Pyrene azide 2
| Cat. # | Quantity | Price | Lead time | Buy this product |
|---|---|---|---|---|
| A2530 | 1 mg | $110 | in stock | |
| B2530 | 5 mg | $210 | in stock | |
| C2530 | 10 mg | $310 | in stock | |
| D2530 | 25 mg |
$410
|
in stock | |
| E2530 | 50 mg |
$695
|
in stock |
This pyrene azide is a derivative of pyreneacetic acid with triethyleneglycol (PEG3) linker.
An alternative pyrene azide with a shorter linker is also available. A detailed description of the fluorophore can be found there.
Absorption and emission spectra of pyrene fluorophore
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BDP 630/650 is a far red emitting fluorophore for Cyanine5 channel. This fluorophore is based on BDP (borondipyrromethene) core, which provides high quantum yield and photostability. This is an amine derivative of this dye.
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BDP 650/665 azide
BDP 650/665 is a red-emitting borondipyrromethene dye. This azide derivative can be conjugated with alkynes and cycloalkynes.General properties
| Appearance: | yellowish solid |
| Molecular weight: | 416.47 |
| CAS number: | 1807512-45-3 |
| Molecular formula: | C24H24N4O3 |
| Solubility: | good solubility in chloroform, dichloromethane, moderate solubility in DMSO, DMF, acetonitrile |
| Quality control: | NMR 1H (95%) |
| Storage conditions: | 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. |
| MSDS: | Download |
| Product specifications |
Spectral properties
| Excitation/absorption maximum, nm: | 343; 326; 313; 276; 265; 242; 234 |
| Emission maximum, nm: | 377; 397 |
Product citations
- Bednarczyk, M.; Peters, J.K.; Kasprzyk, R.; Starek, J.; Warminski, M.; Spiewla, T.; Mugridge, J.S.; Gross, J.D.; Jemielity, J.; Kowalska, J. Fluorescence-Based Activity Screening Assay Reveals Small Molecule Inhibitors of Vaccinia Virus mRNA Decapping Enzyme D9. ACS Chemical Biology, 2022, 17(6), 1460-1471. doi: 10.1021/acschembio.2c00049
- Wanat, P.; Walczak, S.; Wojtczak, B.A.; Nowakowska, M.; Jemielity, J.; Kowalska, J. Ethynyl, 2-Propynyl, and 3-Butynyl C-Phosphonate Analogues of Nucleoside Di- and Triphosphates: Synthesis and Reactivity in CuAAC. Organic Letters, 2015, 17(12), 3062–3065. doi: 10.1021/acs.orglett.5b01346
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