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
sulfo-Cyanine5 NHS ester
Water-soluble sulfo-Cyanine5 succinimidyl ester for labeling various amine-containing molecules in the aqueous phase.sulfo-Cyanine5 carboxylic acid
Water-soluble Cyanine5 carboxylic acid, non-activated fluorescent dye.Perylene azide
Perylene is an extremely bright and photostable fluorescent label with green fluorescence.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
This Product is offered and sold for research purposes only. It has not been tested for safety and efficacy in food, drug, medical device, cosmetic, commercial or any other use. Supply does not express or imply authorization to use for any other purpose, including, without limitation, in vitro diagnostic purposes, in the manufacture of food or pharmaceutical products, in medical devices or in cosmetic products.
The count of items is incorrect.
Your cart is empty
$ 
