Items 31 to 40 of 198 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Ac-LEHD-AFC | 210345-03-2 | sc-311277 sc-311277A | 5 mg 10 mg | $345.00 $682.00 | 1 | |
Ac-LEHD-AFC is a fluorescent compound characterized by its ability to emit light within the 495-570 nm spectrum. This acid halide features a unique structural framework that promotes selective interactions with target molecules, enhancing its reactivity. Its distinct electronic properties contribute to rapid reaction kinetics, making it an effective probe for studying dynamic processes. Additionally, its stability under varying conditions allows for reliable performance in diverse experimental setups. | ||||||
Dansylcadaverine | 10121-91-2 | sc-214851 sc-214851A sc-214851B | 100 mg 250 mg 1 g | $52.00 $89.00 $240.00 | 4 | |
Dansylcadaverine is a fluorescent compound that emits light in the 495-570 nm range, showcasing unique photophysical properties. Its structure facilitates strong hydrogen bonding and π-π stacking interactions, enhancing its affinity for specific biomolecules. The compound exhibits notable quantum yield and photostability, allowing for prolonged observation in various environments. Its distinct electronic configuration also influences its reactivity, making it a valuable tool for probing molecular dynamics. | ||||||
8-Hydroxypyrene-1,3,6-trisulfonic acid, trisodium salt | 27928-00-3 | sc-291738 | 1 g | $119.00 | 3 | |
8-Hydroxypyrene-1,3,6-trisulfonic acid, trisodium salt, is a highly fluorescent compound that emits light in the 495-570 nm range, characterized by its strong solubility in aqueous solutions. The presence of sulfonic acid groups enhances its ionic interactions, promoting stability in various environments. Its unique conjugated system allows for efficient energy transfer and a high degree of photostability, making it suitable for applications requiring consistent fluorescence under varying conditions. | ||||||
3,3′-Dioctadecyloxacarbocyanine perchlorate | 34215-57-1 | sc-214168 | 25 mg | $136.00 | 7 | |
3,3′-Dioctadecyloxacarbocyanine perchlorate is a lipophilic dye known for its remarkable fluorescence in the 495-570 nm range. Its long hydrocarbon chains facilitate strong interactions with lipid membranes, enhancing its ability to partition into biological systems. The compound exhibits unique photophysical properties, including high quantum yield and stability, which are influenced by its rigid structure and effective energy transfer mechanisms. This results in distinct fluorescence characteristics under varying environmental conditions. | ||||||
Ammonium 7-Fluoro-2,1,3-benzoxadiazole-4-sulfonate | 84806-27-9 | sc-210805 | 25 mg | $294.00 | ||
Ammonium 7-Fluoro-2,1,3-benzoxadiazole-4-sulfonate is a fluorescent compound that exhibits strong emission in the 495-570 nm range. Its unique benzoxadiazole core contributes to its exceptional photostability and high molar absorptivity. The sulfonate group enhances solubility in aqueous environments, promoting effective interactions with polar solvents. This compound's distinct electronic properties facilitate rapid excited-state dynamics, leading to efficient energy transfer and fluorescence under diverse conditions. | ||||||
DAF-2 DA (cell permeable) | 205391-02-2 | sc-221526 | 1 mg | $428.00 | 7 | |
DAF-2 DA is a cell-permeable fluorescent probe that emits light in the 495-570 nm range, characterized by its ability to selectively react with reactive oxygen species (ROS). Its unique structure allows for rapid diffusion across cellular membranes, enabling real-time monitoring of oxidative stress. The compound's distinct electron-rich framework enhances its reactivity, facilitating specific interactions with biomolecules and promoting efficient fluorescence signaling in biological systems. | ||||||
Rhodamine 6G | 989-38-8 | sc-280066 sc-280066A sc-280066B sc-280066C sc-280066D | 25 g 100 g 250 g 1 kg 5 kg | $49.00 $141.00 $263.00 $806.00 $2916.00 | 4 | |
Rhodamine 6G is a vibrant fluorescent dye known for its exceptional photostability and high quantum yield, emitting light in the 495-570 nm range. Its unique xanthene structure allows for strong π-π stacking interactions, enhancing its solubility in various solvents. The dye exhibits notable aggregation-induced emission properties, which can lead to distinct fluorescence behavior in different environments. Additionally, its ability to form hydrogen bonds contributes to its reactivity and versatility in various chemical contexts. | ||||||
Coumarin 6 | 38215-36-0 | sc-217955 sc-217955A sc-217955B sc-217955C | 1 g 5 g 10 g 25 g | $92.00 $249.00 $369.00 $779.00 | 3 | |
Coumarin 6 is a fluorescent compound characterized by its strong emission in the 495-570 nm range, attributed to its unique coumarin backbone. This structure facilitates efficient energy transfer and intramolecular charge transfer, enhancing its fluorescence properties. The compound exhibits notable solvatochromism, where its emission spectrum shifts based on solvent polarity. Coumarin 6 also demonstrates significant interactions with metal ions, influencing its photophysical behavior and reactivity in diverse environments. | ||||||
Ac-YVAD-AFC | 219137-85-6 | sc-311282 sc-311282A | 5 mg 10 mg | $166.00 $322.00 | 3 | |
Ac-YVAD-AFC is a synthetic peptide that exhibits fluorescence in the 495-570 nm range, primarily due to its unique amino acid sequence. This compound is designed to interact selectively with specific proteases, leading to a distinct cleavage event that enhances its fluorescent signal. Its structural conformation allows for effective binding to target enzymes, facilitating rapid reaction kinetics. Additionally, Ac-YVAD-AFC's stability in various conditions makes it a versatile tool for studying proteolytic activity. | ||||||
Hydroxystilbamidine bis(methanesulfonate) | 223769-64-0 | sc-300818 | 10 mg | $465.00 | ||
Hydroxystilbamidine bis(methanesulfonate) is a fluorescent compound that emits light in the 495-570 nm range, characterized by its unique stilbene backbone. This compound exhibits strong intermolecular interactions, enhancing its photostability and fluorescence intensity. Its distinct electronic structure allows for efficient energy transfer processes, contributing to its dynamic photophysical properties. The compound's solubility in polar solvents facilitates diverse experimental applications, showcasing its versatility in various chemical environments. | ||||||