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Chemodex
Coumarin 343
150
CHF
CHF 150.00
In stock
CDX-C0073-M500500 mgCHF 150.00
| Product Details | |
|---|---|
| Synonyms | C343; Coumarin 519; 2,3,6,7-Tetrahydro-11-oxo-1H,5H,11H-[1]benzopyrano[6,7,8-ij]quinolizine-10-carboxylic Acid |
| Product Type | Chemical |
| Properties | |
| Formula |
C16H15NO4 |
| MW | 285.29 |
| CAS | 55804-65-4 |
| Purity Chemicals | ≥98% (HPLC) |
| Appearance | Yellow to orange powder. |
| Solubility | Soluble in DMSO or ethanol. Slightly soluble in water. |
| Identity | Determined by 1H-NMR. |
| Declaration | Manufactured by Chemodex. |
| Other Product Data |
Click here for Original Manufacturer Product Datasheet |
| InChi Key | KCDCNGXPPGQERR-UHFFFAOYSA-N |
| Smiles | O=C1OC2=C3C4=C(CCCN4CCC3)C=C2C=C1C(O)=O |
| Shipping and Handling | |
| Shipping | AMBIENT |
| Short Term Storage | +20°C |
| Long Term Storage | +4°C |
| Handling Advice | Protect from light and moisture. |
| Use/Stability | Stable for at least 2 years after receipt when stored at +4°C. |
| Documents | |
| MSDS | Inquire |
| Product Specification Sheet | |
| Datasheet |
 Download PDF |
Description
Coumarin 343, also known as coumarin 519, is a laser dye that exists in neutral or anionic form, depending on the pH of the medium. This compund is not cell-permeable. Coumarin 343 has been used in many different applications that include solution dynamic probes, laser dyes and organic sensitizers in dye-sensitized solar cells. It is a good organic-dye photosensitizer for injecting electrons efficiently into the conduction band of semiconductors, such as TiO2, ZrO2, and ZnO. Coumarin 343 has been used in MALDI and FRET applications. Spectral data: λmax 443nm (EtOH), λex 490nm, λlaser 512-520nm (range).
Product References
(1) K.H. Drexhage, et al.; Optics Commun. 15, 399 (1975) | (2) T. Honda, et al.; Acta Cryt. C52, 679 (1996) | (3) R.J. Cave & E.W. Castner; J. Phys. Chem. A 106, 12117 (2002) | (4) K. Hara, et al.; J. Phys. Chem. B 107, 597 (2003) | (5) M. Arduini, et al.; Chem. Commun. 2003, 1606 (2003) | (6) I. Kondov, et al.; J. Phys. Chem. A 110, 1364 (2006) | (7) X. Zhang, et al.; J. Photochem. Photobiol. A: Chem. 194, 167 (2008) | (8) S.W. Hong & W.H. Jo; Polymer 49, 4180 (2008) | (9) X.K. Hu, et al.; Int. J. Mass Spectr. 278, 69 (2008) | (10) D. Stockwell, et al.; J. Phys. Chem. C 114, 6560 (2010) | (11) V.A. Lapina, et al.; J. Phys. Org. Chem. 30, e3731 (2017) | (12) M. Taniguchi & J.S. Lindsey; Photochem. Photobiol. 94, 290 (2018)