
Pyrene-amido-PEG4-CH2CH2COOH | CAS 1817735-34-4
| Catalog Number | F08-0006 |
| Category | Pyrene Dyes |
| Molecular Formula | C₂₈H₃₃NO₇ |
| Molecular Weight | 495.56 |
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Product Introduction
Pyrene-amido-PEG4-CH2CH2COOH is a polyethylene glycol (PEG)-based PROTAC linker. Pyrene-amido-PEG4-CH2CH2COOH can be used in the synthesis of a series of PROTACs.
Chemical Information
Product Specification
Application
Chemical Information
| Synonyms | Pyrene-PEG4-acid |
| Purity | 98% |
| IUPAC Name | 3-[2-[2-[2-[2-(4,6-dihydropyrene-1-carbonylamino)ethoxy]ethoxy]ethoxy]ethoxy]propanoic acid |
| SMILES | C1C=CC2=C3C1=CCC4=C3C(=C(C=C4)C(=O)NCCOCCOCCOCCOCCC(=O)O)C=C2 |
| InChI | InChI=1S/C28H33NO7/c30-25(31)10-12-33-14-16-35-18-19-36-17-15-34-13-11-29-28(32)24-9-7-22-5-4-20-2-1-3-21-6-8-23(24)27(22)26(20)21/h1,3-4,6-9H,2,5,10-19H2,(H,29,32)(H,30,31) |
| InChIKey | VISZCCCHHXRQSJ-UHFFFAOYSA-N |
| Solubility | DMSO, DMF, DCM |
Product Specification
| Fluorescence Quantum Yield | 1.00 |
| Excitation | 343; 326; 313 |
| Emission | 377; 397 |
| Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Application
Pyrene-amido-PEG4-CH2CH2COOH is a pyrene-based PEG-carboxylic acid conjugation building block designed for fluorescence labeling and materials functionalization. The pyrene chromophore enables strong, environment-sensitive fluorescence useful for tracking hydrophobic or aromatic interactions, while the PEG spacer improves aqueous handling and reduces steric constraints. The terminal carboxylic acid provides a practical handle for coupling into bioconjugates, affinity surfaces, and polymer or nanoparticle platforms used in fluorescence imaging and assay development.
1. Hydrophobic Labeling Probes
Pyrene-amido-PEG4-CH2CH2COOH is used as a fluorescent tag to visualize and quantify hydrophobic or aromatic microenvironments in complex mixtures, including polymer matrices, micelles, and membrane-associated assemblies. Researchers commonly incorporate the pyrene label into labeling strategies where the fluorescence readout reports on local environment changes around the aromatic chromophore. The PEG4 linker helps maintain dispersion in aqueous workflows and supports consistent probe performance during labeling of soft materials and supramolecular systems.
2. Biomaterial Surface Functionalization
Pyrene-amido-PEG4-CH2CH2COOH supports fluorescence-enabled characterization of biomaterials by enabling surface or bulk incorporation of a trackable moiety. In materials science and chemical biology workflows, the carboxylic acid functionality is leveraged to attach the pyrene-containing conjugate to surface chemistries or to prepare labeled polymer coatings and scaffolds for microscopy-based mapping of material distribution. This application is frequently used to confirm coating uniformity, monitor adsorption/retention behavior, and enable spatial studies of labeled constructs in microscopy and imaging readouts.
3. Fluorescent Conjugate Construction
Pyrene-amido-PEG4-CH2CH2COOH is applied as a modular fluorescent component for constructing research-grade conjugates where a pyrene fluorophore is required alongside a PEG spacer and a terminal carboxyl group. Chemical biology groups use the carboxyl handle to integrate the pyrene tag into larger labeling reagents, including PEGylated linkers and fluorescence reporters used to track conjugate localization in experimental imaging workflows. The combination of aromatic fluorescence and flexible PEG spacing makes it useful for building multi-component fluorescent reagents for assay development and material tracing.
4. Microscopy Tracking Of Assemblies
Pyrene-amido-PEG4-CH2CH2COOH is used in fluorescence microscopy to monitor the formation, localization, and stability of labeled assemblies formed from polymers, nanoparticles, or supramolecular components. The pyrene fluorophore provides a bright visualization handle for tracking where the labeled moiety partitions within heterogeneous systems, while the PEG spacer supports compatibility with aqueous sample preparation. This approach is commonly used to study assembly dynamics and distribution patterns in lab-scale imaging experiments where fluorescence contrast is needed to distinguish labeled domains.
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