
Azido-PEG8-amine | CAS 857891-82-8
| Catalog Number | R14-0263 |
| Category | Azides |
| Molecular Formula | C18H38N4O8 |
| Molecular Weight | 438.52 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
Azido-PEG8-amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. It is also a non-cleavable 8 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
Chemical Information
Product Specification
Application
Computed Properties
Patents
Chemical Information
| Synonyms | O-(2-Aminoethyl)-O'-(2-azidoethyl)heptaethylene glycol; N3-PEG8-CH2CH2NH2; Azido-PEG8-NH2; N3-PEG8-NH2; 26-Azido-3,6,9,12,15,18,21,24-octaoxahexacosan-1-amine |
| Purity | ≥90% |
| IUPAC Name | 2-[2-[2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanamine |
| SMILES | C(COCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-])N |
| InChI | InChI=1S/C18H38N4O8/c19-1-3-23-5-7-25-9-11-27-13-15-29-17-18-30-16-14-28-12-10-26-8-6-24-4-2-21-22-20/h1-19H2 |
| InChIKey | ZSFGTBJYBWJOLZ-UHFFFAOYSA-N |
| Appearance | Colorless or Light Yellowish Liquid |
| LogP | 0.54126 |
Product Specification
| Storage | Store at 2-8°C |
| Signal | Warning |
| GHSHazardStatements | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation] H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation] |
| Precautionary Statement Codes | P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 |
Application
Azido-PEG8-amine is a polyethylene glycol (PEG)-spaced primary amine bearing a terminal azide handle, designed for copper-free or copper-mediated azide–alkyne click chemistry workflows and downstream conjugation strategies. The PEG8 spacer provides aqueous solubility and reduces steric constraints, while the azide enables modular attachment of the amine-bearing biomolecule or material to complementary clickable partners such as cyclooctynes or alkynes. This reagent is commonly used as a versatile linker for building functional probes, labeling reagents, and PEGylated conjugates in chemical biology, imaging, and materials research.
1. Bioconjugation Linker Design
Azido-PEG8-amine is widely used as a PEG-based azide linker for assembling bioconjugates where an amine-functional handle must be retained for subsequent coupling to activated esters, isothiocyanates, aldehydes, or other electrophiles. Researchers incorporate the PEG8 spacer to improve conjugate solubility and to help preserve binding or recognition properties of the biomolecule being modified, particularly when multiple functional groups are introduced. The azide group provides a reliable click handle for attaching the conjugate to alkyne-functional probes, surfaces, or carriers under conditions compatible with sensitive biomolecular workflows.
2. Molecular Imaging Probe Building
Azido-PEG8-amine supports the construction of imaging reagents by enabling modular attachment of PEGylated targeting scaffolds or reporter moieties through azide–alkyne click chemistry. In molecular imaging and chemical biology tool development, the reagent is frequently selected to tune hydrophilicity and spacing between a reporter and a biomolecular recognition element, which can improve probe behavior in aqueous labeling and washing steps. The amine functionality further allows incorporation of additional chemistry for chelator installation, fluorophore coupling, or attachment to imaging platforms that require orthogonal functional groups.
3. Surface And Material Functionalization
Azido-PEG8-amine is used to functionalize polymers, nanoparticles, and material surfaces with a clickable azide layer while providing an amine for further derivatization or crosslinking. In biomaterials science, the PEG8 segment helps create a hydrated interface that can reduce nonspecific interactions and improve accessibility of reactive groups on the material surface. Click-compatible patterning and modular assembly workflows often rely on this reagent to introduce azide functionality that can be later coupled to alkyne-bearing linkers, coatings, or bioactive motifs for creating functionalized materials and assay-ready surfaces.
4. Diagnostic Reagent Development
Azido-PEG8-amine is commonly employed in the development of research diagnostic reagents and assay components that require controlled presentation of clickable handles for reagent assembly. The combination of an azide for click coupling and a primary amine for secondary conjugation enables flexible build-up of multicomponent assay systems, including labeled affinity reagents and immobilizable detection formats. Teams developing assay reagents often use the PEG8 spacer to manage steric accessibility and to support consistent conjugate behavior during reagent mixing, incubation, and washing steps.
Computed Properties
| XLogP3 | -1 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 11 |
| Rotatable Bond Count | 26 |
| Exact Mass | 438.26896418 g/mol |
| Monoisotopic Mass | 438.26896418 g/mol |
| Topological Polar Surface Area | 114Ų |
| Heavy Atom Count | 30 |
| Formal Charge | 0 |
| Complexity | 376 |
| 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-2022219409-A2 | Compositions containing nucleic acid nanoparticles and processes related to alteration of their physicochemical characteristics | 2021-04-15 |
| US-2022072141-A1 | Protein-drug conjugates comprising camptothecin analogs and methods of use thereof | 2020-07-13 |
| US-2021330810-A1 | Compositions containing nucleic acid nanoparticles with modular functionality | 2020-04-27 |
| US-11357865-B2 | Compositions containing nucleic acid nanoparticles with modular functionality | 2020-04-27 |
| US-2022370635-A1 | Compositions containing nucleic acid nanoparticles with modular functionality | 2020-04-27 |
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