
HyNic-PEG4-alkyne
| Catalog Number | R01-0244 |
| Category | Alkynes |
| Molecular Formula | C20H30N4O5 |
| Molecular Weight | 406.48 |
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Product Introduction
HyNic-PEG4-alkyne is a bifunctional ADC linker combining hydrazine and alkyne groups for oxime ligation and copper-catalyzed click chemistry, enhancing conjugation versatility and stability.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Purity | >98.0% |
| Shelf Life | 0-4°C for short term (days to weeks), or -20°C for long term (months). |
| IUPAC Name | |
| SMILES | CC(=NNC1=NC=C(C=C1)C(=O)NCCOCCOCCOCCOCC#C)C |
| InChI | InChI=1S/C20H30N4O5/c1-4-8-26-10-12-28-14-15-29-13-11-27-9-7-21-20(25)18-5-6-19(22-16-18)24-23-17(2)3/h1,5-6,16H,7-15H2,2-3H3,(H,21,25)(H,22,24) |
| InChIKey | WJVXRHOIVDGQSZ-UHFFFAOYSA-N |
| Solubility | 10 mm in DMSO |
| Appearance | Oil |
Product Specification
| Storage | Store at -20 °C, keep in dry and avoid sunlight. |
Application
HyNic-PEG4-alkyne is a PEGylated alkyne-bearing click chemistry reagent designed for copper-free and strain-promoted bioorthogonal conjugation workflows. The HyNic (hydrazine/acetylhydrazone) handle combined with a flexible PEG4 spacer provides a practical platform for installing alkyne functionality onto biomolecules, targeting ligands, or surfaces while improving solubility and reducing nonspecific interactions. As an alkyne partner used in SPAAC-style labeling strategies, HyNic-PEG4-alkyne is commonly selected for building imaging probes, diagnostic reagents, and functional biomaterials where controlled conjugation and aqueous compatibility are critical.
1. Biomolecule Labeling Workflows
HyNic-PEG4-alkyne is widely used to introduce a PEG-spaced alkyne handle onto proteins, peptides, and other macromolecular constructs that are subsequently functionalized with complementary cyclooctyne/strained-alkyne partners. Researchers in chemical biology and molecular imaging rely on the PEG4 spacer to help maintain binding-relevant conformations and to improve handling in aqueous buffers during downstream conjugation steps. The HyNic-derived functionality supports robust incorporation of the reagent into labeling pipelines, enabling modular assembly of multi-component probes such as fluorescent, affinity, or enrichment-tagged reagents for analytical assays and mechanistic studies.
2. Molecular Imaging Probe Assembly
HyNic-PEG4-alkyne is used as a key intermediate for preparing imaging-capable conjugates, including fluorescent and luminescent probe families that require reliable, bioorthogonal attachment to a second imaging moiety. The PEG4 linker helps reduce steric hindrance and promotes consistent probe performance when conjugation is performed under mild, bioconjugation-compatible conditions. In molecular imaging research, the reagent’s alkyne functionality supports the rapid generation of probe libraries where different reporter groups can be attached to a shared targeting or scaffold component, streamlining optimization of imaging reagent formats.
3. Targeting Ligand and Affinity Conjugates
HyNic-PEG4-alkyne is commonly incorporated into targeting ligands and affinity reagents to enable site-directed or handle-based construction of conjugates for binding studies and reagent development. The PEG4 spacer is particularly valuable when conjugation must preserve accessibility of recognition elements, such as in antibody fragments, receptor-binding peptides, or small-molecule affinity scaffolds. By providing an alkyne handle for subsequent click coupling, HyNic-PEG4-alkyne supports modular assembly of multivalent constructs used in pull-down workflows, binding characterization, and structured reagent generation for platform screening.
4. Functional Biomaterials Surface Modification
HyNic-PEG4-alkyne is applied in biomaterials science to functionalize polymeric and hydrogel surfaces with alkyne-bearing groups that can be further coupled to complementary clickable chemistries. Materials groups use the PEG4 segment to improve surface hydration and reduce nonspecific adsorption, which is important for reproducible performance in coating, patterning, and surface-based assays. The reagent’s click-ready alkyne functionality makes it suitable for creating functional interfaces such as affinity surfaces, bioactive coatings, and modular material platforms where subsequent attachment of probes, capture ligands, or signaling elements is performed in a controlled, aqueous workflow.
Computed Properties
| XLogP3 | 0.2 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 8 |
| Rotatable Bond Count | 16 |
| Exact Mass | 406.22162007 g/mol |
| Monoisotopic Mass | 406.22162007 g/mol |
| Topological Polar Surface Area | 103Ų |
| Heavy Atom Count | 29 |
| Formal Charge | 0 |
| Complexity | 516 |
| 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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