
Hydroxy-Amino-bis(PEG2-propargyl) | CAS 2100306-77-0
| Catalog Number | R01-0092 |
| Category | Alkynes |
| Molecular Formula | C₁₆H₂₇NO₅ |
| Molecular Weight | 313.39 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
Hydroxy-Amino-bis(PEG2-propargyl) is a polyethylene glycol (PEG)-based PROTAC linker. Hydroxy-Amino-bis(PEG2-propargyl) can be used in the synthesis of a series of PROTACs.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Synonyms | 2-[bis[2-(2-prop-2-ynoxyethoxy)ethyl]amino]ethanol; Ethanol, 2-[bis[2-[2-(2-propyn-1-yloxy)ethoxy]ethyl]amino]-; 2-(4,7,13,16-tetraoxa-10-azanonadeca-1,18-diyn-10-yl)ethan-1-ol |
| Purity | 98% |
| IUPAC Name | 2-[bis[2-(2-prop-2-ynoxyethoxy)ethyl]amino]ethanol |
| SMILES | C#CCOCCOCCN(CCO)CCOCCOCC#C |
| InChI | InChI=1S/C16H27NO5/c1-3-9-19-13-15-21-11-6-17(5-8-18)7-12-22-16-14-20-10-4-2/h1-2,18H,5-16H2 |
| InChIKey | CFAWPKGCJLYIOW-UHFFFAOYSA-N |
Product Specification
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Application
Hydroxy-Amino-bis(PEG2-propargyl) is a multifunctional, PEG-based click chemistry reagent featuring two propargyl termini and an internal hydroxy–amino functionality. As a bis-propargyl compound, it is commonly used as a building block for copper-catalyzed azide–alkyne cycloaddition (CuAAC) and related alkyne-driven conjugation workflows. Its PEG2 spacing and hydrophilic character make it particularly relevant when researchers need to introduce two reactive alkyne handles for multivalent labeling, surface functionalization, or probe assembly in chemical biology and biomaterials programs.
1. Multivalent Probe Labeling
Hydroxy-Amino-bis(PEG2-propargyl) is widely used to generate multivalent chemical probes by coupling to azide-bearing targeting ligands, affinity tags, or imaging handles through CuAAC. The presence of two propargyl groups enables dense functionalization strategies that improve labeling efficiency in assay development and molecular imaging reagent preparation, while the PEG2 chain segments help maintain solubility and reduce nonspecific aggregation during probe handling. Researchers commonly incorporate this reagent into workflows for building modular probe libraries where azide partners can be varied while keeping a consistent bis-alkyne scaffold.
2. Biomolecule And Peptide Conjugation
Hydroxy-Amino-bis(PEG2-propargyl) supports click-based conjugation of biomolecules by providing two alkyne reactive sites that can be installed onto azide-functionalized biomolecular constructs. In chemical biology and proteomics tool development, the bis-propargyl format is useful for creating crosslinked or dual-labeled reagents, such as bifunctional tags for orthogonal downstream processing or for preparing standardized conjugates for assay panels. The PEG2 spacing and hydroxy–amino core are also advantageous in preparing aqueous conjugation mixtures where stable handling and reproducible coupling are important for research-grade reagent workflows.
3. Surface Functionalization For Biomaterials
Hydroxy-Amino-bis(PEG2-propargyl) is used to functionalize polymeric or hydrogel surfaces that carry azide groups, enabling the attachment of bioactive moieties, affinity ligands, or reporter groups via click chemistry. The dual alkyne functionality supports higher surface coverage and multivalent presentation of attached components, which is valuable in biomaterials science for building patterned or densely functionalized materials used in extracellular matrix mimics, cell-interaction studies, and material-based screening platforms. Its PEG2 character helps maintain surface wettability and facilitates consistent reagent performance during coating and washing steps typical of materials preparation.
4. Dual-Handle Linker Construction
Hydroxy-Amino-bis(PEG2-propargyl) serves as a practical dual-handle linker for constructing complex conjugates where two separate azide-bearing components must be incorporated into a single assembly. This usage is common in molecular imaging reagent development and diagnostic reagent chemistry, where researchers need controlled architectures such as bis-functional scaffolds for attaching two reporters, two affinity elements, or a reporter plus a capture handle. The reagent’s bis-propargyl design supports modular assembly strategies that streamline synthesis planning for research tool development, while the PEG2 spacing provides flexibility for reducing steric constraints in multicomponent coupling designs.
Computed Properties
| XLogP3 | -0.8 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 16 |
| Exact Mass | 313.18892296 g/mol |
| Monoisotopic Mass | 313.18892296 g/mol |
| Topological Polar Surface Area | 60.4Ų |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 300 |
| 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