
Propargyl-PEG6-NH2 | CAS 1198080-04-4
| Catalog Number | R01-0203 |
| Category | Alkynes |
| Molecular Formula | C₁₅H₂₉NO₆ |
| Molecular Weight | 319.39 |
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Product Introduction
Propargyl-PEG6-NH2 is a polyethylene glycol (PEG)-based PROTAC linker. Propargyl-PEG6-NH2 can be used in the synthesis of a series of PROTACs.
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | Propargyl-PEG6-amine |
| Purity | 98% |
| IUPAC Name | 2-[2-[2-[2-[2-(2-prop-2-ynoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethanamine |
| SMILES | C#CCOCCOCCOCCOCCOCCOCCN |
| InChI | InChI=1S/C15H29NO6/c1-2-4-17-6-8-19-10-12-21-14-15-22-13-11-20-9-7-18-5-3-16/h1H,3-16H2 |
| InChIKey | USTJDUXGVRIRRT-UHFFFAOYSA-N |
| Solubility | In DMSO: 250 mg/mL (782.74 mM; Need ultrasonic) |
Product Specification
| Storage | Pure form, -20°C, 3 years; In solvent, -80°C, 6 months; -20°C, 1 month |
Application
Propargyl-PEG6-NH2 is a PEG-based alkyne-functional linker designed for copper-free or copper-catalyzed click chemistry workflows, enabling rapid conjugation through its terminal propargyl group. The flexible PEG6 spacer and primary amine handle support compatibility with aqueous labeling, surface immobilization, and biomolecule coupling strategies that benefit from improved solubility and reduced nonspecific interactions. As a versatile building block, it is commonly used to introduce an alkyne “handle” for subsequent bioorthogonal ligation, including rapid assembly of PEGylated probes, materials, and imaging reagents.
1. Bioorthogonal Probe Labeling
Propargyl-PEG6-NH2 is widely used as an alkyne-bearing reagent for installing click-ready functionality onto proteins, peptides, and other biomolecular platforms that are subsequently functionalized with azide-containing reporters. Researchers value the PEG6 chain for maintaining colloidal stability in labeling buffers and for spacing the reactive alkyne away from the biomolecule surface, which can help preserve binding or recognition properties of the labeled construct. This reagent is particularly common in workflows that generate multicomponent chemical probes, such as fluorescent tags, affinity handles, or enrichment reagents, where the alkyne handle is introduced first and the final reporter is attached in a modular, high-throughput manner.
2. Surface and Material Functionalization
Propargyl-PEG6-NH2 supports the creation of alkyne-functional surfaces and polymeric materials used in chemical biology and materials science. The primary amine enables convenient attachment to activated surfaces, coatings, or polymer backbones, while the terminal alkyne provides a reactive site for downstream click conjugation to azide-functional materials, nanoparticles, or biomolecule layers. This approach is frequently adopted for building patterned or functionalized interfaces, including PEGylated coatings that reduce fouling and improve reagent accessibility, as well as for constructing clickable hydrogel or scaffold systems used to organize bioactive ligands and imaging moieties.
3. PEG Linker for Conjugate Assembly
Propargyl-PEG6-NH2 serves as a practical PEG linker for assembling conjugates that require controlled spacing between a target and a reactive click partner. The PEG6 spacer is commonly selected to improve solubility and to mitigate steric crowding when attaching bulky fluorophores, affinity tags, or other chemical groups through click chemistry. In downstream development, the reagent is often used to generate intermediate alkyne-bearing conjugates that can be rapidly diversified by reacting with azide-functional components, supporting iterative optimization of probe architecture for imaging, tracking, or enrichment applications in research settings.
4. Molecular Imaging Reagent Development
Propargyl-PEG6-NH2 is used in the preparation of alkyne-functional imaging reagents and labeling intermediates that are later coupled to azide-bearing imaging reporters. The reagent’s PEG6 segment helps tune hydrophilicity and can improve handling of conjugates in aqueous labeling conditions, which is beneficial when preparing clickable imaging constructs for microscopy, fluorescence-based assays, or other molecular imaging tool development. By introducing a stable alkyne handle with a flexible spacer, Propargyl-PEG6-NH2 enables modular conjugation strategies where the imaging moiety can be selected or exchanged at a later stage, streamlining probe synthesis and enabling consistent reagent formats across experiments.
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