
Propargyl-PEG1-acid | CAS 55683-37-9
| Catalog Number | R01-0221 |
| Category | Alkynes |
| Molecular Formula | C6H8O3 |
| Molecular Weight | 128.13 |
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Product Introduction
Propargyl-PEG1-acid contains a propargyl group with a terminal carboxylic acid. Under the catalysis of copper, propargyl can react with azide-bearing compounds to form stable triazole compounds. The carboxylic acid can form amide bonds in the presence of activators (e.g. EDC, or DCC). It can be used in the synthesis of PROTACs.
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | Propargyl-PEG1-COOH; 3-(prop-2-yn-1-yloxy)propanoic acid |
| Purity | ≥95% |
| IUPAC Name | 3-prop-2-ynoxypropanoic acid |
| SMILES | C#CCOCCC(=O)O |
| InChI | InChI=1S/C6H8O3/c1-2-4-9-5-3-6(7)8/h1H,3-5H2,(H,7,8) |
| InChIKey | GMFDYXLFHSFUHE-UHFFFAOYSA-N |
| Density | 1.1±0.1 g/cm3 |
| Appearance | Pale Yellow or Colorless Oily Matter |
| Boiling Point | 265.8±20.0 °C at 760 mmHg |
Product Specification
| Storage | Store at 2-8°C for short term (days to weeks) or -20°C for long term (months to years) |
| Signal | Danger |
| Precautionary Statement Codes | P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P354+P338, P317, P319, P321, P332+P317, P362+P364, P403+P233, P405, and P501 |
Application
Propargyl-PEG1-acid is a PEG-based propargylated carboxylic acid designed for copper-catalyzed azide–alkyne cycloaddition (CuAAC) click chemistry and related alkyne-mediated bioconjugation workflows. Its short PEG spacer and terminal alkyne provide a convenient handle for attaching biomolecules, polymers, or surfaces while improving aqueous compatibility and reducing nonspecific interactions. This reagent is commonly incorporated into research-grade labeling strategies for generating stable triazole-linked conjugates used in chemical biology, materials functionalization, and molecular imaging tool development.
1. Biomolecule Conjugation
Propargyl-PEG1-acid is widely used to introduce a click-reactive alkyne functionality into proteins, peptides, and other biomolecular building blocks through standard coupling to the carboxylic acid. Researchers use the PEG spacer to help maintain solubility and to moderate steric effects during subsequent CuAAC labeling with azide-bearing partners, enabling efficient generation of triazole-linked conjugates for assay development and mechanistic studies. The resulting conjugates are particularly useful when a flexible, water-compatible linker is desired between the biological targeting element and the downstream tag.
2. Surface And Material Functionalization
Propargyl-PEG1-acid supports the creation of alkyne-functional surfaces and polymer materials that can be patterned or modified via CuAAC with azide-functional coatings, probes, or capture ligands. Material scientists and chemical engineers use the reagent to tether functional groups onto substrates while leveraging the PEG segment to improve wetting and reduce fouling in aqueous environments. This approach is frequently adopted for building modular interfaces such as clickable hydrogels, coatings, and sensor platforms where stable triazole linkages are needed for robust downstream reagent attachment.
3. Molecular Imaging Probe Building
Propargyl-PEG1-acid is commonly employed as an intermediate for assembling alkyne-bearing imaging reagents and diagnostic research tools that are later coupled to azide-functional fluorophores, affinity tags, or scaffold components via CuAAC. The PEG1 spacer helps maintain probe dispersibility and can reduce aggregation tendencies during probe synthesis and handling, which is valuable for consistent labeling workflows. Teams developing molecular imaging toolkits often prefer this reagent because it provides a compact, reactive alkyne handle that integrates cleanly into multi-component probe assembly pipelines.
4. Polymer and Nanocarrier Labeling
Propargyl-PEG1-acid is used to functionalize PEGylated polymers and nanoparticle/nanocarrier platforms with clickable alkyne groups for subsequent attachment of azide-bearing ligands or reporters. In materials and chemical biology labs, the reagent enables modular construction of labeled carriers where the PEG spacer supports colloidal stability and helps preserve reactivity during conjugation steps. The triazole-linked products generated from alkyne–azide coupling are frequently selected for creating reproducible, multi-functional carrier systems used in advanced labeling, tracking, and analytical reagent development.
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