Items 51 to 60 of 157 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Calcein Blue | 54375-47-2 | sc-214650 sc-214650A | 1 g 10 g | $67.00 $362.00 | ||
Calcein Blue is a fluorescent dye that exhibits remarkable photostability and distinct emission characteristics when excited below 380 nm. Its unique structure allows for effective chelation with metal ions, leading to enhanced fluorescence intensity. The compound's ability to form stable complexes influences its photophysical behavior, while its hydrophilic nature promotes solubility in aqueous environments. These properties make it an intriguing candidate for exploring molecular interactions and dynamics in various chemical systems. | ||||||
2′-O-(N′-Methylanthraniloyl)guanosine-3′,5′-cyclic monophosphate sodium salt | 83707-15-7 | sc-221695 | 10 µmol | $209.00 | ||
2'-O-(N'-Methylanthraniloyl)guanosine-3',5'-cyclic monophosphate sodium salt is a cyclic nucleotide that exhibits unique photophysical properties when excited below 380 nm. Its structural configuration facilitates specific interactions with protein kinases, influencing signal transduction pathways. The compound's ability to undergo conformational changes enhances its reactivity, while its ionic nature contributes to solubility in polar solvents, making it a fascinating subject for studying molecular dynamics and enzymatic mechanisms. | ||||||
7-Ethoxycoumarin-3-carbonitrile | 117620-77-6 | sc-210611 | 10 mg | $143.00 | ||
7-Ethoxycoumarin-3-carbonitrile is a fluorescent compound that exhibits intriguing photochemical behavior when excited below 380 nm. Its unique structure allows for strong π-π stacking interactions, enhancing its stability and reactivity in various environments. The presence of the ethoxy and cyano groups influences its electronic properties, leading to distinct absorption and emission characteristics. This compound's ability to participate in electron transfer processes makes it a compelling subject for exploring molecular interactions and reaction kinetics. | ||||||
Ageladine A, TFA | 643020-13-7 | sc-396549 | 200 µg | $364.00 | ||
Ageladine A, TFA is a fascinating compound that exhibits remarkable photophysical properties when excited below 380 nm. Its unique structural features facilitate strong hydrogen bonding and intramolecular interactions, which significantly influence its reactivity. The compound's distinct electronic configuration allows for efficient energy transfer processes, making it an interesting candidate for studying dynamic molecular behavior and reaction pathways in various chemical environments. | ||||||
QUIN 2, Tetrapotassium Salt | 73630-23-6 | sc-202303 | 5 mg | $231.00 | ||
QUIN 2, Tetrapotassium Salt, is a notable compound characterized by its ability to form stable complexes with metal ions, enhancing its reactivity in various chemical systems. Its unique ionic structure promotes strong electrostatic interactions, which can influence solubility and stability in aqueous environments. The compound exhibits distinct fluorescence properties under UV light, allowing for the exploration of energy transfer mechanisms and molecular dynamics in complex mixtures. | ||||||
6-Dodecanoyl-N,N-dimethyl-2-naphthylamine | 74515-25-6 | sc-214371 | 100 mg | $331.00 | 1 | |
6-Dodecanoyl-N,N-dimethyl-2-naphthylamine is a distinctive compound known for its robust hydrophobic interactions and unique photophysical properties. Its naphthyl moiety contributes to significant π-π stacking, enhancing its stability in nonpolar environments. The compound exhibits notable fluorescence under UV excitation, facilitating studies on energy transfer and molecular aggregation. Additionally, its structure allows for versatile reactivity, making it an intriguing subject for exploring reaction kinetics in organic synthesis. | ||||||
FFP-18(AM) | sc-218476 | 1 mg | $357.00 | |||
FFP-18(AM) is an intriguing acid halide characterized by its strong electrophilic nature, which facilitates rapid acylation reactions with nucleophiles. Its unique carbon chain length enhances solubility in organic solvents, promoting efficient interaction with various substrates. The compound exhibits distinct reactivity patterns, particularly in esterification and amidation processes, making it a valuable model for studying reaction mechanisms and kinetics in synthetic organic chemistry. | ||||||
7-HC-6-heptenoate | sc-223737 sc-223737A | 10 mg 50 mg | $74.00 $295.00 | |||
7-HC-6-heptenoate is a notable acid halide distinguished by its conjugated double bond, which imparts unique reactivity in electrophilic addition reactions. This compound's structural features enable selective interactions with nucleophiles, leading to diverse synthetic pathways. Its ability to undergo rapid transesterification and acyl transfer reactions highlights its role in exploring reaction dynamics and mechanistic studies in organic synthesis. The compound's distinct physical properties further enhance its utility in various chemical transformations. | ||||||
Vitamin A | 68-26-8 | sc-280187 sc-280187A | 1 g 10 g | $377.00 $2602.00 | ||
Vitamin A, a vital organic compound, exhibits intriguing photochemical properties, particularly in its interaction with light below 380 nm. Its conjugated system allows for efficient energy absorption, leading to isomerization and potential radical formation. This behavior facilitates unique pathways in photoreactivity, influencing molecular stability and reactivity. Additionally, Vitamin A's hydrophobic nature enhances its solubility in lipid environments, affecting its transport and interaction with biological membranes. | ||||||
Toluidine Blue O | 92-31-9 | sc-206058 sc-206058A sc-206058C sc-206058B | 25 g 100 g 1 kg 250 g | $138.00 $258.00 $1275.00 $367.00 | 5 | |
Toluidine Blue O is a synthetic dye characterized by its strong absorption of light below 380 nm, which facilitates distinct electronic transitions within its aromatic structure. This compound exhibits notable interactions with nucleic acids, leading to intercalation and enhanced fluorescence. Its cationic nature promotes binding to negatively charged surfaces, influencing reaction kinetics and stability in various environments. The dye's solubility in polar solvents further enhances its versatility in diverse chemical contexts. | ||||||