
4CzIPN | CAS 1416881-52-1
| Catalog Number | R12-0005 |
| Category | Non-Functionalized Dyes |
| Molecular Formula | C56H32N6 |
| Molecular Weight | 788.89 |
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Product Introduction
4CzIPN is an organic fluorescent dye. 4CzIPN is a thermally activated delayed fluorescence(TADF)material.
Chemical Information
Application
Chemical Information
| Synonyms | 1,2,3,5-Tetrakis(carbazol-9-yl)-4,6-dicyanobenzene; 1,3-Benzenedicarbonitrile, 2,4,5,6-tetra-9H-carbazol-9-yl-; tetrakis(9H-carbazol-9-yl)benzene-1,3-dicarbonitrile |
| IUPAC Name | 2,4,5,6-tetra(carbazol-9-yl)benzene-1,3-dicarbonitrile |
| SMILES | C1=CC=C2C(=C1)C3=CC=CC=C3N2C4=C(C(=C(C(=C4C#N)N5C6=CC=CC=C6C7=CC=CC=C75)N8C9=CC=CC=C9C1=CC=CC=C18)N1C2=CC=CC=C2C2=CC=CC=C21)C#N |
| InChI | InChI=1S/C56H32N6/c57-33-43-53(59-45-25-9-1-17-35(45)36-18-2-10-26-46(36)59)44(34-58)55(61-49-29-13-5-21-39(49)40-22-6-14-30-50(40)61)56(62-51-31-15-7-23-41(51)42-24-8-16-32-52(42)62)54(43)60-47-27-11-3-19-37(47)38-20-4-12-28-48(38)60/h1-32H |
| InChIKey | PRWATGACIORDEL-UHFFFAOYSA-N |
| Solubility | Soluble in DMSO (Slightly), Methanol (Slightly, Heated, Sonicated) |
| Density | 1.32±0.1 g/cm3 (Predicted) |
| Appearance | Light Yellow to Dark Yellow Solid |
Application
4CzIPN is a carbazole-based organic photocatalyst widely used in visible-light photoredox reactions, including click-type bond-forming transformations that proceed under mild conditions. Its strong absorption in the blue region and robust radical-generating behavior make it a frequent choice for building fluorescently labeled biomolecules and conjugates from functionalized precursors in chemical biology workflows.
1. Bioconjugation Under Light
4CzIPN is used by chemical biology and bioconjugation teams to enable light-driven coupling steps that generate labeled biomolecule conjugates without requiring harsh conditions. Researchers incorporate it into workflows that assemble clickable handles on proteins, peptides, and other biomolecular scaffolds prior to downstream attachment of dyes, affinity tags, or imaging reporters. This approach supports modular probe construction for microscopy and fluorescence-based assays where reaction compatibility with biomolecular functionality is a practical constraint.
2. Fluorescent Probe Construction
4CzIPN supports the development of fluorescent probes by facilitating photochemical assembly of conjugates from dye-bearing building blocks and reactive partners. Probe developers use it during the preparation of fluorescently tagged ligands, labeling reagents, and multicomponent imaging constructs that are subsequently validated by gel-based analysis, fluorescence spectroscopy, and microscopy. Because the reagent is commonly employed in visible-light workflows, it fits well into lab processes that prioritize operational simplicity and compatibility with light-sensitive labeling components.
3. Biomaterial Surface Functionalization
4CzIPN is applied in materials chemistry settings to drive light-mediated coupling chemistry for attaching functional groups to polymeric or surface-supported substrates. Biomaterials researchers use it to prepare surfaces and coatings bearing reactive motifs that can later be used for fluorescent labeling, immobilized affinity reagents, or imaging-compatible material platforms. In these workflows, 4CzIPN helps integrate photochemical steps into surface engineering pipelines used for microscopy studies and fluorescence readouts from engineered materials.
4. Polymer and Nanoparticle Labeling
4CzIPN is used in industrial and research laboratories to support photoredox-driven functionalization of polymers and nanoparticle conjugates used as fluorescence carriers. Teams developing labeled polymer standards, fluorescently tagged nanomaterials, or multivalent imaging reagents employ it to incorporate reactive sites that can be subsequently linked to fluorophores or targeting ligands. This enables scalable reagent preparation for fluorescence imaging experiments and fluorescence-based characterization of labeled materials.
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