Items 111 to 114 of 114 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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2-Chloro-4,6-bis[3-(perfluorohexyl)propyloxy]-1,3,5-triazine | 916770-15-5 | sc-230140 sc-230140A | 1 g 10 g | $205.00 $2000.00 | ||
2-Chloro-4,6-bis[3-(perfluorohexyl)propyloxy]-1,3,5-triazine exhibits remarkable photophysical properties, characterized by strong fluorescence due to its triazine framework, which facilitates efficient energy transfer. The perfluoroalkyl chains enhance hydrophobic interactions, promoting self-assembly in nonpolar environments. Its unique electronic structure allows for selective interactions with various substrates, influencing reaction kinetics and enabling diverse applications in material science and photonics. | ||||||
6-JOE, SE | 113394-23-3 | sc-482037 | 5 mg | $219.00 | ||
6-JOE, SE is a distinctive fluorescein derivative characterized by its exceptional photostability and high quantum yield. Its unique structure allows for efficient energy transfer in various environments, enhancing its fluorescence intensity. The compound exhibits selective interactions with specific biomolecules, facilitating targeted imaging applications. Additionally, its rapid reaction kinetics enable real-time monitoring of dynamic processes, making it a versatile tool in fluorescence-based studies. | ||||||
AMF | 91539-64-9 | sc-482039 | 25 mg | $119.00 | ||
AMF is a notable fluorescein derivative known for its remarkable solubility in polar solvents, which enhances its versatility in diverse experimental conditions. Its unique electronic structure promotes strong intramolecular hydrogen bonding, leading to increased stability and reduced non-radiative decay. The compound's distinct absorption and emission profiles allow for effective multiplexing in fluorescence assays, while its rapid photobleaching resistance supports prolonged observation of dynamic interactions in various systems. | ||||||
6-TET, SE | sc-482043 | 5 mg | $182.00 | |||
6-TET, SE is a distinctive fluorescein derivative characterized by its exceptional photophysical properties, including a high quantum yield and sharp emission spectra. Its unique molecular architecture facilitates efficient energy transfer processes, enhancing fluorescence intensity. The compound exhibits notable stability under varying pH conditions, allowing for reliable performance in diverse environments. Additionally, its ability to form specific interactions with biomolecules enables targeted applications in fluorescence-based studies. |