
AF430 maleimide
| Catalog Number | R01-0048 |
| Category | Alexa Fluor |
| Molecular Formula | C34H45N4F3O8S |
| Molecular Weight | 726.8 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
AF430 is a hydrophilic dye of coumarin nature. The dye is used in flow cytometry.,This maleimide derivative is reactive against thiol groups. Therefore, it allows to label many proteins, including those residing on cell surface.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Synonyms | BP Fluor 430 maleimide |
| Purity | NMR 1H, HPLC-MS (95%) |
| IUPAC Name | [9-[6-[2-(2,5-dioxopyrrol-1-yl)ethylamino]-6-oxohexyl]-8,8-dimethyl-2-oxo-4-(trifluoromethyl)pyrano[3,2-g]quinolin-6-yl]methanesulfonate;triethylazanium |
| SMILES | CC[NH+](CC)CC.CC1(C=C(C2=C(N1CCCCCC(=O)NCCN3C(=O)C=CC3=O)C=C4C(=C2)C(=CC(=O)O4)C(F)(F)F)CS(=O)(=O)[O-])C |
| InChI | InChI=1S/C28H30F3N3O8S.C6H15N/c1-27(2)15-17(16-43(39,40)41)18-12-19-20(28(29,30)31)13-26(38)42-22(19)14-21(18)34(27)10-5-3-4-6-23(35)32-9-11-33-24(36)7-8-25(33)37;1-4-7(5-2)6-3/h7-8,12-15H,3-6,9-11,16H2,1-2H3,(H,32,35)(H,39,40,41);4-6H2,1-3H3 |
| InChIKey | BNLRHNPZRYDBCU-UHFFFAOYSA-N |
| Solubility | Soluble in water, polar organic solvents (DMF, DMSO) |
| Appearance | Yellow solid |
Product Specification
| CF260 | 0.06 |
| CF280 | 0.06 |
| Fluorescence Quantum Yield | 0.23 |
| Mass Spec M+ Increment | 625.2 |
| Excitation | 430 |
| Emission | 542 |
| Storage | Storage: 12 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 maleimide is a maleimide-functional fluorescent dye designed for rapid, thiol-reactive bioconjugation. The maleimide group enables efficient coupling to cysteine-containing biomolecules and thiol-bearing surfaces, while the AF430 fluorophore provides an excitation/emission profile used for fluorescence-based labeling and tracking in chemical biology workflows. This reagent is commonly used to prepare fluorescent conjugates for imaging, assay development, and molecular staining where controlled attachment to sulfhydryl groups is required.
1. Protein Thiol Labeling
AF430 maleimide is widely used in protein labeling workflows where site-specific attachment to accessible cysteine residues is required. Researchers employ it to generate fluorescent protein conjugates for fluorescence microscopy, fluorescence-based binding studies, and labeling controls in biomolecular assays. The maleimide handle supports straightforward conjugate preparation to produce dye-labeled proteins for downstream characterization by fluorescence instruments such as plate readers and gel imaging systems.
2. Peptide And Biomolecule Conjugates
AF430 maleimide supports fluorescent labeling of peptides, peptide-based affinity reagents, and other thiol-containing biomolecules used in chemical biology and biomaterials research. In practice, it is used to build fluorescent probes for tracking biomolecule distribution, monitoring conjugate uptake in experimental systems, and generating labeled ligands for binding experiments. The thiol-reactive chemistry is particularly useful when preparing conjugates that must be compatible with fluorescence readouts without introducing large, non-fluorescent linkers.
3. Surface And Hydrogel Functionalization
AF430 maleimide is also used to functionalize thiol-bearing surfaces and biomaterials, including hydrogels and polymer coatings prepared with reactive sulfhydryl groups. Teams developing fluorescently addressable materials use the dye to visualize coating uniformity, quantify surface labeling, and create fluorescent material standards for microscopy and imaging experiments. This application is common in biomaterials science where stable attachment to thiol-functionalized substrates is needed for reproducible fluorescence imaging of engineered surfaces.
4. Fluorescent Probe Construction
AF430 maleimide is frequently incorporated into fluorescent probe development efforts that rely on thiol-mediated attachment of a fluorophore to a targeting or reporting scaffold. Researchers use the dye to assemble labeled constructs for molecular imaging reagent screening, fluorescence-based detection assay development, and labeling of components in multistep probe workflows. By enabling controlled dye installation on thiol-containing building blocks, AF430 maleimide helps teams generate consistent fluorescent reagents for experimental optimization and method development.
Computed Properties
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 12 |
| Rotatable Bond Count | 13 |
| Exact Mass | 726.29102007 g/mol |
| Monoisotopic Mass | 726.29102007 g/mol |
| Topological Polar Surface Area | 166Ų |
| Heavy Atom Count | 50 |
| 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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