
Propargyl-PEG12-amine | CAS 956348-61-1
| Catalog Number | R01-0198 |
| Category | Alkynes |
| Molecular Formula | C27H53NO12 |
| Molecular Weight | 583.71 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
Propargyl-PEG12-amine is a heterobifunctional PEG linker containing a propargyl group and an amino group. The propargyl group can react with azide in various biomolecules via click chemistry, and the amino group can react with carboxylic acids, activated NHS esters, carbonyls and so on.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Synonyms | Propargyl-PEG24-amine;HC≡C-CH2-PEG12-NH2; Propyne-PEG12-amine; Propyne-PEG12-NH2 |
| Purity | >97% |
| IUPAC Name | 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-prop-2-ynoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanamine |
| SMILES | C#CCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN |
| InChI | InChI=1S/C27H53NO12/c1-2-4-29-6-8-31-10-12-33-14-16-35-18-20-37-22-24-39-26-27-40-25-23-38-21-19-36-17-15-34-13-11-32-9-7-30-5-3-28/h1H,3-28H2 |
| InChIKey | NEVZNOYZXMNIGM-UHFFFAOYSA-N |
| Appearance | White Solid |
Product Specification
| Storage | Store at -18°C |
Application
Propargyl-PEG12-amine is a PEG-based propargylated primary amine designed for copper-free and copper-mediated click chemistry workflows, enabling efficient installation of alkyne handles onto biomolecules and materials. The reagent combines a terminal alkyne for click conjugation with a long, hydrophilic PEG spacer that improves solubility and reduces nonspecific interactions during labeling and surface modification. Its amine functionality further supports straightforward coupling to activated esters, aldehydes, or NHS-activated surfaces, making it a widely used building block for generating clickable PEGylated probes and linkers in chemical biology and materials research.
1. Biomolecule PEGylation
Propargyl-PEG12-amine is commonly used to introduce a PEG spacer and a terminal alkyne into proteins, peptides, and other biomolecular constructs prior to downstream conjugation. Researchers use the amine handle to attach the PEG chain to targeting ligands, scaffolds, or carrier proteins, then employ the alkyne group as a click-compatible handle for attaching fluorophores, affinity tags, or imaging moieties. The PEG12 length is particularly valued in labeling workflows where improved aqueous compatibility and reduced aggregation are important for maintaining reagent performance during probe assembly and analytical characterization.
2. Surface And Material Functionalization
Propargyl-PEG12-amine is frequently applied to functionalize polymeric and inorganic surfaces with click-ready PEG linkers for subsequent attachment of biomolecules or capture reagents. The primary amine enables coupling to activated surfaces and coatings, while the propargyl group provides a defined reactive site for later conjugation to complementary azide-bearing partners. This approach is used in the development of patterned materials, biointerfaces, and assay platforms where controlled surface presentation and minimized nonspecific adsorption benefit from PEG-mediated spacing between the surface and the attached recognition element.
3. Fluorophore And Probe Assembly
Propargyl-PEG12-amine is used as a modular linker to build fluorescent and affinity probes that require a long, flexible spacer between the labeling site and the reporter. By installing the PEG12-alkyne motif onto a scaffold through the amine functionality, probe developers can later perform click conjugation to assemble dye conjugates, enrichment handles, or multivalent imaging reagents. The resulting constructs are often designed to support robust labeling in complex buffers, where the PEG spacer helps maintain solubility and reduces background interactions during probe preparation and use.
4. Multivalent Targeting Constructs
Propargyl-PEG12-amine supports the creation of multivalent chemical biology tools by providing an alkyne-bearing PEG arm that can be clicked onto azide-functional targeting or assembly components. Researchers integrate the amine-bearing PEG linker into larger architectures such as ligand-decorated polymers, modular binding constructs, or scaffolded libraries, then use the alkyne handle to attach additional modules in a controlled, stepwise manner. This strategy is widely adopted in research settings that require flexible spacing and modularity to tune reagent architecture for imaging and binding studies, while keeping conjugation chemistry compatible with common click workflows.
Computed Properties
| XLogP3 | -2.4 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 13 |
| Rotatable Bond Count | 36 |
| Exact Mass | 583.35677613 g/mol |
| Monoisotopic Mass | 583.35677613 g/mol |
| Topological Polar Surface Area | 137Ų |
| Heavy Atom Count | 40 |
| Formal Charge | 0 |
| Complexity | 509 |
| 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 |
Recommended Services
Recommended Articles
- Hoechst Dyes: Definition, Structure, Mechanism and Applications
- Mastering the Spectrum: A Comprehensive Guide to Cy3 and Cy5 Dyes
- Fluorescent Probes: Definition, Structure, Types and Application
- Fluorescent Dyes: Definition, Mechanism, Types and Application
- Coumarin Dyes: Definition, Structure, Benefits, Synthesis and Uses
- Unlocking the Power of Fluorescence Imaging: A Comprehensive Guide
- Cell Imaging: Definitions, Systems, Protocols, Dyes, and Applications
- Lipid Staining: Definition, Principles, Methods, Dyes, and Uses
- Flow Cytometry: Definition, Principles, Protocols, Dyes, and Uses
- Nucleic Acid Staining: Definition, Principles, Dyes, Procedures, and Uses
Recommended Products
Online Inquiry