Pyrene azide 2
| Cat. # | Quantity | Price | Lead time | Buy this product |
|---|---|---|---|---|
| A2530 | 1 mg | $110.00 | in stock | |
| B2530 | 5 mg | $210.00 | in stock | |
| C2530 | 10 mg | $310.00 | in stock | |
| D2530 | 25 mg |
$410.00
|
in stock | |
| E2530 | 50 mg |
$695.00
|
in stock |
This pyrene azide is a derivative of pyreneacetic acid. Contains triethylene glycol 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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Sulfo-Cyanine5.5 NHS ester
Water soluble, sulfonated, far-red sulfo-Cyanine5.5 dye in the form of NHS ester.Coumarin 343 X azide
Coumarin 343 is a blue emitting fluorophore that can serve as a FRET donor for fluorescein (FAM). This azide derivative can be conjugated with alkynes by сlick chemistry. An extended linker arm between the fluorophore and the azide group enhances solubility and provides spatial separation between the dye and the biomolecule.Biotin alkyne
Biotin alkyne is a reactive affinity label which can be attached to biomolecules via click reaction.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
- 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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