Heterobifunctional Crosslinkers
Items 51 to 56 of 56 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Maleimide-PEG12-NHS ester | 1426151-00-9 | sc-397277 sc-397277A | 50 mg 250 mg | $340.00 $750.00 | ||
Maleimide-PEG12-NHS ester is a versatile heterobifunctional reagent featuring a maleimide moiety that selectively reacts with thiols, creating robust thioether bonds. The NHS ester component provides a rapid and efficient pathway for amine coupling, yielding stable amide linkages. The extended PEG chain enhances solubility and flexibility, facilitating improved molecular interactions and reaction kinetics, making it suitable for diverse bioconjugation strategies and complex biomolecule assembly. | ||||||
monodisperse Mal-PEG4-NHS-ester | 756525-99-2 | sc-397273 | 100 mg | $323.00 | ||
Monodisperse Mal-PEG4-NHS-ester is a specialized heterobifunctional linker characterized by its precise molecular weight and uniformity. The NHS ester group enables swift and selective amine coupling, while the maleimide moiety engages thiols, forming stable thioether bonds. Its PEG4 segment enhances solubility and biocompatibility, promoting efficient molecular interactions. This unique combination of functionalities allows for tailored conjugation strategies and optimized reaction dynamics in various applications. | ||||||
Maleimide-PEG8-NHS ester | 756525-93-6 | sc-397276 sc-397276A | 50 mg 250 mg | $206.00 $599.00 | ||
Maleimide-PEG8-NHS ester is a versatile heterobifunctional reagent featuring a polyethylene glycol (PEG) spacer that enhances solubility and flexibility. The NHS ester facilitates rapid and specific reactions with amines, while the maleimide group selectively reacts with thiol-containing compounds, yielding robust thioether linkages. This compound's unique structure promotes efficient conjugation and fine-tuning of molecular interactions, making it ideal for diverse biochemical applications. | ||||||
[N-(2-Maleimidoethyl]diethylenetriaminepentaacetic Acid, Monoamide | 180152-82-3 | sc-218918 | 10 mg | $500.00 | ||
N-(2-Maleimidoethyl]diethylenetriaminepentaacetic Acid, Monoamide is a heterobifunctional compound characterized by its dual reactivity. The maleimide moiety enables selective conjugation with thiols, forming stable thioether bonds, while the diethylenetriaminepentaacetic acid component offers multiple coordination sites for metal ions. This unique combination allows for intricate molecular assembly and enhanced stability in complex biochemical environments, facilitating diverse interaction pathways. | ||||||
2-maleimidoethylamine hydrochloride | 134272-64-3 | sc-265752 sc-265752A sc-265752B | 100 mg 1 g 5 g | $90.00 $311.00 $984.00 | ||
2-Maleimidoethylamine hydrochloride is a heterobifunctional compound characterized by its ability to form stable covalent bonds with thiol groups, enabling selective labeling and cross-linking of biomolecules. Its unique amine and maleimide functionalities facilitate specific interactions, allowing for precise conjugation in complex biochemical environments. The compound's reactivity is influenced by pH and temperature, which can modulate its kinetics, enhancing its utility in various chemical applications. | ||||||
N-(2-Maleimidoethyl)-6-aminohexanamide, Trifluoroacetic Acid Salt | 1185075-13-1 | sc-218916 | 10 mg | $300.00 | ||
N-(2-Maleimidoethyl)-6-aminohexanamide, Trifluoroacetic Acid Salt is a heterobifunctional compound distinguished by its ability to engage in selective cross-linking and conjugation reactions. The maleimide group provides a reactive site for thiol attachment, promoting the formation of robust thioether linkages. Meanwhile, the trifluoroacetic acid salt enhances solubility and stability, facilitating efficient reaction kinetics in various environments, thus enabling complex molecular interactions and assemblies. | ||||||