Amine-Reactive
Items 61 to 66 of 66 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
N-Succinimidyloxycarbonylpentyl Methanethiosulfonate | 76078-81-4 | sc-212285 | 10 mg | $290.00 | ||
N-Succinimidyloxycarbonylpentyl Methanethiosulfonate exhibits distinctive reactivity as an amine, characterized by its ability to form stable thioether linkages through nucleophilic substitution. The presence of the succinimide moiety enhances its electrophilic nature, promoting selective interactions with amines. This compound's unique structure allows for efficient conjugation reactions, facilitating the formation of covalent bonds that can influence molecular assembly and stability in various environments. | ||||||
Fluorescent red 647 reactive | sc-300707 | 1 mg | $399.00 | |||
Fluorescent red 647 reactive exhibits exceptional reactivity as an amine, characterized by its ability to form covalent bonds through nucleophilic attack on electrophilic centers. Its unique fluorophore structure allows for strong light absorption and emission, enhancing detection sensitivity. The compound's high quantum yield and photostability contribute to its effectiveness in various labeling applications, while its selective reactivity enables precise targeting in complex environments. | ||||||
N-Succinimido-(+)-biotin | 35013-72-0 | sc-212274A sc-212274B sc-212274 | 100 mg 250 mg 500 mg | $75.00 $190.00 $340.00 | ||
N-Succinimido-(+)-biotin demonstrates remarkable reactivity as an amine, primarily through its ability to engage in robust amide bond formation. The biotin component enhances its affinity for specific biomolecules, enabling targeted interactions. Its unique structure promotes efficient conjugation with amines, leading to stable adducts. This compound's distinctive molecular interactions facilitate the modulation of biochemical pathways, influencing the dynamics of complex biological systems. | ||||||
Amrubicinol-13C3 (Mixture of Diastereomers) | sc-217645 | 500 µg | $4500.00 | |||
Amrubicinol-13C3 (Mixture of Diastereomers) showcases intriguing behavior as an amine, particularly in its capacity to engage in hydrogen bonding and facilitate electron transfer processes. Its diastereomeric nature introduces diverse steric and electronic effects, influencing reaction kinetics and selectivity in synthetic pathways. The compound's solubility characteristics enhance its interaction with various substrates, promoting unique reactivity profiles in complex chemical environments. | ||||||
N-Maleimidobutyryloxysulphosuccinimide ester | 158018-86-1 | sc-355687 | 100 mg | $265.00 | ||
N-Maleimidobutyryloxysulphosuccinimide ester is a versatile reagent known for its ability to form stable covalent bonds with amines through thiol-ene click chemistry. Its unique structure facilitates rapid reaction kinetics, allowing for efficient conjugation under mild conditions. The sulfonyl group enhances solubility and reactivity, while the maleimide moiety provides specificity in targeting nucleophilic sites. This compound's distinct molecular interactions enable precise modifications in complex biochemical systems. | ||||||
6-HEX, SE | sc-482035 | 5 mg | $137.00 | |||
6-HEX, SE exhibits remarkable properties as an amine, characterized by its ability to form stable complexes through coordination with metal ions. This interaction can significantly alter reaction pathways, enhancing catalytic efficiency. The compound's unique steric configuration influences its nucleophilicity, allowing for selective reactions with electrophiles. Additionally, its polar nature contributes to solvation dynamics, impacting reactivity in diverse chemical systems. | ||||||