
AF430 tetrazine
| Catalog Number | R01-0040 |
| Category | Alexa Fluor |
| Molecular Formula | C32H32N6F3KO6S |
| Molecular Weight | 724.79 |
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Product Introduction
AF430 is a fluorescent dye. AF430 has an excitation maximum at 430 nm and an emission maximum at 542 nm. AF430 is one of the few dyes that absorb between 400 nm and 450 nm. AF430 fluorescence is photostable and pH-insensitive in a broad range of pH values.,Tetrazine residue participates in the fast copper-free click reaction that is well suited to non-toxic in vitro cell labeling and low-concentration applications.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Synonyms | BP Fluor 430 tetrazine |
| Purity | NMR 1H, HPLC-MS (95%) |
| IUPAC Name | potassium;[8,8-dimethyl-9-[6-[[4-(6-methyl-1,2,4,5-tetrazin-3-yl)phenyl]methylamino]-6-oxohexyl]-2-oxo-4-(trifluoromethyl)pyrano[3,2-g]quinolin-6-yl]methanesulfonate |
| SMILES | CC1=NN=C(N=N1)C2=CC=C(C=C2)CNC(=O)CCCCCN3C4=C(C=C5C(=CC(=O)OC5=C4)C(F)(F)F)C(=CC3(C)C)CS(=O)(=O)[O-].[K+] |
| InChI | InChI=1S/C32H33F3N6O6S.K/c1-19-37-39-30(40-38-19)21-10-8-20(9-11-21)17-36-28(42)7-5-4-6-12-41-26-15-27-24(25(32(33,34)35)14-29(43)47-27)13-23(26)22(16-31(41,2)3)18-48(44,45)46;/h8-11,13-16H,4-7,12,17-18H2,1-3H3,(H,36,42)(H,44,45,46);/q;+1/p-1 |
| InChIKey | YUKYIZNJBZINPX-UHFFFAOYSA-M |
| Solubility | Good in water, DMF, DMSO |
| Appearance | Dark orange solid |
Product Specification
| CF260 | 0.06 |
| CF280 | 0.06 |
| Fluorescence Quantum Yield | 0.23 |
| Mass Spec M+ Increment | 658.2 |
| Excitation | 430 |
| Emission | 542 |
| Storage | Storage: 24 months after receival at -20 °C in the Dark. Transportation: at room temperature for up to 3 weeks. Avoid prolonged exposure to light. Desiccate. |
Application
AF430 tetrazine is a tetrazine-based click chemistry reagent designed for bioorthogonal labeling via inverse-electron-demand Diels-Alder reactions with strained alkenes (commonly trans-cyclooctene or bicyclononyne). Its conjugation-ready tetrazine functionality enables rapid construction of fluorescent and affinity-tagged biomolecule conjugates, including imaging reagents and labeling handles for complex biological workflows. AF430 tetrazine is typically selected when researchers need efficient, orthogonal attachment to biomolecules, probes, or surfaces under conditions compatible with fluorescence-based readouts.
1. Fluorescent Probe Conjugation
AF430 tetrazine is used to assemble fluorescent labeling reagents where a tetrazine handle is required for later coupling to strained-alkene partners. Researchers in chemical biology and fluorescence imaging workflows employ it to generate AF430-containing probes for microscopy and spectroscopy-based localization studies, including labeling of proteins, peptides, and other biomolecular constructs that have been engineered to present a complementary strained-alkene group.
2. Biomolecule Labeling Workflows
AF430 tetrazine supports practical bioconjugation workflows that require fast, selective attachment to biomolecules without interfering with native functional groups. In academic and industrial research settings, it is commonly used to functionalize antibodies, antibody fragments, affinity ligands, and carrier proteins that have been pre-equipped with strained-alkene moieties, enabling downstream use in fluorescence-based assays, imaging reagent development, and molecular staining toolchains.
3. Surface And Material Functionalization
AF430 tetrazine is applied in biomaterials and surface engineering efforts where fluorescent tagging of functional materials is needed. Teams working on hydrogel labeling, nanoparticle surface modification, and polymer functionalization use it to install AF430-containing click handles onto substrates or colloidal platforms that carry strained-alkene groups, facilitating fluorescence readouts for material tracking, coating verification, and imaging-guided characterization.
4. Multi-Component Click Assembly
AF430 tetrazine is also leveraged for sequential or modular labeling strategies in probe construction, where a tetrazine component is introduced as one step in a multi-reagent assembly. Researchers building complex imaging reagents, FRET-capable constructs, or multiplexed labeling panels use AF430 tetrazine as a defined coupling module to integrate AF430 into larger conjugate architectures while maintaining compatibility with fluorescence measurement workflows.
Computed Properties
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 14 |
| Rotatable Bond Count | 11 |
| Exact Mass | 724.16931991 g/mol |
| Monoisotopic Mass | 724.16931991 g/mol |
| Topological Polar Surface Area | 176Ų |
| Heavy Atom Count | 49 |
| Formal Charge | 0 |
| Complexity | 1340 |
| 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 | 2 |
| Compound Is Canonicalized | Yes |
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