages or disease progression, providing valuable insights into cellular activities.

Photodynamic Therapy: In medical settings, the distinctive photophysical characteristics of 1,3,5,7,8-Pentamethyl-2-formyl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene are leveraged for photodynamic therapy (PDT). Upon exposure to precise light wavelengths, it triggers the production of reactive oxygen species capable of eradicating targeted cancer cells. This presents a precise and minimally invasive approach for treating specific cancer types, showcasing the potential of this compound in medical applications.

Chemical Sensing: Functioning as a sensitive sensor for detecting various chemical ions and molecules, this compound responds to environmental changes with great sensitivity. Its fluorescence properties can alter in reaction to shifts in pH, binding with metal ions, or changes in solvent polarity. This unique feature is utilized in fabricating sensors for environmental surveillance and biochemical assessments, illustrating its versatility in chemical sensing applications.