
LG-PEG10-azide
| Catalog Number | R14-0012 |
| Category | Azides |
| Molecular Formula | C34H66N4O21 |
| Molecular Weight | 866.9 |
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Product Introduction
LG-PEG10-azide
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| IUPAC Name | (2R,3R,5R)-N-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethyl]-2,3,5,6-tetrahydroxy-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhexanamide |
| SMILES | C(COCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-])NC(=O)C(C(C(C(CO)O)OC1C(C(C(C(O1)CO)O)O)O)O)O |
| InChI | InChI=1S/C34H66N4O21/c35-38-37-2-4-49-6-8-51-10-12-53-14-16-55-18-20-57-22-21-56-19-17-54-15-13-52-11-9-50-7-5-48-3-1-36-33(47)30(45)29(44)32(25(41)23-39)59-34-31(46)28(43)27(42)26(24-40)58-34/h25-32,34,39-46H,1-24H2,(H,36,47)/t25-,26-,27+,28+,29-,30-,31-,32?,34+/m1/s1 |
| InChIKey | OCOLQNCCGCCUGL-NGPHBTBESA-N |
Product Specification
| Storage | -20 °C |
Application
LG-PEG10-azide is a polyethylene glycol (PEG)-functionalized azide reagent designed for copper-free and copper-mediated azide–alkyne click chemistry workflows. As a small PEG conjugation handle, it combines the bioorthogonal azide functionality with a flexible hydrophilic spacer that can improve solubility and reduce nonspecific interactions in labeling and surface modification contexts. LG-PEG10-azide is commonly used as a modular “PEG–azide” building block for attaching biomolecules, polymers, and nanomaterials to alkyne-bearing partners in research-grade chemical biology, biomaterials, and molecular imaging tool development.
1. Bioconjugation Labeling
LG-PEG10-azide is widely used to introduce an azide handle onto proteins, peptides, and other biomolecular platforms that are subsequently coupled to alkyne-functional probes via click chemistry. Researchers favor PEG spacers to help maintain target accessibility, improve aqueous compatibility, and moderate steric effects during probe attachment. This reagent supports modular workflows in chemical biology where labeling density, linker length, and conjugation site availability are tuned by selecting PEG–azide reagents matched to the downstream alkyne partner.
2. Surface Functionalization
LG-PEG10-azide is used to functionalize material surfaces and interfaces with azide groups for later attachment of fluorescent tags, affinity ligands, or biorecognition elements using click-compatible alkyne chemistries. The PEG component helps create a hydrated, antifouling-like interfacial environment that can be advantageous for assays, biosensor coatings, and cell-interaction studies where nonspecific adsorption can otherwise dominate. This makes LG-PEG10-azide a practical choice for engineering azide-bearing coatings on polymers, glass, and other lab-scale substrates intended for probe immobilization.
3. Polymer and Hydrogel Crosslinking
LG-PEG10-azide is commonly incorporated into PEG-based polymer systems and hydrogel formulations to enable click-based network formation or post-gel functionalization with alkyne-bearing crosslinkers and pendant groups. In biomaterials research, the azide functionality provides a versatile handle for spatially controlled modification after material formation, supporting the creation of materials with tailored presentation of bioactive motifs or imaging reporters. The PEG spacer also aligns well with hydrogel design principles that emphasize water compatibility and tunable mechanical/transport behavior.
4. Molecular Imaging Probes
LG-PEG10-azide is used as a PEG–azide intermediate for assembling imaging and detection reagents that require a click-ready azide moiety for coupling to alkyne-functional reporter scaffolds. Molecular imaging tool development often benefits from PEG linkers to improve solubility, reduce aggregation, and provide a flexible distance between the reporter and its conjugation partner, which can be important for probe stability in complex labeling buffers. By supplying a standardized azide handle, LG-PEG10-azide supports reproducible probe construction in research workflows that rely on modular click assembly.
Computed Properties
| XLogP3 | -5.8 |
| Hydrogen Bond Donor Count | 9 |
| Hydrogen Bond Acceptor Count | 23 |
| Rotatable Bond Count | 41 |
| Exact Mass | 866.42195513 g/mol |
| Monoisotopic Mass | 866.42195513 g/mol |
| Topological Polar Surface Area | 316Ų |
| Heavy Atom Count | 59 |
| Formal Charge | 0 |
| Complexity | 1040 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 8 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
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