
Folate-PEG3-azide
| Catalog Number | R14-0333 |
| Category | Azides |
| Molecular Formula | C27H35N11O8 |
| Molecular Weight | 641.64 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
Folate-PEG3-azide is a compound that integrates a folate moiety with a triethylene glycol (PEG3) spacer and an azide functional group. The azide group facilitates participation in copper-catalyzed azide–alkyne cycloaddition (CuAAC) reactions, enabling its use in bioorthogonal chemistry and bioconjugation strategies. This reagent is often applied in the selective targeting and labeling of folate receptor-expressing biomolecules, supporting studies in cellular imaging and targeted delivery systems.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Synonyms | (2S)-2-[(4-{[(2-amino-4-oxo-1,4-dihydropteridin-6-yl)methyl]amino}phenyl)formamido]-4-[(2-{2-[2-(2-azidoethoxy)ethoxy]ethoxy}ethyl)carbamoyl]butanoic acid; L-Glutamine, N2-[4-[[(2-amino-3,4-dihydro-4-oxo-6-pteridinyl)methyl]amino]benzoyl]-N-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethyl]-; N2-[4-[[(2-Amino-3,4-dihydro-4-oxo-6-pteridinyl)methyl]amino]benzoyl]-N-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethyl]-L-glutamine |
| Purity | >90% by HPLC |
| IUPAC Name | (2S)-2-[[4-[(2-amino-4-oxo-3H-pteridin-6-yl)methylamino]benzoyl]amino]-5-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethylamino]-5-oxopentanoic acid |
| SMILES | C1=CC(=CC=C1C(=O)NC(CCC(=O)NCCOCCOCCOCCN=[N+]=[N-])C(=O)O)NCC2=CN=C3C(=N2)C(=O)NC(=N3)N |
| InChI | InChI=1S/C27H35N11O8/c28-27-36-23-22(25(41)37-27)34-19(16-32-23)15-31-18-3-1-17(2-4-18)24(40)35-20(26(42)43)5-6-21(39)30-7-9-44-11-13-46-14-12-45-10-8-33-38-29/h1-4,16,20,31H,5-15H2,(H,30,39)(H,35,40)(H,42,43)(H3,28,32,36,37,41)/t20-/m0/s1 |
| InChIKey | SWFSDYKTNPMWOV-FQEVSTJZSA-N |
| Solubility | DMF and DMSO |
Product Specification
| Storage | -20 °C |
Application
Folate-PEG3-azide is a folate-targeting conjugate bearing a terminal azide handle for copper-free or copper-mediated azide–alkyne click chemistry. The reagent combines a bioactive folate moiety with a flexible PEG3 linker that improves solubility and presentation of the azide for downstream bioconjugation. As a result, Folate-PEG3-azide is widely used to install folate ligands onto probes, surfaces, and biomaterials where controlled attachment via click chemistry is required.
1. Folate-Targeted Probe Labeling
Folate-PEG3-azide is commonly used to generate folate-decorated imaging and detection probes by clicking the azide functionality onto alkyne-bearing reporters such as fluorophores, affinity tags, or imaging handles. Researchers in chemical biology and molecular imaging workflows rely on the PEG spacer to maintain accessibility of the folate ligand while enabling modular swapping of the reporter component. This approach supports rapid probe panel development for studying receptor-mediated binding behaviors in cell-based assays and for optimizing probe architecture prior to instrument measurements.
2. Cell-Targeted Surface Functionalization
Folate-PEG3-azide is used to functionalize culture substrates, microarrays, and biosensor surfaces with folate ligands through click-compatible coupling to alkyne-functional coatings. Biomaterials and diagnostic reagent developers often choose PEG-azide building blocks to achieve uniform ligand spacing and improved wettability, which can be important for reproducible binding readouts across experiments. The resulting folate-presenting surfaces are valuable for studying ligand–receptor interactions, building targeted capture platforms, and creating standardized materials for assay development.
3. Targeted Nanoparticle Conjugation
Folate-PEG3-azide supports the preparation of folate-functionalized nanoparticles and nanocarriers by click conjugation to alkyne-bearing lipid anchors, polymer backbones, or surface ligands. In research settings spanning chemical biology and materials science, the reagent is selected for its modularity: the folate targeting element is introduced as a defined azide-bearing component, while the nanoparticle formulation can be tuned independently. This separation of targeting and carrier design helps teams streamline iterative optimization of particle surface chemistry for downstream labeling, tracking, and binding studies.
4. Receptor-Binding Assay Reagents
Folate-PEG3-azide is frequently incorporated into assay reagent development where folate-decorated constructs are needed as binding reagents, competitive ligands, or reference standards. By using click chemistry to attach the azide-bearing folate to defined alkyne-functional scaffolds, developers can generate consistent multivalent or monovalent presentation formats that are useful for comparing binding trends across experimental conditions. Such constructs are also used to validate assay components in molecular imaging and diagnostic chemistry pipelines that require well-characterized targeting motifs.
Computed Properties
| XLogP3 | -0.9 |
| Hydrogen Bond Donor Count | 6 |
| Hydrogen Bond Acceptor Count | 14 |
| Rotatable Bond Count | 21 |
| Exact Mass | 641.26700712 g/mol |
| Monoisotopic Mass | 641.26700712 g/mol |
| Topological Polar Surface Area | 243Ų |
| Heavy Atom Count | 46 |
| Formal Charge | 0 |
| Complexity | 1080 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| 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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