boron dipyrromethene (bodipy)

BDP 558 568 maleimide is a boron-dipyrromethene (BODIPY) dye that contains a terminal maleimide group.

BDP 558 568 tetrazine is a boron dipyrromethene (BODIPY) dye that contains a terminal tetrazine group.

BDP 630 650 tetrazine is a boron-dipyrromethene (BODIPY) dye that includes a terminal tetrazine group.

BODIPY R6G NHS ester is a chemical compound characterized by the presence of BODIPY (boron dipyrromethene) and Rhodamine 6G structures, combined with an NHS (N-hydroxysuccinimide) ester active group. This composition enables efficient and specific covalent coupling with amino groups on biomolecules such as proteins and nucleic acids, making it suitable for applications in bio-labeling, fluorescence imaging, and biosensing. The compound's unique fluorescent properties allow it to maintain high brightness and stability even in complex biological environments. Its excitation emission wavelengths are 530 nm and 545 nm, respectively.

8-Chloro-1,3,5,7-tetramethyl BODIPY is a fluorescent dye featuring a boron-dipyrromethene core. This compound has methyl and chlorine atom substituents at specific positions on the pyrrole rings. It exhibits a high fluorescence quantum yield and distinct absorption and emission wavelengths. Ex Em(nm)=500 515.

Py-BODIPY is a type of fluorescent dye based on the boron-dipyrromethene (BODIPY) structure that incorporates a pyridine (Py) group. The presence of the pyridine group may enhance the dye's ability to interact with biomolecules or other substrates, thereby broadening its application potential in areas such as biological labeling, bioimaging, and chemical sensing. Ex Em(nm)=508 517.

8-(4-hydroxyphenyl)-1,3,5,7-tetramethyl BODIPY is a fluorescent dye molecule based on the boron-dipyrromethene (BODIPY) structure, known for its high fluorescence quantum yield and excellent photostability. When excited by light at specific wavelengths, it emits bright fluorescence. Its fluorescence properties make it widely applicable in fields such as bioimaging, fluorescent labeling, and sensors. Ex Em(nm)=503 512.

8-Phenyl-2,6-diethyl-1,3,5,7-tetramethyl BODIPY is an organic fluorescent dye molecule, classified within the boron-dipyrromethene (BODIPY) compound family. Ex Em(nm)=525 544.

8-(4-ethynylphenyl)-1,3,5,7-tetramethyl BODIPY is an organic fluorescent dye characterized by an ethynylphenyl group at the 8-position of the boron dipyrromethene (BODIPY) structure and methyl substituents at the 1, 3, 5, and 7 positions. It boasts a high fluorescence quantum yield and specific chemical properties, making it useful for applications such as fluorescence imaging.

8-(4-Anilino) BODIPY is a compound featuring a para-anilino group attached at the 8-position of a boron-dipyrromethene core. It is characterized by a high fluorescence quantum yield, narrow emission bandwidth, and excellent photostability, making it widely applicable in areas such as biological imaging, chemical analysis, and materials science.

Coppersensor 1 (CS1) is a boron dipyrromethene-based fluorescent sensor for selective and sensitive detection of copper(I) ions (Cu + ) in biological samples. Coppersensor 1 can be imaged using any type of fluorescence microscope, including epifluorescence, confocal and multiphoton.

Meso-Benzothiazole-BODIPY 505 515, a boron dipyrromethene (BODIPY)-based fluorescent probe, is utilized in autophagy research, particularly for studying Alzheimer's disease, lysosomal storage disorders, and neurodegenerative diseases [1].

BDP 581 591 alkyne, a moderately hydrophobic borondipyrromethene fluorophore, is designed for specialized applications requiring specific fluorescent properties.

Bodipy TR alkyne, a boron dipyrromethene fluorophore for the ROX (Texas Red) channel, is versatile for applications in microscopy, fluorescence polarization measurements, and other uses. This derivative serves as a terminal alkyne in copper-catalyzed click chemistry.

BODIPY-C12, a boron-dipyrromethene derivative with a lipophilic tail (excitation 490 nm), is a hydrophobic molecule sensitive to the surrounding environment and can be used to quantify viscosity [1].