
Ald-CH2-PEG8-azide | CAS 2353410-13-4
| Catalog Number | R14-0141 |
| Category | Azides |
| Molecular Formula | C18H35N3O9 |
| Molecular Weight | 437.5 |
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Product Introduction
Ald-CH2-PEG8-azide is a monodisperse PEG crosslinker containing an azide group and an aldehyde group. The azide group enables PEGylation via Click Chemistry. PEG8 spacer increases solubility in aqueous media. aldehyde can be used in PEGylation through its reaction with hydrazine or hydrazide forming a hydrolytic acyl hydrozone linkage.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Synonyms | 26-azido-3,6,9,12,15,18,21,24-octaoxahexacosanal |
| Purity | 98% |
| IUPAC Name | 2-[2-[2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]acetaldehyde |
| SMILES | C(COCCOCCOCCOCCOCCOCCOCCOCC=O)N=[N+]=[N-] |
| InChI | InChI=1S/C18H35N3O9/c19-21-20-1-3-23-5-7-25-9-11-27-13-15-29-17-18-30-16-14-28-12-10-26-8-6-24-4-2-22/h2H,1,3-18H2 |
| InChIKey | MDBICGYCCGZSLH-UHFFFAOYSA-N |
| Solubility | Water, DMSO, DCM, DMF |
Product Specification
| Storage | -20 °C |
Application
Ald-CH2-PEG8-azide is a PEG-based azide click chemistry reagent that combines an aldehyde-bearing handle with a terminal azide for bioorthogonal conjugation workflows. As an azide-functionalized linker, it is commonly used in strain-promoted or copper-catalyzed azide–alkyne cycloaddition strategies to install biomolecular or material components with high chemoselectivity. The PEG8 spacer supports improved solubility and reduced nonspecific interactions, making the reagent attractive for preparing functional imaging probes, surface-modified biomaterials, and multicomponent labeling constructs.
1. Bioconjugation Labeling
Ald-CH2-PEG8-azide is widely used as a modular linker for attaching azide-bearing moieties to alkyne-functional partners in click-based bioconjugation workflows. Researchers employ it to introduce a PEG8 spacer between a reactive aldehyde-containing group and the downstream click handle, which can help maintain labeling accessibility on proteins, peptides, and other biomolecules. The aldehyde functionality is frequently leveraged to enable additional conjugation or immobilization steps in parallel with azide-based assembly, supporting streamlined preparation of complex probe sets for chemical biology studies and analytical assays.
2. Molecular Imaging Probes
Ald-CH2-PEG8-azide serves as a practical building block for constructing molecular imaging and detection reagents that require both a flexible PEG linker and an azide for subsequent click installation of reporter tags. In probe development, the reagent is used to generate azide-functional intermediates that can be coupled to alkyne-bearing fluorophores, affinity ligands, or imaging scaffolds, enabling rapid exchange of reporter components without redesigning the entire conjugate. The PEG8 segment helps improve aqueous handling and can reduce aggregation tendencies during probe formulation and downstream optical characterization.
3. Surface and Hydrogel Functionalization
Ald-CH2-PEG8-azide is used to functionalize material surfaces and polymer networks where azide-mediated click coupling provides reliable attachment chemistry to alkyne-functional coatings or crosslinking partners. Biomaterials and materials science groups often incorporate this reagent to introduce PEG8-tethered azide groups that can be patterned or assembled onto surfaces, nanoparticles, or hydrogel matrices via click reactions. The aldehyde-bearing element also supports orthogonal coupling or surface chemistry options during material preparation, enabling multistep architectures such as layered functional coatings and affinity-enabled materials for research-grade assays.
4. Diagnostic Reagent Building Blocks
Ald-CH2-PEG8-azide is commonly applied in the development of diagnostic and analytical reagent components that rely on modular assembly of labeled recognition elements. Teams in reagent development use the azide handle to click-attach reporter or capture functionalities to prepared intermediates, supporting consistent batch-to-batch conjugate construction for assay development. The PEG8 linker is particularly useful when conjugates must remain soluble and accessible in complex assay buffers, while the aldehyde functionality can be used to support additional derivatization steps that align with established reagent manufacturing workflows.
Computed Properties
| XLogP3 | -0.5 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 11 |
| Rotatable Bond Count | 26 |
| Exact Mass | 437.23732970 g/mol |
| Monoisotopic Mass | 437.23732970 g/mol |
| Topological Polar Surface Area | 105Ų |
| Heavy Atom Count | 30 |
| Formal Charge | 0 |
| Complexity | 399 |
| 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 |
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