3-Ethynylperylene
Cat. # | Quantity | Price | Lead time | Buy this product |
---|---|---|---|---|
555B0 | 50 mg | $100 | in stock | |
655B0 | 100 mg | $160 | in stock |
Perylene is PAH (polycyclic aromatic hydrocarbon) containing five fused rings. Planarity of this molecule gives rise to its ruggedness, low solubility of its derivatives, as well as its outstanding fluorescence.
Perylene possesses intense green fluorescence, great photostability, and quantum yield approaching unity. This makes this PAH one of the most promising blocks for the design of new molecular probes, functional materials, and molecular devices.
This molecule contains alkyne group ready for Click Chemistry, as well as for other coupling reactions such as Sonogashira cross-coupling.
Perylene absorption and emission spectra
Recommended protocol
Calculator
Customers also purchased with this product
Alkyne phosphoramidite, 5'-terminal
Alkyne phosphoramidite for the synthesis of oligonucleotides ready for click chemistry.EDC (N-ethyl-N'-(3-dimethylaminopropyl)carbodiimide), coupling grade
Water soluble carbodiimide for the coupling of carboxylic acids with amines.Cyanine3 azide
Azide derivative of Cyanine3 fluorescent dye for сlick сhemistry.General properties
Appearance: | orange solid |
Molecular weight: | 276.33 |
CAS number: | 132196-66-8 |
Molecular formula: | C22H12 |
IUPAC name: | 3-Ethynylperylene |
Solubility: | good in chlorinated organic solvents (DCM, chloroform), moderate in DMF, low in alcohols |
Quality control: | NMR 1H (95%) and 13C, TLC |
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: | 435; 408; 252 |
ε, L⋅mol−1⋅cm−1: | 36000 |
Emission maximum, nm: | 439; 467 |
Fluorescence quantum yield: | 1.0 |
Product citations
- Beri, D.; Jakoby, M.; Howard, I.A.; Busko, D.; Richards, B.S.; Turshatov, A. Improved photon absorption in dye-functionalized silicon nanocrystals synthesized via microwave-assisted hydrosilylation. Dalton Transactions, 2020, 49(7), 2290–2299. doi: 10.1039/c9dt04497c
- Beri, D.; Jakoby, M.; Busko, D.; Richards, B.S.; Turshatov, A. Enhancing Singlet Oxygen Generation in Conjugates of Silicon Nanocrystals and Organic Photosensitizers. Frontiers in Chemistry, 2020, 8, 567. doi: 10.3389/fchem.2020.00567