![{[Name]}](https://resource.bocsci.com/structure/2055022-35-8.gif?v=2025011501)
![{[Name]}](https://resource.bocsci.com/structure/34450-18-5.gif?v=2025011501)
![{[Name]}](https://resource.bocsci.com/structure/944560-99-0.gif?v=2025011501)
![{[Name]}](https://resource.bocsci.com/structure/1351556-81-4.gif?v=2025011501)
![{[Name]}](https://resource.bocsci.com/structure/34993-56-1.gif?v=2025011501)
![{[Name]}](https://resource.bocsci.com/structure/1422023-54-8.gif?v=2025011501)
Inquiry Basket
Propargyl-PEG5-amine | CAS 1589522-46-2
| Catalog Number | R01-0204 |
| Category | Alkynes |
| Molecular Formula | C13H25NO5 |
| Molecular Weight | 275.34 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
Propargyl-PEG5-amine is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Propargyl-PEG5-amine is a PEG-based PROTAC linker can be used in the synthesis of PROTACs.
Chemical Information
Product Specification
Application
Computed Properties
Patents
| Synonyms | Propargyl-PEG5-NH2 |
| Purity | >98.0% |
| Shelf Life | 0-4°C for short term (days to weeks), or -20°C for long term (months). |
| IUPAC Name | 2-[2-[2-[2-(2-prop-2-ynoxyethoxy)ethoxy]ethoxy]ethoxy]ethanamine |
| Canonical SMILES | C#CCOCCOCCOCCOCCOCCN |
| InChI | InChI=1S/C13H25NO5/c1-2-4-15-6-8-17-10-12-19-13-11-18-9-7-16-5-3-14/h1H,3-14H2 |
| InChIKey | BLBTXXAWMPTQOK-UHFFFAOYSA-N |
| Solubility | 10 mm in DMSO |
| Density | 1.0±0.1 g/cm3 |
| Appearance | Colorless Liquid |
| Boiling Point | 360.4±37.0 °C at 760 mmHg |
| Vapor Pressure | 0.0±0.8 mmHg at 25°C |
| LogP | -1.54 |
| Storage | Store at -5°C,keep in dry and avoid sunlight. |
Propargyl-PEG5-amine, a versatile chemical compound widely utilized in various bioconjugation and biomedical research applications, offers a myriad of opportunities. Here are four key applications:
Chemical Biology: A cornerstone in click chemistry reactions, Propargyl-PEG5-amine plays a vital role in conjugating biomolecules. The alkyne group of this compound engages in copper-catalyzed azide-alkyne cycloaddition (CuAAC) with azide-functionalized molecules, enabling precise labeling and modification of peptides, proteins, and nucleic acids with unparalleled specificity and efficiency.
Drug Delivery: In the realm of drug delivery systems, Propargyl-PEG5-amine acts as a pivotal linker connecting drugs to targeting molecules like antibodies or ligands. The polyethylene glycol (PEG) spacer ensures solubility and biocompatibility, while the propargyl group allows for stable conjugation, enhancing the precision and efficacy of the drug delivery vehicle, ultimately revolutionizing targeted drug delivery mechanisms.
Imaging: A catalyst for progress in diagnostic imaging, Propargyl-PEG5-amine plays a crucial role in developing imaging probes. By linking imaging agents such as fluorophores or radioisotopes to biomolecules, this compound enables real-time tracking of biological processes in vivo, particularly valuable in cancer research for visualizing tumor growth and metastasis, pushing the boundaries of diagnostic imaging technology.
Surface Modification: For researchers seeking to functionalize surfaces like nanoparticles, biosensors, and medical devices, Propargyl-PEG5-amine proves indispensable. PEGylation helps mitigate non-specific binding and enhance stability, while the propargyl group facilitates attachment of biological ligands, culminating in the creation of cutting-edge biosensing and diagnostic platforms poised to redefine the landscape of surface modification techniques.
| XLogP3 | -1.3 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 15 |
| Exact Mass | 275.17327290 g/mol |
| Monoisotopic Mass | 275.17327290 g/mol |
| Topological Polar Surface Area | 72.2Ų |
| Heavy Atom Count | 19 |
| Formal Charge | 0 |
| Complexity | 216 |
| 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 |
| Publication Number | Title | Priority Date |
|---|---|---|
| WO-2020152067-A1 | Heterocyclic derivatives | 2019-01-22 |
| US-2022062258-A1 | Heterocyclic derivatives | 2019-01-22 |
| US-2018346457-A1 | Raf-degrading conjugate compounds | 2017-04-28 |
| US-10787443-B2 | RAF-degrading conjugate compounds | 2017-04-28 |
| US-2018207276-A1 | Modified therapeutic agents and compositions thereof | 2015-03-18 |
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
- BODIPY Dyes: Definition, Structure, Synthesis and Uses
- Cyanine Dyes: Definition, Structure, Types and Uses
- Fluorescein Dyes: Definition, Structure, Synthesis and Uses
- Rhodamine Dyes: Definition, Structure, Uses, Excitation and Emission
- 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
- DNA Staining: Definition, Procedures, Benefits, Dyes and Uses
- Cell Staining: Definition, Principles, Protocols, Dyes, and Uses
- Ion Imaging: Definition, Principles, Benefits, Dyes, and Uses
- Fluorescent Labeling: Definition, Principles, Types and Applications
Recommended Products
Online Inquiry
