
BDP TMR azide
| Catalog Number | F01-0019 |
| Category | BODIPY |
| Molecular Formula | C24H27BF2N6O2 |
| Molecular Weight | 480.32 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
BDP TMR is a borondipyrromethene fluorophore (analog of BODIPY® TMR) with excitation and emission wavelengths matching TAMRA dye channels. The dye has a long fluorescence lifetime. This derivative is an azide for Click chemistry labeling.
Chemical Information
Product Specification
Application
Computed Properties
Chemical Information
| Purity | NMR 1H, HPLC-MS (95%) |
| IUPAC Name | N-(3-azidopropyl)-3-[2,2-difluoro-12-(4-methoxyphenyl)-4,6-dimethyl-1-aza-3-azonia-2-boranuidatricyclo[7.3.0.03,7]dodeca-3,5,7,9,11-pentaen-5-yl]propanamide |
| SMILES | [B-]1(N2C(=CC=C2C3=CC=C(C=C3)OC)C=C4[N+]1=C(C(=C4C)CCC(=O)NCCCN=[N+]=[N-])C)(F)F |
| InChI | InChI=1S/C24H27BF2N6O2/c1-16-21(10-12-24(34)29-13-4-14-30-31-28)17(2)32-23(16)15-19-7-11-22(33(19)25(32,26)27)18-5-8-20(35-3)9-6-18/h5-9,11,15H,4,10,12-14H2,1-3H3,(H,29,34) |
| InChIKey | RDEBWDYUAWKFLF-UHFFFAOYSA-N |
| Solubility | good in most organic solvents |
| Appearance | orange to brown solid |
Product Specification
| Fluorescence Quantum Yield | 0.95 |
| Excitation | 545 |
| Emission | 570 |
| 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
BDP TMR azide is a BDP-based tetramethylrhodamine (TMR) fluorescent azide designed for copper-free click chemistry labeling workflows, enabling efficient attachment of the dye to biomolecules, affinity reagents, and polymeric materials. Its bright red emission supports fluorescence microscopy and flow cytometry readouts after conjugate formation, while the azide handle makes it a practical reagent for building targeted fluorescent conjugates and imaging probes.
1. Biomolecule Labeling
BDP TMR azide is used by chemical biology and protein engineering groups to fluorescently label biomolecules through azide-alkyne click conjugation, producing stable, traceable conjugates for imaging and quantification. Researchers commonly incorporate the dye into labeled antibodies, peptides, and nucleic acid-related constructs to track binding interactions, reaction progress, or localization in cell and biochemical assays. The TMR fluorophore provides a strong red-channel signal that is convenient for multiplexing with other fluorophores when spectral crosstalk is managed in the assay design.
2. Fluorescence Microscopy Imaging
BDP TMR azide serves as a fluorescent labeling reagent for fluorescence microscopy studies where red emission is advantageous for background separation and multi-color experimental layouts. In microscopy workflows, the azide functionality supports rapid conjugate construction with alkyne-bearing targeting ligands or biomaterial surfaces, enabling visualization of labeled components in fixed-cell imaging, binding assays, and extracellular matrix or scaffold studies. Imaging teams often choose BDP TMR azide when they need a robust fluorescent tag that can be installed onto custom probes without requiring direct dye incorporation into the biological component during synthesis.
3. Flow Cytometry Dye Conjugates
BDP TMR azide is applied in flow cytometry workflows to generate red fluorescent conjugates for cell-surface and binding assays, where click-installed fluorophores provide consistent labeling across batches. Cytometry users frequently prepare alkyne-functionalized binders (such as affinity reagents or targeting ligands) and then attach BDP TMR azide to produce labeled reagents for measuring binding, uptake, or competitive interactions. The azide click handle supports flexible reagent development, allowing assay teams to rapidly prototype and compare labeling constructs while keeping the fluorescent reporter constant.
4. Polymer And Surface Functionalization
BDP TMR azide is also used to fluorescently functionalize polymers, hydrogels, and other alkyne-bearing biomaterials, enabling visualization of material distribution, coating uniformity, and transport behavior. Materials scientists and biomaterials groups employ the dye to create trackable fluorescent scaffolds for microscopy-based studies of cell-material interactions, diffusion, and surface remodeling. By installing the TMR fluorophore via click chemistry, researchers can tailor labeling density and maintain compatibility with downstream material processing steps used in lab-scale fabrication and assay development.
Computed Properties
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 9 |
| Exact Mass | 480.2256606 g/mol |
| Monoisotopic Mass | 480.2256606 g/mol |
| Topological Polar Surface Area | 60.6Ų |
| Heavy Atom Count | 35 |
| Formal Charge | 0 |
| Complexity | 983 |
| 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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