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Chemodex
1-[4-(Dimethylamino)phenyl]-6-phenyl hexatriene
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| Product Details | |
|---|---|
| Synonyms | DMA-DPH; 4′-(Dimethylamino)diphenylhexatriene |
| Product Type | Chemical |
| Properties | |
| Formula | C20H21N |
| MW | 275.39 |
| CAS | 79849-61-9 |
| Source/Host Chemicals | Synthetic |
| Purity Chemicals | ≥80% (HPLC) |
| Appearance | Yellow powder. |
| Solubility | Soluble in methanol (1 mg/ml). |
| Identity | Determined by 1H-NMR. |
| Declaration | Manufactured by Chemodex. |
| Other Product Data |
Click here for Original Manufacturer Product Datasheet |
| InChi Key | QNBRWGUCMQGGDA-YPXUENLVSA-N |
| Smiles | CN(C)C1=CC=C(/C=C/C=C/C=C/C2=CC=CC=C2)C=C1 |
| Shipping and Handling | |
| Shipping | AMBIENT |
| Short Term Storage | +4°C |
| Long Term Storage | -20°C |
| Handling Advice | Protect from light and moisture. |
| Use/Stability | Stable for at least 2 years after receipt when stored at -20°C. |
| Documents | |
| Product Specification Sheet | |
| Datasheet |
 Download PDF |
Description
1-[4-(dimethylamino)phenyl]-6-phenylhexa-1,3,5-triene (DMA-DPH) is a green-emitting dye that is part of a class of molecules known as "push-pull" chromophores. It can be used as a photoemitter in organic light-emitting diodes (OLEDs) for screen displays and solid-state lighting applications. When dispersed in a polymer matrix, a mixture of neutral DMA-DPH (green emitter) and another chromophore can produce red, green, and blue light. The neutral form of DMA-DPH emits green light, while its protonated form, DMA-DPH_p, emits a high-intensity blue light, which is a key mechanism for producing blue color on demand. This makes DMA-DPH a versatile material for tuning emitted colors in OLEDs. DPH is used as a fluorescent probe to study cell membranes and lipid bilayers.
Product References
(1) F.W. Wang, et al.; Polymer 27, 1529 (1986) | (2) T. Suzuki & M. Kawakita; J. Biochem. 117, 881 (1995) | (3) M. Vasilopoulou, et al.; J. Phys. Conf. Ser. 10, 285 (2005) | (4) M. Vasilopoulou, et al.; Adv. Func. Mat. 17, 3477 (2007) | (5) I.S.K. Ioannis, et al.; Phys. Chem. Chem. Phys. 13, 21273 (2011) | (6) S. Michlewska, et al.; Future Med. Chem. 11, 1741 (2019) | (7) A. Verykios, et al.; J. Phys. D: Appl. Phys. 55, 215106 (2022)