
Ald-C2-PEG4-azide | CAS 2030118-14-8
| Catalog Number | R14-0144 |
| Category | Azides |
| Molecular Formula | C₁₁H₂₁N₃O₅ |
| Molecular Weight | 275.30 |
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Product Introduction
Ald-C2-PEG4-azide is a polyethylene glycol (PEG)-based PROTAC linker. Ald-C2-PEG4-azide can be used in the synthesis of a series of PROTACs.
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | Ald-PEG4-azide;N3-PEG4-CH2CH2CHO |
| Purity | 95% |
| IUPAC Name | 3-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]propanal |
| SMILES | C(COCCOCCOCCOCCN=[N+]=[N-])C=O |
| InChI | InChI=1S/C11H21N3O5/c12-14-13-2-5-17-7-9-19-11-10-18-8-6-16-4-1-3-15/h3H,1-2,4-11H2 |
| InChIKey | QOWLQMPHQXRVBL-UHFFFAOYSA-N |
| Solubility | Water, DMSO, DCM, DMF |
Product Specification
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Application
Ald-C2-PEG4-azide is a PEG-based azide-functionalized click chemistry reagent designed for bioorthogonal conjugation workflows. As an azide partner for copper-catalyzed azide–alkyne cycloaddition (CuAAC), it enables efficient attachment of biomolecules, linkers, or imaging handles to alkyne-bearing targets. The reagent combines an aldehyde-bearing anchor (for carbonyl-reactive coupling strategies) with a flexible PEG4 spacer that improves solubility and reduces steric constraints, making it well suited for downstream labeling, probe assembly, and surface or material functionalization in chemical biology and biomaterials research.
1. PEGylated Probe Labeling
Ald-C2-PEG4-azide is commonly used to introduce an azide handle into PEGylated probes and labeling reagents, supporting modular assembly with alkyne-functional dyes, affinity tags, or reporter scaffolds via CuAAC. The PEG4 spacer helps maintain probe accessibility and can reduce nonspecific interactions during labeling workflows, which is particularly valuable when generating soluble conjugates for analytical assays and microscopy. Researchers frequently incorporate Ald-C2-PEG4-azide into intermediate conjugation steps so that the final reporter attachment is deferred until the appropriate alkyne partner is selected, improving flexibility across probe design iterations.
2. Biomolecule Conjugation Workflows
Ald-C2-PEG4-azide fits into carbonyl-reactive conjugation schemes where aldehyde-containing precursors or aldehyde-functional biomolecule surfaces are used to install a PEG4-azide functionality prior to click coupling. This approach supports the preparation of azide-functional proteins, peptides, or polymer–biomolecule conjugates that can be further coupled to alkyne-bearing ligands, targeting motifs, or detection elements. In chemical biology laboratories, the reagent is often selected to create standardized azide-bearing intermediates that streamline multi-step bioconjugation pipelines, including the generation of reagent sets for comparative labeling studies.
3. Surface and Material Functionalization
Ald-C2-PEG4-azide is used to functionalize polymeric and biomaterials surfaces with azide groups for subsequent CuAAC attachment of alkyne-containing coatings, capture ligands, or fluorescent reporters. The PEG4 spacer can improve the presentation of reactive sites away from the surface, which is advantageous when immobilizing probes on hydrogels, membranes, or other substrate formats where steric crowding can limit coupling efficiency. Materials-focused groups often rely on Ald-C2-PEG4-azide to create stable, click-ready interfaces that support reproducible patterning and modular exchange of surface-bound components.
4. Molecular Imaging and Detection Reagents
Ald-C2-PEG4-azide is frequently incorporated into the build of imaging and detection reagents where an azide handle is required for late-stage conjugation to alkyne-bearing fluorophores or signal reporters. The PEG4 chain contributes to improved aqueous compatibility and can help preserve the optical or binding performance of appended reporters by reducing local steric effects. By using Ald-C2-PEG4-azide as a standardized azide-bearing linker, imaging reagent developers can rapidly generate libraries of conjugates with consistent linker environments, supporting efficient optimization of labeling density and probe architecture for analytical characterization workflows.
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