Items 71 to 80 of 198 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Calcein disodium salt | 108750-13-6 | sc-210999 sc-210999A sc-210999B | 1 g 5 g 25 g | $53.00 $99.00 $359.00 | ||
Calcein disodium salt is a fluorescent compound that emits light in the 495-570 nm range, characterized by its unique chelation properties. The presence of carboxylate groups allows for strong interactions with metal ions, enhancing its fluorescence through metal-to-ligand charge transfer. Its hydrophilic nature, due to the disodium salt form, promotes solubility in aqueous environments, facilitating dynamic interactions in biological systems and influencing reaction kinetics in various chemical processes. | ||||||
DAF-2T | 208850-35-5 | sc-294266 | 1 mg | $411.00 | 1 | |
DAF-2T is a fluorescent dye that exhibits emission in the 495-570 nm range, notable for its robust photostability and high quantum yield. Its unique structure allows for selective binding to specific targets, enhancing its sensitivity in detection applications. The compound's electron-rich framework facilitates intramolecular charge transfer, resulting in distinct spectral properties. Additionally, its lipophilic characteristics enable effective membrane permeability, influencing its behavior in diverse environments. | ||||||
N-(NBD-Aminocaproyl)sphinganine | sc-301239 | 50 µg | $42.00 | |||
N-(NBD-Aminocaproyl)sphinganine is a specialized compound that emits fluorescence in the 495-570 nm range, characterized by its unique ability to form stable complexes with biomolecules. Its structural features promote specific hydrogen bonding interactions, enhancing selectivity in binding assays. The compound's amphiphilic nature contributes to its solubility in various media, while its dynamic conformational flexibility allows for rapid response in biochemical environments, influencing reaction kinetics and molecular interactions. | ||||||
Ac-VEID-AFC | sc-311280 sc-311280A | 5 mg 10 mg | $261.00 $465.00 | 1 | ||
Ac-VEID-AFC is a fluorescent probe that emits light in the 495-570 nm range, distinguished by its capacity to undergo specific enzymatic cleavage. This compound features a unique peptide bond that facilitates selective interactions with proteases, leading to a measurable increase in fluorescence upon substrate hydrolysis. Its hydrophobic characteristics enhance membrane permeability, while the inherent stability of its structure ensures reliable performance in diverse biochemical assays, making it a valuable tool for studying proteolytic activity. | ||||||
2-Aminoacridone | 27918-14-5 | sc-213751 sc-213751A | 25 mg 100 mg | $101.00 $272.00 | ||
2-Aminoacridone is a fluorescent compound that exhibits strong emission in the 495-570 nm range, characterized by its ability to form hydrogen bonds and engage in π-π stacking interactions. These molecular features contribute to its stability and fluorescence intensity. The compound's unique electronic structure allows for efficient energy transfer processes, enhancing its photophysical properties. Additionally, its solubility in various solvents facilitates diverse experimental applications, making it a versatile choice for fluorescence-based studies. | ||||||
3,3′-Dipentyloxacarbocyanine iodide | 53213-81-3 | sc-214164 | 100 mg | $204.00 | ||
3,3'-Dipentyloxacarbocyanine iodide is a cyanine dye notable for its vibrant fluorescence in the 495-570 nm range. Its unique structure enables strong dipole-dipole interactions and effective charge transfer, enhancing its photostability. The compound's extended conjugated system contributes to its distinct absorption characteristics, while its hydrophobic nature influences solubility in organic solvents. These properties make it an intriguing subject for studies in photonics and molecular interactions. | ||||||
C-6 NBD-dihydro-Ceramide | 114301-95-0 | sc-204662 sc-204662A | 1 mg 5 mg | $255.00 $1040.00 | ||
C-6 NBD-dihydro-Ceramide is a fluorescent lipid derivative that exhibits strong emission in the 495-570 nm range. Its unique hydrophobic tail facilitates membrane incorporation, allowing for specific interactions with lipid bilayers. The compound's structural features promote distinct molecular packing and aggregation behaviors, influencing its photophysical properties. Additionally, its ability to form hydrogen bonds enhances stability and reactivity in various environments, making it a subject of interest in biophysical research. | ||||||
5-Carboxy-fluorescein diacetate N-succinimidyl ester | 150206-05-6 | sc-214315 | 5 mg | $158.00 | 1 | |
5-Carboxy-fluorescein diacetate N-succinimidyl ester is a fluorescent compound that emits light in the 495-570 nm range, characterized by its reactive ester groups. These groups enable efficient conjugation to amine-containing biomolecules, facilitating targeted labeling. The compound's unique structure allows for enhanced solubility in aqueous environments, while its carboxylic acid moiety can engage in ionic interactions, influencing its behavior in complex biological systems. Its photostability and distinct excitation properties make it a versatile tool for studying molecular dynamics. | ||||||
QUIN 2, Tetrapotassium Salt | 73630-23-6 | sc-202303 | 5 mg | $231.00 | ||
QUIN 2, Tetrapotassium Salt is a fluorescent chelator that exhibits strong emission in the 495-570 nm range. Its unique structure allows for effective binding with calcium ions, enhancing its fluorescence properties. The compound's ionic nature contributes to its solubility in aqueous solutions, facilitating interactions with various biomolecules. Additionally, its ability to form stable complexes with metal ions influences reaction kinetics, making it a valuable tool for probing cellular processes. | ||||||
6-Dodecanoyl-N,N-dimethyl-2-naphthylamine | 74515-25-6 | sc-214371 | 100 mg | $338.00 | 1 | |
6-Dodecanoyl-N,N-dimethyl-2-naphthylamine is a unique compound characterized by its distinct photophysical properties, particularly its emission in the 495-570 nm range. The presence of the dodecanoyl group enhances its hydrophobic interactions, promoting aggregation in nonpolar environments. This compound exhibits notable stability in various solvents, influencing its reactivity and interaction pathways. Its molecular structure allows for specific π-π stacking interactions, which can affect its electronic properties and fluorescence behavior. | ||||||