
Propargyl-PEG2-amine | CAS 944561-44-8
| Catalog Number | R02-0007 |
| Category | Alkynes |
| Molecular Formula | C7H13NO2 |
| Molecular Weight | 143.18 |
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Product Introduction
Propargyl-PEG2-amine is a small alkyne-functionalized linker used for copper-catalyzed click reactions in ADC construction. It provides a flexible and hydrophilic spacer for site-specific antibody labeling, supporting diverse bioconjugation workflows.
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | Alkyne-PEG2-Amine;2-[2-(2-Propynyloxy)ethoxy]ethylamine; Propyne-PEG2-NH2; 2-(2-(prop-2-yn-1-yloxy)ethoxy)ethan-1-amine |
| Purity | ≥ 95.0 % |
| IUPAC Name | 2-(2-prop-2-ynoxyethoxy)ethanamine |
| SMILES | C#CCOCCOCCN |
| InChI | InChI=1S/C7H13NO2/c1-2-4-9-6-7-10-5-3-8/h1H,3-8H2 |
| InChIKey | GVHLQHHQXWSDDM-UHFFFAOYSA-N |
| Solubility | 10 mm in DMSO |
| Density | 1.0±0.1 g/cm3 |
| Appearance | Colorless to almost colorless clear liquid |
| Boiling Point | 213.8±20.0 °C at 760 mmHg |
| LogP | 0.31180 |
Product Specification
| Storage | Store at -20 °C, keep in dry and avoid sunlight. |
| Signal | Danger |
| Precautionary Statement Codes | P260, P261, P264, P264+P265, P271, P280, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P354+P338, P316, P317, P319, P321, P332+P317, P362+P364, P363, P403+P233, P405, and P501 |
Application
Propargyl-PEG2-amine is a PEG-based primary amine functionalized with a terminal alkyne, making it a versatile handle for copper-free or copper-catalyzed click chemistry workflows, especially where aqueous solubility and bioconjugation compatibility are required. The short, flexible PEG spacer helps reduce nonspecific interactions and improves reagent accessibility to target biomolecules, surfaces, or polymer backbones. As a small-molecule building block, it is commonly incorporated into labeling, surface functionalization, and probe construction pipelines that rely on alkyne–azide coupling to generate stable conjugates for chemical biology and materials research.
1. Biomolecule Labeling
Propargyl-PEG2-amine is widely used as an alkyne-bearing amine for installing clickable functionality onto proteins, peptides, and other biomolecular scaffolds that already contain reactive groups for amide/amine coupling or that can be modified through standard bioconjugation chemistries. The PEG2 spacer supports efficient downstream click conjugation while helping maintain solubility in common labeling buffers, which is particularly valuable for workflows that compare multiple labeling densities or require reproducible probe formation. Researchers use this reagent to generate azide-reactive conjugates for imaging reagents, affinity reagents, and modular assay components where an alkyne handle is the key integration point.
2. Surface And Material Functionalization
Propargyl-PEG2-amine is commonly applied to functionalize polymers, nanoparticles, and planar materials with terminal alkyne groups, enabling subsequent attachment of azide-bearing ligands, dyes, or capture molecules via click chemistry. The amine functionality allows coupling to activated surfaces and scaffold chemistries, while the PEG spacer improves colloidal stability and can reduce surface-associated aggregation that would otherwise complicate conjugation and characterization. In materials science and industrial R&D, this reagent supports the build-out of clickable interfaces for biosensing platforms, customizable coatings, and modular material libraries used in high-throughput reagent development.
3. PEG Linker For Probe Construction
Propargyl-PEG2-amine serves as a compact PEG linker that provides both a reactive amine and a terminal alkyne, making it a practical intermediate for assembling multifunctional chemical probes. Teams in chemical biology and molecular imaging reagent development use it to introduce a controlled, flexible tether between a recognition element (installed through the amine) and a clickable attachment point used to connect to fluorophores, affinity tags, or other reporter modules. The PEG2 spacing is particularly helpful when probe performance depends on minimizing steric hindrance during conjugation and when probe solubility and handling are important for reproducible imaging and assay reagent preparation.
4. Polymer and Macromolecule Conjugation
Propargyl-PEG2-amine is used to introduce alkyne handles into polymer backbones and macromolecular constructs, supporting click-based post-functionalization strategies used in biomaterials and research-grade reagent manufacturing. The amine group enables incorporation through standard coupling to polymer functional groups or activated intermediates, while the terminal alkyne provides a reliable site for subsequent azide-driven assembly of multicomponent materials. This approach is frequently adopted to create clickable polymer coatings, crosslinkable or modular hydrogel components, and conjugate libraries where orthogonal control of functional density and conjugation order is needed for downstream characterization and application development.
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