
Propargyl-PEG2-methylamine | CAS 1835759-76-6
| Catalog Number | R01-0120 |
| Category | Alkynes |
| Molecular Formula | C8H15NO2 |
| Molecular Weight | 157.2 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
Propargyl-PEG2-methylamine is a crosslinker with a propargyl group and methylamine group. The propargyl group forms triazole linkage with azide-bearing compounds or biomolecules in copper catalyzed Click Chemistry reactions. The methylamine group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc.
Chemical Information
Product Specification
Application
Computed Properties
Patents
Chemical Information
| Synonyms | N-methyl-2-(2-prop-2-ynoxyethoxy)ethanamine; Propargyl-PEG2-NHMe; Ethanamine, N-methyl-2-[2-(2-propyn-1-yloxy)ethoxy]- methyl({2-[2-(prop-2-yn-1-yloxy)ethoxy]ethyl})amine |
| Purity | 98% |
| IUPAC Name | N-methyl-2-(2-prop-2-ynoxyethoxy)ethanamine |
| SMILES | CNCCOCCOCC#C |
| InChI | InChI=1S/C8H15NO2/c1-3-5-10-7-8-11-6-4-9-2/h1,9H,4-8H2,2H3 |
| InChIKey | XZTAFUAQYHXUMA-UHFFFAOYSA-N |
| Solubility | Water, DMSO, DCM, DMF |
Product Specification
| Storage | -20 °C |
Application
Propargyl-PEG2-methylamine is a PEG-based propargylated amine designed for copper-free or copper-catalyzed click chemistry workflows, enabling efficient installation of an alkynyl handle onto biomolecules, polymers, and surfaces. As an amine-bearing PEG linker with a terminal alkyne, it is commonly used as a versatile intermediate for subsequent conjugation, including the preparation of fluorescent probes, affinity reagents, and functional materials. Its short, water-compatible PEG spacer supports solubility and reduces steric constraints, which is particularly valuable in bioconjugation and molecular imaging reagent development.
1. Bioconjugation Linker Development
Propargyl-PEG2-methylamine is widely employed as a compact PEG linker to introduce an alkyne functionality into amine-reactive conjugation schemes, supporting downstream click coupling to azide-bearing partners. Researchers use this reagent to build modular bioconjugates for assay development, including labeled antibodies, peptide constructs, and protein conjugates where controlled spacing and aqueous compatibility are important. The PEG2 spacer helps maintain accessibility of the reactive groups and improves handling in typical labeling buffers, making it a practical choice for preparing click-ready biomolecular reagents.
2. Fluorescent Probe And Imaging Tools
Propargyl-PEG2-methylamine is commonly used in the construction of fluorescent probes that require a terminal alkyne for azide-reactive labeling strategies. Molecular imaging and chemical biology groups incorporate this reagent to generate click-compatible dye conjugates, enabling rapid attachment to azide-tagged targeting motifs, imaging scaffolds, or polymeric carriers. The PEG2 methylamine architecture supports straightforward incorporation into labeling workflows while providing a short hydrophilic segment that can improve probe solubility and reduce nonspecific aggregation during probe assembly.
3. Surface Functionalization For Materials
Propargyl-PEG2-methylamine is used to functionalize surfaces and materials with an alkyne handle for subsequent click immobilization of azide-functional coatings, capture ligands, or patterned biomolecular layers. Materials scientists and diagnostic reagent developers often select this reagent to create clickable interfaces on polymer films, hydrogels, and other substrate formats where a PEG spacer improves wetting and reduces steric hindrance at the surface. The resulting alkyne-functional materials are then amenable to modular assembly, allowing rapid exchange of azide-bearing components for platform optimization.
4. Diagnostic Reagent And Assay Platforms
Propargyl-PEG2-methylamine supports the preparation of assay-ready reagents that rely on azide–alkyne click coupling for modular assembly of detection components. In diagnostic reagent development workflows, the reagent is used to introduce an alkyne group into affinity reagents, polymer tags, or signal-generating building blocks that are later coupled to azide-functional reporters. The PEG2 spacer and amine-bearing functionality make it a convenient intermediate for building consistent conjugation architectures across different reagent batches, facilitating scalable assay platform development in research and industrial settings.
Computed Properties
| XLogP3 | -0.4 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 7 |
| Exact Mass | 157.110278721 g/mol |
| Monoisotopic Mass | 157.110278721 g/mol |
| Topological Polar Surface Area | 30.5Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 117 |
| 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-2021260438-A1 | Antibody-drug conjugates comprising anti-b7-h3 antibodies | 2020-06-26 |
| US-2012269766-A1 | Bifunctional molecules with antibody-recruiting and entry inhibitory activity against the human immunodeficiency virus | 2009-10-13 |
| US-2016082102-A1 | Bifunctional molecules with antibody-recruiting and entry inhibitory activity against the human immunodeficiency virus | 2009-10-13 |
| US-9181224-B2 | Bifunctional molecules with antibody-recruiting and entry inhibitory activity against the human immunodeficiency virus | 2009-10-13 |
| US-2012034295-A1 | Chimeric small molecules for the recruitment of antibodies to cancer cells | 2008-05-13 |
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