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NHS-C5-bis-PEG3-azide
| Catalog Number | R14-0329 |
| Category | Azides |
| Molecular Formula | C34H58N10O15 |
| Molecular Weight | 846.88 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
A branched linker with two azides for click chemistry and an NHS activated ester
Chemical Information
Product Specification
Application
| Purity | >90% by HPLC |
| Solubility | DCM, THF, acetonitrile, DMF and DMSO |
| Appearance | Oil |
| Storage | -20 °C |
NHS-C5-bis-PEG3-azide, a versatile bifunctional crosslinker, finds a wide array of applications in biochemical and biomedical fields. Here are four key applications:
Bioconjugation: A foundational tool in bioconjugation, NHS-C5-bis-PEG3-azide is extensively utilized for linking proteins, peptides, and diverse biomolecules. The NHS ester delicately interacts with primary amines, facilitating the attachment of azide groups to biomolecules. This initial conjugation sets the scene for intricate creation of biofunctional molecules through click chemistry-mediated attachment of alkyne-tagged compounds, resulting in multifaceted biomolecular structures.
Drug Delivery: Spearheading targeted drug delivery advancements, NHS-C5-bis-PEG3-azide plays a pivotal role in crafting precise delivery systems. By linking NHS-C5-bis-PEG3-azide to drug compounds and attaching targeting ligands via click chemistry, researchers engineer systems tailored to deliver therapeutic agents precisely to target cells. This targeted drug delivery strategy not only enhances treatment efficacy but also minimizes non-specific effects and treatment-related toxicity.
Imaging: In the domain of biomolecule imaging, NHS-C5-bis-PEG3-azide emerges as a crucial component for labeling. The azide functionality provides the opportunity to attach fluorescent dyes or radiolabels through click chemistry, creating tools for real-time tracking and visualizing biological processes.
Surface Modification: A cornerstone in biomaterial and medical device surface engineering, the compound excels in surface modification. By introducing azide groups to surfaces, subsequent functionalization with alkyne-containing compounds becomes feasible, enabling the immobilization of bioactive ligands or antifouling agents. This strategic enhancement boosts the biocompatibility and functionality of materials utilized in medical sensors and implants.
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