
Propargyl-PEG8-acid | CAS 2055014-94-1
| Catalog Number | R01-0214 |
| Category | Alkynes |
| Molecular Formula | C20H36O10 |
| Molecular Weight | 436.49 |
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Product Introduction
Propargyl-PEG8-acid features an extended PEG8 spacer for improved solubility and reduced aggregation in ADCs. The alkyne group supports efficient click reactions for covalent drug-antibody linkage in bioconjugation applications.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Synonyms | Alkyne-PEG8-COOH; Propargyl-PEG8-COOH; Propargyl-PEG7-CH2CH2COOH; 4,7,10,13,16,19,22,25-Octaoxaoctacos-27-ynoic acid; 4,7,10,13,16,19,22,25-Octaoxaoctacos-27-yn-1-oic acid |
| Purity | ≥95% |
| Shelf Life | ≥ 2 years |
| IUPAC Name | 3-[2-[2-[2-[2-[2-[2-(2-prop-2-ynoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]propanoic acid |
| SMILES | C#CCOCCOCCOCCOCCOCCOCCOCCOCCC(=O)O |
| InChI | InChI=1S/C20H36O10/c1-2-4-23-6-8-25-10-12-27-14-16-29-18-19-30-17-15-28-13-11-26-9-7-24-5-3-20(21)22/h1H,3-19H2,(H,21,22) |
| InChIKey | QZQUQXNQKWZDNM-UHFFFAOYSA-N |
| Solubility | Soluble in DCM, DMF, DMSO, Water |
| Density | 1.1±0.1 g/cm3 |
| Appearance | Pale Yellow or Colorless Oily Matter |
| Boiling Point | 531.0±50.0 °C at 760 mmHg |
| Vapor Pressure | 0.0±3.0 mmHg at 25°C |
| LogP | -2.23 |
Product Specification
| Storage | Store at 2-8°C |
Application
Propargyl-PEG8-acid is a PEG-based alkyne building block designed for copper-free and copper-catalyzed click chemistry workflows, most commonly serving as an alkyne handle for strain-promoted or azide–alkyne cycloaddition conjugation strategies. Its extended, hydrophilic PEG spacer and terminal carboxylic acid support aqueous solubility and downstream coupling to amine- or hydrazide-bearing biomolecules, surfaces, and polymeric materials. As a research-grade reagent, Propargyl-PEG8-acid is frequently used to introduce a defined clickable functionality while maintaining colloidal stability and reducing nonspecific interactions in labeling and materials assembly.
1. Biomolecule PEGylation
Propargyl-PEG8-acid is widely used to install a click-ready PEG spacer onto peptides, proteins, and other biomolecule scaffolds via carboxyl-activated coupling chemistries. The alkyne functionality enables subsequent attachment of azide-bearing tags, including fluorescent reporters, affinity handles, and bioorthogonal probes, while the PEG8 segment helps preserve solubility and improves conjugate behavior in complex buffers. This makes Propargyl-PEG8-acid a practical choice for preparing conjugation-ready bioreagents used in analytical chemistry, chemical biology, and probe development.
2. Surface And Material Functionalization
Propargyl-PEG8-acid supports the creation of clickable interfaces on polymer films, hydrogels, and functionalized nanoparticles by leveraging its terminal carboxylic acid for immobilization or tethering strategies. Once anchored, the alkyne group provides a convenient handle for subsequent reaction with azide-functional materials, enabling stepwise assembly of coatings, multicomponent surfaces, and spatially addressable constructs. In materials research workflows, Propargyl-PEG8-acid is often selected to balance surface hydration with controlled presentation of reactive groups.
3. Imaging Probe Conjugation
Propargyl-PEG8-acid is commonly incorporated into molecular imaging and detection reagent pipelines to generate azide-reactive conjugates that can be labeled with fluorophores or other reporter moieties containing azide functionality. The PEG8 spacer can help modulate steric accessibility of the clickable site, which is valuable when constructing multivalent probes or when conjugating to bulky targeting ligands. Researchers use Propargyl-PEG8-acid to produce well-defined alkyne-bearing intermediates for modular synthesis of imaging and sensing reagents.
4. Polymer and Hydrogel Crosslinking
Propargyl-PEG8-acid is used in polymer chemistry and biomaterials development to introduce alkyne functionality into PEG-containing networks and crosslinkable systems. By coupling the carboxylic acid to polymer backbones or pendant groups, the reagent enables later click-based incorporation of complementary azide components, allowing modular tuning of network composition and labeling density. This approach is particularly useful for generating functional hydrogels and polymer conjugates where maintaining aqueous compatibility and minimizing aggregation are important for downstream characterization and application.
Computed Properties
| XLogP3 | -1.3 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 25 |
| Exact Mass | 436.23084734 g/mol |
| Monoisotopic Mass | 436.23084734 g/mol |
| Topological Polar Surface Area | 111Ų |
| Heavy Atom Count | 30 |
| Formal Charge | 0 |
| Complexity | 410 |
| 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 |
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