1-Ethynyl pyrene
Cat. # | Quantity | Price | Lead time | Buy this product |
---|---|---|---|---|
515B0 | 50 mg | $50 | in stock | |
615B0 | 100 mg | $64 | in stock |
Pyrene is one of the simplest polyaromatic hydrocarbons (PAHs). Pyrene derivatives are known for their ability to intercalate dsDNA.
Pyrene possesses intrinsic fluorescence. When two pyrene residues are located in close proximity, excimer formation can be observed by fluorescence spectroscopy. Pyrene has been therefore used to probe structures of biomolecules.
Ethynylpyrene molecule contains terminal triple bond fragment for click chemistry, as well as other coupling reactions such as Sonogashira coupling.
Absorption and emission spectra of pyrene fluorophore
Recommended protocol
Calculator
Customers also purchased with this product
Cyanine7 NHS ester
Amine reactive NHS ester of near infrared fluorescent dye, an improved analog of Cy7®.
Add this product to your cart and
get free express delivery
get free express delivery
BDP 630/650 alkyne
Alkyne dye for copper-catalyzed click chemistry, containing borondipyrromethene fluorophore BDP 630/650 for the red channel.TAMRA alkyne, 6-isomer
Terminal alkyne for copper-catalyzed click chemistry. Tetramethylrhodamine (TAMRA) is a rhodamine dye which is popular in qPCR and other applications. TAMRA is a also a FRET acceptor for FAM.General properties
Appearance: | light yellow solid |
Molecular weight: | 226.27 |
CAS number: | 34993-56-1 |
Molecular formula: | C18H10 |
Solubility: | good in chloroform, dichloromethane, toluene, low in water |
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: | 343; 326; 313; 276; 265; 242; 234 |
Emission maximum, nm: | 377; 397 |
Product citations
- Vega, B.; Wondraczek, H.; Bretschneider, L.; Näreoja, T.; Fardim, P.; Heinze, T. Preparation of reactive fibre interfaces using multifunctional cellulose derivatives. Carbohydrate Polymers, 2015, 132, 261–273. doi: 10.1016/j.carbpol.2015.05.048
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.
Your item has been added.
View your
cart
or
proceed to checkout
The count of items is incorrect.