
Propargyl-PEG8-bromide | CAS 2055046-25-6
| Catalog Number | R01-0180 |
| Category | Alkynes |
| Molecular Formula | C19H35BrO8 |
| Molecular Weight | 471.38 |
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Product Introduction
Propargyl-PEG8-bromide features a terminal alkyne and bromide for versatile conjugation chemistry. Its long PEG8 spacer enhances hydrophilicity and is suitable for use in ADC linker strategies.
Chemical Information
Product Specification
Application
Computed Properties
Patents
Chemical Information
| Synonyms | Alkyne-PEG8-Br; Propargyl-PEG8-Br |
| Purity | >98.0% |
| Shelf Life | 0-4°C for short term (days to weeks), or -20°C for long term (months). |
| IUPAC Name | |
| SMILES | C#CCOCCOCCOCCOCCOCCOCCOCCOCCBr |
| InChI | InChI=1S/C19H35BrO8/c1-2-4-21-6-8-23-10-12-25-14-16-27-18-19-28-17-15-26-13-11-24-9-7-22-5-3-20/h1H,3-19H2 |
| InChIKey | GKKYPBWKHAGRKT-UHFFFAOYSA-N |
| Solubility | 10 mm in DMSO |
| Appearance | Solid |
Product Specification
| Storage | Store at -20 °C, keep in dry and avoid sunlight. |
Application
Propargyl-PEG8-bromide is a PEG-based alkylating reagent bearing a terminal propargyl group, enabling copper-free or copper-mediated click-compatible conjugation workflows while providing a flexible hydrophilic spacer for biomolecule and surface functionalization. As a PEGylated propargyl bromide, it combines a reactive leaving group for nucleophilic substitution with an alkyne handle that is widely used in click chemistry for attaching labels, linkers, or functional motifs. Its PEG8 chain length is particularly relevant when minimizing nonspecific interactions and improving solubility in probe, material, and assay development.
1. PEG Linker For Conjugates
Propargyl-PEG8-bromide is commonly used as a PEG spacer linker to introduce a clickable alkyne handle onto amine- or thiol-containing substrates through standard PEGylation and alkylation strategies. Researchers and platform teams employ this reagent to build conjugates for chemical biology tools where the PEG segment helps control steric accessibility and reduces aggregation, improving labeling consistency across proteins, peptides, and polymeric carriers. The propargyl functionality supports downstream click coupling to azide-bearing partners, enabling modular assembly of fluorescent tags, affinity handles, or bioorthogonal probes.
2. Surface Functionalization Chemistry
Propargyl-PEG8-bromide is well suited for preparing clickable, antifouling-like surfaces by incorporating PEG spacers that improve wettability and reduce nonspecific adsorption. Materials scientists use it to generate alkyne-functional coatings and patterned interfaces that can subsequently be decorated with azide-bearing biomolecules, nanoparticles, or imaging reagents via click chemistry. This application is frequently adopted in sensor development and biomaterials research where spatially controlled immobilization and stable linker presentation are important for reproducible assay readouts and surface reactivity.
3. Fluorescent Probe And Imaging Labels
Propargyl-PEG8-bromide is frequently selected to create alkyne-bearing intermediates for fluorescent labeling workflows, particularly when longer PEG spacers are needed to tune probe behavior in complex chemical environments. Chemical biology groups use it to attach clickable handles to targeting ligands, carrier scaffolds, or solubilizing components, then perform azide–alkyne coupling to install dyes or imaging moieties. The PEG8 chain can help maintain probe dispersibility and accessibility of the reactive site, which is valuable when constructing multicomponent imaging reagents and ratiometric labeling schemes.
4. Polymer And Nanoparticle Labeling
Propargyl-PEG8-bromide is used to introduce propargyl-functional PEG linkers into polymer systems and nanoparticle formulations, enabling subsequent click-based attachment of functional ligands and reporters. Industrial and academic teams often incorporate PEG spacers to stabilize colloids, adjust surface chemistry, and improve compatibility with aqueous processing steps. By providing an alkyne handle for modular conjugation, the reagent supports scalable preparation of labeled materials such as PEGylated carriers, clickable coatings on particles, and functional polymer conjugates used in research-grade diagnostics and assay development.
Computed Properties
| XLogP3 | -0.1 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 24 |
| Exact Mass | 470.15153 g/mol |
| Monoisotopic Mass | 470.15153 g/mol |
| Topological Polar Surface Area | 73.8Ų |
| Heavy Atom Count | 28 |
| Formal Charge | 0 |
| Complexity | 337 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| WO-2021050612-A1 | Compositions and methods for the treatment of respiratory syncytial virus | 2019-09-09 |
| WO-2020252396-A1 | Compositions and methods for the treatment of respiratory syncytial virus | 2019-06-13 |
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